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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 14, 2003
[Central neurological manifestations during chemotherapy in children]D Orbach, H Brisse, F DozPediatric Blood & Cancer|November 2, 2005
Ifosfamide neurotoxicity: an atypical presentation with psychiatric manifestationsC Kerdudo, D Orbach, J L Sarradet, 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.Annales De Biologie Clinique|February 15, 2001
[Refinement and role of the diagnosis of Gilbert disease with molecular biology]B Le Bihan-Levaufre, J Francoual, P Labrune, 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 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.Revue Des Maladies Respiratoires|December 29, 2004
[Clinical, haemodynamic and genetic features of familial pulmonary arterial hypertension]B Sztrymf, J Francoual, O Sitbon, et al.Pageof 27