The genetic aetiology of late-onset chronic progressive cerebellar ataxia. A population-based study.

scientific article published on 6 March 2009

The genetic aetiology of late-onset chronic progressive cerebellar ataxia. A population-based study. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1007/S00415-009-0015-2
P698PubMed publication ID19259763

P50authorHuw R MorrisQ42586947
Mark WardleQ60680030
Mustapha MuzaimiQ61201541
P2093author name stringNeil P Robertson
Nigel M Williams
Elisa Majounie
P2860cites work???Q64789962
The fragile-X premutation: a maturing perspectiveQ24533443
Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxiaQ24533542
Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populationsQ24539225
Frequency analysis of autosomal dominant cerebellar ataxias in Japanese patients and clinical characterization of spinocerebellar ataxia type 6Q28268233
Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.Q33679836
Gluten ataxia in perspective: epidemiology, genetic susceptibility and clinical characteristicsQ34174932
DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalenceQ34320292
Triplet repeat primed PCR (TP PCR) in molecular diagnostic testing for Friedreich ataxia.Q35789783
High prevalence of spinocerebellar ataxia type 1 (SCA1) in an isolated region of JapanQ43891218
Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.Q43951901
Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study GroupQ44511991
Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.Q46666276
Case control analysis of repeat expansion size in ataxiaQ47264183
Regional differences in genetic subgroup frequency in hereditary cerebellar ataxia, and a morphometrical study of brain MR images in SCA1, MJD and SCA6.Q48166152
The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlatesQ48486744
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia.Q50282467
Screening for FMR-1 premutations in 122 older Flemish males presenting with ataxiaQ50282780
Are (CTG)n expansions at the SCA8 locus rare polymorphisms?Q57970937
Origin of the expansion mutation in myotonic dystrophyQ70765926
Genetic background of apparently idiopathic sporadic cerebellar ataxiaQ73074693
Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutationQ73621643
Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patientsQ74457553
The occurrence of dominant spinocerebellar ataxias among 251 Finnish ataxia patients and the role of predisposing large normal alleles in a genetically isolated populationQ81361572
P433issue3
P304page(s)343-348
P577publication date2009-03-06
P1433published inJournal of NeurologyQ6295649
P1476titleThe genetic aetiology of late-onset chronic progressive cerebellar ataxia. A population-based study
P478volume256

Reverse relations

cites work (P2860)
Q42591553Contactin-associated protein-2 antibodies in non-paraneoplastic cerebellar ataxia
Q35061105FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes
Q38896237Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders
Q34329664Fragile x-associated tremor ataxia syndrome: the expanding clinical picture, pathophysiology, epidemiology, and update on treatment
Q54396826Late onset Alexander's disease presenting as cerebellar ataxia associated with a novel mutation in the GFAP gene.
Q44848424Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patients
Q38194974Multiple system atrophy of the cerebellar type: clinical state of the art.
Q51800676Neuroimaging in Dementia.
Q45073197Quantitative trait loci mapping for conjugated linoleic acid, vaccenic acid and ∆(9) -desaturase in Italian Brown Swiss dairy cattle using selective DNA pooling
Q44457611The Diagnosis and Natural History of Multiple System Atrophy, Cerebellar Type

Search more.