Author Index to Volume 36

Brain & Development 36 (2014) VIII–XIX www.elsevier.com/locate/braindev

Author Index to Volume 36 Abdel Razek, A., Mazroa, J., and Baz, H. Assessment of white matter integrity of autistic preschool children with diffusion weighted MR imaging 28 Abe, Y., see Wakusawa, K. 61 Afroze, B., Amjad, N., Ibrahim, S.H., Humayun, K.N., and Yakob, Y. Adrenal insufficiency in a child with MELAS syndrome 924 Aida, N., see Kato, H. 630 Aihara, M., see Tando, T. 844 Airoldi, G., see Vantaggiato, C. 682 Akaboshi, S., see Shimojima, K. 315 Akalın, H., see Torun, Y.A. 864 Akella, R.R.D., Aoyama, Y., Mori, C., Lingappa, L., Cariappa, R., and Fukao, T. Metabolic encephalopathy in beta-ketothiolase deficiency: The first report from India 537 Akiyama, M., Kobayashi, K., Inoue, T., Akiyama, T., and Yoshinaga, H. Five pediatric cases of ictal fear with variable outcomes 758 Akiyama, T., Kobayashi, K., Higashikage, A., Sato, J., and Yoshinaga, H. CSF/plasma ratios of amino acids: Reference data and transports in children 3 Akiyama, T., see Akiyama, M. 758 Akiyoshi, K., see Yamada, H. 254 Akutagawa, O., see Ishii, H. 380 Alehan, F., see Saygi, S. 137 Amano, M., see Nomura, K. 778 Amjad, N., see Afroze, B. 924 Ancora, G., see Capretti, M.G. 203 Andrade, C.S., Otaduy, M.C.G., Valente, K.D.R., Park, E.J., Kanas, A.F., da Silva Filho, M.R.M., Tsunemi, M.H., and Leite, C.C. Widespread pH abnormalities in patients with malformations of cortical development and epilepsy: A phosphorus-31 brain MR spectroscopy study 899 Antoniazzi, L., see Bonanni, P. 826 Anzai, R., see Kato, H. 630 Aoki, Y., see Wakusawa, K. 61 Aoki, Y., see Saito, Y. 878 Aoyagi, K., see Tando, T. 844 Aoyama, Y., see Akella, R.R.D. 537 Arantes, P.R., see Borlot, F. 585 Arhan, E.P., see Deg˘erliyurt, A. 690 Arıca, B., see Bektas, O. 130 Arima, M., see Itoh, M. 89 Arima, M., see Itoh, M. 388 Arndt, K., see Tan, C.A. 351 Arpin, D.J., see Kurz, M.J. 870 Arrigoni, F., see Vantaggiato, C. 682 Arvinda, H.R., see Sonam, K. 807 Asano, M., see Ishitobi, M. 823 Atac, F.B., see Saygi, S. 137 Auladell, M., see Boronat, S. 801 Azumakawa, K., see Fukui, M. 80 doi:10.1016/S0387-7604(14)00233-2

Azzolini, S., Nosadini, M., Balzarin, M., Sartori, S., Suppiej, A., Mardari, R., Greggio, N.A., and Toldo, I. Delayed myelination is not a constant feature of Allan–Herndon–Dudley syndrome: Report of a new case and review of the literature 716

Baba, H., see Toda, K. 641 Balasubramaniam, S., see Chen, B.C. 593 Balestri, P., see Grosso, S. 932 Balzarin, M., see Azzolini, S. 716 Bao, X., see Xu, X. 676 Barkovich, A.J., see Takanashi, J. 259 Bassi, M.T., see Vantaggiato, C. 682 Baz, H., see Abdel Razek, A. 28 Bektas, O., Arıca, B., Teber, S., Yılmaz, A., Zeybek, H., Kaymak, S., and Deda, G. Chloral hydrate and/or hydroxyzine for sedation in pediatric EEG recording 130 Benrhouma, H., see Rebai, I. 921 Bergamino, L., see Renna, S. 70 Bernhard, M.K., see Mettin, R.R. 306 Bertola, D.R., see Borlot, F. 585 Bertossi, C., Cassina, M., De Palma, L., Vecchi, M., Rossato, S., Toldo, I., Dona`, M., Murgia, A., Boniver, C., and Sartori, S. 14q12 duplication including FOXG1: Is there a common age-dependent epileptic phenotype? 402 Bertrando, S., see Grosso, S. 932 Bharath, M.M. S., see Sonam, K. 807 Bianchi, S., see Pavlidis, E. 837 Bindu, P.S., see Sonam, K. 807 Bladowska, J., ak, T., Zimny, A., Zacharzewska-Gondek, A., Gondek, T.M., Szewczyk, P., Noga, L., Noczyn´ska, A., and Sa˛siadek, M.J. Assessment of metabolic changes within normal appearing gray and white matter in children with growth hormone deficiency: Magnetic resonance spectroscopy and hormonal correlation 770 Blagosklonov, O., see Magnin, E. 711 Boltshauser, E., see Poretti, A. 88 Bonanni, P., Volzone, A., Randazzo, G., Antoniazzi, L., Rampazzo, A., Scarpa, M., and Nobili, L. Nocturnal frontal lobe epilepsy in mucopolysaccharidosis 826 Bonini, F., Egeo, G., Fattouch, J., Fanella, M., Morano, A., Giallonardo, A.T., and di Bonaventura, C. Natural evolution from idiopathic photosensitive occipital lobe epilepsy to idiopathic generalized epilepsy in an untreated young patient 346 Boniver, C., see Bertossi, C. 402 Borgatti, R., see Vantaggiato, C. 682 Borgohain, R., see Cherian, A. 892 Borkowska, A.R., Francuz, P., Soluch, P., and Wolak, T. Brain activation in teenagers with isolated spelling disorder during tasks involving spelling assessment and comparison of pseudowords. fMRI study 786

Author Index to Volume 36 Borlot, F., Arantes, P.R., Quaio, C.R., da Silva Franco, J.F., Lourenc¸o, C.M., Bertola, D.R., and Kim, C.A. New insights in mucopolysaccharidosis type VI: Neurological perspective 585 Boronat, S., Caruso, P., Auladell, M., Van Eeghen, A., and Thiele, E.A. Arachnoid cysts in tuberous sclerosis complex 801 Boulahdour, H., see Magnin, E. 711 Bresolin, N., see Vantaggiato, C. 682 Brown, W. T., see Mazur-Kolecka, B. 322 Burroughs, S.A., see Nair, S. 505 Cantalupo, G., see Pavlidis, E. 837 Cantalupo, G., Spagnoli, C., Cerasti, D., Piccolo, B., Crisi, G., and Pisani, F. Tapia’s syndrome secondary to laterocervical localization of diffuse large cell lymphoma 548 Cantoni, O., see Vantaggiato, C. 682 Capretti, M.G., Lanari, M., Tani, G., Ancora, G., Sciutti, R., Marsico, C., Lazzarotto, T., Gabrielli, L., Guerra, B., Corvaglia, L., and Faldella, G. Role of cerebral ultrasound and magnetic resonance imaging in newborns with congenital cytomegalovirus infection 203 Cariappa, R., see Akella, R.R.D. 537 Caruso, P., see Boronat, S. 801 Cassina, M., see Bertossi, C. 402 Castelli, M., see Vantaggiato, C. 682 Catone, G., see Coppola, G. 541 Cavanna, A.E., see Crossley, E. 45 Ceballos-Picot, I., see Rebai, I. 921 Cerasti, D., see Cantalupo, G. 548 Chae, J.-H., see Kim, J.S. 510 Chae, J.-H., see Kim, S.H. 734 Chan, D., see Shiraishi, H. 21 Chang, Y.-C., see Hsu, M.-H. 248 Chaturvedi, S.K., see Dhiman, V. 287 Chehade, H., see Fluss, J. 84 Chen, B.C., Balasubramaniam, S., McGownc, I.N., O’Neill, J.P., Chng, G.S., Keng, W.T., Ngu, L.H., and Duley, J.A. Treatment of Lesch–Nyhan disease with S-adenosylmethionine: Experience with five young Malaysians, including a girl 593 Chen, H., see Li, X. 653 Chen, J., see Dai, Y. 228 Cheng, L., Wang, S.-H., Jia, N., Xie, M., and Liao, X.-M. Environmental stimulation influence the cognition of developing mice by inducing changes in oxidative and apoptosis status 51 Cheng, L., see Li, X. 653 Cheng, Q., see Dai, Y. 228 Cheon, J.-E., see Kim, S.H. 734 Cherian, A., Jabeen, S.A., Kandadai, R.M., Iype, T., Moturi, P., Reddy, M., Kanikannan, M.A., Borgohain, R., and Padmanabhan, S. Epilepsy with myoclonic absences in siblings 892 Chiu, C.-H., see Hung, P.-C. 634 Chng, G.S., see Chen, B.C. 593 Cho, S.-R., see Lee, H.S. 764 Choi, J., see Kim, J.S. 510 Choi, Y.-S., see Lee, H.S. 764 Citterio, A., see Vantaggiato, C. 682 Cohen, I.L., see Mazur-Kolecka, B. 322 Coppola, G., D’Amico, A., Pironti, E., Martino, F., Santoro, E., Di Paolo, N., Isone, C., and Catone, G. Brainstem arteriovenous malformation presenting with dyspraxic handwriting in a young girl 541 Cornacchione, S., see Grosso, S. 932 Corvaglia, L., see Capretti, M.G. 203 Crisi, G., see Cantalupo, G. 548 Cristina, E., see Renna, S. 70 Crossley, E., Seri, S., Stern, J.S., Robertson, M.M., and Cavanna, A.E. Premonitory urges for tics in adult patients with Tourette syndrome 45 Curatolo, P., see Lo-Castro, A. 185

