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Showing results (1051-1060 of 1,067) with videos related to
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Journal of Neuromuscular Diseases
|
November 14, 2022
Telemedicine in Neuromuscular Diseases During Covid-19 Pandemic: ERN-NMD European Survey
Lynda El-Hassar, Ahmed Amara, Benoit Sanson, et al.
Nature Genetics
|
May 6, 2020
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes
Andrea Cortese, Yi Zhu, Adriana P Rebelo, et al.
Nature Communications
|
April 28, 2022
Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy
Hong Joo Kim, Payam Mohassel, Sandra Donkervoort, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 12, 2018
Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy
Alicia Alonso-Jimenez, Rosemarie H M J M Kroon, Aida Alejaldre-Monforte, et al.
American Journal of Human Genetics
|
April 16, 2021
A form of muscular dystrophy associated with pathogenic variants in JAG2
Sandra Coppens, Alison M Barnard, Sanna Puusepp, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 9, 2018
Muscle MRI in patients with dysferlinopathy: pattern recognition and implications for clinical trials
Jordi Diaz-Manera, Roberto Fernandez-Torron, Jaume LLauger, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 27, 2022
Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study
Marianela Schiava, Chiseko Ikenaga, Rocío Nur Villar-Quiles, et al.
Neurology. Genetics
|
July 18, 2025
Muscle Biopsy Findings in Valosin-Containing Protein Multisystem Proteinopathy
Marianela Schiava, Yolande Parkhurst, Matthew Henderson, et al.
Journal of Neurology
|
August 21, 2023
Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP-mediated disease reveals characteristic features useful for diagnosis
Diana Esteller, Marianela Schiava, José Verdú-Díaz, et al.
Neurology
|
January 11, 2019
Assessment of disease progression in dysferlinopathy: A 1-year cohort study
Ursula Moore, Marni Jacobs, Meredith K James, et al.
Page
of 107
Search research articles
Search
Showing results (1051-1060 of 1,067) with videos related to
Sort By:
Page
of 107
Journal of Neuromuscular Diseases
|
November 14, 2022
Telemedicine in Neuromuscular Diseases During Covid-19 Pandemic: ERN-NMD European Survey
Lynda El-Hassar, Ahmed Amara, Benoit Sanson, et al.
Nature Genetics
|
May 6, 2020
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes
Andrea Cortese, Yi Zhu, Adriana P Rebelo, et al.
Nature Communications
|
April 28, 2022
Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy
Hong Joo Kim, Payam Mohassel, Sandra Donkervoort, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 12, 2018
Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy
Alicia Alonso-Jimenez, Rosemarie H M J M Kroon, Aida Alejaldre-Monforte, et al.
American Journal of Human Genetics
|
April 16, 2021
A form of muscular dystrophy associated with pathogenic variants in JAG2
Sandra Coppens, Alison M Barnard, Sanna Puusepp, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 9, 2018
Muscle MRI in patients with dysferlinopathy: pattern recognition and implications for clinical trials
Jordi Diaz-Manera, Roberto Fernandez-Torron, Jaume LLauger, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 27, 2022
Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study
Marianela Schiava, Chiseko Ikenaga, Rocío Nur Villar-Quiles, et al.
Neurology. Genetics
|
July 18, 2025
Muscle Biopsy Findings in Valosin-Containing Protein Multisystem Proteinopathy
Marianela Schiava, Yolande Parkhurst, Matthew Henderson, et al.
Journal of Neurology
|
August 21, 2023
Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP-mediated disease reveals characteristic features useful for diagnosis
Diana Esteller, Marianela Schiava, José Verdú-Díaz, et al.
Neurology
|
January 11, 2019
Assessment of disease progression in dysferlinopathy: A 1-year cohort study
Ursula Moore, Marni Jacobs, Meredith K James, et al.
Page
of 107