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Early Human Development|April 25, 1997
Newborn screening for homocystinuriaS E Snyderman, C SansaricqPediatric Research|June 1, 2001
Influence of metabolic control on growth in homocystinuria due to cystathionine B-synthase deficiencyA K Topaloglu, C Sansaricq, S E SnydermanJournal of Inherited Metabolic Disease|January 1, 1987
Successful long term therapy of biopterin deficiencyS E Snyderman, C Sansaricq, M T PulmonesAmerican Journal of Medical Genetics|November 1, 1992
Comparison of phenylketonuric and nonphenylketonuric sibs from untreated pregnancies in a mother with phenylketonuriaH L Levy, D Lobbregt, C Sansaricq, et al.The Journal of Pediatrics|November 1, 1979
The nutritional therapy of histidinemiaS E Snyderman, C Sansaricq, P M Norton, et al.Pediatric Research|September 1, 1984
The relationship between the branched chain amino acids and their alpha-ketoacids in maple syrup urine diseaseS E Snyderman, F Goldstein, C Sansaricq, et al.The Journal of Pediatrics|July 1, 1981
Plasma and cerebrospinal fluid amino acid concentrations in phenylketonuria during the newborn periodS E Snyderman, C Sansaricq, P M Norton, et al.Molecular Genetics and Metabolism|December 14, 2005
Cerebral glucose metabolism in adults with early treated classic phenylketonuriaM P Wasserstein, S E Snyderman, C Sansaricq, et al.Acta Paediatrica Scandinavica|March 1, 1975
Cystine deficiency during dietotherapy of homocystinemiaC Sansaricq, S Garg, P M Norton, et al.Journal of Child Neurology|July 1, 1995
Baclofen in the treatment of polymyoclonus and ataxia in a patient with homocystinuriaY Awaad, C Sansaricq, J Moroney, et al.Pageof 3