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Showing results (91-100 of 98) with videos related to

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Revue Neurologique|June 9, 2000
[Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene]M Fardeau, P Vicart, A Caron, et al.
Heart (British Cardiac Society)|July 16, 2004
Reliable detection of early myocardial dysfunction by tissue Doppler echocardiography in Becker muscular dystrophyC Meune, O Pascal, H M Bécane, et al.
Pacing and Clinical Electrophysiology : PACE|January 4, 2001
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutationH M Bécane, G Bonne, S Varnous, et al.
Journal Des Maladies Vasculaires|October 7, 2005
[Intermittent claudications]F Becker, J P Boissel, C Boissier, et al.
Nature Genetics|March 18, 1999
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophyG Bonne, M R Di Barletta, S Varnous, et al.
Neurology|August 28, 2002
Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophyA J van der Kooi, G Bonne, B Eymard, et al.
Revue Neurologique|September 7, 2015
Myofibrillar myopathies: State of the art, present and future challengesA Béhin, E Salort-Campana, K Wahbi, et al.
Annals of Neurology|August 12, 2000
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C geneG Bonne, E Mercuri, A Muchir, et al.
Pageof 10

Showing results (91-100 of 98) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 98 results.
Revue Neurologique|June 9, 2000
[Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene]M Fardeau, P Vicart, A Caron, et al.
Heart (British Cardiac Society)|July 16, 2004
Reliable detection of early myocardial dysfunction by tissue Doppler echocardiography in Becker muscular dystrophyC Meune, O Pascal, H M Bécane, et al.
Pacing and Clinical Electrophysiology : PACE|January 4, 2001
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutationH M Bécane, G Bonne, S Varnous, et al.
Journal Des Maladies Vasculaires|October 7, 2005
[Intermittent claudications]F Becker, J P Boissel, C Boissier, et al.
Nature Genetics|March 18, 1999
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophyG Bonne, M R Di Barletta, S Varnous, et al.
Neurology|August 28, 2002
Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophyA J van der Kooi, G Bonne, B Eymard, et al.
Revue Neurologique|September 7, 2015
Myofibrillar myopathies: State of the art, present and future challengesA Béhin, E Salort-Campana, K Wahbi, et al.
Annals of Neurology|August 12, 2000
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C geneG Bonne, E Mercuri, A Muchir, et al.
Pageof 10