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L Capel

Showing results (1-10 of 18) with videos related to

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Nursing Mirror|September 8, 1977
Rhinitis and its managementL Capel
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.
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.
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.
FEBS Letters|December 2, 1996
Oxidized low-density lipoprotein induces the production of interleukin-8 by endothelial cellsC Claise, M Edeas, 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.
Clinical Genetics|November 4, 2004
Allelic heterogeneity of Crigler-Najjar type I syndrome: a study of 24 casesF M Petit, V Gajdos, J Francoual, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Nursing Mirror|September 8, 1977
Rhinitis and its managementL Capel
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.
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.
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.
FEBS Letters|December 2, 1996
Oxidized low-density lipoprotein induces the production of interleukin-8 by endothelial cellsC Claise, M Edeas, 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.
Clinical Genetics|November 4, 2004
Allelic heterogeneity of Crigler-Najjar type I syndrome: a study of 24 casesF M Petit, V Gajdos, J Francoual, et al.
Pageof 2