IX

da Silva Filho, M.R.M., see Andrade, C.S. 899 da Silva Franco, J.F., see Borlot, F. 585 Dai, Y., Li, W., Zhong, M., Chen, J., Liu, Y., Cheng, Q., and Li, T. Preconditioning and post-treatment with cobalt chloride in rat model of perinatal hypoxic–ischemic encephalopathy 228 Das, S., see Tan, C.A. 351 de Coulon, G., see Fluss, J. 84 De Palma, L., see Bertossi, C. 402 Deda, G., see Bektas, O. 130 Deg˘erliyurt, A., Teber, S., Karakaya, G., Gu¨ven, A., *eker, E.D., Arhan, E.P., and * ayli, T.R. Pseudotumor cerebri/idiopathic intracranial hypertension in children: An experience of a tertiary care hospital 690 Dhiman, V., Sinha, S., Rawat, V.S., Vijaysagar, K.J., Thippeswamy, H., Srinath, S., Chaturvedi, S.K., and Satishchandra, P. Children with psychogenic non-epileptic seizures (PNES): A detailed semiologic analysis and modified new classification 287 di Bonaventura, C., see Bonini, F. 346 Di Paolo, N., see Coppola, G. 541 Di Pietro, P., see Renna, S. 70 Dias, A.I., see Rocha, S. 176 Ding, Y., see Ma, Y.-Y. 394 Ding, Y., see Wang, Q. 813 Doi, K., see Inokuchi, R. 626 Dona`, M., see Bertossi, C. 402 Doneda, C., see Vantaggiato, C. 682 D’Amico, A., see Coppola, G. 541 Duley, J.A., see Chen, B.C. 593 Egami, C., see Ohya, T. 241 Egeo, G., see Bonini, F. 346 Ekici, A., see Kocak, O. 167 Elix, H., see Mettin, R.R. 306 Emi, S., see Hasegawa, S. 608 Emoto, Y., see Yamamoto, T. 479 Endo, W., see Wakusawa, K. 61 Endo, W., see Nakayama, T. 532 Endo, W., see Sato, H. 268 Endo, Y., Saito, Y., Otsuki, T., Takahashi, A., Nakata, Y., Okada, K., Hirozane, M., Kaido, T., Kaneko, Y., Takada, E., Okazaki, T., Enokizono, T., Saito, T., Komaki, H., Nakagawa, E., Sugai, K., and Sasaki, M. Persistent verbal and behavioral deficits after resection of the left supplementary motor area in epilepsy surgery 74 Enoki, H., see Nakamura, K. 272 Enokizono, T., see Endo, Y. 74 Eom, S., see Lee, Y.-J. 496 Erdem, R., see Saygi, S. 137 Erol, I., see Saygi, S. 137 Evangeliou, A., see Gkampeta, A. 411 Faivre, L., see Magnin, E. 711 Faldella, G., see Capretti, M.G. 203 Falsaperla, R., see Pavone, P. 739 Fanella, M., see Bonini, F. 346 Fattouch, J., see Bonini, F. 346 Ferna´ndez-Jae´n, A., see Ferna´ndez-Mayoralas, D.M. 413 Ferna´ndez-Mayoralas, D.M., Ferna´ndez-Jae´n, A., and Ferna´ndezPerrone, A.L. Expanding spectrum of electroclinical findings in patients with karyotype 47,XYY 413 Ferna´ndez-Perrone, A.L., see Ferna´ndez-Mayoralas, D.M. 413 Ferreira, A.C., see Rocha, S. 176 Flores-Sarnat, L., see Sarnat, H.B. 463 Flory, M., see Mazur-Kolecka, B. 322

X

Author Index to Volume 36

Fluss, J., Kern, I., de Coulon, G., Gonzalez, E., and Chehade, H. Vitamin D deficiency: A forgotten treatable cause of motor delay and proximal myopathy 84 Fontana, A., see Mangano, S. 408 Frackowiak, J., see Mazur-Kolecka, B. 322 Franceschini, R., see Grosso, S. 932 Francuz, P., see Borkowska, A.R. 786 Frattini, D., see Fusco, C. 183 Fry, N.R., see Noble, J.J. 294 Fujii, T., see Hayashi, A. 830 Fujii, Y., Ishikawa, N., Kobayashi, Y., Kobayashi, M., and Kato, M. Compound heterozygosity in GPR56 with bilateral frontoparietal polymicrogyria 528 Fujimori, A., Itoh, K., Goto, S., Hirakawa, H., Wang, B., Kokubo, T., Kito, S., Tsukamoto, S., and Fushiki, S. Disruption of Aspm causes microcephaly with abnormal neuronal differentiation 661 Fujimoto, K., Nagai, T., Okazaki, S., Kawajiri, M., and Tomiwa, K. Development and verification of child observation sheet for 5-yearold children 107 Fujioka, T., see Ishii, H. 380 Fujisawa, T.X., see Yatsuga, C. 620 Fujita, K., see Nishiyama, M. 928 Fujita, T., see Inoue, T. 613 Fukahori, Y., see Yamamoto, T. 479 Fukao, T., see Akella, R.R.D. 537 Fukasawa, T., Suzuki, M., Kato, T., Hayakawa, F., Miura, K., Kidokoro, H., Kubota, T., Okumura, A., Maruyama, K., Hishikawa, Y., Itomi, K., Negoro, T., Watanabe, K., and Natsume, J. Characteristics of epilepsy occurring in the first four months 752 Fukui, M., Shimakawa, S., Tanabe, T., Nomura, S., Kashiwagi, M., Azumakawa, K., and Tamai, H. Partial seizures during ACTH therapy in a cryptogenic West syndrome patient 80 Fukui, M., see Nomura, S. 399 Fukumoto, R., see Nomura, K. 778 Fukunaga, S., see Takahashi, K. 670 Funato, M., see Li, J. 472 Furione, M., see Renna, S. 70 Furukawa, T., see Shimojima, K. 315 Fusco, C., Russo, A., Invernizzi, F., Frattini, D., Pisani, F., and Garavaglia, B. Novel phenotype in a family with infantile convulsions and paroxysmal choreoathetosis syndrome and PRRT2 gene mutation 183 Fushiki, S., see Fujimori, A. 661 Gabrielli, L., see Capretti, M.G. 203 Garavaglia, B., see Fusco, C. 183 Gayathri, N., see Sonam, K. 807 Giallonardo, A.T., see Bonini, F. 346 Gkampeta, A., Pavlidou, E., Evangeliou, A., and Pavlou, E. Ketosis and EEG improvement following viral gastroenteritis in patient with West syndrome 411 Gondek, T.M., see Bladowska, J. 770 Gonzalez, E., see Fluss, J. 84 Gonzalez, M., see Mazur-Kolecka, B. 322 Goto, M., Komaki, H., Saito, T., Saito, Y., Nakagawa, E., Sugai, K., Sasaki, M., Nishino, I., and Goto, Y. MELAS phenotype associated with m.3302A>G mutation in mitochondrial tRNALeu(UUR) gene 180 Goto, S., see Fujimori, A. 661 Goto, T., see Ishitobi, M. 823 Goto, Y., see Goto, M. 180 Gough, M., see Noble, J.J. 294 Gouider-Khouja, N., see Rebai, I. 921 Govindaraju, C., see Sonam, K. 807 Greggio, N.A., see Azzolini, S. 716 Grosso, S., Cornacchione, S., Romano, D., Bertrando, S., Franceschini, R., and Balestri, P. Optic perineuritis: A further cause of visual loss and disc edema in children 932

Guerra, B., see Capretti, M.G. 203 Guidarelli, A., see Vantaggiato, C. 682 Gunshin, M., see Inokuchi, R. 626 Gu¨ven, A., see Deg˘erliyurt, A. 690 Haginoya, K., see Shiraishi, H. 21 Haginoya, K., see Wakusawa, K. 61 Haginoya, K., see Nakayama, T. 532 Hamada, A., see Yatsuga, C. 620 Hamano, H., see Takahashi, K. 670 Hara, M., Nishi, Y., Yamashita, Y., Hirata, R., Takahashi, S., Nagamitsu, S., Hosoda, H., Kangawa, K., Kojima, M., and Matsuishi, T. Relation between circulating levels of GH, IGF-1, ghrelin and somatic growth in Rett syndrome 794 Hara, T., see Torisu, H. 342 Harahap, N.I.F., see Yamamoto, T. 914 Hasegawa, S., see Oka, M. 16 Hasegawa, S., see Momonaka, H. 484 Hasegawa, S., see Takahashi, K. 670 Hasegawa, S., see Kajimoto, M. 637 Hasegawa, S., Matsushige, T., Inoue, H., Takahara, M., Kajimoto, M., Momonaka, H., Oka, M., Isumi, H., Emi, S., Hayashi, M., and Ichiyama, T. Serum and cerebrospinal fluid levels of visinin-like protein-1 in acute encephalopathy with biphasic seizures and late reduced diffusion 608 Hashimoto, S., see Kawamura, Y. 601 Hata, D., see Kumakura, A. 725 Hatagaki, C., see Nomura, K. 778 Hattori, H., see Hikita, N. 159 Hattori, T., see Seto, T. 359 Hayakawa, F., see Kato, T. 372 Hayakawa, F., see Tsuji, T. 555 Hayakawa, F., see Fukasawa, T. 752 Hayakawa, M., see Tsuji, T. 555 Hayashi, A., Kawakita, R., Kumada, T., Nozaki, F., Hiejima, I., Miyajima, T., Kusunoki, T., and Fujii, T. Pathological fracture and pyogenic osteomyelitis in a patient with type 2 Gaucher disease 830 Hayashi, K., see Kondo, H. 730 Hayashi, M., see Okoshi, Y. 707 Hayashi, M., see Hasegawa, S. 608 Hayashi, M., see Okoshi, Y. 907 Hayashi, M., see Itoh, M. 89 Hayashi, M., see Itoh, M. 388 Hidaka, Y., see Saida, K. 721 Hiejima, I., see Hayashi, A. 830 Higashikage, A., see Akiyama, T. 3 Hikita, N., Hattori, H., Kato, M., Sakuma, S., Morotomi, Y., Ishida, H., Seto, T., Tanaka, K., Shimono, T., Shintaku, H., and Tokuhara, D. A case of TUBA1A mutation presenting with lissencephaly and Hirschsprung disease 159 Hikita, N., see Seto, T. 359 Hino-Fukuyo, N., see Nakayama, T. 143 Hino-Fukuyo, N., see Nakayama, T. 532 Hino-Fukuyo, N., see Sato, H. 268 Hirabayashi, K., see Saida, K. 721 Hirakawa, H., see Fujimori, A. 661 Hiraki, K., see Yasumura, A. 97 Hirano, M., see Saida, K. 721 Hirata, R., see Hara, M. 794 Hiratani, M., see Ishitobi, M. 823 Hirose, S., see Inoue, T. 613 Hirozane, M., see Endo, Y. 74 Hirsch, W., see Mettin, R.R. 306 Hishikawa, Y., see Fukasawa, T. 752 Holmes, G.L., see Nair, S. 505 Hoshika, A., see Ishii, H. 380

