Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10

Annals of Neurology

Volumn 50, Issue 2, 2001, Pages 234-239

  Rasmussen, Astrid ^a   Matsuura, Tohru ^b,c   Ruano, Luis ^a   Yescas, Petra ^a   Ochoa, Adriana ^a   Ashizawa, Tetsuo ^b,c   Alonso, Elisa ^a  

^a NATIONAL INSTITUTE OF NEUROLOGY AND NEUROSURGERY   (Mexico)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c MICHAEL E DEBAKEY VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BEHAVIOR DISORDER; BRAIN ATROPHY; CEREBELLAR ATAXIA; CLINICAL ARTICLE; CLINICAL FEATURE; DYSKINESIA; FEMALE; GENETIC ANALYSIS; HUMAN; MALE; MEXICO; NERVE CONDUCTION; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE REPEAT; ONSET AGE; POLYNEUROPATHY; PRIORITY JOURNAL; SEIZURE; SPINOCEREBELLAR DEGENERATION;

ADOLESCENT; ADULT; AGE OF ONSET; BRAIN; ELECTROENCEPHALOGRAPHY; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MEXICO; PEDIGREE; PSYCHOLOGICAL TESTS; SPINOCEREBELLAR ATAXIAS;

EID: 0034902760     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.1081     Document Type: Article

References (23)

1. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias
2. Clinical features and classification of the inherited ataxias
3. Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia
4. Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy
5. Large expansion of ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10
6. Molecular diagnosis of spinocerebellar ataxias in Mexican population
7. Expansion of an unstable trinucleotide repeat in spinocerebellar ataxia type 1
8. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2 gene on human chromosome 12
9. Identification of the gene for spinocerebellar ataxia type 2 (SCA2) using a direct identification of repeat expansion and cloning technique (DIRECT)
10. Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
11. CAG repeat expansion in a novel gene in Machado-Joseph disease at chromosome 14q32.1
12. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A voltage-dependent calcium channel
13. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion
14. An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
15. Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12
16. Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): Clinical description and genetic localisation to chromosome 16q22.1
17. Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11
18. Autosomal dominant cerebellar ataxia type III: Linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3
19. Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation
20. A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S205 on chromosome 19q13.4-qter
21. Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22
22. Neurocysticercosis as the main cause of late-onset epilepsy in Mexico
23. Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotype