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Lev G Goldfarb

Showing results (11-20 of 51) with videos related to

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Journal of Neuropathology and Experimental Neurology|January 18, 2012
Kuru: genes, cannibals and neuropathologyPawel P Liberski, Beata Sikorska, Shirley Lindenbaum, et al.
Folia Neuropathologica|July 21, 2009
Viliuisk encephalomyelitis in Eastern Siberia - analysis of 390 casesLev G Goldfarb, Vsevolod A Vladimirtsev, Fyodor A Platanov, et al.
Neurology|December 8, 2010
Dominant-negative effects of a novel mutation in the filamin myopathyPeter F M van der Ven, Zagaa Odgerel, Dieter O Fürst, et al.
Acta Neuropathologica|October 31, 2012
Filamin C-related myopathies: pathology and mechanismsDieter O Fürst, Lev G Goldfarb, Rudolf A Kley, et al.
Muscle & Nerve|July 19, 2012
Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late-onset cerebellar ataxiaGiorgio Tasca, Zagaa Odgerel, Mauro Monforte, et al.
Annals of Neurology|September 3, 2002
Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathyAyush Dagvadorj, Robert B Petersen, Hee Suk Lee, et al.
Neuromuscular Disorders : NMD|June 30, 2006
Distinct phenotypic features and gender-specific disease manifestations in a Spanish family with desmin L370P mutationManuel Arias, Julio Pardo, Patricia Blanco-Arias, et al.
Autophagy|December 15, 2012
Impairment of protein degradation in myofibrillar myopathy caused by FLNC/filamin C mutationsRudolf A Kley, Peter F M van der Ven, Montse Olivé, et al.
Neuromuscular Disorders : NMD|October 25, 2008
Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patientMontse Olivé, Alexey Shatunov, Laura Gonzalez, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|May 5, 2009
Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama diseaseSergiu C Blumen, Vivian E Drory, Menachem Sadeh, et al.
Pageof 6

Showing results (11-20 of 51) with videos related to

Sort By:
Pageof 6
Journal of Neuropathology and Experimental Neurology|January 18, 2012
Kuru: genes, cannibals and neuropathologyPawel P Liberski, Beata Sikorska, Shirley Lindenbaum, et al.
Folia Neuropathologica|July 21, 2009
Viliuisk encephalomyelitis in Eastern Siberia - analysis of 390 casesLev G Goldfarb, Vsevolod A Vladimirtsev, Fyodor A Platanov, et al.
Neurology|December 8, 2010
Dominant-negative effects of a novel mutation in the filamin myopathyPeter F M van der Ven, Zagaa Odgerel, Dieter O Fürst, et al.
Acta Neuropathologica|October 31, 2012
Filamin C-related myopathies: pathology and mechanismsDieter O Fürst, Lev G Goldfarb, Rudolf A Kley, et al.
Muscle & Nerve|July 19, 2012
Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late-onset cerebellar ataxiaGiorgio Tasca, Zagaa Odgerel, Mauro Monforte, et al.
Annals of Neurology|September 3, 2002
Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathyAyush Dagvadorj, Robert B Petersen, Hee Suk Lee, et al.
Neuromuscular Disorders : NMD|June 30, 2006
Distinct phenotypic features and gender-specific disease manifestations in a Spanish family with desmin L370P mutationManuel Arias, Julio Pardo, Patricia Blanco-Arias, et al.
Autophagy|December 15, 2012
Impairment of protein degradation in myofibrillar myopathy caused by FLNC/filamin C mutationsRudolf A Kley, Peter F M van der Ven, Montse Olivé, et al.
Neuromuscular Disorders : NMD|October 25, 2008
Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patientMontse Olivé, Alexey Shatunov, Laura Gonzalez, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|May 5, 2009
Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama diseaseSergiu C Blumen, Vivian E Drory, Menachem Sadeh, et al.
Pageof 6