Author Index to Volume 36 Hosoda, H., see Hara, M. 794 Hsia, S.-H., see Hung, P.-C. 356 Hsu, M.-H., Huang, C.-C., Hung, P.-L., Huang, H.-M., Huang, L.-T., Huang, C.-C., Sheen, J.-M., Huang, S.-C., and Chang, Y.-C. Paraneoplastic neurological disorders in children with benign ovarian tumors 248 Hu, L.-Y., see Ma, Y.-Y. 394 Huang, C.-C., see Hsu, M.-H. 248 Huang, H.-M., see Hsu, M.-H. 248 Huang, L.-T., see Hsu, M.-H. 248 Huang, S.-C., see Hsu, M.-H. 248 Humayun, K.N., see Afroze, B. 924 Hung, P.-C., Wang, H.-S., Hsia, S.-H., and Wong, A.M.-C. Plasmapheresis as adjuvant therapy in Stevens–Johnson syndrome and hepatic encephalopathy 356 Hung, P.-C., Wang, H.-S., Chiu, C.-H., and Wong, A.M.-C. Cervical spinal cord compression in a child with cervicofacial actinomycosis 634 Hung, P.-L., see Hsu, M.-H. 248 Hwang, H., see Kim, J.S. 510 Hwang, Y.S., see Kim, S.H. 734 Hwang, Y.S., see Kim, J.S. 510 Iai, M., see Kato, H. 630 Ibrahim, S.H., see Afroze, B. 924 Ichihashi, K., see Okamoto, N. 523 Ichiyama, T., see Momonaka, H. 484 Ichiyama, T., see Hasegawa, S. 608 Ichiyama, T., see Kajimoto, M. 637 Ichiyama, T., see Takahashi, K. 670 Ichiyama, T., see Oka, M. 16 Ide, S., see Itoh, M. 388 Ideguchi, H., see Inoue, T. 613 Iemura, A., see Matsuoka, M. 35 Ihara, Y., see Inoue, T. 613 Ihira, M., see Kawamura, Y. 601 Iijima, K., see Matsuo, K. 10 Ikeda, S., see Yatsuga, C. 620 Ikematsu, K., see Yamamoto, T. 479 Imai, H., see Saida, K. 721 Inaba, Y., see Saida, K. 721 Inagaki, M., see Inoue, Y. 700 Inagaki, M., see Kaga, M. 284 Inagaki, M., see Yasumura, A. 97 Inokuchi, R., Nakamura, K., Mizuno, N., Sato, H., Shinohara, K., Matsubara, T., Doi, K., Ishii, T., Gunshin, M., Nakajima, S., and Yahagi, N. Adult-onset seizures in a patient with Down syndrome and portosystemic shunt 626 Inoue, H., see Momonaka, H. 484 Inoue, H., see Oka, M. 16 Inoue, H., see Hasegawa, S. 608 Inoue, H., see Kajimoto, M. 637 Inoue, K., see Takanashi, J. 259 Inoue, N., see Matsuo, K. 10 Inoue, T., see Akiyama, M. 758 Inoue, T., Ihara, Y., Tomonoh, Y., Nakamura, N., Ninomiya, S., Fujita, T., Ideguchi, H., Yasumoto, S., Zhang, B., and Hirose, S. Early onset and focal spike discharges as indicators of poor prognosis for myoclonic-astatic epilepsy 613 Inoue, T., see Itoh, M. 388 Inoue, Y., Ito, K., Kita, Y., Inagaki, M., Kaga, M., and Swanson, J.M. Psychometric properties of Japanese version of the Swanson, Nolan, and Pelham, version-IV Scale-Teacher Form: A study of school children in community samples 700 Inui, T., see Wakusawa, K. 61 Invernizzi, F., see Fusco, C. 183

XI

Isaka, K., see Ishii, H. 380 Ishibashi, K., see Seto, T. 359 Ishida, H., see Hikita, N. 159 Ishii, H., Takami, T., Fujioka, T., Mizukaki, N., Kondo, A., Sunohara, D., Hoshika, A., Akutagawa, O., and Isaka, K. Comparison of changes in cerebral and systemic perfusion between appropriate- and small-for-gestational-age infants during the first three days after birth 380 Ishii, M., see Nonoda, Y. 194 Ishii, S., see Tando, T. 844 Ishii, T., see Inokuchi, R. 626 Ishii, Y., see Ohya, T. 241 Ishikawa, N., see Oka, M. 16 Ishikawa, N., see Fujii, Y. 528 Ishitobi, M., Kawatani, M., Asano, M., Kosaka, H., Goto, T., Hiratani, M., and Wada, Y. Quetiapine responsive catatonia in an autistic patient with comorbid bipolar disorder and idiopathic basal ganglia calcification 823 Ishiyama, A., see Saito, Y. 878 Ishiyama, A., see Saito, Y. 337 Ishizaki, Y., see Torisu, H. 342 Isobe, K., see Nakamura, S. 563 Isobe, K., see Kusaka, T. 277 Isone, C., see Coppola, G. 541 Isumi, H., see Hasegawa, S. 608 Isumi, H., see Oka, M. 16 Ito, K., Nakata, Y., Matsuda, H., Sugai, K., Watanabe, M., Kamiya, K., Kimura, Y., Shigemoto, Y., Okazaki, M., Sasaki, M., and Sato, N. Evaluation of FDG-PET and ECD-SPECT in patients with subcortical band heterotopia 578 Ito, K., see Inoue, Y. 700 Ito, S., see Itoh, M. 388 Itoh, K., see Fujimori, A. 661 Itoh, M., Iwasaki, Y., Hayashi, M., and Arima, M. Reply to the Letter: ‘‘Nationwide survey of Arima syndrome: Revised diagnostic criteria from epidemiological analysis’’ 89 Itoh, M., Iwasaki, Y., Ohno, K., Inoue, T., Hayashi, M., Ito, S., Matsuzaka, T., Ide, S., and Arima, M. Nationwide survey of Arima syndrome: Revised diagnostic criteria from epidemiological analysis 388 Itoh, S., see Kusaka, T. 277 Itoh, S., see Nakamura, S. 563 Itomi, K., see Fukasawa, T. 752 Iwaki, M., see Wakusawa, K. 61 Iwasaki, M., see Nakayama, T. 532 Iwasaki, M., see Kawai, K. 124 Iwasaki, M., see Matsuoka, M. 35 Iwasaki, T., see Nonoda, Y. 194 Iwasaki, Y., see Itoh, M. 89 Iwasaki, Y., see Itoh, M. 388 Iype, T., see Cherian, A. 892 Izumi, S., see Shiihara, T. 489 Izumi, T., see Yamada, H. 254 Jabeen, S.A., see Cherian, A. 892 Jenkin, G., see Li, J. 472 Jenkins, E.C., see Mazur-Kolecka, B. 322 Jia, N., see Cheng, L. 51 Jiang, L., see Xie, L. 153 Jiang, L., see Li, X. 653 Jiang, Y., see Xu, X. 676 Jiang, Z.D., and Wilkinson, A.R. Impaired function of the auditory brainstem in term neonates with hyperbilirubinemia 212 Jimbo, E., see Saito, M. 64 Jinnai, W., see Nakamura, S. 563 Jinnou, H., see Nakamura, K. 272 Joshi, S., see Roy, S. 219

XII

Author Index to Volume 36

Joshi, S., see Rathod, R. 853 Ju, J., see Ma, Y.-Y. 394 Kaczmarski, W., see Mazur-Kolecka, B. 322 Kaga, M., see Inoue, Y. 700 Kaga, M., see Yasumura, A. 97 Kaga, M. New Year’s Greeting from the former Editor-in-Chief of Brain & Development 1 Kaga, M., Inagaki, M., and Ohta, R. Epidemiological study of Landau–Kleffner syndrome (LKS) in Japan 284 Kaga, Y., see Tando, T. 844 Kaido, T., see Endo, Y. 74 Kajimoto, M., see Momonaka, H. 484 Kajimoto, M., Hasegawa, S., Nomura, S., Inoue, H., Matsushige, T., and Ichiyama, T. An 11-year-old girl with recurrent bacterial meningitis due to liquorrhea caused by bone malformation of the skull base 637 Kajimoto, M., see Oka, M. 16 Kajimoto, M., see Hasegawa, S. 608 Kakuma, T., see Matsuoka, M. 35 Kale, A., see Rathod, R. 853 Kale, A., see Roy, S. 219 Kamei, Y., see Li, J. 472 Kamiya, K., see Ito, K. 578 Kamiya, T., see Kouwaki, M. 572 Kanas, A.F., see Andrade, C.S. 899 Kanda, S., see Okoshi, Y. 707 Kandadai, R.M., see Cherian, A. 892 Kaneko, Y., see Endo, Y. 74 Kaneko, Y., see Shiraishi, H. 21 Kanemura, H., see Tando, T. 844 Kang, H.-C., see Lee, Y.-J. 496 Kang, H.-C., see Yoon, J.-R. 163 Kangawa, K., see Hara, M. 794 Kanikannan, M.A., see Cherian, A. 892 Karakaya, G., see Deg˘erliyurt, A. 690 Karakukcu, M., see Torun, Y.A. 864 Kasapcopur, O., see Uluduz, D. 884 Kashiwagi, M., see Fukui, M. 80 Kashiwagi, M., see Tanabe, T. 301 Kashiwagi, M., Tanabe, T., Shimakawa, S., Nakamura, M., Murata, S., Shabana, K., Shinohara, J., Odanaka, Y., Matsumura, H., Maki, K., Okumura, K., Okasora, K., and Tamai, H. Clinicoradiological spectrum of reversible splenial lesions in children 330 Kato, H., Miyake, F., Shimbo, H., Ohya, M., Sugawara, H., Aida, N., Anzai, R., Takagi, M., Okuda, M., Takano, K., Wada, T., Iai, M., Yamashita, S., and Osaka, H. Urine screening for patients with developmental disabilities detected a patient with creatine transporter deficiency due to a novel missense mutation in SLC6A8 630 Kato, M., see Fujii, Y. 528 Kato, M., see Shiihara, T. 489 Kato, M., see Hikita, N. 159 Kato, T., Tsuji, T., Hayakawa, F., Kubota, T., Kidokoro, H., Natsume, J., Watanabe, K., and Okumura, A. A new electroencephalogram classification with reduced recording time in asphyxiated term infants 372 Kato, T., see Fukasawa, T. 752 Kato, T., see Tsuji, T. 555 Kawai, K., Morino, M., and Iwasaki, M. Modification of vertical hemispherotomy for refractory epilepsy 124 Kawajiri, M., see Fujimoto, K. 107 Kawakita, R., see Hayashi, A. 830 Kawamura, Y., Ohashi, M., Ihira, M., Hashimoto, S., Taniguchi, K., and Yoshikawa, T. Nationwide survey of rotavirus-associated encephalopathy and sudden unexpected death in Japan 601 Kawano, S., see Matsuo, K. 10 Kawatani, M., see Ishitobi, M. 823

