The aetiology of sporadic adult-onset ataxia

Brain

Volumn 125, Issue 5, 2002, Pages 961-968

  Abele, M ^a   Burk K ^b   Schols L ^c   Schwartz, S ^a   Besenthal, I ^b   Dichgans, J ^b   Zuhlke C ^d   Riess, O ^e   Klockgether, T ^a  

^a UNIVERSITY OF BONN   (Germany)

^b UNIVERSITY OF TÜBINGEN   (Germany)

^c ST JOSEF HOSPITAL   (Germany)

^d UNIVERSITY OF LÜBECK   (Germany)

^e UNIVERSITY OF ROSTOCK   (Germany)

Author keywords

Antigliadin antibodies; Friedreich's ataxia; Multiple system atrophy; Spinocerebellar ataxia

Indexed keywords

ATAXIN 3; GENE PRODUCT; GLIADIN ANTIBODY; GLUTAMATE DECARBOXYLASE ANTIBODY; PROTEIN SCA2; PROTEIN SCA6; UNCLASSIFIED DRUG;

ACHILLES REFLEX; ADULT; AGED; ANTIBODY BLOOD LEVEL; ARTICLE; ATAXIA; BABINSKI REFLEX; CLINICAL FEATURE; COMORBIDITY; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE COURSE; DYSPHAGIA; FAMILY HISTORY; FEMALE; FRIEDREICH ATAXIA; GENE MUTATION; HEREDITY; HUMAN; MAJOR CLINICAL STUDY; MALE; ONSET AGE; PREVALENCE; PRIORITY JOURNAL; SHY DRAGER SYNDROME; SPINOCEREBELLAR DEGENERATION; VIBRATION SENSE;

EID: 0036238233     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/awf107     Document Type: Article

References (38)

1. Cerebellar ataxia with glutamic acid decarboxylase autoantibodies
2. Recessive ataxia with ocular apraxia: Review of 22 Portuguese patients
3. Autosomal recessive spastic ataxia of Charlevoix-Saguenay
4. Sporadic cerebellar ataxia associated with gluten sensitivity
5. Gluten sensitivity in sporadic and hereditary cerebellar ataxia
6. Celial disease and idiopathic cerebellar ataxia
7. Clinical and genetic abnormalities in patients with Friedreich's ataxia
8. Differential stability of the (GAA)n tract in the Friedreich ataxia (STM7) gene
9. Consensus statement on the diagnosis of multiple system atrophy
10. Evolution of sporadic olivopontocerebellar atrophy into multiple system atrophy
11. Does cryptic gluten sensitivity play a part in neurological illness?
12. Clinical, radiological, neurophysiological, and neuropathological characteristics of gluten ataxia
13. "Idiopathic" late onset cerebellar ataxia. A clinical and genetic study of 36 cases
14. Absence of mutations in ATM, the gene responsible for ataxia telangiectasia in patients with cerebellar ataxia
15. Cerebellar ataxia with anti-glutamic acid decarboxylase antibodies: Study of 14 patients
16. 1A voltage-dependent calcium channel gene and clinical variations in Japanese population
17. Idiopathic cerebellar ataxia of late onset: Natural history and MRI morphology
18. Late-onset Friedreich's ataxia. Molecular genetics, clinical neurophysiology, and magnetic resonance imaging
19. Absence of SCA1 mutation in idiopathic cerebellar ataxia
20. The natural history of degenerative ataxia: A retrospective study in 466 patients
21. An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
22. Spinocerebellar ataxia type 6. Molecular and clinical features of 35 Japanese patients including one homozygous for the CAG repeat expansion
23. Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families
24. The distribution of oligodendroglial inclusions in multiple system atrophy and its relevance to clinical symptomatology
25. Idiopathic cerebellar ataxia associated with celiac disease: Lack of distinctive neurological features
26. Spinocerebellar ataxias in Spanish patients: Genetic analysis of familial and sporadic cases
27. Multiple system atrophy-the nature of the beast
28. SCA2 trinucleotide expansion in German SCA patients
29. SCA6 is caused by moderate CAG expansion in the alpha1 A-voltage-dependent calcium channel gene
30. Autoantibodies to glutamic acid decarboxylase in three patients with cerebellar ataxia, late-onset insulin-dependent diabetes mellitus, and polyendocrine autoimmunity
31. Spinocerebellar ataxia type 1: Clinical and neurophysiological characteristics in German kindreds
32. Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients
33. Genetic background of apparently idiopathic sporadic cerebellar ataxia
34. Spinocerebellar ataxia type 6: Genotype and phenotype in German kindreds
35. Multiple system atrophy: Natural history, MRI morphology, and dopamine receptor imaging with 123IBZM-SPECT
36. Autoantibody screening in subacute cerebellar ataxia
37. Clinical features and natural history of multiple system atrophy. An analysis of 100 cases
38. Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia