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Archives of Disease in Childhood
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September 18, 1999
Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert syndrome
P 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 literature
P 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 deficiency
P Labrune, J Zittoun, I Duvaltier, et al.
Prenatal Diagnosis
|
July 17, 1998
Prenatal diagnosis of glycogen storage disease type Ia by restriction enzyme digestion
P 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 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.
American Journal of Medical Genetics
|
December 10, 1999
Jeune syndrome and liver disease: report of three cases treated with ursodeoxycholic acid
P Labrune, M Fabre, P Trioche, et al.
Joint Bone Spine
|
April 26, 2003
Gouty tendinitis revealing glycogen storage disease Type Ia in two adolescents
Céline 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.
Page
of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
Archives of Disease in Childhood
|
September 18, 1999
Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert syndrome
P 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 literature
P 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 deficiency
P Labrune, J Zittoun, I Duvaltier, et al.
Prenatal Diagnosis
|
July 17, 1998
Prenatal diagnosis of glycogen storage disease type Ia by restriction enzyme digestion
P 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 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.
American Journal of Medical Genetics
|
December 10, 1999
Jeune syndrome and liver disease: report of three cases treated with ursodeoxycholic acid
P Labrune, M Fabre, P Trioche, et al.
Joint Bone Spine
|
April 26, 2003
Gouty tendinitis revealing glycogen storage disease Type Ia in two adolescents
Céline 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.
Page
of 3