Kawatani, M., see Kometani, H. 551 Kaymak, S., see Bektas, O. 130 Keevil, S.F., see Noble, J.J. 294 Kemse, N., see Rathod, R. 853 Keng, W.T., see Chen, B.C. 593 Kern, I., see Fluss, J. 84 Khaire, A., see Rathod, R. 853 Khaire, A., see Roy, S. 219 Khan, N.A., see Sonam, K. 807 Kidokoro, H., see Tsuji, T. 555 Kidokoro, H., see Kato, T. 372 Kidokoro, H., see Fukasawa, T. 752 Kiess, W., see Mettin, R.R. 306 Kihara, M., see Kondo, H. 730 Kikuchi, A., see Nakayama, T. 532 Kikuchi, A., see Nakayama, T. 143 Kim, B.-N., see Kim, S.H. 734 Kim, C.A., see Borlot, F. 585 Kim, C.J., see Lee, B.H. 171 Kim, D.-S., see Lee, Y.-J. 496 Kim, G.-H., see Lee, B.H. 171 Kim, H., see Kim, J.S. 510 Kim, H.D., see Lee, Y.-J. 496 Kim, H.D., see Yoon, J.-R. 163 Kim, I.-O., see Kim, S.H. 734 Kim, J.H., see Lee, B.H. 171 Kim, J.S., Kim, H., Lim, B.C., Chae, J.-H., Choi, J., Kim, K.J., Hwang, Y.S., and Hwang, H. Lacosamide as an adjunctive therapy in pediatric patients with refractory focal epilepsy 510 Kim, K.J., see Kim, J.S. 510 Kim, K.J., see Kim, S.H. 734 Kim, M., see Lee, H.S. 764 Kim, S.-M., see Lee, H.S. 764 Kim, S.H., Lee, J.S., Lim, B.C., Kim, K.J., Hwang, Y.S., Park, J.D., Cheon, J.-E., Kim, I.-O., Kim, B.-N., and Chae, J.-H. A female carrier of ornithine carbamoyltransferase deficiency masquerading as attention deficit-hyperactivity disorder 734 Kim, Y.-M., see Lee, B.H. 171 Kimura, Y., see Ito, K. 578 Kita, Y., see Inoue, Y. 700 Kitani, S., see Matsuoka, M. 35 Kito, S., see Fujimori, A. 661 Kizaki, Z., see Kondo, H. 730 Kobata, K., see Li, J. 472 Kobayashi, K., see Akiyama, M. 758 Kobayashi, K., see Akiyama, T. 3 Kobayashi, M., see Fujii, Y. 528 Kobayashi, S., see Wakusawa, K. 61 Kobayashi, T., see Nakayama, T. 532 Kobayashi, T., see Sato, H. 268 Kobayashi, Y., see Fujii, Y. 528 Kobayashi, Y., see Matsuo, K. 10 Kocak, O., Yarar, C., Yakut, A., Ekici, A., Yimenicioglu, S., and Saylisoy, S. Akathisia in association with herpes simplex encephalitis relapse and opercular syndrome in children 167 Koda, T., see Matsuo, K. 10 Kodera, H., see Nakamura, K. 272 Koike, K., see Saida, K. 721 Kojima, M., see Hara, M. 794 Kojima, S., see Nomura, K. 778 Kokubo, N., see Yasumura, A. 97 Kokubo, T., see Fujimori, A. 661 Komaki, H., see Endo, Y. 74 Komaki, H., see Goto, M. 180 Komaki, H., see Saito, Y. 878 Komaki, H., see Saito, Y. 337

Author Index to Volume 36 Kometani, H., Kawatani, M., Ohta, G., Okazaki, S., Ogura, K., Yasutomi, M., Tanizawa, A., and Ohshima, Y. Marked elevation of interleukin-6 in mild encephalopathy with a reversible splenial lesion (MERS) associated with acute focal bacterial nephritis caused by Enterococcus faecalis 551 Komoike, Y., see Shimojima, K. 315 Komur, M., Unal, S., Okuyaz, C., and Ozgur, A. Moyamoya syndrome associated with sickle cell trait in a child 545 Kondo, A., see Ishii, H. 380 Kondo, H., Tanda, K., Tabata, C., Hayashi, K., Kihara, M., Kizaki, Z., Taniguchi-Ikeda, M., Mori, M., Murayama, K., and Ohtake, A. Leigh syndrome with Fukuyama congenital muscular dystrophy: A case report 730 Kosaka, H., see Ishitobi, M. 823 Kouwaki, M., Yokochi, M., Kamiya, T., and Yokochi, K. Spontaneous movements in the supine position of preterm infants with intellectual disability 572 Koyano, K., see Nakamura, S. 563 Koyano, K., see Kusaka, T. 277 Kraoua, I., see Rebai, I. 921 Kubo, Y., see Yamamoto, T. 914 Kubota, M., see Shiihara, T. 489 Kubota, T., see Kato, T. 372 Kubota, T., see Tsuji, T. 555 Kubota, T., see Fukasawa, T. 752 Kumada, T., see Hayashi, A. 830 Kumakura, A., Takahashi, S., Okajima, K., and Hata, D. A haploinsufficiency of FOXG1 identified in a boy with congenital variant of Rett syndrome 725 Kurashige, T., see Yamamoto, T. 914 Kure, S., see Sato, H. 268 Kure, S., see Nakayama, T. 532 Kure, S., see Nakayama, T. 143 Kuriu, Y., see Yamamoto, T. 479 Kurokawa, T., see Saida, K. 721 Kurokawa, T. In the memory of Professor Cesare T. Lombroso with great gratitude 275 Kurz, M.J., Wilson, T.W., and Arpin, D.J. An fNIRS exploratory investigation of the cortical activity during gait in children with spastic diplegic cerebral palsy 870 Kusaka, T., Isobe, K., Yasuda, S., Koyano, K., Nakamura, S., Nakamura, M., Ueno, M., Miki, T., and Itoh, S. Evaluation of cerebral circulation and oxygen metabolism in infants using nearinfrared light 277 Kusaka, T., see Nakamura, S. 563 Kusunoki, T., see Hayashi, A. 830 Lai, P.S., see Yamamoto, T. 914 Lanari, M., see Capretti, M.G. 203 Lazzarotto, T., see Capretti, M.G. 203 Lee, B.H., Kim, Y.-M., Kim, J.H., Kim, G.-H., Lee, B.S., Kim, C.J., Yoo, H.J., and Yoo, H.-W. Histological, biochemical, and genetic characterization of early-onset fulminating sialidosis type 2 in a Korean neonate with hydrops fetalis 171 Lee, B.S., see Lee, B.H. 171 Lee, E.J., see Yoon, J.-R. 163 Lee, H.S., Song, J., Min, K., Choi, Y.-S., Kim, S.-M., Cho, S.-R., and Kim, M. Short-term effects of erythropoietin on neurodevelopment in infants with cerebral palsy: A pilot study 764 Lee, J.H., see Yoon, J.-R. 163 Lee, J.S., see Lee, Y.-J. 496 Lee, J.S., see Kim, S.H. 734 Lee, Y.-J., Lee, J.S., Kang, H.-C., Kim, D.-S., Shim, K.-W., Eom, S., and Kim, H.D. Outcomes of epilepsy surgery in childhood-onset epileptic encephalopathy 496 Leite, C.C., see Andrade, C.S. 899 Lewis, A.P., see Noble, J.J. 294

