- Email: [email protected]
Subject index to volume 2
Subject Index to Volume
Abnormal pupil, 407 Acquired hydrocephalus, 171 Adrenoleucodystrophy , 45 Agenesis of the corpus callosum, 379 Alpha frequency, 33 Alpha2 -macroglo bulin, 107 Aneurysm, 95 Annual Meeting, Japanese Society of Child Neurology, 207 Anticonvulsants, 239 Aphasia, 8 1 Arteriovenous malformation , 95 Ataxia, 365 Audiometry, 45 Auditory brain stern audiometry, 45 Auditory brain stern response, 45 Auditory evoked potentials , 33 Autosomal-recessive inheritance, 387 Bilirubin encephalopathy, 45, 219 Brain stern response, 45 Brazelton criteria, 3 Carrier detection and creatine phosphokinase, 87 Cavernous hemangioma , 95 CCT-scan , 107 ,2 29 Cerebellar dysgenesis , 345 Cerebellar heterotopia, 345 Cerebellum, 345,359 Cerebral angiography, 95 Cerebral palsy, 45,133 Cerebrospinal fluid dynamics , 171 Cere brovascular diseases , 95 Child aphasia, 81 Chronically ill children, 127 Clumsy children, 69 Coiling of the cord and encephalopathy , 40 I Congenital defects monitoring system, 143 Congenital fiber type disproportion,119 Congenital hydrocephalus , 171
2
Congenital muscular dystrophy , 87 , 191 Congenital myopathy , 119, 387 Congenital rubella syndrome, 401 Congestive cardiomyopathy, 124 Connection specificity , 2 9 Creatine phosphokinase, 87 Developing brain, 29 Development, 33 Development of auditory function, 45 Developmental disabilities, 69, 143 , 149 Developmental language disability, 73 Develo pmental scale of auditory function, 45 Disseminated intravascular coagulation, 327 Down syndrome, 45 Duchenne muscular dystrophy, . 87 Dying children, 127 Dysgnosia, 69 Dyspraxia, 69 Early intervention, 133 , 143, 148 EEG , 33 , 73 , 81 , 407 EEG evolution, 373 Electrical activity , 33 Electron microscopy , 107, 191, 387 Epilepsy-aphasia, 81 Evoked potentials, 33 , 45 Experimental hydrocephalus, 171 External ophthalmoplegia, 407
F antz technique, 15
Guillain-Barre syndrome (GBS) , 407 Gunn rats as a model, 219 Handicapped child, 73, 127 Hearing disturbances, 45 Heterotaxia, 345 Hydranencephaly , 327 Hydrocephalus, 95,171,401 Hyperbilirubinemia, 219 Hypertrophic grisea, 345 Hypomelanotic spots, 107 Hypsarrhythmia, 379
I nborn errors of metabolism, 143 Infantile neuroaxonal dystrophy, 29 Infantile spasm, 45,379 Intelligence scores , 57 Kernicterus, 45 , 219 L anguage development, 73 Latency, 45,137 Leucodystrophy, 45 , 359 Low birth ",;,eight, 15 , 57 Malformations, 95, 171 Mass screening programs, 143 Maternal and child health, 143 Mental retardation, 45 Metachromatic leukodystrophy, 359 Minimal brain dysfunction, 57, 69 Minor cerebellar disturbance, 69 Minor brain dysfunction , 57,69 Moro reflex, 1 5 Moyarnoya syndrome, 95 Muscle biopsy, 119,191,387 Muscular dystrophy, 87,119, 387 Myelination , 337 , 401 Myoglobinemia, 87
Fetal brain , 345 Friedreich's ataxia, 365 Fukuyama type CMD, 119, 191 Necrosis, 401 Full-term, 3,15 Neurobehavioral assessment, 3, IS Genetic counseling, 236 Great vein of Galen , 95
418 Brain & Development, Vol 2, No 4, 1980
Neurocutaneous syndrome, 95, 107 Neurological examination, 3 Neuronal depletion, 359 Non-medical help to families with a sick child, 127 Nonverbal child, 73 Oligodendrocyte, 337 Oligosymptomatic cases, 107 Opaque fiber, 191 Opening address, I Ophthalmoplegia, 407 Ophthalmologic defects in prematures, 57 Overnight polygraphy, 379 Parasomnia, 353 Paroxysmal discharges, 33 Pathogenesis of bilirubin encephalopathy, 219 Phacomatosis, 95,107 Photic driving, 33 Plan tar grasp, 137 Plasticity, 29 Polygraphy, 379 Positive spikes, 33
Prematurity, 57 Prenatally and postnatally acquired arterial lesions, 95 Preterm, 3, IS Prevalence, 353 Progressive muscular dystrophy, 87,191,387 Prospective study, 55 Rigid spine syndrome, 119 Round table discussion, 149 Second International Symposium on Developmental Disabilities, 1,95 Seizure resembling infantile spasms, 379 Sensory evoked potentials, 33 Sensory input, 133 Sequel of hyperbilirubinemia, 219 Skin biopsy, 107 Sleep, 353 Sleep disturbances, 353 Sleep-talking, 353 Sleep-wake cycle, 33 Slow posterior rhythm, 33
Somniloquy, 353 Spinal cord, 228, 337 Spindle, 373 Spinocerebellar degeneration, 365 Spontaneous intracerebral hem orrhage, 95 Support to the whole family, 127 Synapse formation, 29 Teeth enamel defects, 107 Trace alternant, 33,373 Trisomy D J syndrome, 345 Tuberous sclerosis, 107 Tubular structure, 191 Twin, 327 Ultrastructure, 191 Ventral suspension, 15 Visual acuity, IS Visual evoked potentials, 33 Visual function, IS Visual preference, 15 Visual orientation, 15
