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Your search keyword '"Cerebellar Ataxia epidemiology"' showing total 129 results

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129 results on '"Cerebellar Ataxia epidemiology"'

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1. Ataxias in Brazil: 17 years of experience in an ataxia center.

2. Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia-experience from an Italian cohort.

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3. Etiologies and clinical characteristics of acute ataxia in a single national children's medical center.

4. Natural History and Phenotypic Spectrum of GAA-FGF14 Sporadic Late-Onset Cerebellar Ataxia (SCA27B).

5. Genetic heterogeneity within a consanguineous family involving TTPA and SETX genes.

6. Autosomal Recessive Cerebellar Ataxias in Europe: Frequency, Onset, and Severity in 677 Patients.

7. Unravelling the etiology of sporadic late-onset cerebellar ataxia in a cohort of 205 patients: a prospective study.

8. Prevalence of Fragile X-Associated Tremor/Ataxia Syndrome in Patients with Cerebellar Ataxia in Japan.

9. Risk factors for the occurrence and recurrence of acute cerebellar ataxia: a retrospective observational study.

10. Impacts of the COVID-19 Pandemic on the Mental Health and Motor Deficits in Cuban Patients with Cerebellar Ataxias.

11. Genetic spectrum and clinical features in a cohort of Chinese patients with autosomal recessive cerebellar ataxias.

12. The presence of dysphagia in patients with cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS): a subjective and objective study.

13. Overwhelming genetic heterogeneity and exhausting molecular diagnostic process in chronic and progressive ataxias: facing it up with an algorithm, a gene, a panel at a time.

14. Management of Patients with Cerebellar Ataxia During the COVID-19 Pandemic: Current Concerns and Future Implications.

15. Relationship between ataxia and inferior cerebellar peduncle injury in patients with cerebral infarct.

16. Deafness and Vestibulopathy in Cerebellar Diseases: a Practical Approach.

17. Childhood-onset cerebellar ataxia in Japan: A questionnaire-based survey.

18. The Working Life of People with Degenerative Cerebellar Ataxia.

19. A case series of hereditary cerebellar ataxias in a highly consanguineous population from Northeast Brazil.

20. High Degree of Genetic Heterogeneity for Hereditary Cerebellar Ataxias in Australia.

21. Prevalence and phenotype of the c.1529C>T SPG7 variant in adult-onset cerebellar ataxia in Italy.

22. The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.

23. Sporadic adult-onset ataxia.

24. Eye movements in essential tremor patients with parkinsonian and cerebellar signs.

25. Adult Onset Sporadic Cerebellar Ataxia in Singapore: Diagnostic Outcomes of Paraneoplastic Antibody Testing and Early Clinical Features of Paraneoplastic Cerebellar Degeneration.

26. Cerebellar Cortical Abiotrophy in Young Labrador-Retrievers.

27. Decrease of Horizontal Canal Vestibulo-Oculomotor Reflex Gain in the Elderly with Dysequilibrium without Lifetime Vertigo.

28. Cerebellar ataxia in progressive supranuclear palsy: An autopsy study of PSP-C.

29. Is multiple system atrophy with cerebellar ataxia (MSA-C) like spinocerebellar ataxia and multiple system atrophy with parkinsonism (MSA-P) like Parkinson's disease? - A saccade study on pathophysiology.

30. Prevalence of Autoantibodies and the Efficacy of Immunotherapy for Autoimmune Cerebellar Ataxia.

31. Natural history of multiple system atrophy in the USA: a prospective cohort study.

32. Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.

33. Strategy for the surgical treatment of vestibular schwannomas in patients with neurofibromatosis type 2.

34. Drug-induced cerebellar ataxia: a systematic review.

35. Gluten ataxia in Japan.

36. The prevalence of familial hemiplegic migraine with cerebellar ataxia and spinocerebellar ataxia type 6 in Portugal.

37. Purkinje cell cytoplasmic antibody type 1 (anti-Yo) autoimmunity in a child with Down syndrome.

38. The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.

39. De novo partial deletion in GRID2 presenting with complicated spastic paraplegia.

41. The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.

42. Characterization of cerebellar ataxia in chronic alcoholics using the International Cooperative Ataxia Rating Scale (ICARS).

43. Prevalence rate and functional status of cerebellar ataxia in Korea.

44. MERRF and Kearns-Sayre overlap syndrome due to the mitochondrial DNA m.3291T>C mutation.

45. Epidemiological evidence for a link between vertigo and migraine.

46. Nationwide population-based epidemiologic study on cerebellar ataxia in Taiwan.

47. Gluten sensitivity: associated sporadic cerebellar ataxia in Taiwan.

48. Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias.

49. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond.

50. Lesions in early cerebellar development--do they matter?