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Brain & Development|January 26, 2020
Clinical practice with steroid therapy for Duchenne muscular dystrophy: An expert survey in Asia and OceaniaFumi Takeuchi, Harumasa Nakamura, Naohiro Yonemoto, et al.
JAMA Neurology|February 19, 2014
Mutations in GNAL: a novel cause of craniocervical dystoniaKishore R Kumar, Katja Lohmann, Ikuo Masuho, et al.
Journal of Neurology|February 10, 2018
Defining spasticity: a new approach considering current movement disorders terminology and botulinum toxin therapyDirk Dressler, Roongroj Bhidayasiri, Saeed Bohlega, et al.
Annals of Neurology|April 12, 2019
A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonismAna Westenberger, Charles Jourdan Reyes, Gerard Saranza, et al.
International Journal of Molecular Sciences|February 26, 2022
Transcriptional Alterations in X-Linked Dystonia-Parkinsonism Caused by the SVA RetrotransposonJelena Pozojevic, Shela Marie Algodon, Joseph Neos Cruz, et al.
Nature Communications|May 29, 2021
Identifying genetic modifiers of age-associated penetrance in X-linked dystonia-parkinsonismBjörn-Hergen Laabs, Christine Klein, Jelena Pozojevic, et al.
Brain : a Journal of Neurology|June 23, 2026
Relative frequencies of muscle specific kinase antibody myasthenia in 46 centres worldwideAngela Vincent, Rehab Badi, Nina Barisic, et al.
Cell|February 24, 2018
Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome AssemblyTatsiana Aneichyk, William T Hendriks, Rachita Yadav, et al.
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