Results 151 to 160 of about 83,390 (218)

Coenzyme Q10 and spinocerebellar ataxias

Movement Disorders, 2015
R. Lo, K. Figueroa, S. Pulst, Chi-Ying R. Lin, S. Perlman, G. Wilmot, C. Gomez, J. Schmahmann, H. Paulson, V. Shakkottai, S. Ying, T. Zesiewicz, K. Bushara, M. Geschwind, Guangbin Xia, S. Subramony, T. Ashizawa, S. Kuo   +17 more
semanticscholar   +1 more source

Spinocerebellar ataxias in Venezuela: genetic epidemiology and their most likely ethnic descent

Journal of Human Genetics, 2015
I. Paradisi, Vassiliki Ikonomu, S. Arias
semanticscholar   +1 more source

Disturbed calcium signaling in spinocerebellar ataxias and Alzheimer's disease.

Seminars in Cell and Developmental Biology, 2015
P. Egorova, E. Popugaeva, I. Bezprozvanny   +2 more
semanticscholar   +1 more source

The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerability

Journal of Neurology Neurosurgery & Psychiatry, 2014
K. Hekman, C. Gomez
semanticscholar   +1 more source

Changes in CB1 and CB2 receptors in the post‐mortem cerebellum of humans affected by spinocerebellar ataxias

British Journal of Pharmacology, 2014
C. Rodríguez-Cueto, C. Benito, J. Fernández-Ruiz, J. Romero, Mariluz Hernández-Gálvez, M. Gómez‐Ruíz   +5 more
semanticscholar   +1 more source

Spinocerebellar ataxia

Neurobiology of Disease, 2018
van der Stijl, Rogier, Withoff, Sebo, Verbeek, Dineke S.   +2 more
openaire   +1 more source

SCAview: an Intuitive Visual Approach to the Integrative Analysis of Clinical Data in Spinocerebellar Ataxias. [PDF]

Cerebellum
Uebachs M, Wegner P, Schaaf S, Kugai S, Jacobi H, Kuo SH, Ashizawa T, Fluck J, EUROSCA study group, ESMI study group, RISCA study group, CRC-SCA study group, SCA Registry study group, Klockgether T, Faber J.   +14 more
europepmc   +1 more source

Spinocerebellar ataxias

, 1994
openaire   +1 more source

Spinocerebellar ataxia [PDF]

Nature Reviews Disease Primers, 2019
The spinocerebellar ataxias (SCAs) are a genetically heterogeneous group of autosomal dominantly inherited progressive disorders, the clinical hallmark of which is loss of balance and coordination accompanied by slurred speech; onset is most often in adult life. Genetically, SCAs are grouped as repeat expansion SCAs, such as SCA3/Machado-Joseph disease
Thomas Klockgether, Caterina Mariotti, Henry L Paulson   +2 more
exaly   +6 more sources