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C Caillaud

Showing results (41-50 of 80) with videos related to

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American Journal of Human Genetics|April 1, 1989
Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiencyS Lyonnet, C Caillaud, F Rey, et al.
Human Molecular Genetics|April 10, 1999
Adenoviral gene therapy of the Tay-Sachs disease in hexosaminidase A-deficient knock-out miceJ E Guidotti, A Mignon, G Haase, et al.
Scandinavian Journal of Rheumatology|December 17, 2009
Bone and joint involvement in Fabry diseaseK Sacre, Olivier Lidove, B Giroux Leprieur, et al.
Oecologia|February 20, 2014
Coexistence in space and time of sexual and asexual populations of the cereal aphid Sitobion avenaeCharles-Antoine Dedryver, Maurice Hullé, Jean-François Le Gallic, et al.
Medicine and Science in Sports and Exercise|February 1, 1996
Influence of post-surgery time after cardiac transplantation on exercise responsesJ Mercier, N Ville, P Wintrebert, et al.
American Journal of Human Genetics|June 1, 1991
Single-strand conformation polymorphism for detection of mutations and base substitutions in phenylketonuriaP Labrune, D Melle, F Rey, et al.
Human Mutation|January 1, 1997
Metachromatic leukodystrophy: identification of the first deletion in exon 1 and of nine novel point mutations in the arylsulfatase A geneR Draghia, F Letourneur, C Drugan, et al.
International Journal of Sports Medicine|May 1, 1994
Release of cytokines by blood monocytes during strenuous exerciseA Rivier, J Pène, P Chanez, et al.
Neurology|November 9, 2000
Juvenile and adult-onset acid maltase deficiency in France: genotype-phenotype correlationP Laforêt, M Nicolino, P B Eymard, et al.
British Journal of Sports Medicine|July 28, 2005
Response of bone metabolism related hormones to a single session of strenuous exercise in active elderly subjectsL Maïmoun, D Simar, D Malatesta, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|April 1, 1989
Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiencyS Lyonnet, C Caillaud, F Rey, et al.
Human Molecular Genetics|April 10, 1999
Adenoviral gene therapy of the Tay-Sachs disease in hexosaminidase A-deficient knock-out miceJ E Guidotti, A Mignon, G Haase, et al.
Scandinavian Journal of Rheumatology|December 17, 2009
Bone and joint involvement in Fabry diseaseK Sacre, Olivier Lidove, B Giroux Leprieur, et al.
Oecologia|February 20, 2014
Coexistence in space and time of sexual and asexual populations of the cereal aphid Sitobion avenaeCharles-Antoine Dedryver, Maurice Hullé, Jean-François Le Gallic, et al.
Medicine and Science in Sports and Exercise|February 1, 1996
Influence of post-surgery time after cardiac transplantation on exercise responsesJ Mercier, N Ville, P Wintrebert, et al.
American Journal of Human Genetics|June 1, 1991
Single-strand conformation polymorphism for detection of mutations and base substitutions in phenylketonuriaP Labrune, D Melle, F Rey, et al.
Human Mutation|January 1, 1997
Metachromatic leukodystrophy: identification of the first deletion in exon 1 and of nine novel point mutations in the arylsulfatase A geneR Draghia, F Letourneur, C Drugan, et al.
International Journal of Sports Medicine|May 1, 1994
Release of cytokines by blood monocytes during strenuous exerciseA Rivier, J Pène, P Chanez, et al.
Neurology|November 9, 2000
Juvenile and adult-onset acid maltase deficiency in France: genotype-phenotype correlationP Laforêt, M Nicolino, P B Eymard, et al.
British Journal of Sports Medicine|July 28, 2005
Response of bone metabolism related hormones to a single session of strenuous exercise in active elderly subjectsL Maïmoun, D Simar, D Malatesta, et al.
Pageof 8