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Neuromuscular Disorders : NMD
|
October 27, 2009
Immunolabelling and flow cytometry as new tools to explore dysferlinopathies
N 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 expression
S 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 dystrophy
C 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 decay
M Krahn, C Pécheux, F Chapon, et al.
Neurology
|
July 20, 2007
New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation
A 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 13q12
D Jung, F Leturcq, Y Sunada, et al.
Neuromuscular Disorders : NMD
|
December 1, 1996
From adhalinopathies to alpha-sarcoglycanopathies: an overview
M 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 India
F 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.
Page
of 5
Search research articles
Search
Showing results (31-40 of 50) with videos related to
Sort By:
Page
of 5
Neuromuscular Disorders : NMD
|
October 27, 2009
Immunolabelling and flow cytometry as new tools to explore dysferlinopathies
N 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 expression
S 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 dystrophy
C 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 decay
M Krahn, C Pécheux, F Chapon, et al.
Neurology
|
July 20, 2007
New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation
A 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 13q12
D Jung, F Leturcq, Y Sunada, et al.
Neuromuscular Disorders : NMD
|
December 1, 1996
From adhalinopathies to alpha-sarcoglycanopathies: an overview
M 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 India
F 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.
Page
of 5