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Lev G Goldfarb

Showing results (41-50 of 51) with videos related to

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FEBS Letters|June 28, 2005
Hsp27-2D-gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathiesChristoph S Clemen, Dirk Fischer, Udo Roth, et al.
Journal of the Neurological Sciences|June 18, 2003
Viliuisk encephalomyelitis: intrathecal synthesis of oligoclonal IgGAlison J E Green, Tatiana M Sivtseva, Al'bina P Danilova, et al.
American Journal of Human Genetics|April 12, 2003
Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type VAnthony Antonellis, Rachel E Ellsworth, Nyamkhishig Sambuughin, et al.
BMC Neurology|November 1, 2015
Adult-onset autosomal dominant spastic paraplegia linked to a GTPase-effector domain mutation of dynamin 2Nyamkhishig Sambuughin, Lev G Goldfarb, Tatiana M Sivtseva, et al.
Neuromuscular Disorders : NMD|May 11, 2006
Different early pathogenesis in myotilinopathy compared to primary desminopathyDirk Fischer, Christoph S Clemen, Montse Olivé, et al.
Epidemiology (Cambridge, Mass.)|December 17, 2009
Epidemiology of Viliuisk encephalomyelitis in Eastern SiberiaHee Suk Lee, Svetlana N Zhdanova, Vsevolod A Vladimirtsev, et al.
Journal of Neuropathology and Experimental Neurology|July 28, 2022
The Location of Disease-Causing DES Variants Determines the Severity of Phenotype and the Morphology of Sarcoplasmic AggregatesAndré Macedo Serafim Silva, Patricia Rodrigo, Cristiane Araújo Martins Moreno, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathyAlexey Shatunov, Montse Olivé, Zagaa Odgerel, et al.
Brain : a Journal of Neurology|September 11, 2012
Pathophysiology of protein aggregation and extended phenotyping in filaminopathyRudolf A Kley, Piraye Serdaroglu-Oflazer, Yvonne Leber, et al.
Neuromuscular Disorders : NMD|June 17, 2011
Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathyMontse Olivé, Zagaa Odgerel, Amaia Martínez, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
FEBS Letters|June 28, 2005
Hsp27-2D-gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathiesChristoph S Clemen, Dirk Fischer, Udo Roth, et al.
Journal of the Neurological Sciences|June 18, 2003
Viliuisk encephalomyelitis: intrathecal synthesis of oligoclonal IgGAlison J E Green, Tatiana M Sivtseva, Al'bina P Danilova, et al.
American Journal of Human Genetics|April 12, 2003
Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type VAnthony Antonellis, Rachel E Ellsworth, Nyamkhishig Sambuughin, et al.
BMC Neurology|November 1, 2015
Adult-onset autosomal dominant spastic paraplegia linked to a GTPase-effector domain mutation of dynamin 2Nyamkhishig Sambuughin, Lev G Goldfarb, Tatiana M Sivtseva, et al.
Neuromuscular Disorders : NMD|May 11, 2006
Different early pathogenesis in myotilinopathy compared to primary desminopathyDirk Fischer, Christoph S Clemen, Montse Olivé, et al.
Epidemiology (Cambridge, Mass.)|December 17, 2009
Epidemiology of Viliuisk encephalomyelitis in Eastern SiberiaHee Suk Lee, Svetlana N Zhdanova, Vsevolod A Vladimirtsev, et al.
Journal of Neuropathology and Experimental Neurology|July 28, 2022
The Location of Disease-Causing DES Variants Determines the Severity of Phenotype and the Morphology of Sarcoplasmic AggregatesAndré Macedo Serafim Silva, Patricia Rodrigo, Cristiane Araújo Martins Moreno, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathyAlexey Shatunov, Montse Olivé, Zagaa Odgerel, et al.
Brain : a Journal of Neurology|September 11, 2012
Pathophysiology of protein aggregation and extended phenotyping in filaminopathyRudolf A Kley, Piraye Serdaroglu-Oflazer, Yvonne Leber, et al.
Neuromuscular Disorders : NMD|June 17, 2011
Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathyMontse Olivé, Zagaa Odgerel, Amaia Martínez, et al.
Pageof 6