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H Ogier

Showing results (11-20 of 127) with videos related to

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Archives Francaises De Pediatrie|January 1, 1983
[Phenylalanine-restricted diet. The portion-by-weight system]E Depondt, H Ogier, A Munnich, et al.
Molecular Genetics and Metabolism|April 5, 2001
Long-term treatment with sodium phenylbutyrate in ornithine transcarbamylase-deficient patientsA B Burlina, H Ogier, H Korall, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 1999
[Favorable outcome of treatment with NTBC of acute liver insufficiency disclosing hereditary tyrosinemia type I]E Barkaoui, D Debray, D Habès, et al.
European Journal of Pediatrics|March 1, 1992
Nutritional vitamin B12 deficiency: two cases detected by routine newborn urinary screeningJ L Michaud, B Lemieux, H Ogier, et al.
European Journal of Pediatrics|May 20, 1998
Remethylation defects: guidelines for clinical diagnosis and treatmentH Ogier de Baulny, M Gérard, J M Saudubray, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 1999
[Diagnosis of states of ketosis in pediatrics]H Ogier de Baulny, I Husson, P Castelnau, et al.
Progress in Clinical and Biological Research|January 1, 1982
New trends in the treatment of inborn errors of metabolism: an overviewJ Frézal, A Munnich, H Ogier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 27, 2010
[Should a metabolic work-up be performed in autism?]M Schiff, R Delorme, J-F Benoist, et al.
Human Pathology|May 1, 1992
A congenital anomaly of vitamin B12 metabolism: a study of three casesP Russo, J Doyon, E Sonsino, et al.
Revue D'Electroencephalographie Et De Neurophysiologie Clinique|December 1, 1981
[Convulsive seizures in the neonatal metabolic diseases (author's transl)]F Moussalli-Salefranque, J Mises, P Plouin, et al.
Pageof 13

Showing results (11-20 of 127) with videos related to

Sort By:
Pageof 13
Archives Francaises De Pediatrie|January 1, 1983
[Phenylalanine-restricted diet. The portion-by-weight system]E Depondt, H Ogier, A Munnich, et al.
Molecular Genetics and Metabolism|April 5, 2001
Long-term treatment with sodium phenylbutyrate in ornithine transcarbamylase-deficient patientsA B Burlina, H Ogier, H Korall, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 1999
[Favorable outcome of treatment with NTBC of acute liver insufficiency disclosing hereditary tyrosinemia type I]E Barkaoui, D Debray, D Habès, et al.
European Journal of Pediatrics|March 1, 1992
Nutritional vitamin B12 deficiency: two cases detected by routine newborn urinary screeningJ L Michaud, B Lemieux, H Ogier, et al.
European Journal of Pediatrics|May 20, 1998
Remethylation defects: guidelines for clinical diagnosis and treatmentH Ogier de Baulny, M Gérard, J M Saudubray, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 1999
[Diagnosis of states of ketosis in pediatrics]H Ogier de Baulny, I Husson, P Castelnau, et al.
Progress in Clinical and Biological Research|January 1, 1982
New trends in the treatment of inborn errors of metabolism: an overviewJ Frézal, A Munnich, H Ogier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 27, 2010
[Should a metabolic work-up be performed in autism?]M Schiff, R Delorme, J-F Benoist, et al.
Human Pathology|May 1, 1992
A congenital anomaly of vitamin B12 metabolism: a study of three casesP Russo, J Doyon, E Sonsino, et al.
Revue D'Electroencephalographie Et De Neurophysiologie Clinique|December 1, 1981
[Convulsive seizures in the neonatal metabolic diseases (author's transl)]F Moussalli-Salefranque, J Mises, P Plouin, et al.
Pageof 13