Results 121 to 130 of about 1,015 (189)

A Novel Compound Heterozygous Mutation in Aprataxin Causes Slowly Progressive Ataxia without Oculomotor Apraxia. [PDF]

open access: yesMov Disord Clin Pract
Satolli S   +6 more
europepmc   +1 more source

Gait and cognitive disorders revealing massive neurocysticercosis: a case report. [PDF]

open access: yesOxf Med Case Reports
Rabearisoa PH   +3 more
europepmc   +1 more source

Exploring the Pathogenicity of SETX I1942T Variant in Ataxia with Oculomotor Apraxia Type 2 Through Segregation Analysis. [PDF]

open access: yesMov Disord Clin Pract
Ros-Arlanzón P   +4 more
europepmc   +1 more source

Pick's disease presenting as progressive apraxia of speech: Atypical clinical and neuroimaging features in three autopsy-confirmed cases. [PDF]

open access: yesClin Neurol Neurosurg
Jones KE   +9 more
europepmc   +1 more source

Apraxic deficits predict general cognitive impairment in patients with biomarker-verified Alzheimer's pathology. [PDF]

open access: yesJ Neurol
Schmidt CC   +10 more
europepmc   +1 more source

Evaluation of higher cognitive functions following posterior quadrant disconnection in the non-dominant hemisphere: a Case Report. [PDF]

open access: yesFront Hum Neurosci
Kawase N   +10 more
europepmc   +1 more source

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