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Human Molecular Genetics|August 25, 2021
Myotonic dystrophy type 1 (DM1) clinical subtypes and CTCF site methylation status flanking the CTG expansion are mutant allele length-dependentFernando Morales, Eyleen Corrales, Baili Zhang, et al.Neurology. Genetics|August 28, 2020
Variant repeats within the DMPK CTG expansion protect function in myotonic dystrophy type 1Jacob N Miller, Ellen van der Plas, Mark Hamilton, et al.Frontiers in Neurology|October 19, 2018
Outcome Measures for Central Nervous System Evaluation in Myotonic Dystrophy Type 1 May Be Confounded by Deficits in Motor Function or InsightMark J Hamilton, John McLean, Sarah Cumming, et al.Human Molecular Genetics|September 21, 2022
Spanish HTT gene study reveals haplotype and allelic diversity with possible implications for germline expansion dynamics in Huntington diseaseAinara Ruiz de Sabando, Edurne Urrutia Lafuente, Arkaitz Galbete, et al.Human Molecular Genetics|July 1, 2020
Longitudinal increases in somatic mosaicism of the expanded CTG repeat in myotonic dystrophy type 1 are associated with variation in age-at-onsetFernando Morales, Melissa Vásquez, Eyleen Corrales, et al.Acta Neurologica Scandinavica|January 1, 2020
Activities of daily living in myotonic dystrophy type 1Erik Landfeldt, Nikoletta Nikolenko, Cecilia Jimenez-Moreno, et al.Journal of Neurology|June 17, 2020
Change over time in ability to perform activities of daily living in myotonic dystrophy type 1Erik Landfeldt, Nikoletta Nikolenko, Cecilia Jimenez-Moreno, et al.Journal of Huntington'S Disease|December 23, 2025
Genetic testing for Huntington's disease: Past, present and future. How could genetic data be used to improve clinical practice?Davina J Hensman Moss, Rhiannon Ireland, Guy Chapman, et al.Brain : a Journal of Neurology|June 20, 2019
MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1Michael Flower, Vilija Lomeikaite, Marc Ciosi, et al.Neuroimage. Clinical|December 8, 2018
Structural white matter networks in myotonic dystrophy type 1Maud van Dorst, Kees Okkersen, Roy P C Kessels, et al.Pageof 10