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Seminars in Neonatology : SN|June 19, 2002
Branched-chain organic aciduriasH Ogier de Baulny, J M SaudubrayEuropean 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|May 7, 1999
[Severe lactic acidosis disease disclosing milk-protein intolerance to cows' milk]C Rizk, L Valdes, H Ogier de Baulny, et al.Journal of Inherited Metabolic Disease|May 4, 2005
Methylmalonic and propionic acidaemias: management and outcomeH Ogier de Baulny, J F Benoist, O Rigal, et al.European Journal of Pediatrics|September 4, 1998
Long-term treatment of persistent hyperinsulinaemic hypoglycaemia of infancy with diazoxide: a retrospective review of 77 cases and analysis of efficacy-predicting criteriaG Touati, F Poggi-Travert, H Ogier de Baulny, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 11, 2002
[Hematologic manifestations of inborn errors of metabolism]P de Lonlay, O Fenneteau, G Touati, et al.Molecular Genetics and Metabolism|September 15, 2011
Molecular characterization of 82 patients with pyruvate dehydrogenase complex deficiency. Structural implications of novel amino acid substitutions in E1 proteinA Imbard, A Boutron, C Vequaud, et al.Annales De Dermatologie Et De Venereologie|March 30, 1999
[Extensive Mongolian spot related to Hurler disease]M Rybojad, I Moraillon, H Ogier de Baulny, et al.Journal of Inherited Metabolic Disease|June 10, 2006
Methylmalonic and propionic acidurias: management without or with a few supplements of specific amino acid mixtureG Touati, V Valayannopoulos, K Mention, et al.Archives of Disease in Childhood|January 1, 1997
In vivo functional investigations of lactic acid in patients with respiratory chain disordersG Touati, O Rigal, A Lombès, et al.Pageof 28