XIII

Li, J., Kobata, K., Kamei, Y., Okazaki, Y., Nishihara, M., Wada, H., Tamai, H., Funato, M., and Jenkin, G. Nucleated red blood cell counts: An early predictor of brain injury and 2-year outcome in neonates with hypoxic–ischemic encephalopathy in the era of cooling-based treatment 472 Li, T., see Dai, Y. 228 Li, W., see Dai, Y. 228 Li, X., see Wang, Q. 813 Li, X., Jiang, L., Cheng, L., and Chen, H. Dibutyl phthalate-induced neurotoxicity in the brain of immature and mature rat offspring 653 Li, X.-Y., see Ma, Y.-Y. 394 Li, X.-Y., see Wu, T.-F. 264 Liao, X.-M., see Cheng, L. 51 Lim, B.C., see Kim, S.H. 734 Lim, B.C., see Kim, J.S. 510 Lin, Q., see Xu, X. 676 Lingappa, L., see Akella, R.R.D. 537 Liu, X., see Xu, X. 676 Liu, Y., see Dai, Y. 228 Liu, Y., see Wang, Q. 813 Liu, Y.-P., see Ma, Y.-Y. 394 Liu, Y.-P., see Wu, T.-F. 264 Lo-Castro, A., and Curatolo, P. Epilepsy associated with autism and attention deficit hyperactivity disorder: Is there a genetic link? 185 Lossin, C. Corrigendum to ‘‘A catalog of SCN1A variants’’ [Brain Dev. 2009 Feb;31(2):114–30] 90 Lourenc¸o, C.M., see Borlot, F. 585 Ma, Y.-Y., Wu, T.-F., Liu, Y.-P., Wang, Q., Li, X.-Y., Ding, Y., Song, J.-Q., Shi, X.-Y., Zhang, W.-N., Zhao, M., Hu, L.-Y., Ju, J., Wang, Z.-L., Yang, Y.-L., and Zou, L.-P. Two compound frameshift mutations in succinate dehydrogenase gene of a Chinese boy with encephalopathy 394 Maeba, S., see Takahashi, K. 670 Maeda, M., see Matsuoka, M. 35 Magnin, E., Blagosklonov, O., Sylvestre, G., Minot, D., Thevenon, J., Faivre, L., Boulahdour, H., Thauvin-Robinet, C., and Rumbach, L. Neuropsychological and neuroimaging phenotype induced by a CAMTA1 mutation 711 Maki, K., see Kashiwagi, M. 330 Malk, K., Metsa¨ranta, M., and Vanhatalo, S. Drug effects on endogenous brain activity in preterm babies 116 Mangano, G.R., see Mangano, S. 408 Mangano, S., Fontana, A., Spitaleri, C., and Mangano, G.R. Benign nocturnal alternating hemiplegia of childhood: A new case with unusual findings 408 Marazzi, M.G., see Renna, S. 70 Mardari, R., see Azzolini, S. 716 Marsico, C., see Capretti, M.G. 203 Martino, F., see Coppola, G. 541 Maruyama, A., see Nishiyama, M. 928 Maruyama, K., see Tsuji, T. 555 Maruyama, K., see Fukasawa, T. 752 Mascaretti, M., see Renna, S. 70 Matoba, R., see Yamamoto, T. 479 Matsubara, T., see Inokuchi, R. 626 Matsuda, H., see Ito, K. 578 Matsuda, Y., see Saito, Y. 337 Matsuishi, T., see Matsuoka, M. 35 Matsuishi, T., see Hara, M. 794 Matsuishi, T., see Ohya, T. 241 Matsumoto, A., see Saito, M. 64 Matsumoto, N., see Takanashi, J. 259 Matsumoto, N., see Nakamura, K. 272 Matsumoto, N., see Okamoto, N. 523 Matsumoto, N., see Nakayama, T. 532 Matsumura, H., see Kashiwagi, M. 330

XIV

Author Index to Volume 36

Matsuo, K., Morioka, I., Oda, M., Kobayashi, Y., Nakamachi, Y., Kawano, S., Nagasaka, M., Koda, T., Yokota, T., Morikawa, S., Miwa, A., Shibata, A., Minematsu, T., Inoue, N., Yamada, H., and Iijima, K. Quantitative evaluation of ventricular dilatation using computed tomography in infants with congenital cytomegalovirus infection 10 Matsuo, M., see Yamamoto, T. 914 Matsuo, M., Ohno, K., and Ohtsuka, F. Characterization of early onset neurofibromatosis type 2 148 Matsuoka, M., Nagamitsu, S., Iwasaki, M., Iemura, A., Yamashita, Y., Maeda, M., Kitani, S., Kakuma, T., Uchimura, N., and Matsuishi, T. High incidence of sleep problems in children with developmental disorders: Results of a questionnaire survey in a Japanese elementary school 35 Matsushige, T., see Oka, M. 16 Matsushige, T., see Kajimoto, M. 637 Matsushige, T., see Hasegawa, S. 608 Matsushige, T., see Momonaka, H. 484 Matsushita, N., see Seto, T. 359 Matsuura, N., see Yatsuga, C. 620 Matsuzaka, T., see Itoh, M. 388 Mazroa, J., see Abdel Razek, A. 28 Mazur-Kolecka, B., Cohen, I.L., Gonzalez, M., Jenkins, E.C., Kaczmarski, W., Brown, W. T., Flory, M., and Frackowiak, J. Autoantibodies against neuronal progenitors in sera from children with autism 322 McGownc, I.N., see Chen, B.C. 593 Merkenschlager, A., see Mettin, R.R. 306 Metsa¨ranta, M., see Malk, K. 116 Mettin, R.R., Merkenschlager, A., Bernhard, M.K., Elix, H., Hirsch, W., Kiess, W., and Syrbe, S. Wide spectrum of clinical manifestations in children with tuberous sclerosis complex – Follow-up of 20 children 306 Miki, T., see Kusaka, T. 277 Miki, T., see Nakamura, S. 563 Min, K., see Lee, H.S. 764 Minematsu, T., see Matsuo, K. 10 Minot, D., see Magnin, E. 711 Miura, K., see Fukasawa, T. 752 Miwa, A., see Matsuo, K. 10 Miya, K., Takahashi, Y., and Mori, H. Anti-NMDAR autoimmune encephalitis 645 Miyajima, T., see Hayashi, A. 830 Miyake, F., see Kato, H. 630 Miyake, N., see Nakamura, K. 272 Miyake, T., see Shiihara, T. 489 Miyata, A., see Saito, Y. 337 Miyata, R., see Okoshi, Y. 907 Mizuguchi, M. Greetings from the new Editor-in-Chief 2 Mizuguchi, T., see Okamoto, N. 523 Mizukaki, N., see Ishii, H. 380 Mizuno, N., see Inokuchi, R. 626 Momoi, M.Y., see Okamoto, N. 523 Momoi, M.Y., see Saito, M. 64 Momonaka, H., Hasegawa, S., Matsushige, T., Inoue, H., Kajimoto, M., Okada, S., Nakatsuka, K., Morishima, T., and Ichiyama, T. High mobility group box 1 in patients with 2009 pandemic H1N1 influenza-associated encephalopathy 484 Momonaka, H., see Hasegawa, S. 608 Morano, A., see Bonini, F. 346 Mori, C., see Akella, R.R.D. 537 Mori, H., see Takanashi, J. 259 Mori, H., see Miya, K. 645 Mori, M., see Kondo, H. 730 Mori, Y., see Nomura, K. 778 Morikawa, S., see Matsuo, K. 10 Morikawa, S., see Yamamoto, T. 914

Morimoto, T., see Nakayama, T. 143 Morino, M., see Kawai, K. 124 Morioka, I., see Matsuo, K. 10 Morishima, T., see Momonaka, H. 484 Morita, K., see Ohya, T. 241 Morotomi, Y., see Hikita, N. 159 Morse, R.P., see Nair, S. 505 Motoyama, M., see Takahashi, K. 670 Mott, S.H., see Nair, S. 505 Moturi, P., see Cherian, A. 892 Muramatsu, M., see Yatsuga, C. 620 Murata, S., see Kashiwagi, M. 330 Murayama, K., see Kondo, H. 730 Murgia, A., see Bertossi, C. 402 Nagai, T., see Fujimoto, K. 107 Nagamitsu, S., see Ohya, T. 241 Nagamitsu, S., see Matsuoka, M. 35 Nagamitsu, S., see Hara, M. 794 Nagappa, M., see Sonam, K. 807 Nagasaka, M., see Matsuo, K. 10 Nagase, H., see Nishiyama, M. 928 Nagashima, M., see Saito, M. 64 Nair, S., Morse, R.P., Mott, S.H., Burroughs, S.A., and Holmes, G.L. Transitory effect of spike and spike-and-wave discharges on EEG power in children 505 Nakagawa, E., see Shiraishi, H. 21 Nakagawa, E., see Saito, Y. 878 Nakagawa, E., see Yasumura, A. 97 Nakagawa, E., see Goto, M. 180 Nakagawa, E., see Saito, Y. 337 Nakagawa, E., see Endo, Y. 74 Nakai, Y., Takashima, R., Takiguchi, T., and Takada, S. Speech intonation in children with autism spectrum disorder 516 Nakajima, H., see Yamamoto, T. 914 Nakajima, S., see Inokuchi, R. 626 Nakamachi, Y., see Matsuo, K. 10 Nakamura, K., see Inokuchi, R. 626 Nakamura, K., Nishiyama, K., Kodera, H., Nakashima, M., Tsurusaki, Y., Miyake, N., Matsumoto, N., Saitsu, H., Jinnou, H., Ohki, S., Yokochi, K., Okanishi, T., and Enoki, H. A de novo CASK mutation in pontocerebellar hypoplasia type 3 with early myoclonic epilepsy and tetralogy of Fallot 272 Nakamura, M., see Nakamura, S. 563 Nakamura, M., see Kashiwagi, M. 330 Nakamura, M., see Kusaka, T. 277 Nakamura, N., see Inoue, T. 613 Nakamura, S., see Kusaka, T. 277 Nakamura, S., Kusaka, T., Koyano, K., Miki, T., Ueno, M., Jinnai, W., Yasuda, S., Nakamura, M., Okada, H., Isobe, K., and Itoh, S. Relationship between early changes in cerebral blood volume and electrocortical activity after hypoxic–ischemic insult in newborn piglets 563 Nakasato, N., see Shiraishi, H. 21 Nakashima, M., see Nakamura, K. 272 Nakata, Y., see Endo, Y. 74 Nakata, Y., see Ito, K. 578 Nakatsuka, K., see Momonaka, H. 484 Nakayama, T., see Sato, H. 268 Nakayama, T., Saitsu, H., Endo, W., Kikuchi, A., Uematsu, M., Haginoya, K., Hino-Fukuyo, N., Kobayashi, T., Iwasaki, M., Tominaga, T., Kure, S., and Matsumoto, N. RBPJ is disrupted in a case of proximal 4p deletion syndrome with epilepsy 532 Nakayama, T., Tanaka, S., Uematsu, M., Kikuchi, A., Hino-Fukuyo, N., Morimoto, T., Sakamoto, O., Tsuchiya, S., and Kure, S. Effect of a blackout in pediatric patients with home medical devices during the 2011 eastern Japan earthquake 143

