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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 deficiency
S 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 mice
J E Guidotti, A Mignon, G Haase, et al.
Scandinavian Journal of Rheumatology
|
December 17, 2009
Bone and joint involvement in Fabry disease
K 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 avenae
Charles-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 responses
J 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 phenylketonuria
P 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 gene
R Draghia, F Letourneur, C Drugan, et al.
International Journal of Sports Medicine
|
May 1, 1994
Release of cytokines by blood monocytes during strenuous exercise
A Rivier, J Pène, P Chanez, et al.
Neurology
|
November 9, 2000
Juvenile and adult-onset acid maltase deficiency in France: genotype-phenotype correlation
P 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 subjects
L Maïmoun, D Simar, D Malatesta, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 80) with videos related to
Sort By:
Page
of 8
American Journal of Human Genetics
|
April 1, 1989
Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency
S 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 mice
J E Guidotti, A Mignon, G Haase, et al.
Scandinavian Journal of Rheumatology
|
December 17, 2009
Bone and joint involvement in Fabry disease
K 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 avenae
Charles-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 responses
J 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 phenylketonuria
P 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 gene
R Draghia, F Letourneur, C Drugan, et al.
International Journal of Sports Medicine
|
May 1, 1994
Release of cytokines by blood monocytes during strenuous exercise
A Rivier, J Pène, P Chanez, et al.
Neurology
|
November 9, 2000
Juvenile and adult-onset acid maltase deficiency in France: genotype-phenotype correlation
P 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 subjects
L Maïmoun, D Simar, D Malatesta, et al.
Page
of 8