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H Ogier de Baulny

Showing results (1-10 of 34) with videos related to

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Seminars in Neonatology : SN|June 19, 2002
Branched-chain organic aciduriasH Ogier de Baulny, J M Saudubray
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.
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.
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.
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.
Journal of Inherited Metabolic Disease|October 13, 2009
Mitochondria and diabetes mellitus: untangling a conflictive relationship?M Schiff, S Loublier, A Coulibaly, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|October 2, 2007
[Mitochondrial neurogastrointestinal encephalomyopathy]P Rousset, M Elmaleh-Bergès, H Ogier de Baulny, et al.
The Journal of Pediatrics|November 1, 1995
Neonatal hyperammonemia caused by a defect of carnitine-acylcarnitine translocaseH Ogier de Baulny, A Slama, G Touati, et al.
Journal of Inherited Metabolic Disease|May 11, 1999
Holocarboxylase synthetase deficiency: report of a case with onset in late infancyE Touma, T Suormala, E R Baumgartner, 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.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Seminars in Neonatology : SN|June 19, 2002
Branched-chain organic aciduriasH Ogier de Baulny, J M Saudubray
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.
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.
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.
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.
Journal of Inherited Metabolic Disease|October 13, 2009
Mitochondria and diabetes mellitus: untangling a conflictive relationship?M Schiff, S Loublier, A Coulibaly, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|October 2, 2007
[Mitochondrial neurogastrointestinal encephalomyopathy]P Rousset, M Elmaleh-Bergès, H Ogier de Baulny, et al.
The Journal of Pediatrics|November 1, 1995
Neonatal hyperammonemia caused by a defect of carnitine-acylcarnitine translocaseH Ogier de Baulny, A Slama, G Touati, et al.
Journal of Inherited Metabolic Disease|May 11, 1999
Holocarboxylase synthetase deficiency: report of a case with onset in late infancyE Touma, T Suormala, E R Baumgartner, 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.
Pageof 4