Author Index to Volume 36 Nara, T., see Wakusawa, K. 61 Natsume, J., see Kato, T. 372 Natsume, J., see Fukasawa, T. 752 Negoro, T., see Fukasawa, T. 752 Ngu, L.H., see Chen, B.C. 593 Niihori, T., see Wakusawa, K. 61 Ninomiya, S., see Inoue, T. 613 Nisari, M., see Torun, Y.A. 864 Nishi, Y., see Hara, M. 794 Nishida, Y., see Yamamoto, T. 914 Nishihara, M., see Li, J. 472 Nishimura, N., see Yamamoto, T. 914 Nishino, I., see Goto, M. 180 Nishio, H., see Yamamoto, T. 914 Nishitani, S., see Yatsuga, C. 620 Nishiyama, K., see Nakamura, K. 272 Nishiyama, M., Fujita, K., Maruyama, A., and Nagase, H. Two cases of traumatic head injury mimicking acute encephalopathy with biphasic seizures and late reduced diffusion 928 Nobili, L., see Bonanni, P. 826 Noble, J.J., Fry, N.R., Lewis, A.P., Keevil, S.F., Gough, M., and Shortland, A.P. Lower limb muscle volumes in bilateral spastic cerebral palsy 294 Noczyn´ska, A., see Bladowska, J. 770 Noda, S., see Saida, K. 721 Noga, L., see Bladowska, J. 770 Nomura, K., Okada, K., Noujima, Y., Kojima, S., Mori, Y., Amano, M., Ogura, M., Hatagaki, C., Shibata, Y., and Fukumoto, R. A clinical study of attention-deficit/hyperactivity disorder in preschool children—prevalence and differential diagnoses 778 Nomura, S., see Kajimoto, M. 637 Nomura, S., see Fukui, M. 80 Nomura, S., Shimakawa, S., Fukui, M., Tanabe, T., and Tamai, H. Lamotrigine for intractable migraine-like headaches in Sturge– Weber syndrome 399 Nomura, Y., see Takanashi, J. 259 Nonoda, Y., Iwasaki, T., and Ishii, M. The efficacy of gabapentin in children of partial seizures and the blood levels 194 Nosadini, M., see Azzolini, S. 716 Noujima, Y., see Nomura, K. 778 Nozaki, F., see Hayashi, A. 830 Nurputra, D.K., see Yamamoto, T. 914 Oda, M., see Matsuo, K. 10 Odanaka, Y., see Kashiwagi, M. 330 Ogura, K., see Kometani, H. 551 Ogura, M., see Nomura, K. 778 Ohashi, M., see Kawamura, Y. 601 Ohki, S., see Nakamura, K. 272 Ohno, K., see Matsuo, M. 148 Ohno, K., see Itoh, M. 388 Ohshima, Y., see Kometani, H. 551 Ohshita, T., see Yamamoto, T. 914 Ohta, G., see Kometani, H. 551 Ohta, R., see Kaga, M. 284 Ohtake, A., see Kondo, H. 730 Ohtsuka, F., see Matsuo, M. 148 Ohya, M., see Kato, H. 630 Ohya, T., Morita, K., Yamashita, Y., Egami, C., Ishii, Y., Nagamitsu, S., and Matsuishi, T. Impaired exploratory eye movements in children with Asperger’s syndrome 241 Oka, M., Hasegawa, S., Matsushige, T., Inoue, H., Kajimoto, M., Ishikawa, N., Isumi, H., and Ichiyama, T. Tau protein concentrations in the cerebrospinal fluid of children with acute disseminated encephalomyelitis 16 Oka, M., see Hasegawa, S. 608 Okada, H., see Nakamura, S. 563

XV

Okada, K., see Endo, Y. 74 Okada, K., see Nomura, K. 778 Okada, S., see Momonaka, H. 484 Okajima, K., see Kumakura, A. 725 Okamoto, N., Yamagata, T., Yada, Y., Ichihashi, K., Matsumoto, N., Momoi, M.Y., and Mizuguchi, T. Williams–Beuren syndrome with brain malformation and hypertrophic cardiomyopathy 523 Okanishi, T., see Nakamura, K. 272 Okasora, K., see Kashiwagi, M. 330 Okazaki, M., see Ito, K. 578 Okazaki, S., see Kometani, H. 551 Okazaki, S., see Fujimoto, K. 107 Okazaki, T., see Endo, Y. 74 Okazaki, Y., see Li, J. 472 Okoshi, Y., Hayashi, M., Kanda, S., and Yamamoto, T. An autopsy case of microencephaly, bizarre putaminal lesion, and cerebellar atrophy with heart and liver diseases 707 Okoshi, Y., Tanuma, N., Miyata, R., and Hayashi, M. Melatonin alterations and brain acetylcholine lesions in sleep disorders in Cockayne syndrome 907 Okuda, M., see Kato, H. 630 Okumura, A., see Tsuji, T. 555 Okumura, A., see Fukasawa, T. 752 Okumura, A., see Kato, T. 372 Okumura, K., see Kashiwagi, M. 330 Okuyaz, C., see Komur, M. 545 Onal, M., see Torun, Y.A. 864 Ono, K., see Toda, K. 641 Ono, T., see Toda, K. 641 O’Neill, J.P., see Chen, B.C. 593 Osaka, H., see Takanashi, J. 259 Osaka, H., see Kato, H. 630 Oshiro, M., see Tsuji, T. 555 Otaduy, M.C.G., see Andrade, C.S. 899 Otsubo, H., see Shiraishi, H. 21 Otsuki, T., see Endo, Y. 74 Ozdemir, M.A., see Torun, Y.A. 864 Ozge, A., see Uluduz, D. 884 Ozgur, A., see Komur, M. 545 Ozkul, Y., see Torun, Y.A. 864 Padmanabhan, S., see Cherian, A. 892 Park, E.J., see Andrade, C.S. 899 Park, J.D., see Kim, S.H. 734 Patıroglu, T., see Torun, Y.A. 864 Pavlidis, E., Cantalupo, G., Bianchi, S., Piccolo, B., and Pisani, F. Epileptic features in Cornelia de Lange syndrome: Case report and literature review 837 Pavlidou, E., see Gkampeta, A. 411 Pavlou, E., see Gkampeta, A. 411 Pavone, L., see Pavone, P. 739 Pavone, P., Striano, P., Falsaperla, R., Pavone, L., and Ruggieri, M. Infantile spasms syndrome, West syndrome and related phenotypes: What we know in 2013 739 Piccolo, B., see Pavlidis, E. 837 Piccolo, B., see Cantalupo, G. 548 Piralla, A., see Renna, S. 70 Pirlo, D., see Renna, S. 70 Pironti, E., see Coppola, G. 541 Pisani, F., see Fusco, C. 183 Pisani, F., see Cantalupo, G. 548 Pisani, F., see Pavlidis, E. 837 Poretti, A., and Boltshauser, E. Nationwide survey of Arima syndrome: A note of doubt 88 Qin, J., see Xu, X. 676 Quaio, C.R., see Borlot, F. 585

XVI

Author Index to Volume 36

Rampazzo, A., see Bonanni, P. 826 Randazzo, G., see Bonanni, P. 826 Randhir, K., see Roy, S. 219 Rapin, I., see Shetreat-Klein, M. 91 Rathod, R., Khaire, A., Kemse, N., Kale, A., and Joshi, S. Maternal omega-3 fatty acid supplementation on vitamin B12 rich diet improves brain omega-3 fatty acids, neurotrophins and cognition in the Wistar rat offspring 853 Rawat, V.S., see Dhiman, V. 287 Rebai, I., Kraoua, I., Benrhouma, H., Rouissi, A., Turki, I., CeballosPicot, I., and Gouider-Khouja, N. Lesch Nyhan syndrome: A novel complex mutation in a Tunisian child 921 Reddy, M., see Cherian, A. 892 Reeder, A., see Tan, C.A. 351 Renna, S., Bergamino, L., Pirlo, D., Rossi, A., Furione, M., Piralla, A., Mascaretti, M., Cristina, E., Marazzi, M.G., and Di Pietro, P. A case of neonatal human parechovirus encephalitis with a favourable outcome 70 Resch, L., see Sarnat, H.B. 463 Robertson, M.M., see Crossley, E. 45 Rocha, S., Ferreira, A.C., Dias, A.I., Vieira, J.P., and Sequeira, S. Sulfite oxidase deficiency – An unusual late and mild presentation 176 Romaniello, R., see Vantaggiato, C. 682 Romano, D., see Grosso, S. 932 Rossato, S., see Bertossi, C. 402 Rossi, A., see Renna, S. 70 Rouissi, A., see Rebai, I. 921 Roy, S., Sable, P., Khaire, A., Randhir, K., Kale, A., and Joshi, S. Effect of maternal micronutrients (folic acid and vitamin B12) and omega 3 fatty acids on indices of brain oxidative stress in the offspring 219 Ruggieri, M., see Pavone, P. 739 Rumbach, L., see Magnin, E. 711 Russo, A., see Fusco, C. 183 Sable, P., see Roy, S. 219 Saida, K., Inaba, Y., Hirano, M., Satake, W., Toda, T., Suzuki, Y., Sudo, A., Noda, S., Hidaka, Y., Hirabayashi, K., Imai, H., Kurokawa, T., and Koike, K. A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese child 721 Saip, S., see Uluduz, D. 884 Saito, A., see Shimojima, K. 315 Saito, K., see Yamamoto, T. 914 Saito, M., Yamagata, T., Matsumoto, A., Shiba, Y., Nagashima, M., Taniguchi, S., Jimbo, E., and Momoi, M.Y. MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus 64 Saito, T., see Saito, Y. 337 Saito, T., see Endo, Y. 74 Saito, T., see Goto, M. 180 Saito, T., see Saito, Y. 878 Saito, Y., see Endo, Y. 74 Saito, Y., Aoki, Y., Takeshita, E., Saito, T., Sugai, K., Komaki, H., Nakagawa, E., Ishiyama, A., Takanoha, S., Wada, S., and Sasaki, M. Hypophosphatemia is a common complication in severely disabled individuals with neurological disorders and is caused by infection, refeeding and Fanconi syndrome 878 Saito, Y., Matsuda, Y., Sugai, K., Nakagawa, E., Ishiyama, A., Saito, T., Komaki, H., Sasaki, M., and Miyata, A. Effects of clonazepam on self-induced photoparoxysmal responses 337 Saito, Y., see Goto, M. 180 Saitoh, S., see Shiraishi, H. 21 Saitsu, H., see Takanashi, J. 259 Saitsu, H., see Nakamura, K. 272 Saitsu, H., see Nakayama, T. 532

