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Human Molecular Genetics
|
October 19, 2018
The epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neurons
Mattéa J Finelli, Davide Aprile, Enrico Castroflorio, et al.
Journal of Neuromuscular Diseases
|
February 5, 2019
Reliability and Validity of Self-Report Questionnaires as Indicators of Fatigue in RYR1-Related Disorders
Anna Kuo, Joshua J Todd, Jessica W Witherspoon, et al.
Plos One
|
February 5, 2025
Treatment with the CCR5 antagonist OB-002 reduces lung pathology, but does not prevent disease in a Syrian hamster model of SARS-CoV-2 infection
Bryce M Warner, Robert Vendramelli, Amrit S Boese, et al.
Skeletal Muscle
|
August 22, 2025
NAD<sup>+</sup> dyshomeostasis in RYR1-related myopathies
Tokunbor A Lawal, Willa Riekhof, Linda Groom, et al.
Molecular Psychiatry
|
September 19, 2024
Both GEF domains of the autism and developmental epileptic encephalopathy-associated Trio protein are required for proper tangential migration of GABAergic interneurons
Lara Eid, Ludmilla Lokmane, Praveen K Raju, et al.
Journal of Neurology
|
August 30, 2018
Correlation of phenotype with genotype and protein structure in RYR1-related disorders
Joshua J Todd, Vatsala Sagar, Tokunbor A Lawal, et al.
The Review of Scientific Instruments
|
October 4, 2018
Next-generation diamond cell and applications to single-crystal neutron diffraction
Bianca Haberl, Sachith Dissanayake, Yan Wu, et al.
Frontiers in Neurology
|
March 21, 2018
Novel Variants in Individuals with <i>RYR1</i>-Related Congenital Myopathies: Genetic, Laboratory, and Clinical Findings
Joshua J Todd, Muslima S Razaqyar, Jessica W Witherspoon, et al.
The Journal of Neuroscience Nursing : Journal of the American Association of Neuroscience Nurses
|
June 9, 2020
Assessing Motor Function in Congenital Muscular Dystrophy Patients Using Accelerometry
Tokunbor A Lawal, Joshua J Todd, Jeffrey S Elliott, et al.
Journal of Neuropathology and Experimental Neurology
|
April 9, 2014
Clinical, pathologic, and mutational spectrum of dystroglycanopathy caused by LARGE mutations
Katherine G Meilleur, Kristen Zukosky, Livija Medne, et al.
Page
of 23
Search research articles
Search
Showing results (191-200 of 225) with videos related to
Sort By:
Page
of 23
Human Molecular Genetics
|
October 19, 2018
The epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neurons
Mattéa J Finelli, Davide Aprile, Enrico Castroflorio, et al.
Journal of Neuromuscular Diseases
|
February 5, 2019
Reliability and Validity of Self-Report Questionnaires as Indicators of Fatigue in RYR1-Related Disorders
Anna Kuo, Joshua J Todd, Jessica W Witherspoon, et al.
Plos One
|
February 5, 2025
Treatment with the CCR5 antagonist OB-002 reduces lung pathology, but does not prevent disease in a Syrian hamster model of SARS-CoV-2 infection
Bryce M Warner, Robert Vendramelli, Amrit S Boese, et al.
Skeletal Muscle
|
August 22, 2025
NAD<sup>+</sup> dyshomeostasis in RYR1-related myopathies
Tokunbor A Lawal, Willa Riekhof, Linda Groom, et al.
Molecular Psychiatry
|
September 19, 2024
Both GEF domains of the autism and developmental epileptic encephalopathy-associated Trio protein are required for proper tangential migration of GABAergic interneurons
Lara Eid, Ludmilla Lokmane, Praveen K Raju, et al.
Journal of Neurology
|
August 30, 2018
Correlation of phenotype with genotype and protein structure in RYR1-related disorders
Joshua J Todd, Vatsala Sagar, Tokunbor A Lawal, et al.
The Review of Scientific Instruments
|
October 4, 2018
Next-generation diamond cell and applications to single-crystal neutron diffraction
Bianca Haberl, Sachith Dissanayake, Yan Wu, et al.
Frontiers in Neurology
|
March 21, 2018
Novel Variants in Individuals with <i>RYR1</i>-Related Congenital Myopathies: Genetic, Laboratory, and Clinical Findings
Joshua J Todd, Muslima S Razaqyar, Jessica W Witherspoon, et al.
The Journal of Neuroscience Nursing : Journal of the American Association of Neuroscience Nurses
|
June 9, 2020
Assessing Motor Function in Congenital Muscular Dystrophy Patients Using Accelerometry
Tokunbor A Lawal, Joshua J Todd, Jeffrey S Elliott, et al.
Journal of Neuropathology and Experimental Neurology
|
April 9, 2014
Clinical, pathologic, and mutational spectrum of dystroglycanopathy caused by LARGE mutations
Katherine G Meilleur, Kristen Zukosky, Livija Medne, et al.
Page
of 23