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Showing results (1031-1040 of 1,067) with videos related to
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Journal of Cachexia, Sarcopenia and Muscle
|
February 23, 2022
Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles
Laura Le Gall, William J Duddy, Cecile Martinat, et al.
Brain : a Journal of Neurology
|
February 11, 2020
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion
Andrea Cortese, Stefano Tozza, Wai Yan Yau, et al.
Annals of Neurology
|
May 10, 2019
A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs)
Davide Pareyson, Tanya Stojkovic, Mary M Reilly, et al.
United European Gastroenterology Journal
|
November 27, 2024
Endoscopic retrograde cholangiopancreatography training conditions, results from a pan-European survey: Between vision and reality
Karim Hamesch, Oscar Cahyadi, Stavros Dimitriadis, et al.
Acta Neuropathologica
|
July 8, 2017
Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues
Valérie Biancalana, Sophie Scheidecker, Marguerite Miguet, et al.
Orphanet Journal of Rare Diseases
|
October 27, 2021
A multicenter cross-sectional French study of the impact of COVID-19 on neuromuscular diseases
Lucie Isoline Pisella, Sara Fernandes, Guilhem Solé, et al.
European Heart Journal
|
March 22, 2021
Association between prophylactic angiotensin-converting enzyme inhibitors and overall survival in Duchenne muscular dystrophy-analysis of registry data
Raphaël Porcher, Isabelle Desguerre, Helge Amthor, et al.
Annals of Neurology
|
February 12, 2021
Assessing Dysferlinopathy Patients Over Three Years With a New Motor Scale
Marni B Jacobs, Meredoith K James, Linda P Lowes, et al.
American Journal of Human Genetics
|
October 18, 2016
Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization
Gina L O'Grady, Heather A Best, Tamar E Sztal, et al.
Frontiers in Neurology
|
April 1, 2022
Assessing the Relationship of Patient Reported Outcome Measures With Functional Status in Dysferlinopathy: A Rasch Analysis Approach
Anna G Mayhew, Meredith K James, Ursula Moore, et al.
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of 107
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Showing results (1031-1040 of 1,067) with videos related to
Sort By:
Page
of 107
Journal of Cachexia, Sarcopenia and Muscle
|
February 23, 2022
Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles
Laura Le Gall, William J Duddy, Cecile Martinat, et al.
Brain : a Journal of Neurology
|
February 11, 2020
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion
Andrea Cortese, Stefano Tozza, Wai Yan Yau, et al.
Annals of Neurology
|
May 10, 2019
A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs)
Davide Pareyson, Tanya Stojkovic, Mary M Reilly, et al.
United European Gastroenterology Journal
|
November 27, 2024
Endoscopic retrograde cholangiopancreatography training conditions, results from a pan-European survey: Between vision and reality
Karim Hamesch, Oscar Cahyadi, Stavros Dimitriadis, et al.
Acta Neuropathologica
|
July 8, 2017
Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues
Valérie Biancalana, Sophie Scheidecker, Marguerite Miguet, et al.
Orphanet Journal of Rare Diseases
|
October 27, 2021
A multicenter cross-sectional French study of the impact of COVID-19 on neuromuscular diseases
Lucie Isoline Pisella, Sara Fernandes, Guilhem Solé, et al.
European Heart Journal
|
March 22, 2021
Association between prophylactic angiotensin-converting enzyme inhibitors and overall survival in Duchenne muscular dystrophy-analysis of registry data
Raphaël Porcher, Isabelle Desguerre, Helge Amthor, et al.
Annals of Neurology
|
February 12, 2021
Assessing Dysferlinopathy Patients Over Three Years With a New Motor Scale
Marni B Jacobs, Meredoith K James, Linda P Lowes, et al.
American Journal of Human Genetics
|
October 18, 2016
Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization
Gina L O'Grady, Heather A Best, Tamar E Sztal, et al.
Frontiers in Neurology
|
April 1, 2022
Assessing the Relationship of Patient Reported Outcome Measures With Functional Status in Dysferlinopathy: A Rasch Analysis Approach
Anna G Mayhew, Meredith K James, Ursula Moore, et al.
Page
of 107