Sakai, Y., see Torisu, H. 342 Sakamoto, O., see Nakayama, T. 143 Sakamoto, O., see Sato, H. 268 Sakuma, S., see Hikita, N. 159 Sanefuji, M., see Torisu, H. 342 Sano, F., see Tando, T. 844 Santoro, E., see Coppola, G. 541 Sarnat, H.B., Resch, L., Flores-Sarnat, L., and Yu, W. Precocious synapses in 13.5-week fetal holoprosencephalic cortex and cyclopean retina 463 Sartori, S., see Bertossi, C. 402 Sartori, S., see Azzolini, S. 716 Sasaki, M., see Ito, K. 578 Sasaki, M., see Saito, Y. 878 Sasaki, M., see Takanashi, J. 259 Sasaki, M., see Goto, M. 180 Sasaki, M., see Endo, Y. 74 Sasaki, M., see Saito, Y. 337 Sa˛siadek, M.J., see Bladowska, J. 770 Satake, W., see Saida, K. 721 Satishchandra, P., see Dhiman, V. 287 Sato, H., Uematsu, M., Endo, W., Nakayama, T., Kobayashi, T., Hino-Fukuyo, N., Sakamoto, O., Shintaku, H., and Kure, S. Early replacement therapy in a first Japanese case with autosomal recessive guanosine triphosphate cyclohydrolase I deficiency with a novel point mutation 268 Sato, H., see Inokuchi, R. 626 Sato, H., see Yamamoto, T. 914 Sato, J., see Akiyama, T. 3 Sato, N., see Ito, K. 578 Saygi, S., Alehan, F., Atac, F.B., Erol, I., Verdi, H., and Erdem, R. Multidrug resistance 1 (MDR1) 3435C/T genotyping in childhood drug-resistant epilepsy 137 *ayli, T.R., see Deg˘erliyurt, A. 690 Saylisoy, S., see Kocak, O. 167 Scarpa, M., see Bonanni, P. 826 Sciutti, R., see Capretti, M.G. 203 *eker, E.D., see Deg˘erliyurt, A. 690 Sequeira, S., see Rocha, S. 176 Seri, S., see Crossley, E. 45 Seto, T., Takesada, H., Matsushita, N., Ishibashi, K., Tsuyuguchi, N., Shimono, T., Hikita, N., Hattori, T., Tanaka, K., and Shintaku, H. Twelve-year-old girl with intracranial epidural abscess and sphenoiditis 359 Seto, T., see Hikita, N. 159 Shabana, K., see Kashiwagi, M. 330 Sheen, J.-M., see Hsu, M.-H. 248 Shetreat-Klein, M., Shinnar, S., and Rapin, I. Abnormalities of joint mobility and gait in children with autism spectrum disorders 91 Shi, X.-Y., see Ma, Y.-Y. 394 Shiba, Y., see Saito, M. 64 Shibata, A., see Matsuo, K. 10 Shibata, Y., see Nomura, K. 778 Shibayama, H., see Takanashi, J. 259 Shigemoto, Y., see Ito, K. 578 Shiihara, T., Miyake, T., Izumi, S., Sugihara, S., Watanabe, M., Takanashi, J., Kubota, M., and Kato, M. Serum and CSF biomarkers in acute pediatric neurological disorders 489 Shim, K.-W., see Lee, Y.-J. 496 Shimada, S., see Shimojima, K. 315 Shimakawa, S., see Tanabe, T. 301 Shimakawa, S., see Nomura, S. 399 Shimakawa, S., see Fukui, M. 80 Shimakawa, S., see Kashiwagi, M. 330 Shimbo, H., see Kato, H. 630 Shimojima, K., see Torisu, H. 342

Author Index to Volume 36 Shimojima, K., Shimada, S., Tamasaki, A., Akaboshi, S., Komoike, Y., Saito, A., Furukawa, T., and Yamamoto, T. Novel compound heterozygous mutations of POLR3A revealed by whole-exome sequencing in a patient with hypomyelination 315 Shimono, T., see Seto, T. 359 Shimono, T., see Hikita, N. 159 Shinnar, S., see Shetreat-Klein, M. 91 Shinohara, J., see Kashiwagi, M. 330 Shinohara, K., see Inokuchi, R. 626 Shinohara, K., see Yatsuga, C. 620 Shintaku, H., see Seto, T. 359 Shintaku, H., see Hikita, N. 159 Shintaku, H., see Sato, H. 268 Shiraishi, H., Haginoya, K., Nakagawa, E., Saitoh, S., Kaneko, Y., Nakasato, N., Chan, D., and Otsubo, H. Magnetoencephalography localizing spike sources of atypical benign partial epilepsy 21 Shortland, A.P., see Noble, J.J. 294 Sinha, S., see Sonam, K. 807 Sinha, S., see Dhiman, V. 287 Soluch, P., see Borkowska, A.R. 786 Sonam, K., Khan, N.A., Bindu, P.S., Taly, A.B., Gayathri, N., Bharath, M.M. S., Govindaraju, C., Arvinda, H.R., Nagappa, M., Sinha, S., and Thangaraj, K. Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutations 807 Song, J., see Lee, H.S. 764 Song, J., see Wang, Q. 813 Song, J.-Q., see Ma, Y.-Y. 394 Song, J.-Q., see Wu, T.-F. 264 Spagnoli, C., see Cantalupo, G. 548 Spitaleri, C., see Mangano, S. 408 Srinath, S., see Dhiman, V. 287 Stein, J., see Tan, C.A. 351 Stern, J.S., see Crossley, E. 45 Striano, P., see Pavone, P. 739 Sudo, A., see Saida, K. 721 Sugai, K., see Goto, M. 180 Sugai, K., see Saito, Y. 878 Sugai, K., see Endo, Y. 74 Sugai, K., see Saito, Y. 337 Sugai, K., see Ito, K. 578 Sugawara, H., see Kato, H. 630 Sugawara, M., see Torisu, H. 342 Sugihara, S., see Shiihara, T. 489 Sugita, K., see Tando, T. 844 Sun, H., see Xu, X. 676 Sunohara, D., see Ishii, H. 380 Suppiej, A., see Azzolini, S. 716 Suzuki, M., see Fukasawa, T. 752 Suzuki, Y., see Saida, K. 721 Suzuki, Y. Obituary 835 Swanson, J.M., see Inoue, Y. 700 Sylvestre, G., see Magnin, E. 711 Syrbe, S., see Mettin, R.R. 306 Szewczyk, P., see Bladowska, J. 770 Tabata, C., see Kondo, H. 730 Tada, H., and Takanashi, J. MR spectroscopy in 18q- syndrome suggesting other than hypomyelination 57 Takada, E., see Endo, Y. 74 Takada, S., see Nakai, Y. 516 Takagi, M., see Kato, H. 630 Takahara, M., see Hasegawa, S. 608 Takahashi, A., see Endo, Y. 74

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Takahashi, K., Hasegawa, S., Maeba, S., Fukunaga, S., Motoyama, M., Hamano, H., and Ichiyama, T. Serum tau protein level serves as a predictive factor for neurological prognosis in neonatal asphyxia 670 Takahashi, S., see Kumakura, A. 725 Takahashi, S., see Hara, M. 794 Takahashi, Y., see Miya, K. 645 Takami, T., see Ishii, H. 380 Takanashi, J., see Tada, H. 57 Takanashi, J., Osaka, H., Saitsu, H., Sasaki, M., Mori, H., Shibayama, H., Tanaka, M., Nomura, Y., Terao, Y., Inoue, K., Matsumoto, N., and Barkovich, A.J. Different patterns of cerebellar abnormality and hypomyelination between POLR3A and POLR3B mutations 259 Takanashi, J., see Shiihara, T. 489 Takanashi, J., see Yamamoto, T. 914 Takano, K., see Kato, H. 630 Takanoha, S., see Saito, Y. 878 Takashima, R., see Nakai, Y. 516 Takesada, H., see Seto, T. 359 Takeshima, Y., see Yamamoto, T. 914 Takeshita, E., see Saito, Y. 878 Takeuchi, A., see Yamamoto, T. 914 Takiguchi, T., see Nakai, Y. 516 Taly, A.B., see Sonam, K. 807 Tamai, H., see Nomura, S. 399 Tamai, H., see Li, J. 472 Tamai, H., see Fukui, M. 80 Tamai, H., see Kashiwagi, M. 330 Tamai, H., see Tanabe, T. 301 Tamasaki, A., see Shimojima, K. 315 Tan, C.A., Topper, S., Ward Melver, C., Stein, J., Reeder, A., Arndt, K., and Das, S. The first case of CDK5RAP2-related primary microcephaly in a non-consanguineous patient identified by next generation sequencing 351 Tanabe, T., Kashiwagi, M., Shimakawa, S., Tamai, H., and Wakamiya, E. Outpatient screening of Japanese children with epilepsy for attention-deficit/hyperactivity disorder (AD/HD) 301 Tanabe, T., see Kashiwagi, M. 330 Tanabe, T., see Nomura, S. 399 Tanabe, T., see Fukui, M. 80 Tanaka, H., see Yamamoto, T. 479 Tanaka, K., see Seto, T. 359 Tanaka, K., see Hikita, N. 159 Tanaka, M., see Takanashi, J. 259 Tanaka, S., see Nakayama, T. 143 Tanaka, S., see Wakusawa, K. 61 Tanda, K., see Kondo, H. 730 Tando, T., Kaga, Y., Ishii, S., Aoyagi, K., Sano, F., Kanemura, H., Sugita, K., and Aihara, M. Developmental changes in frontal lobe function during a verbal fluency task: A multi-channel nearinfrared spectroscopy study 844 Tani, G., see Capretti, M.G. 203 Taniguchi-Ikeda, M., see Kondo, H. 730 Taniguchi, K., see Kawamura, Y. 601 Taniguchi, S., see Saito, M. 64 Tanizawa, A., see Kometani, H. 551 Tanuma, N., see Okoshi, Y. 907 Tavsanli, M.E., see Uluduz, D. 884 Teber, S., see Bektas, O. 130 Teber, S., see Deg˘erliyurt, A. 690 Temel, G.O., see Uluduz, D. 884 Terao, Y., see Takanashi, J. 259 Thangaraj, K., see Sonam, K. 807

