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H Ogier

Showing results (71-80 of 127) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1994
[Mid-term outcome of 2 cases with maple syrup urine disease: role of liver transplantation in the treatment]J C Netter, G Cossarizza, C Narcy, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Functional characterization of novel mutations in the human cytochrome b geneF Legros, E Chatzoglou, P Frachon, et al.
Archives Francaises De Pediatrie|December 1, 1981
[Lysinuric protein intolerance: a severe hyperammonemia secondary to l-arginine deficiency (author's transl)]]F X Coude, H Ogier, C Charpentier, et al.
Histochemistry and Cell Biology|January 1, 1995
Immunohistochemical analysis of muscle cytochrome c oxidase deficiency in childrenS Possekel, A Lombes, H Ogier de Baulny, et al.
The Journal of Pediatrics|May 1, 1983
Diet-responsive proconvertin (factor VII) deficiency in homocystinuriaA Munnich, J M Saudubray, M D Dautzenberg, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|December 1, 1985
Absence of hepatic peroxisomes in a case of infantile Refsum's diseaseH Ogier, F Roels, A Cornelis, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 24, 2011
[Sjögren-Larsson syndrome: 2 case reports]C Galoin-Bertail, H Ogier de Baulny, R Wanders, et al.
Human Genetics|January 1, 1981
Neonatal glutaric aciduria type II: an X-linked recessive inherited disorderF X Coude, H Ogier, C Charpentier, et al.
Lancet (London, England)|December 10, 1983
Antenatal diagnosis of combined xanthine and sulphite oxidase deficienciesH Ogier, S K Wadman, J L Johnson, et al.
Journal of Inherited Metabolic Disease|April 22, 2009
Early-onset hyperargininaemia: a severe disorder?M Schiff, J-F Benoist, M L Cardoso, et al.
Pageof 13

Showing results (71-80 of 127) with videos related to

Sort By:
Pageof 13
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1994
[Mid-term outcome of 2 cases with maple syrup urine disease: role of liver transplantation in the treatment]J C Netter, G Cossarizza, C Narcy, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Functional characterization of novel mutations in the human cytochrome b geneF Legros, E Chatzoglou, P Frachon, et al.
Archives Francaises De Pediatrie|December 1, 1981
[Lysinuric protein intolerance: a severe hyperammonemia secondary to l-arginine deficiency (author's transl)]]F X Coude, H Ogier, C Charpentier, et al.
Histochemistry and Cell Biology|January 1, 1995
Immunohistochemical analysis of muscle cytochrome c oxidase deficiency in childrenS Possekel, A Lombes, H Ogier de Baulny, et al.
The Journal of Pediatrics|May 1, 1983
Diet-responsive proconvertin (factor VII) deficiency in homocystinuriaA Munnich, J M Saudubray, M D Dautzenberg, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|December 1, 1985
Absence of hepatic peroxisomes in a case of infantile Refsum's diseaseH Ogier, F Roels, A Cornelis, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 24, 2011
[Sjögren-Larsson syndrome: 2 case reports]C Galoin-Bertail, H Ogier de Baulny, R Wanders, et al.
Human Genetics|January 1, 1981
Neonatal glutaric aciduria type II: an X-linked recessive inherited disorderF X Coude, H Ogier, C Charpentier, et al.
Lancet (London, England)|December 10, 1983
Antenatal diagnosis of combined xanthine and sulphite oxidase deficienciesH Ogier, S K Wadman, J L Johnson, et al.
Journal of Inherited Metabolic Disease|April 22, 2009
Early-onset hyperargininaemia: a severe disorder?M Schiff, J-F Benoist, M L Cardoso, et al.
Pageof 13