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D Mathews

Showing results (351-360 of 450) with videos related to

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Experimental Neurology|June 6, 2022
Deep cerebellar stimulation enhances cognitive recovery after prefrontal traumatic brain injury in rodentHugh H Chan, Olivia Hogue, Nicole D Mathews, et al.
Kidney International|February 3, 2012
Post-streptococcal glomerulonephritis is a strong risk factor for chronic kidney disease in later lifeWendy E Hoy, Andrew V White, Alison Dowling, et al.
Neurology|August 9, 2020
Motor outcome measures in patients with <i>FKRP</i> mutations: A longitudinal follow-upAmber M Gedlinske, Carrie M Stephan, Shelley R H Mockler, et al.
Frontiers in Public Health|December 12, 2022
Using implementation mapping for the adoption and implementation of <i>Target:BP</i> in community health centersMelissa A Valerio-Shewmaker, Natalia I Heredia, Catherine Pulicken, et al.
EMBO Molecular Medicine|March 6, 2023
An innovative hematopoietic stem cell gene therapy approach benefits CLN1 disease in the mouse modelMarco Peviani, Sabyasachi Das, Janki Patel, et al.
BMC Neurology|March 16, 2024
Defining clinical endpoints in limb girdle muscular dystrophy: a GRASP-LGMD studyAmy Doody, Lindsay Alfano, Jordi Diaz-Manera, et al.
Radiation Protection Dosimetry|November 17, 2020
Ct Dosimetry for The Australian Cohort Data Linkage StudyZoe Brady, Anna Forsythe, Jasmine McBain-Miller, et al.
Annals of Clinical and Translational Neurology|April 17, 2025
UDP-glucose dehydrogenase variants cause dystroglycanopathyAnna M Reelfs, Carrie M Stephan, Theresa M Czech, et al.
Journal of the Neurological Sciences|June 10, 2011
Mortality in Friedreich ataxiaAmy Y Tsou, Erin K Paulsen, Sarah J Lagedrost, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 1, 1994
The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the diseaseS T Winokur, U Bengtsson, J Feddersen, et al.
Pageof 45

Showing results (351-360 of 450) with videos related to

Sort By:
Pageof 45
Experimental Neurology|June 6, 2022
Deep cerebellar stimulation enhances cognitive recovery after prefrontal traumatic brain injury in rodentHugh H Chan, Olivia Hogue, Nicole D Mathews, et al.
Kidney International|February 3, 2012
Post-streptococcal glomerulonephritis is a strong risk factor for chronic kidney disease in later lifeWendy E Hoy, Andrew V White, Alison Dowling, et al.
Neurology|August 9, 2020
Motor outcome measures in patients with <i>FKRP</i> mutations: A longitudinal follow-upAmber M Gedlinske, Carrie M Stephan, Shelley R H Mockler, et al.
Frontiers in Public Health|December 12, 2022
Using implementation mapping for the adoption and implementation of <i>Target:BP</i> in community health centersMelissa A Valerio-Shewmaker, Natalia I Heredia, Catherine Pulicken, et al.
EMBO Molecular Medicine|March 6, 2023
An innovative hematopoietic stem cell gene therapy approach benefits CLN1 disease in the mouse modelMarco Peviani, Sabyasachi Das, Janki Patel, et al.
BMC Neurology|March 16, 2024
Defining clinical endpoints in limb girdle muscular dystrophy: a GRASP-LGMD studyAmy Doody, Lindsay Alfano, Jordi Diaz-Manera, et al.
Radiation Protection Dosimetry|November 17, 2020
Ct Dosimetry for The Australian Cohort Data Linkage StudyZoe Brady, Anna Forsythe, Jasmine McBain-Miller, et al.
Annals of Clinical and Translational Neurology|April 17, 2025
UDP-glucose dehydrogenase variants cause dystroglycanopathyAnna M Reelfs, Carrie M Stephan, Theresa M Czech, et al.
Journal of the Neurological Sciences|June 10, 2011
Mortality in Friedreich ataxiaAmy Y Tsou, Erin K Paulsen, Sarah J Lagedrost, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 1, 1994
The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the diseaseS T Winokur, U Bengtsson, J Feddersen, et al.
Pageof 45