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Nucleic Acids Research
|
November 21, 2007
Ex vivo correction of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a mutation in the selenocysteine codon
M Rederstorff, V Allamand, P Guicheney, et al.
American Journal of Medical Genetics. Part A
|
August 21, 2007
Ehlers-Danlos syndrome due to tenascin-X deficiency: muscle weakness and contractures support overlap with collagen VI myopathies
N C Voermans, G J Jenniskens, B C Hamel, et al.
American Journal of Hypertension
|
February 1, 1993
Proliferation and Na+/H+ antiport activity in human fibroblasts from type I diabetic patients with nephropathy
K Soussan, E Dausse, T Hannedouche, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
October 1, 1994
[Physiopathology of mitral mechanics in hypertrophic cardiomyopathy. Groupe de travail "Cardiomyopathies et insuffisance cardiaque" de la Société Française de Cardiologie]
A Hagège, M Desnos, M Komajda, et al.
European Journal of Biochemistry
|
December 12, 2001
Human synemin gene generates splice variants encoding two distinct intermediate filament proteins
M Titeux, V Brocheriou, Z Xue, et al.
Journal of Molecular and Cellular Cardiology
|
September 1, 1996
Exclusion of KCNE1 (IsK) as a candidate gene for Jervell and Lange-Nielsen syndrome
F Tesson, C Donger, I Denjoy, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
June 22, 2005
[Catecholinergic ventricular tachycardia in children]
I Denjoy, A Postma, J M Lupoglazoff, et al.
European Journal of Human Genetics : EJHG
|
May 31, 2007
Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects
L Gouas, V Nicaud, S Chaouch, et al.
Clinical Neuropathology
|
January 10, 2009
Dynamin 2-related centronuclear myopathy: clinical, histological and genetic aspects of further patients and review of the literature
M Jeub, M Bitoun, P Guicheney, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
August 1, 1995
Readjusting the localization of long QT syndrome gene on chromosome 11p15
E Dausse, I Denjoy, P Kahlem, et al.
Page
of 15
Search research articles
Search
Showing results (71-80 of 143) with videos related to
Sort By:
Page
of 15
Nucleic Acids Research
|
November 21, 2007
Ex vivo correction of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a mutation in the selenocysteine codon
M Rederstorff, V Allamand, P Guicheney, et al.
American Journal of Medical Genetics. Part A
|
August 21, 2007
Ehlers-Danlos syndrome due to tenascin-X deficiency: muscle weakness and contractures support overlap with collagen VI myopathies
N C Voermans, G J Jenniskens, B C Hamel, et al.
American Journal of Hypertension
|
February 1, 1993
Proliferation and Na+/H+ antiport activity in human fibroblasts from type I diabetic patients with nephropathy
K Soussan, E Dausse, T Hannedouche, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
October 1, 1994
[Physiopathology of mitral mechanics in hypertrophic cardiomyopathy. Groupe de travail "Cardiomyopathies et insuffisance cardiaque" de la Société Française de Cardiologie]
A Hagège, M Desnos, M Komajda, et al.
European Journal of Biochemistry
|
December 12, 2001
Human synemin gene generates splice variants encoding two distinct intermediate filament proteins
M Titeux, V Brocheriou, Z Xue, et al.
Journal of Molecular and Cellular Cardiology
|
September 1, 1996
Exclusion of KCNE1 (IsK) as a candidate gene for Jervell and Lange-Nielsen syndrome
F Tesson, C Donger, I Denjoy, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
June 22, 2005
[Catecholinergic ventricular tachycardia in children]
I Denjoy, A Postma, J M Lupoglazoff, et al.
European Journal of Human Genetics : EJHG
|
May 31, 2007
Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects
L Gouas, V Nicaud, S Chaouch, et al.
Clinical Neuropathology
|
January 10, 2009
Dynamin 2-related centronuclear myopathy: clinical, histological and genetic aspects of further patients and review of the literature
M Jeub, M Bitoun, P Guicheney, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
August 1, 1995
Readjusting the localization of long QT syndrome gene on chromosome 11p15
E Dausse, I Denjoy, P Kahlem, et al.
Page
of 15