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Results:
1-5
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Results: 5
SUCCINYL-COA-3-KETOACID COA-TRANSFERASE DEFICIENCY
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
NEWBORN SCREENING FOR HOMOCYSTINURIA
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
A CASE OF 2-METHYL, 3-HYDROXY BUTYRYL-COA DEHYDROGENASE-DEFICIENCY
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
BACLOFEN IN THE TREATMENT OF POLYMYOCLONUS AND ATAXIA IN A PATIENT WITH HOMOCYSTINURIA
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
MOLECULAR-BASIS OF PHENOTYPIC VARIATION IN PATIENTS WITH ARGININEMIA
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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