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P Labrune

Showing results (61-70 of 122) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1989
Crigler-Najjar type II disease inheritance: a family studyP Labrune, A Myara, C Hennion, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 1, 1991
Fatal liver failure in two children with Niemann-Pick disease type BP Labrune, P Bedossa, P Huguet, et al.
Archives Francaises De Pediatrie|March 1, 1990
[Sclerosing cholangitis revealing histiocytosis X]I Neveu, P Labrune, P Huguet, et al.
Acta Paediatrica Scandinavica|June 1, 1990
Recurrent enterocolitis-like symptoms as the possible presenting manifestations of neonatal Brucella melitensis infectionP Labrune, B Jabir, J F Magny, et al.
Clinical Genetics|May 23, 2006
Crigler-Najjar type II syndrome may result from several types and combinations of mutations in the UGT1A1 geneF Petit, V Gajdos, L Capel, 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.
Archives Francaises De Pediatrie|May 1, 1986
[Medical treatment of staphylococcal epiduritis]B Bader, P Labrune, M Zerah, 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.
Pageof 13

Showing results (61-70 of 122) with videos related to

Sort By:
Pageof 13
Journal of Inherited Metabolic Disease|January 1, 1989
Crigler-Najjar type II disease inheritance: a family studyP Labrune, A Myara, C Hennion, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 1, 1991
Fatal liver failure in two children with Niemann-Pick disease type BP Labrune, P Bedossa, P Huguet, et al.
Archives Francaises De Pediatrie|March 1, 1990
[Sclerosing cholangitis revealing histiocytosis X]I Neveu, P Labrune, P Huguet, et al.
Acta Paediatrica Scandinavica|June 1, 1990
Recurrent enterocolitis-like symptoms as the possible presenting manifestations of neonatal Brucella melitensis infectionP Labrune, B Jabir, J F Magny, et al.
Clinical Genetics|May 23, 2006
Crigler-Najjar type II syndrome may result from several types and combinations of mutations in the UGT1A1 geneF Petit, V Gajdos, L Capel, 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.
Archives Francaises De Pediatrie|May 1, 1986
[Medical treatment of staphylococcal epiduritis]B Bader, P Labrune, M Zerah, 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.
Pageof 13