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Journal of Inherited Metabolic Disease
|
January 1, 1989
Crigler-Najjar type II disease inheritance: a family study
P 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 B
P 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 infection
P 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 gene
F 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 cases
P 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 patients
P 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 deficiency
P Labrune, J Zittoun, I Duvaltier, et al.
Page
of 13
Search research articles
Search
Showing results (61-70 of 122) with videos related to
Sort By:
Page
of 13
Journal of Inherited Metabolic Disease
|
January 1, 1989
Crigler-Najjar type II disease inheritance: a family study
P 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 B
P 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 infection
P 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 gene
F 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 cases
P 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 patients
P 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 deficiency
P Labrune, J Zittoun, I Duvaltier, et al.
Page
of 13