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C Walter

Showing results (601-610 of 860) with videos related to

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Neuromuscular Disorders : NMD|October 16, 2009
Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblastsJouni Vesa, Hailing Su, Giles D Watts, et al.
Human Molecular Genetics|August 4, 2009
Evaluation of the therapeutic potential of carbonic anhydrase inhibitors in two animal models of dystrophin deficient muscular dystrophyJean Giacomotto, Cordula Pertl, Caroline Borrel, et al.
Neuromuscular Disorders : NMD|January 11, 2005
Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophyMaggie C Walter, Thomas N Witt, Beate Schlotter Weigel, et al.
Journal of Biomedical Semantics|April 13, 2019
Moonstone: a novel natural language processing system for inferring social risk from clinical narrativesMike Conway, Salomeh Keyhani, Lee Christensen, et al.
Neuromuscular Disorders : NMD|November 20, 2020
Tasks and interfaces in primary and specialized palliative care for Duchenne muscular dystrophy - A patients' perspectiveMaria Janisch, Kristin Boehme, Simone Thiele, et al.
Integrative Organismal Biology (Oxford, England)|June 12, 2025
Comparative Study of Sun Compass Orientation in Migrating Anadromous versus Resident Freshwater Threespine Sticklebacks (<i>Gasterosteus aculeatus</i>)L Spiecker, M Laurien, F Schröder, et al.
Substance Abuse : Research and Treatment|December 13, 2021
Changes in Substance Use Among People Seeking Alcohol and Other Drug Treatment During the COVID-19 Pandemic: Evaluating Mental Health Outcomes and ResilienceMolly Carlyle, Janni Leung, Zoe C Walter, et al.
Neuromuscular Disorders : NMD|December 18, 2003
A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammationSabine Krause, Beate Schlotter-Weigel, Maggie C Walter, et al.
Journal of Neuromuscular Diseases|May 31, 2021
Health-related Quality of Life and Satisfaction with German Health Care Services in Patients with Charcot-Marie-Tooth NeuropathyElisabeth Schorling, Katja C Senn, Simone Thiele, et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|August 21, 2016
Unexpected genomic relationships between Bacillus anthracis strains from Bangladesh and Central EuropeFarzana Islam Rume, Chowdhury Rafiqul Ahsan, Paritosh Kumar Biswas, et al.
Pageof 86

Showing results (601-610 of 860) with videos related to

Sort By:
Pageof 86
Neuromuscular Disorders : NMD|October 16, 2009
Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblastsJouni Vesa, Hailing Su, Giles D Watts, et al.
Human Molecular Genetics|August 4, 2009
Evaluation of the therapeutic potential of carbonic anhydrase inhibitors in two animal models of dystrophin deficient muscular dystrophyJean Giacomotto, Cordula Pertl, Caroline Borrel, et al.
Neuromuscular Disorders : NMD|January 11, 2005
Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophyMaggie C Walter, Thomas N Witt, Beate Schlotter Weigel, et al.
Journal of Biomedical Semantics|April 13, 2019
Moonstone: a novel natural language processing system for inferring social risk from clinical narrativesMike Conway, Salomeh Keyhani, Lee Christensen, et al.
Neuromuscular Disorders : NMD|November 20, 2020
Tasks and interfaces in primary and specialized palliative care for Duchenne muscular dystrophy - A patients' perspectiveMaria Janisch, Kristin Boehme, Simone Thiele, et al.
Integrative Organismal Biology (Oxford, England)|June 12, 2025
Comparative Study of Sun Compass Orientation in Migrating Anadromous versus Resident Freshwater Threespine Sticklebacks (<i>Gasterosteus aculeatus</i>)L Spiecker, M Laurien, F Schröder, et al.
Substance Abuse : Research and Treatment|December 13, 2021
Changes in Substance Use Among People Seeking Alcohol and Other Drug Treatment During the COVID-19 Pandemic: Evaluating Mental Health Outcomes and ResilienceMolly Carlyle, Janni Leung, Zoe C Walter, et al.
Neuromuscular Disorders : NMD|December 18, 2003
A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammationSabine Krause, Beate Schlotter-Weigel, Maggie C Walter, et al.
Journal of Neuromuscular Diseases|May 31, 2021
Health-related Quality of Life and Satisfaction with German Health Care Services in Patients with Charcot-Marie-Tooth NeuropathyElisabeth Schorling, Katja C Senn, Simone Thiele, et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|August 21, 2016
Unexpected genomic relationships between Bacillus anthracis strains from Bangladesh and Central EuropeFarzana Islam Rume, Chowdhury Rafiqul Ahsan, Paritosh Kumar Biswas, et al.
Pageof 86