Results 221 to 226 of about 6,741 (226)

Regional differences in genetic subgroup frequency in hereditary cerebellar ataxia, and a morphometrical study of brain MR images in SCA1, MJD and SCA6

Journal of the Neurological Sciences, 1999
Utako Nagaoka, Toru Kawanami
exaly  

Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: Genetic, clinical, and positron emission tomography findings

Movement Disorders, 2009
Jifeng Guo, Li-Fang Lei, Xin-Xiang Yan   +2 more
exaly  

CRISPR-based gene activation for the study and treatment of MJD/SCA3

A doença de Machado-Joseph (DMJ) é uma doença neurodegenerativa caracterizada por uma expansão anormal do tripleto CAG no gene MJD 1/ATXN3, que resulta num trato de poliglutamina alargado no interior da proteína ataxina-3. Este aumento perigoso da função causa neurodegeneração em várias regiões do cérebro através de uma variedade de vias patogénicas ...
openaire   +1 more source

MicroRNA profiling in the serums of SCA3/MJD patients

International Journal of Neuroscience, 2014
Yuting Shi, Fengzhen Huang, Beisha Tang   +2 more
exaly  

P30.34 Abnormal offset cortical potential in Machado-Joseph disease (MJD)

Clinical Neurophysiology, 2006
M.K. Lu, C.H. Tsai, C.S. Liu, Y.J. Chen, C.C. Lee   +4 more
openaire   +1 more source

Natural History of Oculomotor Neurophysiology in Ataxic and Pre-ataxic Carriers of SCA3/MJD

Case Medical Research, 2020
openaire   +1 more source