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Nature Genetics
|
July 1, 1993
Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11
L Carrier, C Hengstenberg, J S Beckmann, et al.
European Journal of Clinical Investigation
|
June 1, 1988
Platelet serotonin content and plasma tryptophan in peri- and postmenopausal women: variations with plasma oestrogen levels and depressive symptoms
P Guicheney, D Léger, J Barrat, et al.
Journal of Hypertension
|
March 1, 1989
Phenylephrine, vasopressin and angiotensin II as determinants of proto-oncogene and heat-shock protein gene expression in adult rat heart and aorta
J M Moalic, C Bauters, D Himbert, et al.
Neuromuscular Disorders : NMD
|
November 2, 1999
Genetic heterogeneity of congenital muscular dystrophy with rigid spine syndrome
B Moghadaszadeh, H Topaloglu, L Merlini, et al.
Neuromuscular Disorders : NMD
|
October 29, 2000
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci
B Talim, A Ferreiro, B Cormand, et al.
Human Genetics
|
April 1, 1997
The role of immunocytochemistry and linkage analysis in the prenatal diagnosis of merosin-deficient congenital muscular dystrophy
I Naom, M D'Alessandro, C Sewry, et al.
American Journal of Human Genetics
|
October 3, 1998
Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic)
C Donger, E Krejci, A P Serradell, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
September 28, 1998
[QT interval and drugs. Recommendation for drug prescription for patients with long QT syndrome. Clinical Research Group of INSERM 4940 12: Diagnostic Clinic of Congenital Long QT Syndrome]
J Y Le Heuzey, J M Davy, J Weissenburger, et al.
European Heart Journal
|
May 6, 1998
Familial hypertrophic cardiomyopathy. Cardiac ultrasonic abnormalities in genetically affected subjects without echocardiographic evidence of left ventricular hypertrophy
A A Hagège, O Dubourg, M Desnos, et al.
Nature Genetics
|
February 1, 1997
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
N Neyroud, F Tesson, I Denjoy, et al.
Page
of 15
Search research articles
Search
Showing results (101-110 of 143) with videos related to
Sort By:
Page
of 15
Nature Genetics
|
July 1, 1993
Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11
L Carrier, C Hengstenberg, J S Beckmann, et al.
European Journal of Clinical Investigation
|
June 1, 1988
Platelet serotonin content and plasma tryptophan in peri- and postmenopausal women: variations with plasma oestrogen levels and depressive symptoms
P Guicheney, D Léger, J Barrat, et al.
Journal of Hypertension
|
March 1, 1989
Phenylephrine, vasopressin and angiotensin II as determinants of proto-oncogene and heat-shock protein gene expression in adult rat heart and aorta
J M Moalic, C Bauters, D Himbert, et al.
Neuromuscular Disorders : NMD
|
November 2, 1999
Genetic heterogeneity of congenital muscular dystrophy with rigid spine syndrome
B Moghadaszadeh, H Topaloglu, L Merlini, et al.
Neuromuscular Disorders : NMD
|
October 29, 2000
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci
B Talim, A Ferreiro, B Cormand, et al.
Human Genetics
|
April 1, 1997
The role of immunocytochemistry and linkage analysis in the prenatal diagnosis of merosin-deficient congenital muscular dystrophy
I Naom, M D'Alessandro, C Sewry, et al.
American Journal of Human Genetics
|
October 3, 1998
Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic)
C Donger, E Krejci, A P Serradell, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
September 28, 1998
[QT interval and drugs. Recommendation for drug prescription for patients with long QT syndrome. Clinical Research Group of INSERM 4940 12: Diagnostic Clinic of Congenital Long QT Syndrome]
J Y Le Heuzey, J M Davy, J Weissenburger, et al.
European Heart Journal
|
May 6, 1998
Familial hypertrophic cardiomyopathy. Cardiac ultrasonic abnormalities in genetically affected subjects without echocardiographic evidence of left ventricular hypertrophy
A A Hagège, O Dubourg, M Desnos, et al.
Nature Genetics
|
February 1, 1997
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
N Neyroud, F Tesson, I Denjoy, et al.
Page
of 15