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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 myopathiesHaiyan 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) geneHaiyan 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 immunotherapiesMichal 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 myopathiesChristoph Bachmann, Faiza Noreen, Nicol C Voermans, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 23, 2025
Alzheimer's Imaging ConsortiumPrithvi Arunachalam, Francesca Treves, Leonard Pieperhoff, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 25, 2025
BiomarkersPrithvi 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 miceSmita Ghare, Dennis Warner, Jeffrey Warner, et al.
Annals of Neurology|September 15, 2010
RYR1 mutations are a common cause of congenital myopathies with central nucleiJ M Wilmshurst, S Lillis, H Zhou, et al.
European Journal of Neurology|May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout lifeM 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 DiseaseAgata Fant, Sara Trova, Edoardo Monfrini, et al.
Pageof 104

Showing results (1011-1020 of 1,035) with videos related to

Sort By:
Pageof 104
Brain : a Journal of Neurology|May 8, 2007
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathiesHaiyan 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) geneHaiyan 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 immunotherapiesMichal 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 myopathiesChristoph Bachmann, Faiza Noreen, Nicol C Voermans, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 23, 2025
Alzheimer's Imaging ConsortiumPrithvi Arunachalam, Francesca Treves, Leonard Pieperhoff, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 25, 2025
BiomarkersPrithvi 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 miceSmita Ghare, Dennis Warner, Jeffrey Warner, et al.
Annals of Neurology|September 15, 2010
RYR1 mutations are a common cause of congenital myopathies with central nucleiJ M Wilmshurst, S Lillis, H Zhou, et al.
European Journal of Neurology|May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout lifeM 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 DiseaseAgata Fant, Sara Trova, Edoardo Monfrini, et al.
Pageof 104