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P Divry

Showing results (51-60 of 114) with videos related to

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Archives Francaises De Pediatrie|August 1, 1981
[Plasma concentrations of amino acids, urea nitrogen and ammonia in 1 to 2 month-old low birth weight premature infant (author's transl)]L Sann, D Rigal, P Divry, et al.
Medecine Legale Et Dommage Corporel|October 1, 1974
[Case of fatal trichloroethane 1,1,1 poisoning]J M Rouzioux, H Thozet, P Divry, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
N-acetylaspartic aciduria: report of three new cases in children with a neurological syndrome associating macrocephaly and leukodystrophyP Divry, C Vianey-Liaud, C Gay, et al.
Archives Francaises De Pediatrie|March 1, 1975
[A form of late propionic acidemia]P Guibaud, P Divry, G Marcon, et al.
Pediatrie|January 1, 1993
[Citrullinemia: management and clinical course. Apropos of a familial case]C Gay, H Tronchon, P Divry, et al.
Journal of Inherited Metabolic Disease|January 1, 1978
Propionyl-CoA-carboxylase determination: study of enzyme parameters in cultured skin fibroblasts from enzyme-deficient and normal subjectsP Divry, M O Rolland, N Dingeon, et al.
Pediatric Neurology|May 1, 1993
Mevalonic aciduria in 3 siblings: a new recognizable metabolic encephalopathyJ Mancini, N Philip, B Chabrol, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Canavan disease: findings in four new casesH Michelakakis, S Giouroukos, P Divry, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Diagnosis of inborn errors of metabolism by acylcarnitine profiling in blood using tandem mass spectrometryC Vianey-Saban, N Guffon, F Delolne, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
A new case of methylmalonic aciduria with unexplained negative urinary methylmalonic colorimetric testC Charpentier, M Coude, J L Perignon, et al.
Pageof 12

Showing results (51-60 of 114) with videos related to

Sort By:
Pageof 12
Archives Francaises De Pediatrie|August 1, 1981
[Plasma concentrations of amino acids, urea nitrogen and ammonia in 1 to 2 month-old low birth weight premature infant (author's transl)]L Sann, D Rigal, P Divry, et al.
Medecine Legale Et Dommage Corporel|October 1, 1974
[Case of fatal trichloroethane 1,1,1 poisoning]J M Rouzioux, H Thozet, P Divry, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
N-acetylaspartic aciduria: report of three new cases in children with a neurological syndrome associating macrocephaly and leukodystrophyP Divry, C Vianey-Liaud, C Gay, et al.
Archives Francaises De Pediatrie|March 1, 1975
[A form of late propionic acidemia]P Guibaud, P Divry, G Marcon, et al.
Pediatrie|January 1, 1993
[Citrullinemia: management and clinical course. Apropos of a familial case]C Gay, H Tronchon, P Divry, et al.
Journal of Inherited Metabolic Disease|January 1, 1978
Propionyl-CoA-carboxylase determination: study of enzyme parameters in cultured skin fibroblasts from enzyme-deficient and normal subjectsP Divry, M O Rolland, N Dingeon, et al.
Pediatric Neurology|May 1, 1993
Mevalonic aciduria in 3 siblings: a new recognizable metabolic encephalopathyJ Mancini, N Philip, B Chabrol, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Canavan disease: findings in four new casesH Michelakakis, S Giouroukos, P Divry, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Diagnosis of inborn errors of metabolism by acylcarnitine profiling in blood using tandem mass spectrometryC Vianey-Saban, N Guffon, F Delolne, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
A new case of methylmalonic aciduria with unexplained negative urinary methylmalonic colorimetric testC Charpentier, M Coude, J L Perignon, et al.
Pageof 12