Subject Index 419
Abnormal pupil, 407 Acquired hydrocephalus, 171 Adrenoleucodystrophy , 45 Agenesis of the corpus callosum, 379 Alpha frequency, 33 Alpha2 -macroglo bulin, 107 Aneurysm, 95 Annual Meeting, Japanese Society of Child Neurology, 207 Anticonvulsants, 239 Aphasia, 8 1 Arteriovenous malformation , 95 Ataxia, 365 Audiometry, 45 Auditory brain stern audiometry, 45 Auditory brain stern response, 45 Auditory evoked potentials , 33 Autosomal-recessive inheritance, 387 Bilirubin encephalopathy, 45, 219 Brain stern response, 45 Brazelton criteria, 3 Carrier detection and creatine phosphokinase, 87 Cavernous hemangioma , 95 CCT-scan , 107 ,2 29 Cerebellar dysgenesis , 345 Cerebellar heterotopia, 345 Cerebellum, 345,359 Cerebral angiography, 95 Cerebral palsy, 45,133 Cerebrospinal fluid dynamics , 171 Cere brovascular diseases , 95 Child aphasia, 81 Chronically ill children, 127 Clumsy children, 69 Coiling of the cord and encephalopathy , 40 I Congenital defects monitoring system, 143 Congenital fiber type disproportion,119 Congenital hydrocephalus , 171
2
Congenital muscular dystrophy , 87 , 191 Congenital myopathy , 119, 387 Congenital rubella syndrome, 401 Congestive cardiomyopathy, 124 Connection specificity , 2 9 Creatine phosphokinase, 87 Developing brain, 29 Development, 33 Development of auditory function, 45 Developmental disabilities, 69, 143 , 149 Developmental language disability, 73 Develo pmental scale of auditory function, 45 Disseminated intravascular coagulation, 327 Down syndrome, 45 Duchenne muscular dystrophy, . 87 Dying children, 127 Dysgnosia, 69 Dyspraxia, 69 Early intervention, 133 , 143, 148 EEG , 33 , 73 , 81 , 407 EEG evolution, 373 Electrical activity , 33 Electron microscopy , 107, 191, 387 Epilepsy-aphasia, 81 Evoked potentials, 33 , 45 Experimental hydrocephalus, 171 External ophthalmoplegia, 407
F antz technique, 15
Guillain-Barre syndrome (GBS) , 407 Gunn rats as a model, 219 Handicapped child, 73, 127 Hearing disturbances, 45 Heterotaxia, 345 Hydranencephaly , 327 Hydrocephalus, 95,171,401 Hyperbilirubinemia, 219 Hypertrophic grisea, 345 Hypomelanotic spots, 107 Hypsarrhythmia, 379
I nborn errors of metabolism, 143 Infantile neuroaxonal dystrophy, 29 Infantile spasm, 45,379 Intelligence scores , 57 Kernicterus, 45 , 219 L anguage development, 73 Latency, 45,137 Leucodystrophy, 45 , 359 Low birth ",;,eight, 15 , 57 Malformations, 95, 171 Mass screening programs, 143 Maternal and child health, 143 Mental retardation, 45 Metachromatic leukodystrophy, 359 Minimal brain dysfunction, 57, 69 Minor cerebellar disturbance, 69 Minor brain dysfunction , 57,69 Moro reflex, 1 5 Moyarnoya syndrome, 95 Muscle biopsy, 119,191,387 Muscular dystrophy, 87,119, 387 Myelination , 337 , 401 Myoglobinemia, 87
Fetal brain , 345 Friedreich's ataxia, 365 Fukuyama type CMD, 119, 191 Necrosis, 401 Full-term, 3,15 Neurobehavioral assessment, 3, IS Genetic counseling, 236 Great vein of Galen , 95
418 Brain & Development, Vol 2, No 4, 1980
Neurocutaneous syndrome, 95, 107 Neurological examination, 3 Neuronal depletion, 359 Non-medical help to families with a sick child, 127 Nonverbal child, 73 Oligodendrocyte, 337 Oligosymptomatic cases, 107 Opaque fiber, 191 Opening address, I Ophthalmoplegia, 407 Ophthalmologic defects in prematures, 57 Overnight polygraphy, 379 Parasomnia, 353 Paroxysmal discharges, 33 Pathogenesis of bilirubin encephalopathy, 219 Phacomatosis, 95,107 Photic driving, 33 Plan tar grasp, 137 Plasticity, 29 Polygraphy, 379 Positive spikes, 33
Prematurity, 57 Prenatally and postnatally acquired arterial lesions, 95 Preterm, 3, IS Prevalence, 353 Progressive muscular dystrophy, 87,191,387 Prospective study, 55 Rigid spine syndrome, 119 Round table discussion, 149 Second International Symposium on Developmental Disabilities, 1,95 Seizure resembling infantile spasms, 379 Sensory evoked potentials, 33 Sensory input, 133 Sequel of hyperbilirubinemia, 219 Skin biopsy, 107 Sleep, 353 Sleep disturbances, 353 Sleep-talking, 353 Sleep-wake cycle, 33 Slow posterior rhythm, 33
Somniloquy, 353 Spinal cord, 228, 337 Spindle, 373 Spinocerebellar degeneration, 365 Spontaneous intracerebral hem orrhage, 95 Support to the whole family, 127 Synapse formation, 29 Teeth enamel defects, 107 Trace alternant, 33,373 Trisomy D J syndrome, 345 Tuberous sclerosis, 107 Tubular structure, 191 Twin, 327 Ultrastructure, 191 Ventral suspension, 15 Visual acuity, IS Visual evoked potentials, 33 Visual function, IS Visual preference, 15 Visual orientation, 15
Subject Index 419