25 results for “ataxia”. Showing 25 of 39,449.
Dominant ataxias and Friedreich ataxia: an update.
ataxias (spinocerebellar ataxias) are one major group of ataxias. Spinocerebellar
Friedreich's ataxia. Revision of the phenotype according to molecular genetics.
ataxia symptoms and nine patients with an atypical Friedreich's ataxia
Postural Tremor and Ataxia Progression in Spinocerebellar Ataxias.
ataxia progression. Genetic interactions between ataxia genes might influence the brain
Progression characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS): a 2 year cohort study.
Ataxia (SARA). Secondary outcomes were the Inventory of Non-Ataxia
Accuracy of clinical diagnostic criteria for Friedreich's ataxia.
Ataxia was studied in 142 patients with progressive unremitting ataxia
Genes involved in hereditary ataxias.
ataxia (FRDA), the most common type of autosomal recessive ataxia
Bacillus subtilis Histidine Kinase KinC Activates Biofilm Formation by Controlling Heterogeneity of Single-Cell Responses.
ataxia (FRDA) is characterized by progressive ataxia with onset from
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ataxia (FRDA) is characterized by progressive ataxia with onset from
Marked variation in the cardiomyopathy associated with Friedreich's ataxia.
ataxia, a recessively inherited disorder characterised by spinocerebellar degeneration. Individuals
Episodic ataxias 1 and 2.
ataxia type 1 (EA1) is characterized by brief episodes of ataxia
ATM loss disrupts the autophagy-lysosomal pathway.
ataxia telangiectasia mutated) protein is found associated with multiple organelles
The natural history of degenerative ataxia: a retrospective study in 466 patients.
ataxia (FRDA, n = 83), early onset cerebellar ataxia (EOCA, n = 30), autosomal
Friedreich's ataxia GAA repeat expansion in patients with recessive or sporadic ataxia.
ataxia (FRDA) expanded repeat and provide preliminary guidance for future
ClearSpeechTogether: a Rater Blinded, Single, Controlled Feasibility Study of Speech Intervention for People with Progressive Ataxia.
ataxias. This feasibility study targeted people with progressive ataxia and mild
Early onset cerebellar ataxia with retained tendon reflexes: a clinical and genetic study of a disorder distinct from Friedreich's ataxia.
ataxia. Other important differences from Friedreich's ataxia are absence
Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features.
ataxia are described. Onset of symptoms was before the age of 25 (mean
Sensory ataxia and cardiac hypertrophy caused by neurovascular oxidative stress in chemogenetic transgenic mouse lines.
ataxia caused by oxidative stress and mitochondrial dysfunction in neurons
Diabetes in Friedreich ataxia.
ataxia. In this Supplement article, we review the clinical data
How is disease progress in Friedreich's ataxia best measured? A study of four rating scales.
ataxia (FRDA), the most common genetic cause of ataxia, is characterised
Superior cerebellar peduncle atrophy in Friedreich's ataxia correlates with disease symptoms.
ataxia (FRDA) is the most common early onset inherited ataxia
Future Prospects of Gene Therapy for Friedreich's Ataxia.
ataxia is an autosomal recessive neurogenetic disease that is mainly
Patient-reported, psychosocial and health economic outcomes in mild to moderate Friedreich's ataxia: baseline results of the PROFA study.
ataxia (FA) is the most common autosomal recessive ataxia. Little
A mild case of Friedreich ataxia: lymphocyte and sural nerve analysis for GAA repeat length reveals somatic mosaicism.
ataxia (FRDA) is an autosomal recessive, neurodegenerative disease, characterized by progressive
PLS3 Overexpression Delays Ataxia in <i>Chp1</i> Mutant Mice.
ataxia. In this study, we aimed to determine whether PLS3
Cardiac energetics correlates to myocardial hypertrophy in Friedreich's ataxia.
ataxia is a neurodegenerative disease frequently associated with hypertrophic cardiomyopathy