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Pediatric Research
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September 1, 1984
The relationship between the branched chain amino acids and their alpha-ketoacids in maple syrup urine disease
S E Snyderman, F Goldstein, C Sansaricq, et al.
Pediatrics
|
December 1, 1972
The use of neomycin in the treatment of methylmalonic aciduria
S 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 period
S 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 family
C 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 neurotoxicity
J Korein, C Sansaricq, M Kalmijn, et al.
Acta Paediatrica Scandinavica
|
March 1, 1975
Cystine deficiency during dietotherapy of homocystinemia
C Sansaricq, S Garg, P M Norton, et al.
Clinical Pediatrics
|
August 1, 1984
Familial congenital short small bowel with associated defects. A long-term survival
C Sansaricq, W J Chen, M Manka, et al.
Molecular Genetics and Metabolism
|
December 14, 2005
Cerebral glucose metabolism in adults with early treated classic phenylketonuria
M 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 homocystinuria
Y Awaad, C Sansaricq, J Moroney, et al.
Archives of Dermatology
|
September 1, 1977
Azaribine, homocystinemia, and thrombosis
J L Shupack, A J Grieco, A M Epstein, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 32) with videos related to
Sort By:
Page
of 4
Pediatric Research
|
September 1, 1984
The relationship between the branched chain amino acids and their alpha-ketoacids in maple syrup urine disease
S E Snyderman, F Goldstein, C Sansaricq, et al.
Pediatrics
|
December 1, 1972
The use of neomycin in the treatment of methylmalonic aciduria
S 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 period
S 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 family
C 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 neurotoxicity
J Korein, C Sansaricq, M Kalmijn, et al.
Acta Paediatrica Scandinavica
|
March 1, 1975
Cystine deficiency during dietotherapy of homocystinemia
C Sansaricq, S Garg, P M Norton, et al.
Clinical Pediatrics
|
August 1, 1984
Familial congenital short small bowel with associated defects. A long-term survival
C Sansaricq, W J Chen, M Manka, et al.
Molecular Genetics and Metabolism
|
December 14, 2005
Cerebral glucose metabolism in adults with early treated classic phenylketonuria
M 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 homocystinuria
Y Awaad, C Sansaricq, J Moroney, et al.
Archives of Dermatology
|
September 1, 1977
Azaribine, homocystinemia, and thrombosis
J L Shupack, A J Grieco, A M Epstein, et al.
Page
of 4