Works about ATAXIA
Results: 2964
Ataxia With Vitamin E Deficiency: Case Series, Vitamin E Therapy Response, Founder Effect, and In Silico Analysis.
- Published in:
- Clinical Genetics, 2025, v. 107, n. 3, p. 366, doi. 10.1111/cge.14658
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- Article
Longitudinal Imaging Biomarkers Correlate with Progressive Motor Deficit in the Mouse Model of Charlevoix‐Saguenay Ataxia.
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- Annals of Neurology, 2025, v. 97, n. 3, p. 425, doi. 10.1002/ana.27146
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- Article
Goal‐Directed Rehabilitation Versus Standard Care for Individuals with Hereditary Cerebellar Ataxia: A Multicenter, Single‐Blind, Randomized Controlled Superiority Trial.
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- Annals of Neurology, 2025, v. 97, n. 3, p. 409, doi. 10.1002/ana.27130
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- Article
Physiological and Molecular Pathology of Aminoglycoside Ototoxicity.
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- Volta Review, 2005, v. 105, n. 3, p. 325
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- Article
A Case Report of Plasmapheresis in Paraneoplastic Cerebellar Ataxia Associated With Anti-Tr Antibody.
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- Therapeutic Apheresis & Dialysis, 2006, v. 10, n. 1, p. 90, doi. 10.1111/j.1744-9987.2006.00348.x
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- Article
Dietary Vitamin E Deficiency Increases Anxiety-Like Behavior in Juvenile and Adult Rats.
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- Bioscience, Biotechnology & Biochemistry, 2011, v. 75, n. 10, p. 1894, doi. 10.1271/bbb.110190
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- Article
Effects of Sex and Gender on Adaptation to Space: Neurosensory Systems.
- Published in:
- 2014
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- Journal Article
Ataxin active site determination using spectral distribution of electron ion interaction potentials of amino acids.
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- Medical & Biological Engineering & Computing, 2010, v. 48, n. 4, p. 303, doi. 10.1007/s11517-010-0587-0
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- Article
The coding region of TP53INP2, a gene expressed in the developing nervous system, is not altered in a family with autosomal recessive non‐progressive infantile ataxia on chromosome 20q11‐q13.
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- Developmental Dynamics, 2007, v. 236, n. 3, p. 843, doi. 10.1002/dvdy.21064
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- Article
Brown-Vialetto-Van Laere Syndrome: Clinical and Neuropathologic Findings with Immunohistochemistry for C20orf54 in Three Affected Patients.
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- 2013
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- Publication type:
- Case Study
CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report.
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- Journal of Headache & Pain, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s10194-021-01297-5
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- Article
First case of feline spongiform encephalopathy in a captive cheetah born in France: PrP<sup>sc</sup> analysis in various tissues revealed unexpected targeting of kidney and adrenal gland.
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- Histochemistry & Cell Biology, 2003, v. 119, n. 5, p. 415, doi. 10.1007/s00418-003-0524-5
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- Article
Bilateral parietal lesions disrupt the beneficial effects of prism adaptation: evidence from a patient with optic ataxia.
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- Experimental Brain Research, 2008, v. 187, n. 2, p. 295, doi. 10.1007/s00221-008-1303-2
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- Article
Trace eyeblink conditioning in patients with cerebellar degeneration: comparison of short and long trace intervals.
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- Experimental Brain Research, 2008, v. 187, n. 1, p. 85, doi. 10.1007/s00221-008-1283-2
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- Article
Eyeblink conditioning in patients with hereditary ataxia: a one-year follow-up study.
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- Experimental Brain Research, 2005, v. 162, n. 3, p. 332, doi. 10.1007/s00221-004-2181-x
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- Article
Mono-Limb Ataxia Caused by Motor Cortical Infarction: Case Report and Review of the Literature.
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- Cerebrovascular Diseases, 2013, v. 36, n. 5/6, p. 462, doi. 10.1159/000354861
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- Article
Anterior Inferior Cerebellar Artery Territorial Infarction Caused by Vertebral Artery Dissection.
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- Cerebrovascular Diseases, 2013, v. 35, n. 6, p. 592, doi. 10.1159/000350729
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- Article
Dyssynergic Defecation and Anal Sphincter Disorders in Children in High-Resolution Anorectal Manometry Investigation.
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- 2020
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- Publication type:
- journal article
Fragile-X-associated Tremor/Ataxia Syndrome (FXTAS) in a Female with FMR1 Premutation: Case Report.
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- 2022
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- Publication type:
- Case Study
Effects of Gluteus Maximus Muscle Strength on Ataxia, Gait, and Equilibrium in Multiple Sclerosis.
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- European Journal of Therapeutics, 2023, v. 29, n. 1, p. 81, doi. 10.58600/eurjther-199
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- Article
Research Highlights.
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- Nature Immunology, 2006, v. 7, n. 8, p. 801, doi. 10.1038/ni0806-801
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- Article
Vestibular disorders of dogs and cats.
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- Practica Veterinara.ro, 2015, n. 21, p. 24
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- Article
A Null Mutation of the Serotonin 6 Receptor Alters Acute Responses to Ethanol.
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- Neuropsychopharmacology, 2006, v. 31, n. 8, p. 1801, doi. 10.1038/sj.npp.1301030
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- Article
Effects of flow rate and gas mixture on the welfare of weaned and neonate pigs during gas euthanasia.
