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Nature Genetics
|
October 1, 1996
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene
V Nigro, E de Sá Moreira, G Piluso, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
May 29, 2009
Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients
F Rinaldi, A Botta, L Vallo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
November 24, 2006
High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithm
L Morandi, C Angelini, A Prelle, et al.
International Journal of Cardiology
|
May 23, 1997
Autonomic nervous system imbalance and left ventricular systolic dysfunction as potential candidates for arrhythmogenesis in Becker muscular dystrophy
V Ducceschi, G Nigro, B Sarubbi, et al.
Muscle & Nerve
|
March 1, 1995
Evaluation of the cardiomyopathy in Becker muscular dystrophy
G Nigro, L I Comi, L Politano, et al.
Human Mutation
|
June 29, 2004
Molecular diagnosis in LGMD2A: mutation analysis or protein testing?
M Fanin, L Fulizio, A C Nascimbeni, et al.
Human Molecular Genetics
|
April 1, 1997
Identification of the Syrian hamster cardiomyopathy gene
V Nigro, Y Okazaki, A Belsito, et al.
Neuromuscular Disorders : NMD
|
March 21, 2001
Evaluation of cardiac and respiratory involvement in sarcoglycanopathies
L Politano, V Nigro, L Passamano, et al.
Human Molecular Genetics
|
August 1, 1996
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein
V Nigro, G Piluso, A Belsito, et al.
Annals of Neurology
|
August 1, 1997
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample
M Mora, L Cartegni, C Di Blasi, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 36) with videos related to
Sort By:
Page
of 4
Nature Genetics
|
October 1, 1996
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene
V Nigro, E de Sá Moreira, G Piluso, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
May 29, 2009
Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients
F Rinaldi, A Botta, L Vallo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
November 24, 2006
High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithm
L Morandi, C Angelini, A Prelle, et al.
International Journal of Cardiology
|
May 23, 1997
Autonomic nervous system imbalance and left ventricular systolic dysfunction as potential candidates for arrhythmogenesis in Becker muscular dystrophy
V Ducceschi, G Nigro, B Sarubbi, et al.
Muscle & Nerve
|
March 1, 1995
Evaluation of the cardiomyopathy in Becker muscular dystrophy
G Nigro, L I Comi, L Politano, et al.
Human Mutation
|
June 29, 2004
Molecular diagnosis in LGMD2A: mutation analysis or protein testing?
M Fanin, L Fulizio, A C Nascimbeni, et al.
Human Molecular Genetics
|
April 1, 1997
Identification of the Syrian hamster cardiomyopathy gene
V Nigro, Y Okazaki, A Belsito, et al.
Neuromuscular Disorders : NMD
|
March 21, 2001
Evaluation of cardiac and respiratory involvement in sarcoglycanopathies
L Politano, V Nigro, L Passamano, et al.
Human Molecular Genetics
|
August 1, 1996
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein
V Nigro, G Piluso, A Belsito, et al.
Annals of Neurology
|
August 1, 1997
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample
M Mora, L Cartegni, C Di Blasi, et al.
Page
of 4