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P Guicheney

Showing results (101-110 of 143) with videos related to

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Nature Genetics|July 1, 1993
Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11L 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 symptomsP 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 aortaJ M Moalic, C Bauters, D Himbert, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Genetic heterogeneity of congenital muscular dystrophy with rigid spine syndromeB 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 lociB 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 dystrophyI 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 hypertrophyA 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 syndromeN Neyroud, F Tesson, I Denjoy, et al.
Pageof 15

Showing results (101-110 of 143) with videos related to

Sort By:
Pageof 15
Nature Genetics|July 1, 1993
Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11L 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 symptomsP 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 aortaJ M Moalic, C Bauters, D Himbert, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Genetic heterogeneity of congenital muscular dystrophy with rigid spine syndromeB 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 lociB 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 dystrophyI 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 hypertrophyA 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 syndromeN Neyroud, F Tesson, I Denjoy, et al.
Pageof 15