Results 101 to 110 of about 25,975 (129)

Cerebellar ataxia-onset ALS with <i>SOD1</i> D91A mutation: a rare phenotype. [PDF]

Front Neurol
Shevchuk DV, Nuzhnyi EP, Fedotova EY, Ershova MV, Minaev IV, Anikin GA, Protsenko AR, Abramycheva NY, Zakharova MN, Illarioshkin SN.   +9 more
europepmc   +1 more source

Spectrum of Dystonia in Spinocerebellar Ataxia. [PDF]

Tremor Other Hyperkinet Mov (N Y)
Yellaturi SR, Mukherjee A, Pandey S.
europepmc   +1 more source

Amyotrophic lateral sclerosis -plus patient with an intermediate-length <i>CACNA1A</i> allele: a Case Report. [PDF]

Front Genet
Gao X, Wang T, Chen S, Ma Y, Wei Q, Li C, Shang H, Chen X.   +7 more
europepmc   +1 more source

Diagnostic redirection in dementia-first spinocerebellar ataxia type 17: a family-based case report and focused literature review. [PDF]

Front Neurosci
Zhang S, Zhang X, Li L, Zhou B, Shao W.
europepmc   +1 more source

Phenotype and Genetics of Spinocerebellar Ataxia Type 27B: Novel Movement-disorder Features, Cognitive Impairment, and Repeat Expansion Findings. [PDF]

Cerebellum
Rashedi R, Peemöller F, Erdmann H, Gelderblom M, Hidding U, Ganos C, Chen R, Abicht A, Zittel S.   +8 more
europepmc   +1 more source

Recurrent acute liver failure in infancy - a novel <i>SCYL1</i> mutation: A case report. [PDF]

World J Clin Pediatr
Zourob D, Teneiji AA, Miqdady M, Al Atrash E.   +3 more
europepmc   +1 more source

Mapping the Disrupted Connectome in Spinocerebellar Ataxia Type 3: A Network-Based Statistics Study Identifying Novel Therapeutic Targets for Neuromodulation. [PDF]

CNS Neurosci Ther
Ou L, Zhou C, Wang X, Shi L, Ou P, Xiang C, Chen H, Chen X, Wang B, Chen W, Wang J, Long Z, Liu C.   +12 more
europepmc   +1 more source

Spinocerebellar Ataxia Type 12: Spectrums of Movement Disorders and Clinical Features.

Neurodegener Dis
Rafiei MA, Sadeghzadeh S, Salari M, Etemadifar M.   +3 more
europepmc   +1 more source