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P Trioche

Showing results (1-10 of 23) with videos related to

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La Revue Du Praticien|March 21, 1998
[Neonatal jaundice. Physiopathology, etiology, diagnosis]P Trioche, P Labrune
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Gilbert's disease in 1998]P Labrune, P Trioche
European Journal of Pediatrics|November 1, 1996
Ondansetron for pruritus in child with chronic cholestasisP Trioche, D Samuel, M Odièvre, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 1, 1997
Hepatocellular adenomas in glycogen storage disease type I and III: a series of 43 patients and review of the literatureP Labrune, P Trioche, I Duvaltier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 30, 2007
[Hepatomegaly: diagnosis approach]P Labrune, P Trioche-Eberschweiler, A Mollet-Boudjemline, et al.
Human Mutation|August 14, 1999
Identification of three novel mutations (Q54P, W70X and T108I) in the glucose-6-phosphatase gene of patients with glycogen storage disease type Ia. Mutation in brief no. 256. OnlineP Trioche, J Francoual, J Chalas, et al.
Journal of Inherited Metabolic Disease|May 9, 2000
Apolipoprotein E polymorphism and serum concentrations in patients with glycogen storage disease type IaP Trioche, J Francoual, L Capel, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 15, 2000
Azathioprine-induced lung toxicity and efficacy of cyclosporin A in a young girl with type 2 autoimmune hepatitisF Perreaux, D Zenaty, F Capron, et al.
Hypertension in Pregnancy|December 10, 1999
Implication of apolipoprotein E and the L-arginine-nitric oxide system in preeclampsiaJ Francoual, F Audibert, C Claise, et al.
Neuropediatrics|April 1, 1997
Moyamoya disease in a child with glycogen storage disease type IaF Goutières, M Bourgeois, P Trioche, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
La Revue Du Praticien|March 21, 1998
[Neonatal jaundice. Physiopathology, etiology, diagnosis]P Trioche, P Labrune
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Gilbert's disease in 1998]P Labrune, P Trioche
European Journal of Pediatrics|November 1, 1996
Ondansetron for pruritus in child with chronic cholestasisP Trioche, D Samuel, M Odièvre, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 1, 1997
Hepatocellular adenomas in glycogen storage disease type I and III: a series of 43 patients and review of the literatureP Labrune, P Trioche, I Duvaltier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 30, 2007
[Hepatomegaly: diagnosis approach]P Labrune, P Trioche-Eberschweiler, A Mollet-Boudjemline, et al.
Human Mutation|August 14, 1999
Identification of three novel mutations (Q54P, W70X and T108I) in the glucose-6-phosphatase gene of patients with glycogen storage disease type Ia. Mutation in brief no. 256. OnlineP Trioche, J Francoual, J Chalas, et al.
Journal of Inherited Metabolic Disease|May 9, 2000
Apolipoprotein E polymorphism and serum concentrations in patients with glycogen storage disease type IaP Trioche, J Francoual, L Capel, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 15, 2000
Azathioprine-induced lung toxicity and efficacy of cyclosporin A in a young girl with type 2 autoimmune hepatitisF Perreaux, D Zenaty, F Capron, et al.
Hypertension in Pregnancy|December 10, 1999
Implication of apolipoprotein E and the L-arginine-nitric oxide system in preeclampsiaJ Francoual, F Audibert, C Claise, et al.
Neuropediatrics|April 1, 1997
Moyamoya disease in a child with glycogen storage disease type IaF Goutières, M Bourgeois, P Trioche, et al.
Pageof 3