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F Leturcq

Showing results (31-40 of 50) with videos related to

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Neuromuscular Disorders : NMD|October 27, 2009
Immunolabelling and flow cytometry as new tools to explore dysferlinopathiesN Wein, M Krahn, S Courrier, et al.
Human Molecular Genetics|May 23, 1998
Mutations in Emery-Dreifuss muscular dystrophy and their effects on emerin protein expressionS Manilal, D Recan, C A Sewry, 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.
Clinical Genetics|November 6, 2007
Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decayM Krahn, C Pécheux, F Chapon, et al.
Neurology|July 20, 2007
New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutationA Yanagisawa, C Bouchet, P Y K Van den Bergh, et al.
FEBS Letters|February 26, 1996
Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12D Jung, F Leturcq, Y Sunada, et al.
Neuromuscular Disorders : NMD|December 1, 1996
From adhalinopathies to alpha-sarcoglycanopathies: an overviewM Jeanpierre, A Carrié, F Piccolo, et al.
Human Molecular Genetics|December 1, 1996
A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of IndiaF Piccolo, M Jeanpierre, F Leturcq, et al.
Brain : a Journal of Neurology|October 8, 1998
Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain)M Urtasun, A Sáenz, C Roudaut, et al.
Neurology|May 31, 2007
Multitissular involvement in a family with LMNA and EMD mutations: Role of digenic mechanism?R Ben Yaou, A Toutain, T Arimura, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Neuromuscular Disorders : NMD|October 27, 2009
Immunolabelling and flow cytometry as new tools to explore dysferlinopathiesN Wein, M Krahn, S Courrier, et al.
Human Molecular Genetics|May 23, 1998
Mutations in Emery-Dreifuss muscular dystrophy and their effects on emerin protein expressionS Manilal, D Recan, C A Sewry, 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.
Clinical Genetics|November 6, 2007
Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decayM Krahn, C Pécheux, F Chapon, et al.
Neurology|July 20, 2007
New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutationA Yanagisawa, C Bouchet, P Y K Van den Bergh, et al.
FEBS Letters|February 26, 1996
Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12D Jung, F Leturcq, Y Sunada, et al.
Neuromuscular Disorders : NMD|December 1, 1996
From adhalinopathies to alpha-sarcoglycanopathies: an overviewM Jeanpierre, A Carrié, F Piccolo, et al.
Human Molecular Genetics|December 1, 1996
A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of IndiaF Piccolo, M Jeanpierre, F Leturcq, et al.
Brain : a Journal of Neurology|October 8, 1998
Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain)M Urtasun, A Sáenz, C Roudaut, et al.
Neurology|May 31, 2007
Multitissular involvement in a family with LMNA and EMD mutations: Role of digenic mechanism?R Ben Yaou, A Toutain, T Arimura, et al.
Pageof 5