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Results: 5

Authors: SNYDERMAN SE SANSARICQ C MIDDLETON B
Citation: Se. Snyderman et al., SUCCINYL-COA-3-KETOACID COA-TRANSFERASE DEFICIENCY, Pediatrics, 101(4), 1998, pp. 709-711

Authors: SNYDERMAN SE SANSARICQ C
Citation: Se. Snyderman et C. Sansaricq, NEWBORN SCREENING FOR HOMOCYSTINURIA, Early human development, 48(1-2), 1997, pp. 203-207

Authors: SANSARICQ C HEILBRONER P SNYDERMAN SE FISH I FOREM S
Citation: C. Sansaricq et al., A CASE OF 2-METHYL, 3-HYDROXY BUTYRYL-COA DEHYDROGENASE-DEFICIENCY, Annals of neurology, 40(2), 1996, pp. 124-124

Authors: AWAAD Y SANSARICQ C MORONEY J FISH I KYRIAKAKOS A SNYDERMAN SE
Citation: Y. Awaad et al., BACLOFEN IN THE TREATMENT OF POLYMYOCLONUS AND ATAXIA IN A PATIENT WITH HOMOCYSTINURIA, Journal of child neurology, 10(4), 1995, pp. 294-296

Authors: UCHINO T SNYDERMAN SE LAMBERT M QURESHI IA SHAPIRA SK SANSARICQ C SMIT LME JAKOBS C MATSUDA I
Citation: T. Uchino et al., MOLECULAR-BASIS OF PHENOTYPIC VARIATION IN PATIENTS WITH ARGININEMIA, Human genetics, 96(3), 1995, pp. 255-260
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