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Cerebellum (London, England)|December 16, 2022
Patients' Perspective in Hereditary AtaxiaSorina Gorcenco, Christin Karremo, Andreas PuschmannJournal of Neurology|October 3, 2023
Clinical and genetic analyses of a Swedish patient series diagnosed with ataxiaSorina Gorcenco, Efthymia Kafantari, Joel Wallenius, et al.American Journal of Human Genetics|November 30, 2023
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine diseaseJoel Wallenius, Efthymia Kafantari, Emma Jhaveri, et al.Science Translational Medicine|October 22, 2020
Toward allele-specific targeting therapy and pharmacodynamic marker for spinocerebellar ataxia type 3Mercedes Prudencio, Hector Garcia-Moreno, Karen R Jansen-West, et al.Pageof 1