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Lev G Goldfarb

Showing results (31-40 of 51) with videos related to

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Neuromuscular Disorders : NMD|July 8, 2010
Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutationZagaa Odgerel, Anna Sarkozy, Hee-Suk Lee, et al.
Journal of Neurology|March 3, 2004
A series of West European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desminAyush Dagvadorj, Montse Olivé, Jean-Andoni Urtizberea, et al.
Human Genetics|December 3, 2003
Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathyAnna Kaminska, Sergei V Strelkov, Bertrand Goudeau, et al.
Brain : a Journal of Neurology|May 17, 2006
Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23Alexey Shatunov, Nyamkhishig Sambuughin, Joseph Jankovic, et al.
Neuromuscular Disorders : NMD|March 1, 2003
Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutationsMarinos C Dalakas, Ayush Dagvadorj, Bertrand Goudeau, et al.
Neurogenetics|April 24, 2016
Genetic fitness and selection intensity in a population affected with high-incidence spinocerebellar ataxia type 1Fedor A Platonov, Kathrin Tyryshkin, Dmitriy G Tikhonov, et al.
Journal of Neuropathology and Experimental Neurology|July 11, 2006
Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP depositsMonica Colucci, Francisco J Moleres, Zhi-Liang Xie, et al.
Emerging Infectious Diseases|February 7, 2008
Family clustering of Viliuisk encephalomyelitis in traditional and new geographic regionsVsevolod A Vladimirtsev, Raisa S Nikitina, Neil Renwick, et al.
Human Mutation|July 26, 2006
Variable pathogenic potentials of mutations located in the desmin alpha-helical domainBertrand Goudeau, Fernando Rodrigues-Lima, Dirk Fischer, et al.
Brain : a Journal of Neurology|July 15, 2005
Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutationsKumaraswamy Sivakumar, Theodoros Kyriakides, Imke Puls, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Neuromuscular Disorders : NMD|July 8, 2010
Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutationZagaa Odgerel, Anna Sarkozy, Hee-Suk Lee, et al.
Journal of Neurology|March 3, 2004
A series of West European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desminAyush Dagvadorj, Montse Olivé, Jean-Andoni Urtizberea, et al.
Human Genetics|December 3, 2003
Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathyAnna Kaminska, Sergei V Strelkov, Bertrand Goudeau, et al.
Brain : a Journal of Neurology|May 17, 2006
Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23Alexey Shatunov, Nyamkhishig Sambuughin, Joseph Jankovic, et al.
Neuromuscular Disorders : NMD|March 1, 2003
Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutationsMarinos C Dalakas, Ayush Dagvadorj, Bertrand Goudeau, et al.
Neurogenetics|April 24, 2016
Genetic fitness and selection intensity in a population affected with high-incidence spinocerebellar ataxia type 1Fedor A Platonov, Kathrin Tyryshkin, Dmitriy G Tikhonov, et al.
Journal of Neuropathology and Experimental Neurology|July 11, 2006
Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP depositsMonica Colucci, Francisco J Moleres, Zhi-Liang Xie, et al.
Emerging Infectious Diseases|February 7, 2008
Family clustering of Viliuisk encephalomyelitis in traditional and new geographic regionsVsevolod A Vladimirtsev, Raisa S Nikitina, Neil Renwick, et al.
Human Mutation|July 26, 2006
Variable pathogenic potentials of mutations located in the desmin alpha-helical domainBertrand Goudeau, Fernando Rodrigues-Lima, Dirk Fischer, et al.
Brain : a Journal of Neurology|July 15, 2005
Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutationsKumaraswamy Sivakumar, Theodoros Kyriakides, Imke Puls, et al.
Pageof 6