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P Trioche

Showing results (11-20 of 23) with videos related to

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Archives of Disease in Childhood|September 18, 1999
Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert syndromeP Trioche, J Chalas, J Francoual, et al.
American Journal of Medical Genetics|December 31, 1997
Severe brain and limb defects with possible autosomal recessive inheritance: a series of six cases and review of the literatureP Labrune, P Trioche, C Fallet-Bianco, et al.
European Journal of Pediatrics|September 15, 1999
Haemolytic uraemic syndrome and pulmonary hypertension in a patient with methionine synthase deficiencyP Labrune, J Zittoun, I Duvaltier, et al.
Prenatal Diagnosis|July 17, 1998
Prenatal diagnosis of glycogen storage disease type Ia by restriction enzyme digestionP Trioche, J Francoual, F Audibert, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Allelic heterogeneity of glycogen storage disease type Ib in French patients: a study of 11 casesP Trioche, F Petit, J Francoual, et al.
Human Mutation|November 3, 2000
Genetic heterogeneity of glycogen storage disease type Ia in France: a study of 48 patientsP Trioche, J Francoual, J Chalas, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 6, 2005
[Factors predicting serious bacterial infections in febrile infants less than three months old: multivariate analysis]V Gajdos, L Foix L'Hélias, A Mollet-Boudjemline, et al.
American Journal of Medical Genetics|December 10, 1999
Jeune syndrome and liver disease: report of three cases treated with ursodeoxycholic acidP Labrune, M Fabre, P Trioche, et al.
Joint Bone Spine|April 26, 2003
Gouty tendinitis revealing glycogen storage disease Type Ia in two adolescentsCéline Carvès, Anne Duquenoy, Fabienne Toutain, et al.
Gastroenterologie Clinique Et Biologique|August 25, 2001
[Genetic incidence of Gilbert's syndrome in France]B Le Bihan-Levaufre, J Francoual, J Chalas, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Archives of Disease in Childhood|September 18, 1999
Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert syndromeP Trioche, J Chalas, J Francoual, et al.
American Journal of Medical Genetics|December 31, 1997
Severe brain and limb defects with possible autosomal recessive inheritance: a series of six cases and review of the literatureP Labrune, P Trioche, C Fallet-Bianco, et al.
European Journal of Pediatrics|September 15, 1999
Haemolytic uraemic syndrome and pulmonary hypertension in a patient with methionine synthase deficiencyP Labrune, J Zittoun, I Duvaltier, et al.
Prenatal Diagnosis|July 17, 1998
Prenatal diagnosis of glycogen storage disease type Ia by restriction enzyme digestionP Trioche, J Francoual, F Audibert, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Allelic heterogeneity of glycogen storage disease type Ib in French patients: a study of 11 casesP Trioche, F Petit, J Francoual, et al.
Human Mutation|November 3, 2000
Genetic heterogeneity of glycogen storage disease type Ia in France: a study of 48 patientsP Trioche, J Francoual, J Chalas, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 6, 2005
[Factors predicting serious bacterial infections in febrile infants less than three months old: multivariate analysis]V Gajdos, L Foix L'Hélias, A Mollet-Boudjemline, et al.
American Journal of Medical Genetics|December 10, 1999
Jeune syndrome and liver disease: report of three cases treated with ursodeoxycholic acidP Labrune, M Fabre, P Trioche, et al.
Joint Bone Spine|April 26, 2003
Gouty tendinitis revealing glycogen storage disease Type Ia in two adolescentsCéline Carvès, Anne Duquenoy, Fabienne Toutain, et al.
Gastroenterologie Clinique Et Biologique|August 25, 2001
[Genetic incidence of Gilbert's syndrome in France]B Le Bihan-Levaufre, J Francoual, J Chalas, et al.
Pageof 3