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Z Argov

Showing results (101-110 of 112) with videos related to

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American Journal of Medical Genetics|April 15, 2000
Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammationE M McNally, C T Ly, H Rosenmann, et al.
Neurology|August 19, 2007
GNE protein expression and subcellular distribution are unaltered in HIBMS Krause, A Aleo, S Hinderlich, et al.
Neuromuscular Disorders : NMD|September 11, 2007
Dysferlinopathy in the Jews of the Caucasus: a frequent mutation in the dysferlin geneE Leshinsky-Silver, Z Argov, L Rozenboim, et al.
American Journal of Human Genetics|August 1, 1994
Common mutations in the phosphofructokinase-M gene in Ashkenazi Jewish patients with glycogenesis VII--and their population frequencyJ B Sherman, N Raben, C Nicastri, et al.
American Journal of Medical Genetics|December 1, 1986
Magnetic resonance spectroscopy of normal and diseased musclesB Chance, D P Younkin, R Kelley, et al.
Brain : a Journal of Neurology|May 29, 2000
Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Clinical and genetic featuresZ Argov, M Sadeh, K Mazor, et al.
Neurology|July 28, 2004
Polymyositis: an overdiagnosed entityF W Miller, L G Rider, P H Plotz, et al.
Human Molecular Genetics|April 10, 1999
Dysferlin is a plasma membrane protein and is expressed early in human developmentL V Anderson, K Davison, J A Moss, et al.
European Journal of Neurology|January 31, 2026
EAN 2024 Guideline on the Diagnostic Approach to Oligo/Asymptomatic HyperCKemiaT Kyriakides, K Aleksovska, C Angelini, et al.
Nature Genetics|September 10, 1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BR Bashir, S Britton, T Strachan, et al.
Pageof 12

Showing results (101-110 of 112) with videos related to

Sort By:
Pageof 12
American Journal of Medical Genetics|April 15, 2000
Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammationE M McNally, C T Ly, H Rosenmann, et al.
Neurology|August 19, 2007
GNE protein expression and subcellular distribution are unaltered in HIBMS Krause, A Aleo, S Hinderlich, et al.
Neuromuscular Disorders : NMD|September 11, 2007
Dysferlinopathy in the Jews of the Caucasus: a frequent mutation in the dysferlin geneE Leshinsky-Silver, Z Argov, L Rozenboim, et al.
American Journal of Human Genetics|August 1, 1994
Common mutations in the phosphofructokinase-M gene in Ashkenazi Jewish patients with glycogenesis VII--and their population frequencyJ B Sherman, N Raben, C Nicastri, et al.
American Journal of Medical Genetics|December 1, 1986
Magnetic resonance spectroscopy of normal and diseased musclesB Chance, D P Younkin, R Kelley, et al.
Brain : a Journal of Neurology|May 29, 2000
Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Clinical and genetic featuresZ Argov, M Sadeh, K Mazor, et al.
Neurology|July 28, 2004
Polymyositis: an overdiagnosed entityF W Miller, L G Rider, P H Plotz, et al.
Human Molecular Genetics|April 10, 1999
Dysferlin is a plasma membrane protein and is expressed early in human developmentL V Anderson, K Davison, J A Moss, et al.
European Journal of Neurology|January 31, 2026
EAN 2024 Guideline on the Diagnostic Approach to Oligo/Asymptomatic HyperCKemiaT Kyriakides, K Aleksovska, C Angelini, et al.
Nature Genetics|September 10, 1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BR Bashir, S Britton, T Strachan, et al.
Pageof 12