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Volker Straub

Showing results (61-70 of 374) with videos related to

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Neuromuscular Disorders : NMD|March 2, 2026
Decoding genetic complexity in glycogen storage diseases: three novel variants in SLC37A4, GAA, and PHKG2 identified in an Iranian cohortFatemeh Alian, Volker Straub, Ana Töpf, et al.
Neurology|September 8, 2019
Fat oxidation is impaired during exercise in lipin-1 deficiencyDaniel Raaschou-Pedersen, Karen L Madsen, Mads G Stemmerik, et al.
Neuromuscular Disorders : NMD|November 11, 2008
Sarcoglycanopathies: can muscle immunoanalysis predict the genotype?Lars Klinge, Gabriele Dekomien, Ahmed Aboumousa, et al.
Neuromuscular Disorders : NMD|April 27, 2023
A homozygous loss of function variant in POPDC3: From invalidating exercise intolerance to a limb-girdle muscular dystrophy phenotypeWillem De Ridder, Geert de Vries, Kristof Van Schil, et al.
Neurology|July 4, 2014
The burden of Duchenne muscular dystrophy: an international, cross-sectional studyErik Landfeldt, Peter Lindgren, Christopher F Bell, et al.
European Journal of Heart Failure|August 3, 2010
Intolerance to ß-blockade in a mouse model of δ-sarcoglycan-deficient muscular dystrophy cardiomyopathyRalf Bauer, Alison Blain, Elizabeth Greally, et al.
Neuromuscular Disorders : NMD|March 1, 2015
Conserved expression of truncated telethonin in a patient with limb-girdle muscular dystrophy 2GRita Barresi, Charlotte Morris, Judith Hudson, et al.
Journal of Neuromuscular Diseases|February 13, 2016
Compliance to Care Guidelines for Duchenne Muscular DystrophyErik Landfeldt, Peter Lindgren, Christopher F Bell, et al.
Muscle & Nerve|March 8, 2021
Elevation of fast but not slow troponin I in the circulation of patients with Becker and Duchenne muscular dystrophyBenjamin L Barthel, Dan Cox, Marissa Barbieri, et al.
Orphanet Journal of Rare Diseases|October 24, 2013
The TREAT-NMD care and trial site registry: an online registry to facilitate clinical research for neuromuscular diseasesSunil Rodger, Hanns Lochmüller, Adrian Tassoni, et al.
Pageof 38

Showing results (61-70 of 374) with videos related to

Sort By:
Pageof 38
Neuromuscular Disorders : NMD|March 2, 2026
Decoding genetic complexity in glycogen storage diseases: three novel variants in SLC37A4, GAA, and PHKG2 identified in an Iranian cohortFatemeh Alian, Volker Straub, Ana Töpf, et al.
Neurology|September 8, 2019
Fat oxidation is impaired during exercise in lipin-1 deficiencyDaniel Raaschou-Pedersen, Karen L Madsen, Mads G Stemmerik, et al.
Neuromuscular Disorders : NMD|November 11, 2008
Sarcoglycanopathies: can muscle immunoanalysis predict the genotype?Lars Klinge, Gabriele Dekomien, Ahmed Aboumousa, et al.
Neuromuscular Disorders : NMD|April 27, 2023
A homozygous loss of function variant in POPDC3: From invalidating exercise intolerance to a limb-girdle muscular dystrophy phenotypeWillem De Ridder, Geert de Vries, Kristof Van Schil, et al.
Neurology|July 4, 2014
The burden of Duchenne muscular dystrophy: an international, cross-sectional studyErik Landfeldt, Peter Lindgren, Christopher F Bell, et al.
European Journal of Heart Failure|August 3, 2010
Intolerance to ß-blockade in a mouse model of δ-sarcoglycan-deficient muscular dystrophy cardiomyopathyRalf Bauer, Alison Blain, Elizabeth Greally, et al.
Neuromuscular Disorders : NMD|March 1, 2015
Conserved expression of truncated telethonin in a patient with limb-girdle muscular dystrophy 2GRita Barresi, Charlotte Morris, Judith Hudson, et al.
Journal of Neuromuscular Diseases|February 13, 2016
Compliance to Care Guidelines for Duchenne Muscular DystrophyErik Landfeldt, Peter Lindgren, Christopher F Bell, et al.
Muscle & Nerve|March 8, 2021
Elevation of fast but not slow troponin I in the circulation of patients with Becker and Duchenne muscular dystrophyBenjamin L Barthel, Dan Cox, Marissa Barbieri, et al.
Orphanet Journal of Rare Diseases|October 24, 2013
The TREAT-NMD care and trial site registry: an online registry to facilitate clinical research for neuromuscular diseasesSunil Rodger, Hanns Lochmüller, Adrian Tassoni, et al.
Pageof 38