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L Politano

Showing results (21-30 of 36) with videos related to

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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 geneV 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 patientsF 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 algorithmL 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 dystrophyV Ducceschi, G Nigro, B Sarubbi, et al.
Muscle & Nerve|March 1, 1995
Evaluation of the cardiomyopathy in Becker muscular dystrophyG 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 geneV Nigro, Y Okazaki, A Belsito, et al.
Neuromuscular Disorders : NMD|March 21, 2001
Evaluation of cardiac and respiratory involvement in sarcoglycanopathiesL 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 glycoproteinV 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 sampleM Mora, L Cartegni, C Di Blasi, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Nature Genetics|October 1, 1996
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan geneV 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 patientsF 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 algorithmL 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 dystrophyV Ducceschi, G Nigro, B Sarubbi, et al.
Muscle & Nerve|March 1, 1995
Evaluation of the cardiomyopathy in Becker muscular dystrophyG 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 geneV Nigro, Y Okazaki, A Belsito, et al.
Neuromuscular Disorders : NMD|March 21, 2001
Evaluation of cardiac and respiratory involvement in sarcoglycanopathiesL 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 glycoproteinV 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 sampleM Mora, L Cartegni, C Di Blasi, et al.
Pageof 4