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Volker Straub

Showing results (141-150 of 374) with videos related to

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Biochemical and Biophysical Research Communications|March 9, 2002
Deficiency of alpha-dystroglycan in muscle-eye-brain diseaseHiroki Kano, Kazuhiro Kobayashi, Ralf Herrmann, et al.
Neuropediatrics|December 22, 2020
Three Individuals with PURA Syndrome in a Cohort of Patients with Neuromuscular DiseaseMagdalena Mroczek, Dimitrios Zafeiriou, Juliana Gurgel-Gianetti, et al.
Journal of Cachexia, Sarcopenia and Muscle|December 28, 2019
Longitudinal serum biomarker screening identifies malate dehydrogenase 2 as candidate prognostic biomarker for Duchenne muscular dystrophyMirko Signorelli, Burcu Ayoglu, Camilla Johansson, et al.
Neuromuscular Disorders : NMD|March 26, 2026
Phenotypic characterization of dominantly inherited distal nebulin myopathyFranclo Henning, Kireshnee Naidu, Pearl Thomas, et al.
Nucleic Acid Therapeutics|November 17, 2021
Long-Term Safety and Efficacy Data of Golodirsen in Ambulatory Patients with Duchenne Muscular Dystrophy Amenable to Exon 53 Skipping: A First-in-human, Multicenter, Two-Part, Open-Label, Phase 1/2 TrialLaurent Servais, Eugenio Mercuri, Volker Straub, et al.
Neuromuscular Disorders : NMD|April 17, 2010
Revertant fibres and dystrophin traces in Duchenne muscular dystrophy: implication for clinical trialsVirginia Arechavala-Gomeza, Maria Kinali, Lucy Feng, et al.
International Journal of Molecular Sciences|July 27, 2024
An Integrated Transcriptomics and Genomics Approach Detects an X/Autosome Translocation in a Female with Duchenne Muscular DystrophyAlba Segarra-Casas, Vicente A Yépez, German Demidov, et al.
Journal of Neurology|May 28, 2017
Respiratory involvement in ambulant and non-ambulant patients with facioscapulohumeral muscular dystrophySandra Moreira, Libby Wood, Debbie Smith, et al.
Human Molecular Genetics|December 17, 2013
Mutations in the collagen XII gene define a new form of extracellular matrix-related myopathyDebbie Hicks, Golara Torabi Farsani, Steven Laval, et al.
The American Journal of Pathology|January 13, 2011
Long-term blocking of calcium channels in mdx mice results in differential effects on heart and skeletal muscleLouise H Jørgensen, Alison Blain, Elizabeth Greally, et al.
Pageof 38

Showing results (141-150 of 374) with videos related to

Sort By:
Pageof 38
Biochemical and Biophysical Research Communications|March 9, 2002
Deficiency of alpha-dystroglycan in muscle-eye-brain diseaseHiroki Kano, Kazuhiro Kobayashi, Ralf Herrmann, et al.
Neuropediatrics|December 22, 2020
Three Individuals with PURA Syndrome in a Cohort of Patients with Neuromuscular DiseaseMagdalena Mroczek, Dimitrios Zafeiriou, Juliana Gurgel-Gianetti, et al.
Journal of Cachexia, Sarcopenia and Muscle|December 28, 2019
Longitudinal serum biomarker screening identifies malate dehydrogenase 2 as candidate prognostic biomarker for Duchenne muscular dystrophyMirko Signorelli, Burcu Ayoglu, Camilla Johansson, et al.
Neuromuscular Disorders : NMD|March 26, 2026
Phenotypic characterization of dominantly inherited distal nebulin myopathyFranclo Henning, Kireshnee Naidu, Pearl Thomas, et al.
Nucleic Acid Therapeutics|November 17, 2021
Long-Term Safety and Efficacy Data of Golodirsen in Ambulatory Patients with Duchenne Muscular Dystrophy Amenable to Exon 53 Skipping: A First-in-human, Multicenter, Two-Part, Open-Label, Phase 1/2 TrialLaurent Servais, Eugenio Mercuri, Volker Straub, et al.
Neuromuscular Disorders : NMD|April 17, 2010
Revertant fibres and dystrophin traces in Duchenne muscular dystrophy: implication for clinical trialsVirginia Arechavala-Gomeza, Maria Kinali, Lucy Feng, et al.
International Journal of Molecular Sciences|July 27, 2024
An Integrated Transcriptomics and Genomics Approach Detects an X/Autosome Translocation in a Female with Duchenne Muscular DystrophyAlba Segarra-Casas, Vicente A Yépez, German Demidov, et al.
Journal of Neurology|May 28, 2017
Respiratory involvement in ambulant and non-ambulant patients with facioscapulohumeral muscular dystrophySandra Moreira, Libby Wood, Debbie Smith, et al.
Human Molecular Genetics|December 17, 2013
Mutations in the collagen XII gene define a new form of extracellular matrix-related myopathyDebbie Hicks, Golara Torabi Farsani, Steven Laval, et al.
The American Journal of Pathology|January 13, 2011
Long-term blocking of calcium channels in mdx mice results in differential effects on heart and skeletal muscleLouise H Jørgensen, Alison Blain, Elizabeth Greally, et al.
Pageof 38