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Journal of the Neurological Sciences|October 5, 2007
Oxidative stress is induced in female carriers of X-linked adrenoleukodystrophyMarion Deon, Angela Sitta, Alethea G Barschak, et al.
Archives of Neurology|December 14, 2011
The APOE ε2 allele increases the risk of earlier age at onset in Machado-Joseph diseaseConceição Bettencourt, Mafalda Raposo, Nadiya Kazachkova, et al.
Annals of Neurology|September 26, 2020
CAG Repeat Size Influences the Progression Rate of Spinocerebellar Ataxia Type 3Vanessa B Leotti, Jeroen J de Vries, Camila M Oliveira, et al.
Movement Disorders Clinical Practice|October 27, 2018
Clinical Scales Predict Significant Videofluoroscopic Dysphagia in Machado Joseph Disease PatientsAline D Russo, Estela R Reckziegel, Ana C Krum-Santos, et al.
Arquivos De Neuro-Psiquiatria|October 24, 2006
White matter lesions in Fabry disease before and after enzyme replacement therapy: a 2-year follow-upLaura B Jardim, Flávio Aesse, Leonardo M Vedolin, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|March 14, 2015
Protective effect of antioxidants on DNA damage in leukocytes from X-linked adrenoleukodystrophy patientsDesirèe P Marchetti, Bruna Donida, Helen T da Rosa, et al.
Biochimica Et Biophysica Acta|November 17, 2011
Globotriaosylceramide is correlated with oxidative stress and inflammation in Fabry patients treated with enzyme replacement therapyGiovana B Biancini, Camila S Vanzin, Daiane B Rodrigues, et al.
Cerebellum (London, England)|March 17, 2012
Sequence analysis of 5' regulatory regions of the Machado-Joseph disease gene (ATXN3)Conceição Bettencourt, Mafalda Raposo, Nadiya Kazachkova, et al.
Neuromolecular Medicine|September 15, 2017
Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the MutationGiovana B Bampi, Rafael Bisso-Machado, Tábita Hünemeier, et al.
Cerebellum (London, England)|January 15, 2019
Ophthalmological and Neurologic Manifestations in Pre-clinical and Clinical Phases of Spinocerebellar Ataxia Type 7Pietro B Azevedo, Anastácia G Rocha, Leda M N Keim, et al.
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