XVIII

Author Index to Volume 36

Thauvin-Robinet, C., see Magnin, E. 711 Thevenon, J., see Magnin, E. 711 Thiele, E.A., see Boronat, S. 801 Thippeswamy, H., see Dhiman, V. 287 Toda, K., Baba, H., Ono, T., and Ono, K. The utility of diffusion tensor imaging tractography for post-operative evaluation of a patient with hemispherotomy performed for intractable epilepsy 641 Toda, S., see Yamamoto, T. 914 Toda, T., see Saida, K. 721 Togashi, N., see Wakusawa, K. 61 Tohyama, Y., see Yamamoto, T. 914 Tokuhara, D., see Hikita, N. 159 Toldo, I., see Bertossi, C. 402 Toldo, I., see Azzolini, S. 716 Tominaga, T., see Nakayama, T. 532 Tomiwa, K., see Fujimoto, K. 107 Tomoda, A., see Yatsuga, C. 620 Tomonoh, Y., see Inoue, T. 613 Topper, S., see Tan, C.A. 351 Torisu, H., Watanabe, K., Shimojima, K., Sugawara, M., Sanefuji, M., Ishizaki, Y., Sakai, Y., Yamashita, H., Yamamoto, T., and Hara, T. Girl with a PRRT2 mutation and infantile focal epilepsy with bilateral spikes 342 Torun, Y.A., Ozdemir, M.A., Ulger, H., Nisari, M., Akalın, H., Patıroglu, T., Ozkul, Y., Onal, M., and Karakukcu, M. Erythropoietin improves brain development in short-term hypoxia in rat embryo cultures 864 Toyohisa, D., see Yatsuga, C. 620 Tsuchiya, S., see Nakayama, T. 143 Tsuji, T., see Kato, T. 372 Tsuji, T., Okumura, A., Kidokoro, H., Hayakawa, F., Kubota, T., Maruyama, K., Kato, T., Oshiro, M., Hayakawa, M., and Watanabe, K. Differences between periventricular hemorrhagic infarction and periventricular leukomalacia 555 Tsukamoto, S., see Fujimori, A. 661 Tsunemi, M.H., see Andrade, C.S. 899 Tsurusaki, Y., see Nakamura, K. 272 Tsuyuguchi, N., see Seto, T. 359 Turki, I., see Rebai, I. 921 Uchimura, N., see Matsuoka, M. 35 Uematsu, M., see Nakayama, T. 532 Uematsu, M., see Nakayama, T. 143 Uematsu, M., see Sato, H. 268 Ueno, M., see Kusaka, T. 277 Ueno, M., see Nakamura, S. 563 Ulger, H., see Torun, Y.A. 864 Uluduz, D., Tavsanli, M.E., Uygunog˘lu, U., Saip, S., Kasapcopur, O., Ozge, A., and Temel, G.O. Primary headaches in pediatric patients with chronic rheumatic disease 884 Umehara, T., see Yamamoto, T. 479 Unal, S., see Komur, M. 545 Uygunog˘lu, U., see Uluduz, D. 884 Valente, K.D.R., see Andrade, C.S. 899 Van Eeghen, A., see Boronat, S. 801 Vanhatalo, S., see Malk, K. 116 Vantaggiato, C., Cantoni, O., Guidarelli, A., Romaniello, R., Citterio, A., Arrigoni, F., Doneda, C., Castelli, M., Airoldi, G., Bresolin, N., Borgatti, R., and Bassi, M.T. Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agents 682 Vecchi, M., see Bertossi, C. 402 Verdi, H., see Saygi, S. 137

Vieira, J.P., see Rocha, S. 176 Vijaysagar, K.J., see Dhiman, V. 287 Volzone, A., see Bonanni, P. 826 Wada, H., see Li, J. 472 Wada, S., see Saito, Y. 878 Wada, T., see Kato, H. 630 Wada, Y., see Ishitobi, M. 823 Wakamiya, E., see Tanabe, T. 301 Wakusawa, K., Kobayashi, S., Abe, Y., Tanaka, S., Endo, W., Inui, T., Iwaki, M., Watanabe, S., Togashi, N., Nara, T., Niihori, T., Aoki, Y., and Haginoya, K. A girl with Cardio-facio-cutaneous syndrome complicated with status epilepticus and acute encephalopathy 61 Wang, B., see Fujimori, A. 661 Wang, H.-S., see Hung, P.-C. 634 Wang, H.-S., see Hung, P.-C. 356 Wang, Q., see Ma, Y.-Y. 394 Wang, Q., see Wu, T.-F. 264 Wang, Q., Li, X., Ding, Y., Liu, Y., Song, J., and Yang, Y. Clinical and mutational spectra of 23 Chinese patients with glutaric aciduria type 1 813 Wang, S., see Xu, X. 676 Wang, S.-H., see Cheng, L. 51 Wang, Z.-L., see Ma, Y.-Y. 394 Ward Melver, C., see Tan, C.A. 351 Watanabe, K., see Fukasawa, T. 752 Watanabe, K., see Torisu, H. 342 Watanabe, K., see Kato, T. 372 Watanabe, K., see Tsuji, T. 555 Watanabe, K. Neurophysiological aspects of neonatal seizures 363 Watanabe, M., see Shiihara, T. 489 Watanabe, M., see Ito, K. 578 Watanabe, S., see Wakusawa, K. 61 Wilkinson, A.R., see Jiang, Z.D. 212 Wilson, T.W., see Kurz, M.J. 870 Wolak, T., see Borkowska, A.R. 786 Wong, A.M.-C, see Hung, P.-C. 634 Wong, A.M.-C., see Hung, P.-C. 356 Wu, T.-F., Liu, Y.-P., Li, X.-Y., Wang, Q., Song, J.-Q., and Yang, Y.-L. Prenatal diagnosis of citrullinemia type 1: A Chinese family with a novel mutation of the ASS1 gene 264 Wu, T.-F., see Ma, Y.-Y. 394 Wu, X., see Xu, X. 676 Wu, Y., see Xu, X. 676 Xie, L., and Jiang, L. Arterial ischemic stroke and hemorrhagic stroke in Chinese children: A retrospective analysis 153 Xie, M., see Cheng, L. 51 Xiong, H., see Xu, X. 676 Xu, X., Zhang, Y., Sun, H., Liu, X., Yang, X., Xiong, H., Jiang, Y., Bao, X., Wang, S., Yang, Z., Wu, Y., Qin, J., Lin, Q., and Wu, X. Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations 676 Yada, Y., see Okamoto, N. 523 Yahagi, N., see Inokuchi, R. 626 Yakob, Y., see Afroze, B. 924 Yakut, A., see Kocak, O. 167 Yamada, H., Akiyoshi, K., and Izumi, T. The ominous sequence in patients with tuberous sclerosis complex 254 Yamada, H., see Yamamoto, T. 914 Yamada, H., see Matsuo, K. 10 Yamagata, T., see Okamoto, N. 523 Yamagata, T., see Saito, M. 64

Author Index to Volume 36 Yamamoto, H., see Yasumura, A. 97 Yamamoto, T., Tanaka, H., Emoto, Y., Umehara, T., Fukahori, Y., Kuriu, Y., Matoba, R., and Ikematsu, K. Carnitine palmitoyltransferase 2 gene polymorphism is a genetic risk factor for sudden unexpected death in infancy 479 Yamamoto, T., Sato, H., Lai, P.S., Nurputra, D.K., Harahap, N.I.F., Morikawa, S., Nishimura, N., Kurashige, T., Ohshita, T., Nakajima, H., Yamada, H., Nishida, Y., Toda, S., Takanashi, J., Takeuchi, A., Tohyama, Y., Kubo, Y., Saito, K., Takeshima, Y., Matsuo, M., and Nishio, H. Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patients 914 Yamamoto, T., see Torisu, H. 342 Yamamoto, T., see Okoshi, Y. 707 Yamamoto, T., see Shimojima, K. 315 Yamashita, H., see Torisu, H. 342 Yamashita, S., see Kato, H. 630 Yamashita, Y., see Hara, M. 794 Yamashita, Y., see Matsuoka, M. 35 Yamashita, Y., see Ohya, T. 241 Yang, X., see Xu, X. 676 Yang, Y., see Wang, Q. 813 Yang, Y.-L., see Wu, T.-F. 264 Yang, Y.-L., see Ma, Y.-Y. 394 Yang, Z., see Xu, X. 676 Yarar, C., see Kocak, O. 167 Yasuda, S., see Kusaka, T. 277 Yasuda, S., see Nakamura, S. 563 Yasumoto, S., see Inoue, T. 613 Yasumura, A., Kokubo, N., Yamamoto, H., Yasumura, Y., Nakagawa, E., Kaga, M., Hiraki, K., and Inagaki, M. Neurobehavioral and hemodynamic evaluation of Stroop and reverse Stroop interference in children with attention-deficit/hyperactivity disorder 97

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Yasumura, Y., see Yasumura, A. 97 Yasutomi, M., see Kometani, H. 551 Yatsuga, C., Toyohisa, D., Fujisawa, T.X., Nishitani, S., Shinohara, K., Matsuura, N., Ikeda, S., Muramatsu, M., Hamada, A., and Tomoda, A. No association between catechol-O-methyltransferase (COMT) genotype and attention deficit hyperactivity disorder (ADHD) in Japanese children 620 Yılmaz, A., see Bektas, O. 130 Yimenicioglu, S., see Kocak, O. 167 Yokochi, K., see Kouwaki, M. 572 Yokochi, K., see Nakamura, K. 272 Yokochi, M., see Kouwaki, M. 572 Yokota, T., see Matsuo, K. 10 Yoo, H.-W., see Lee, B.H. 171 Yoo, H.J., see Lee, B.H. 171 Yoon, J.-R., Lee, E.J., Kim, H.D., Lee, J.H., and Kang, H.-C. Polyunsaturated fatty acid-enriched diet therapy for a child with epilepsy 163 Yoshikawa, T., see Kawamura, Y. 601 Yoshinaga, H., see Akiyama, M. 758 Yoshinaga, H., see Akiyama, T. 3 Yu, W., see Sarnat, H.B. 463 Zacharzewska-Gondek, A., see Bladowska, J. 770 _ Zak, T., see Bladowska, J. 770 Zeybek, H., see Bektas, O. 130 Zhang, B., see Inoue, T. 613 Zhang, W.-N., see Ma, Y.-Y. 394 Zhang, Y., see Xu, X. 676 Zhao, M., see Ma, Y.-Y. 394 Zhong, M., see Dai, Y. 228 Zimny, A., see Bladowska, J. 770 Zou, L.-P., see Ma, Y.-Y. 394