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H Ogier

Showing results (21-30 of 127) with videos related to

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Archives Francaises De Pediatrie|March 1, 1987
[Hemorrhagic shock syndrome with encephalopathy]F Hervé, H Bakchine, H Le Loc'h, et al.
Annales De Medecine Interne|January 1, 1987
[Research methods in metabolic myopathies in children]A Lombes, H Ogier, J P Bonnefont, et al.
Skeletal Radiology|March 21, 1998
Carbohydrate-deficient glycoprotein syndrome type I: a new cause of dysostosis multiplexC Garel, C Baumann, M Besnard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Protein glycosylation deficiency: clinical presentation]H Ogier de Baulny, F Poggi-Travert, M Besnard, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 15, 2001
Infantile spasms and Menkes diseaseI Sfaello, P Castelnau, N Blanc, 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 Francaises De Pediatrie|November 1, 1993
[Neonatal hemolytic-uremic syndrome, methylmalonic aciduria and homocystinuria caused by intracellular vitamin B 12 deficiency. Value of etiological diagnosis]C Chenel, C Wood, E Gourrier, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1985
Anatomo-pathological findings in a case of combined deficiency of sulphite oxidase and xanthine oxidase with a defect of molybdenum cofactorA Roth, C Nogues, J P Monnet, et al.
European Journal of Biochemistry|July 15, 1987
Dietary and hormonal regulation of L-type pyruvate kinase gene expression in rat small intestineH Ogier, A Munnich, S Lyonnet, et al.
Annales De Medecine Interne|January 1, 1980
[Alopecia, chronic candidodis, mental retardation and repeated ketoacidosic comas curable by biotin administration: multiple carboxylases deficiency (author's transl)]A Munnich, J M Saudubray, H Ogier, et al.
Pageof 13

Showing results (21-30 of 127) with videos related to

Sort By:
Pageof 13
Archives Francaises De Pediatrie|March 1, 1987
[Hemorrhagic shock syndrome with encephalopathy]F Hervé, H Bakchine, H Le Loc'h, et al.
Annales De Medecine Interne|January 1, 1987
[Research methods in metabolic myopathies in children]A Lombes, H Ogier, J P Bonnefont, et al.
Skeletal Radiology|March 21, 1998
Carbohydrate-deficient glycoprotein syndrome type I: a new cause of dysostosis multiplexC Garel, C Baumann, M Besnard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Protein glycosylation deficiency: clinical presentation]H Ogier de Baulny, F Poggi-Travert, M Besnard, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 15, 2001
Infantile spasms and Menkes diseaseI Sfaello, P Castelnau, N Blanc, 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 Francaises De Pediatrie|November 1, 1993
[Neonatal hemolytic-uremic syndrome, methylmalonic aciduria and homocystinuria caused by intracellular vitamin B 12 deficiency. Value of etiological diagnosis]C Chenel, C Wood, E Gourrier, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1985
Anatomo-pathological findings in a case of combined deficiency of sulphite oxidase and xanthine oxidase with a defect of molybdenum cofactorA Roth, C Nogues, J P Monnet, et al.
European Journal of Biochemistry|July 15, 1987
Dietary and hormonal regulation of L-type pyruvate kinase gene expression in rat small intestineH Ogier, A Munnich, S Lyonnet, et al.
Annales De Medecine Interne|January 1, 1980
[Alopecia, chronic candidodis, mental retardation and repeated ketoacidosic comas curable by biotin administration: multiple carboxylases deficiency (author's transl)]A Munnich, J M Saudubray, H Ogier, et al.
Pageof 13