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Showing results (91-100 of 143) with videos related to

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Neuropediatrics|May 6, 2004
Collagen VI status and clinical severity in Ullrich congenital muscular dystrophy: phenotype analysis of 11 families linked to the COL6 lociE Demir, A Ferreiro, P Sabatelli, et al.
Circulation|December 31, 1997
KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndromeC Donger, I Denjoy, M Berthet, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|July 4, 2001
[T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)]J M Lupoglazoff, I Denjoy, M Berthet, et al.
Annals of Neurology|June 14, 2000
Partial laminin alpha2 chain deficiency in a patient with myopathy resembling inclusion body myositisC Di Blasi, M Mora, D Pareyson, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 15, 1999
[Congenital long QT syndrome. The value of genetics in prognostic evaluation]I Denjoy, J M Lupoglazoff, C Donger, et al.
American Journal of Human Genetics|June 19, 1998
Identification of a new locus for a peculiar form of congenital muscular dystrophy with early rigidity of the spine, on chromosome 1p35-36B Moghadaszadeh, I Desguerre, H Topaloglu, et al.
Neuromuscular Disorders : NMD|June 19, 1998
Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblingsH Topaloğlu, B Talim, N Vignier, et al.
Neurology|May 12, 2004
Clinical and histologic findings in autosomal centronuclear myopathyP-Y Jeannet, G Bassez, B Eymard, et al.
Journal of Molecular and Cellular Cardiology|August 1, 1996
A mutation in HERG associated with notched T waves in long QT syndromeE Dausse, M Berthet, I Denjoy, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 25, 2004
[Neonatal forms of congenital long QT syndrome]J M Lupoglazoff, I Denjoy, E Villain, et al.
Pageof 15

Showing results (91-100 of 143) with videos related to

Sort By:
Pageof 15
Neuropediatrics|May 6, 2004
Collagen VI status and clinical severity in Ullrich congenital muscular dystrophy: phenotype analysis of 11 families linked to the COL6 lociE Demir, A Ferreiro, P Sabatelli, et al.
Circulation|December 31, 1997
KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndromeC Donger, I Denjoy, M Berthet, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|July 4, 2001
[T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)]J M Lupoglazoff, I Denjoy, M Berthet, et al.
Annals of Neurology|June 14, 2000
Partial laminin alpha2 chain deficiency in a patient with myopathy resembling inclusion body myositisC Di Blasi, M Mora, D Pareyson, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 15, 1999
[Congenital long QT syndrome. The value of genetics in prognostic evaluation]I Denjoy, J M Lupoglazoff, C Donger, et al.
American Journal of Human Genetics|June 19, 1998
Identification of a new locus for a peculiar form of congenital muscular dystrophy with early rigidity of the spine, on chromosome 1p35-36B Moghadaszadeh, I Desguerre, H Topaloglu, et al.
Neuromuscular Disorders : NMD|June 19, 1998
Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblingsH Topaloğlu, B Talim, N Vignier, et al.
Neurology|May 12, 2004
Clinical and histologic findings in autosomal centronuclear myopathyP-Y Jeannet, G Bassez, B Eymard, et al.
Journal of Molecular and Cellular Cardiology|August 1, 1996
A mutation in HERG associated with notched T waves in long QT syndromeE Dausse, M Berthet, I Denjoy, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 25, 2004
[Neonatal forms of congenital long QT syndrome]J M Lupoglazoff, I Denjoy, E Villain, et al.
Pageof 15