Results 11 to 20 of about 47,850 (263)

Acute Cerebellar Ataxia Associated with Modest Elevation of Anti-GAD Antibodies in a Young Patient

open access: yesTremor and Other Hyperkinetic Movements, 2019
Background: Anti-GAD-related cerebellar ataxia has rarely been described as an acute cause of autoimmune ataxia. Phenomenology Shown: A young female who acutely developed anti-GAD-associated ataxia with magnetic resonance imaging (MRI) showing ...
Juliana Gomez, Dongkwan Jin
doaj   +1 more source

Clinical spectrum of early onset cerebellar ataxia with retained tendon reflexes: an autosomal recessive ataxia not to be missed

open access: yesArquivos de Neuro-Psiquiatria, 2013
Autosomal recessive cerebellar ataxias are a heterogeneous group of neurological disorders. In 1981, a neurological entity comprised by early onset progressive cerebellar ataxia, dysarthria, pyramidal weakness of the limbs and retained or increased upper
Jose Luiz Pedroso   +4 more
doaj   +1 more source

Cerebellar cognitive disorder parallels cerebellar motor symptoms in Friedreich ataxia

open access: yesAnnals of Clinical and Translational Neurology, 2020
Dentate nuclei (DN) are involved in cerebellar modulation of motor and cognitive functions, whose impairment causes ataxia and cerebellar cognitive affective syndrome (CCAS).
Gilles Naeije   +5 more
doaj   +1 more source

Cerebellar glutamatergic system impacts spontaneous motor recovery by regulating Gria1 expression

open access: yesnpj Regenerative Medicine, 2022
Peripheral nerve injury (PNI) often results in spontaneous motor recovery; however, how disrupted cerebellar circuitry affects PNI-associated motor recovery is unknown.
Pallavi Asthana   +11 more
doaj   +1 more source

Cerebellar Transcranial Magnetic Stimulation Improves Ataxia in Minamata Disease

open access: yesCase Reports in Neurology, 2019
Minamata disease (MD) is a form of intoxication involving the central nervous system and is caused by ingesting seafood from methylmercury-contaminated areas in Japan.
Masaaki Nakamura   +4 more
doaj   +1 more source

Inferior cerebellar hypoplasia resembling a Dandy-Walker-like malformation in purebred Eurasier dogs with familial non-progressive ataxia: a retrospective and prospective clinical cohort study. [PDF]

open access: yesPLoS ONE, 2015
Cerebellar malformations can be inherited or caused by insults during cerebellar development. To date, only sporadic cases of cerebellar malformations have been reported in dogs, and the genetic background has remained obscure.
Filipa Bernardino   +8 more
doaj   +1 more source

Is Ataxia an Underestimated Symptom of Huntington's Disease?

open access: yesFrontiers in Neurology, 2020
Background: Huntington's disease (HD) is a progressive disorder characterized by motor, cognitive and psychiatric features. Cerebellar ataxia is classically considered as uncommon in HD clinical spectrum.Objective: To determine the prevalence of ...
Gustavo L. Franklin   +22 more
doaj   +1 more source

Ataxia-telangiectasia mutated plays an important role in cerebellar integrity and functionality

open access: yesNeural Regeneration Research, 2023
Accumulating evidence indicates that ataxia-telangiectasia mutated kinase is critical for maintaining cellular homeostasis and that it has both nuclear and cytoplasmic functions. However, the functions of ataxia-telangiectasia mutated that when lost lead
Yulia Mitiagin, Ari Barzilai
doaj   +1 more source

Idiopathic very late-onset cerebellar ataxia: a Brazilian case series

open access: yesArquivos de Neuro-Psiquiatria, 2015
The authors present a Brazilian case series of eight patients with idiopathic very-late onset (mean 75.5 years old) cerebellar ataxia, featuring predominantly gait ataxia, associated with cerebellar atrophy.Method: 26 adult patients with a diagnosis of ...
Hélio A. G. Teive   +5 more
doaj   +1 more source

Genetic and clinical features of cerebellar ataxia with RFC1 biallelic repeat expansions in Japan

open access: yesFrontiers in Neurology, 2022
The recessive intronic pentanucleotide repeat AAGGG expansion of replication factor complex subunit 1 (RFC1) is associated with cerebellar ataxia, sensory neuropathy, and vestibular areflexia syndrome.
Masahiro Ando   +18 more
doaj   +1 more source

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