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Showing results (1011-1020 of 1,035) with videos related to
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Brain : a Journal of Neurology
|
May 8, 2007
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies
Haiyan Zhou, Heinz Jungbluth, Caroline A Sewry, et al.
Neuromuscular Disorders : NMD
|
January 19, 2010
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Haiyan Zhou, Suzanne Lillis, Ryan E Loy, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
May 22, 2013
Adoptive transfer of tumor-infiltrating lymphocytes in patients with metastatic melanoma: intent-to-treat analysis and efficacy after failure to prior immunotherapies
Michal J Besser, Ronnie Shapira-Frommer, Orit Itzhaki, et al.
Human Mutation
|
April 2, 2019
Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathies
Christoph Bachmann, Faiza Noreen, Nicol C Voermans, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 23, 2025
Alzheimer's Imaging Consortium
Prithvi Arunachalam, Francesca Treves, Leonard Pieperhoff, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Biomarkers
Prithvi Arunachalam, Francesca Treves, Leonard Pieperhoff, et al.
Alcohol, Clinical & Experimental Research
|
January 5, 2025
Impact of chronic ethanol consumption and SARS-COV-2 on the liver and intestine: A pilot dose-response study in mice
Smita Ghare, Dennis Warner, Jeffrey Warner, et al.
Annals of Neurology
|
September 15, 2010
RYR1 mutations are a common cause of congenital myopathies with central nuclei
J M Wilmshurst, S Lillis, H Zhou, et al.
European Journal of Neurology
|
May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout life
M Snoeck, B G M van Engelen, B Küsters, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 30, 2025
Compound Heterozygous Structural Variants in Cases with Unsolved PRKN-Associated Parkinson's Disease
Agata Fant, Sara Trova, Edoardo Monfrini, et al.
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of 104
Search research articles
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Showing results (1011-1020 of 1,035) with videos related to
Sort By:
Page
of 104
Brain : a Journal of Neurology
|
May 8, 2007
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies
Haiyan Zhou, Heinz Jungbluth, Caroline A Sewry, et al.
Neuromuscular Disorders : NMD
|
January 19, 2010
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Haiyan Zhou, Suzanne Lillis, Ryan E Loy, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
May 22, 2013
Adoptive transfer of tumor-infiltrating lymphocytes in patients with metastatic melanoma: intent-to-treat analysis and efficacy after failure to prior immunotherapies
Michal J Besser, Ronnie Shapira-Frommer, Orit Itzhaki, et al.
Human Mutation
|
April 2, 2019
Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathies
Christoph Bachmann, Faiza Noreen, Nicol C Voermans, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 23, 2025
Alzheimer's Imaging Consortium
Prithvi Arunachalam, Francesca Treves, Leonard Pieperhoff, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Biomarkers
Prithvi Arunachalam, Francesca Treves, Leonard Pieperhoff, et al.
Alcohol, Clinical & Experimental Research
|
January 5, 2025
Impact of chronic ethanol consumption and SARS-COV-2 on the liver and intestine: A pilot dose-response study in mice
Smita Ghare, Dennis Warner, Jeffrey Warner, et al.
Annals of Neurology
|
September 15, 2010
RYR1 mutations are a common cause of congenital myopathies with central nuclei
J M Wilmshurst, S Lillis, H Zhou, et al.
European Journal of Neurology
|
May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout life
M Snoeck, B G M van Engelen, B Küsters, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 30, 2025
Compound Heterozygous Structural Variants in Cases with Unsolved PRKN-Associated Parkinson's Disease
Agata Fant, Sara Trova, Edoardo Monfrini, et al.
Page
of 104