On the move

2. Gahl WA, Kaiser-Kupfer MI. Complications of nephropathic cystinosis after renal failure. Pediatr Nephrol 1987;1:260-8. 3. Gagnadoux MF, Charbit M, Guest G, Arsan A, Broyer M. Clinical evaluation of 70 pediatric renal transplants after 10 to 17 years. Ann Pediatr (Paris) 1991;38:413-7. 4. Ehrich JHH, Brodehl J, Byrd DI, Hossfeld S, Hoyer PF, Leipert K-P, et al. Renal transplantation in 22 children with nephropathic cystinosis. Pediatr Nephrol 1991;5:707-14. 5. Thoene JG, Oshima RG, Crawhall JC, Olson D, Schneider JA. Cystinosis. Intracellular cystine depletion by aminothiols in vitro and in vivo. J Clin Invest 1976;58:180-9. 6. Pisoni RL, Thoene JG, Christensen HN. Detection and characterization of carrier-mediated cationic amino acid transport in lysosomes of normal and cystinotic human fibroblasts: role in therapeutic cystine removal. J Biol Chem 1985;260:4791-8.

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7. Kleta R, Bernardini I, Ueda M, Varade WS, Phornphutkul C, Krasnewich D, Gahl WA. Long-term follow-up of well-treated nephropathic cystinosis patients. J Pediatr 2004;145:555-60. 8. Smolin LA, Clark KF, Thoene JG, Gahl WA, Schneider JA. A comparison of the effectiveness of cysteamine and phosphocysteamine in elevating plasma cysteamine concentration and decreasing leukocyte free cystine in nephropathic cystinosis. Pediatr Res 1988;23:616-20. 9. Sonies B, Ekman EF, Andersson H, Adamson M, Kaler S, Markello T, et al. Swallowing dysfunction in nephropathic cystinosis. N Engl J Med 1990; 323:565-70. 10. Dohil R, Newbury R, Sellers Z, Deutsch R, Schneider JA. The evaluation and treatment of gastrointestinal disease in children with cystinosis receiving cysteamine. J Pediatr 2003;143:224-30.

The Journal of Pediatrics  October 2004