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Volker Straub

Showing results (111-120 of 374) with videos related to

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Annals of Neurology|October 27, 2004
Cardiac and respiratory failure in limb-girdle muscular dystrophy 2IMaja Poppe, John Bourke, Michelle Eagle, et al.
Neuromuscular Disorders : NMD|June 28, 2008
Caveolinopathy--new mutations and additional symptomsAhmed Aboumousa, Jessica Hoogendijk, Richard Charlton, et al.
Disease Models & Mechanisms|November 23, 2019
A comparison of the bone and growth phenotype of <i>mdx</i>, <i>mdx:Cmah<sup>-/-</sup></i> and <i>mdx:Utrn</i><i><sup>+/-</sup></i> murine models with the C57BL/10 wild-type mouseClaire L Wood, Karla J Suchacki, Rob van 't Hof, et al.
Nucleic Acid Therapeutics|August 11, 2017
Development of Exon Skipping Therapies for Duchenne Muscular Dystrophy: A Critical Review and a Perspective on the Outstanding IssuesAnnemieke Aartsma-Rus, Volker Straub, Robert Hemmings, et al.
Neuromuscular Disorders : NMD|April 26, 2020
Expanding the disease phenotype of ADSSL1-associated myopathy in non-Korean patientsMagdalena Mroczek, Hacer Durmus, Sunita Bijarnia-Mahay, et al.
Neurology|February 8, 2020
Accuracy of a machine learning muscle MRI-based tool for the diagnosis of muscular dystrophiesJosé Verdú-Díaz, Jorge Alonso-Pérez, Claudia Nuñez-Peralta, et al.
Neuromuscular Disorders : NMD|July 3, 2021
The phenotypic and genotypic features of a Scottish cohort with McArdle diseaseSacha E Gandhi, Cheryl Longman, Richard K H Petty, et al.
Muscle & Nerve|January 19, 2010
Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscleLars Klinge, John Harris, Caroline Sewry, et al.
Neuromuscular Disorders : NMD|May 26, 2020
Collagen VI-related limb-girdle syndrome caused by frequent mutation in COL6A3 gene with conflicting reports of pathogenicityJanis Stavusis, Ieva Micule, Nathan T Wright, et al.
NMR in Biomedicine|July 15, 2024
Probing diffusion of water and metabolites to assess white matter microstructure in Duchenne muscular dystrophyRosanne Govaarts, Nathalie Doorenweerd, Chloé F Najac, et al.
Pageof 38

Showing results (111-120 of 374) with videos related to

Sort By:
Pageof 38
Annals of Neurology|October 27, 2004
Cardiac and respiratory failure in limb-girdle muscular dystrophy 2IMaja Poppe, John Bourke, Michelle Eagle, et al.
Neuromuscular Disorders : NMD|June 28, 2008
Caveolinopathy--new mutations and additional symptomsAhmed Aboumousa, Jessica Hoogendijk, Richard Charlton, et al.
Disease Models & Mechanisms|November 23, 2019
A comparison of the bone and growth phenotype of <i>mdx</i>, <i>mdx:Cmah<sup>-/-</sup></i> and <i>mdx:Utrn</i><i><sup>+/-</sup></i> murine models with the C57BL/10 wild-type mouseClaire L Wood, Karla J Suchacki, Rob van 't Hof, et al.
Nucleic Acid Therapeutics|August 11, 2017
Development of Exon Skipping Therapies for Duchenne Muscular Dystrophy: A Critical Review and a Perspective on the Outstanding IssuesAnnemieke Aartsma-Rus, Volker Straub, Robert Hemmings, et al.
Neuromuscular Disorders : NMD|April 26, 2020
Expanding the disease phenotype of ADSSL1-associated myopathy in non-Korean patientsMagdalena Mroczek, Hacer Durmus, Sunita Bijarnia-Mahay, et al.
Neurology|February 8, 2020
Accuracy of a machine learning muscle MRI-based tool for the diagnosis of muscular dystrophiesJosé Verdú-Díaz, Jorge Alonso-Pérez, Claudia Nuñez-Peralta, et al.
Neuromuscular Disorders : NMD|July 3, 2021
The phenotypic and genotypic features of a Scottish cohort with McArdle diseaseSacha E Gandhi, Cheryl Longman, Richard K H Petty, et al.
Muscle & Nerve|January 19, 2010
Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscleLars Klinge, John Harris, Caroline Sewry, et al.
Neuromuscular Disorders : NMD|May 26, 2020
Collagen VI-related limb-girdle syndrome caused by frequent mutation in COL6A3 gene with conflicting reports of pathogenicityJanis Stavusis, Ieva Micule, Nathan T Wright, et al.
NMR in Biomedicine|July 15, 2024
Probing diffusion of water and metabolites to assess white matter microstructure in Duchenne muscular dystrophyRosanne Govaarts, Nathalie Doorenweerd, Chloé F Najac, et al.
Pageof 38