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Movement Disorders : Official Journal of the Movement Disorder Society|April 21, 2012
Abnormal response to cortical activation in early stages of Huntington diseaseFanny Mochel, Tra-My N'Guyen, Dinesh Deelchand, et al.
Frontiers in Genetics|October 17, 2019
Genetic Testing in Prion Disease: Psychological Consequences of the Decisions to Know or Not to KnowMathias Schwartz, Jean-Philippe Brandel, Marie Lise Babonneau, et al.
Archives of Cardiovascular Diseases|December 18, 2021
Characterizing cardiac phenotype in Friedreich's ataxia: The CARFA studyLise Legrand, Jonathan W Weinsaft, Francoise Pousset, et al.
Scientific Reports|June 24, 2021
Multiparametric characterization of white matter alterations in early stage Huntington diseaseIsaac M Adanyeguh, Francesca Branzoli, Cécile Delorme, et al.
Annals of Neurology|August 1, 2018
In vivo characterization of white matter pathology in premanifest huntington's diseaseJiaying Zhang, Sarah Gregory, Rachael I Scahill, et al.
European Journal of Human Genetics : EJHG|June 16, 2016
Prenatal testing in Huntington disease: after the test, choices recommenceHanane Bouchghoul, Stéphane-Françoise Clément, Danièle Vauthier, et al.
Frontiers in Neuroscience|November 21, 2018
Altered Intracortical T<sub>1</sub>-Weighted/T<sub>2</sub>-Weighted Ratio Signal in Huntington's DiseaseChristopher D Rowley, Sarah J Tabrizi, Rachael I Scahill, et al.
American Journal of Cardiovascular Drugs : Drugs, Devices, and Other Interventions|October 26, 2019
Predictors of Left Ventricular Dysfunction in Friedreich's Ataxia in a 16-Year Observational StudyLise Legrand, Abdourahmane Diallo, Marie-Lorraine Monin, et al.
The Journal of Biological Chemistry|November 30, 2011
Early alterations of brain cellular energy homeostasis in Huntington disease modelsFanny Mochel, Brandon Durant, Xingli Meng, et al.
Archives of Neurology|August 20, 2003
Subtle cognitive impairment but no dementia in patients with spastin mutationsChantal M E Tallaksen, Elodie Guichart-Gomez, Patrice Verpillat, et al.
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