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Frontiers in Neurology|July 19, 2021
Cognitive Deficits, Apathy, and Hypersomnolence Represent the Core Brain Symptoms of Adult-Onset Myotonic Dystrophy Type 1Jacob N Miller, Alison Kruger, David J Moser, et al.Ebiomedicine|February 15, 2024
Phenome-wide analysis reveals epistatic associations between APOL1 variants and chronic kidney disease and multiple other disordersWalt E Adamson, Harry Noyes, Paul Johnson, et al.Neurology|May 24, 2019
Lower extremity muscle pathology in myotonic dystrophy type 1 assessed by quantitative MRILinda Heskamp, Marlies van Nimwegen, Marieke J Ploegmakers, et al.Stem Cell Research & Therapy|September 15, 2024
Ameliorated cellular hallmarks of myotonic dystrophy in hybrid myotubes from patient and unaffected donor cellsRenée H L Raaijmakers, C Rosanne M Ausems, Marieke Willemse, et al.Neuromuscular Disorders : NMD|July 7, 2023
Longitudinal changes in white matter as measured with diffusion tensor imaging in adult-onset myotonic dystrophy type 1Timothy R Koscik, Ellen van der Plas, Jeffrey D Long, et al.Frontiers in Neurology|February 7, 2022
Blood-Based Markers of Neuronal Injury in Adult-Onset Myotonic Dystrophy Type 1Ellen van der Plas, Jeffrey D Long, Timothy R Koscik, et al.Journal of Huntington'S Disease|February 13, 2021
Huntington's Disease Pathogenesis: Two Sequential ComponentsEun Pyo Hong, Marcy E MacDonald, Vanessa C Wheeler, et al.Journal of Huntington'S Disease|February 13, 2021
Approaches to Sequence the HTT CAG Repeat Expansion and Quantify Repeat Length VariationMarc Ciosi, Sarah A Cumming, Afroditi Chatzi, et al.Human Molecular Genetics|September 13, 2022
Individual-specific levels of CTG•CAG somatic instability are shared across multiple tissues in myotonic dystrophy type 1Fernando Morales, Eyleen Corrales, Melissa Vásquez, et al.Plos Genetics|March 8, 2013
MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease miceStéphanie Tomé, Kevin Manley, Jodie P Simard, et al.Pageof 10