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Journal of Pediatric Gastroenterology and Nutrition|May 1, 1988
Cholesterol ester storage disease: clinical, biochemical, and pathological studies of four new casesD D'Agostino, L Bay, G Gallo, et al.Developmental Medicine and Child Neurology|December 1, 1991
Krabbe disease in monozygotic tripletsH A Arroyo, J Grippo, A Taratuto, et al.The American Journal of Pediatric Hematology/Oncology|January 1, 1983
Neuropsychological study in patients with ALL. Two different CNS prevention therapies--cranial irradiation plus IT methotrexate vs. IT methotrexate aloneS Pavlovsky, N Fisman, R Arizaga, et al.American Journal of Medical Genetics|June 13, 1997
Patient with an Xp21 contiguous gene deletion syndrome in association with agenesis of the corpus callosumS E Baranzini, G del Rey, N Nigro, et al.Medicina|January 1, 1992
[Chronic hexosaminidase A deficiency associated with pure sensory peripheral neuropathy]R E Sica, M I García Erro, H A Molina, et al.European Journal of Pediatrics|February 1, 2000
Familial neonatal SIDS revealing carnitine-acylcarnitine translocase deficiencyJ M Nuoffer, P de Lonlay, C Costa, et al.Artificial Organs|August 9, 2001
Culture of porcine hepatocytes: the dogma of exogenous matrix revisitedA Lorenti, M Barbich, A Hidalgo, et al.American Journal of Medical Genetics|December 18, 1998
Mutation analysis of Gaucher disease patients from Argentina: high prevalence of the RecNciI mutationB Cormand, T L Harboe, L Gort, et al.Medicina|January 1, 1997
[Severe cardiac failure in Kearns-Sayre syndrome]D Consalvo, F Villegas, A M Villa, et al.Medicina|January 1, 1996
[Autoimmune hypoglycemia syndrome with specific anti-human insulin antibodies]J C Cresto, J E Abdenur, N Chamoles, et al.Pageof 2