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V Straub

Showing results (71-80 of 92) with videos related to

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Developmental Cell|November 16, 2001
Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1A Yoshida, K Kobayashi, H Manya, et al.
Neuromuscular Disorders : NMD|July 5, 2011
Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring disease progression in Duchenne muscular dystrophy (DMD)V D Nadarajah, M van Putten, A Chaouch, et al.
Neurology|December 29, 2005
Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 geneH Jungbluth, H Zhou, L Hartley, et al.
Neuromuscular Disorders : NMD|December 17, 2017
Corrigendum to "A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophy" [Neuromuscular disorders 27/11 (2017) 1043-1046]P Y K Van den Bergh, Y Sznajer, V Van Parys, et al.
Human Molecular Genetics|May 1, 1997
Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chainV Allamand, Y Sunada, M A Salih, et al.
Neuromuscular Disorders : NMD|August 15, 2017
A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophyP Y K Van den Bergh, Y Sznajer, V Van Parys, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolateF Duclos, O Broux, N Bourg, et al.
The Journal of Biological Chemistry|December 13, 1996
Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophyD Jung, F Duclos, B Apostol, et al.
Journal of Medical Genetics|May 4, 2004
Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndromeD Beltran-Valero de Bernabé, T Voit, C Longman, et al.
Neuromuscular Disorders : NMD|October 26, 2002
98th ENMC International Workshop on Congenital Muscular Dystrophy (CMD), 7th Workshop of the International Consortium on CMD, 2nd Workshop of the MYO CLUSTER project GENRE. 26-28th October, 2001, Naarden, The NetherlandsF Muntoni, E Bertini, C Bönnemann, et al.
Pageof 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Developmental Cell|November 16, 2001
Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1A Yoshida, K Kobayashi, H Manya, et al.
Neuromuscular Disorders : NMD|July 5, 2011
Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring disease progression in Duchenne muscular dystrophy (DMD)V D Nadarajah, M van Putten, A Chaouch, et al.
Neurology|December 29, 2005
Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 geneH Jungbluth, H Zhou, L Hartley, et al.
Neuromuscular Disorders : NMD|December 17, 2017
Corrigendum to "A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophy" [Neuromuscular disorders 27/11 (2017) 1043-1046]P Y K Van den Bergh, Y Sznajer, V Van Parys, et al.
Human Molecular Genetics|May 1, 1997
Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chainV Allamand, Y Sunada, M A Salih, et al.
Neuromuscular Disorders : NMD|August 15, 2017
A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophyP Y K Van den Bergh, Y Sznajer, V Van Parys, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolateF Duclos, O Broux, N Bourg, et al.
The Journal of Biological Chemistry|December 13, 1996
Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophyD Jung, F Duclos, B Apostol, et al.
Journal of Medical Genetics|May 4, 2004
Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndromeD Beltran-Valero de Bernabé, T Voit, C Longman, et al.
Neuromuscular Disorders : NMD|October 26, 2002
98th ENMC International Workshop on Congenital Muscular Dystrophy (CMD), 7th Workshop of the International Consortium on CMD, 2nd Workshop of the MYO CLUSTER project GENRE. 26-28th October, 2001, Naarden, The NetherlandsF Muntoni, E Bertini, C Bönnemann, et al.
Pageof 10