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- Journal of Animal Science, 2014, v. 92, n. 2, p. 793, doi. 10.2527/jas.2013-6598
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- Article
The Training and Support Programme for parents of children with ataxia: parents' perspectives.
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- Early Child Development & Care, 2007, v. 177, n. 5, p. 507, doi. 10.1080/03004430600576689
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- Publication type:
- Article
Obsessive-compulsive disorder as a first manifestation of Ataxia with Oculomotor Apraxia type 2 due to a novel mutation of SETX gene.
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- Neurological Sciences, 2025, v. 46, n. 1, p. 469, doi. 10.1007/s10072-024-07761-9
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- Article
Genetic aspects of ataxias in a cohort of Turkish patients.
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- Neurological Sciences, 2024, v. 45, n. 9, p. 4349, doi. 10.1007/s10072-024-07484-x
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- Article
Clinical features of adult patients with positive NMDAR-IgG coexisting with MOG-IgG.
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- Neurological Sciences, 2024, v. 45, n. 9, p. 4481, doi. 10.1007/s10072-024-07474-z
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- Article
Imbalance and gait impairment in Parkinson's disease: discussing postural instability and ataxia.
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- Neurological Sciences, 2024, v. 45, n. 4, p. 1377, doi. 10.1007/s10072-023-07205-w
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- Publication type:
- Article
Autosomal recessive spino-cerebellar ataxia type 10 (SCAR10): clinical presentation associated with c.289delA ANO10 gene variant.
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- Neurological Sciences, 2024, v. 45, n. 3, p. 1283, doi. 10.1007/s10072-023-07104-0
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- Article
Italian cross-cultural adaptation of the patient-reported outcome measure of ataxia.
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- Neurological Sciences, 2023, v. 44, n. 8, p. 2773, doi. 10.1007/s10072-023-06714-y
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- Article
Seizures and central vestibular nystagmus as the initial presentation of leukoencephalopathy with ataxia (LKPAT).
- Published in:
- Neurological Sciences, 2023, v. 44, n. 3, p. 1083, doi. 10.1007/s10072-022-06464-3
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- Article
Comorbidities in Friedreich ataxia: incidence and manifestations from early to advanced disease stages.
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- 2022
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- Publication type:
- journal article
Fluctuating ataxia caused by mitochondrial tRNA (Lys) gene m.8363G > A variant.
- Published in:
- Neurological Sciences, 2022, v. 43, n. 11, p. 6589, doi. 10.1007/s10072-022-06246-x
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- Article
Investigation of postural control and spatiotemporal parameters of gait during dual tasks in ataxic individuals.
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- 2022
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- Publication type:
- journal article
Spastic paraplegia type 46: novel and recurrent GBA2 gene variants in a compound heterozygous Italian patient with spastic ataxia phenotype.
- Published in:
- Neurological Sciences, 2021, v. 42, n. 11, p. 4741, doi. 10.1007/s10072-021-05463-0
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- Article
Ataxia with oculomotor apraxia type 2 (AOA2): an eye movement study of two siblings.
- Published in:
- 2021
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- Publication type:
- Letter
A novel SACS p.Pro4154GlnfsTer20 mutation in a family with autosomal recessive spastic ataxia of Charlevoix-Saguenay.
- Published in:
- Neurological Sciences, 2021, v. 42, n. 7, p. 2969, doi. 10.1007/s10072-021-05117-1
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- Article
A case of novel CACNA1A mutation causing type 2 episodic ataxia.
- Published in:
- 2021
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- Publication type:
- Case Study
A novel PNPLA6 mutation in a Turkish family with intractable Holmes tremor and spastic ataxia.
- Published in:
- Neurological Sciences, 2021, v. 42, n. 4, p. 1535, doi. 10.1007/s10072-020-04869-6
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- Publication type:
- Article
NGS-based detection of a novel mutation in PRKCG (SCA14) in sporadic adult-onset ataxia plus dystonic tremor.
- Published in:
- 2020
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- Publication type:
- Letter
Spinocerebellar ataxia type 48: last but not least.
- Published in:
- 2020
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- Publication type:
- journal article
Reversible cerebellar MRI hyperintensities and ataxia associated with hypomagnesemia: a case report with review of the literature.
- Published in:
- 2020
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- Publication type:
- Case Study
Paraneoplastic sensorimotor neuropathy associated with mediastinal germ cell tumor: favorable outcome after high-dose intravenous immunoglobulin therapy.
- Published in:
- 2020
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- Publication type:
- Case Study
A case of Friedreich ataxia in an adolescent with 16p11.2 microdeletion syndrome.
- Published in:
- 2020
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- Publication type:
- Case Study
Correction to: Reversible cerebellar MRI hyperintensities and ataxia associated with hypomagnesemia: a case report with review of the literature.
- Published in:
- 2020
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- Publication type:
- corrected article
Sporadic adult-onset spinocerebellar ataxias : Reply: Degenerative and acquired sporadic adult-onset ataxia https://doi.org/10.1007/s10072-019-03856-w.
- Published in:
- 2019
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- Publication type:
- Letter
Wilson's disease: a reversible cause of ataxia.
- Published in:
- 2018
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- Publication type:
- Case Study
Bálint syndrome caused by bilateral medial occipital infarcts.
- Published in:
- 2018
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- Publication type:
- Case Study
Ocular flutter, generalized myoclonus, and ataxia associated with anti-GM1, GD1a, and GD1b antibodies in a 6-year-old child.
- Published in:
- 2018
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- Publication type:
- Case Study