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C Sansaricq

Showing results (11-20 of 32) with videos related to

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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.
Pediatrics|December 1, 1972
The use of neomycin in the treatment of methylmalonic aciduriaS E Snyderman, C Sansaricq, P Norton, 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.
Journal of Inherited Metabolic Disease|April 8, 2006
Biochemical and molecular diagnosis of lipoamide dehydrogenase deficiency in a North American Ashkenazi Jewish familyC Sansaricq, S Pardo, M Balwani, et al.
The International Journal of Neuroscience|November 1, 1994
Maple syrup urine disease: clinical, EEG, and plasma amino acid correlations with a theoretical mechanism of acute neurotoxicityJ Korein, C Sansaricq, M Kalmijn, et al.
Acta Paediatrica Scandinavica|March 1, 1975
Cystine deficiency during dietotherapy of homocystinemiaC Sansaricq, S Garg, P M Norton, et al.
Clinical Pediatrics|August 1, 1984
Familial congenital short small bowel with associated defects. A long-term survivalC Sansaricq, W J Chen, M Manka, 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.
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.
Archives of Dermatology|September 1, 1977
Azaribine, homocystinemia, and thrombosisJ L Shupack, A J Grieco, A M Epstein, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
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.
Pediatrics|December 1, 1972
The use of neomycin in the treatment of methylmalonic aciduriaS E Snyderman, C Sansaricq, P Norton, 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.
Journal of Inherited Metabolic Disease|April 8, 2006
Biochemical and molecular diagnosis of lipoamide dehydrogenase deficiency in a North American Ashkenazi Jewish familyC Sansaricq, S Pardo, M Balwani, et al.
The International Journal of Neuroscience|November 1, 1994
Maple syrup urine disease: clinical, EEG, and plasma amino acid correlations with a theoretical mechanism of acute neurotoxicityJ Korein, C Sansaricq, M Kalmijn, et al.
Acta Paediatrica Scandinavica|March 1, 1975
Cystine deficiency during dietotherapy of homocystinemiaC Sansaricq, S Garg, P M Norton, et al.
Clinical Pediatrics|August 1, 1984
Familial congenital short small bowel with associated defects. A long-term survivalC Sansaricq, W J Chen, M Manka, 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.
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.
Archives of Dermatology|September 1, 1977
Azaribine, homocystinemia, and thrombosisJ L Shupack, A J Grieco, A M Epstein, et al.
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