Type 8 spinocerebellar ataxia. A report of a family;Ataxia espinocerebelosa tipo 8. Descripción de una familia

Revista de Neurologia

Volumn 33, Issue 2, 2001, Pages 150-152

  Sempere, A P ^a   Millan J M ^a   Royo Vilanova, C ^a   Medrano, V ^a  

^a HOSPITAL VEGA BAJA   (Spain)

Author keywords

Dysarthria; Hereditary ataxias; Spinocerebellar ataxia

Indexed keywords

ADULT; ARTICLE; BRAIN DISEASE; CASE REPORT; CEREBELLUM ATROPHY; DIFFERENTIAL DIAGNOSIS; DYSARTHRIA; FEMALE; GAIT; HEREDITARY ATAXIA; HUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; SPINOCEREBELLAR DEGENERATION; TRINUCLEOTIDE REPEAT;

EID: 0034825995     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: 10.33588/rn.3302.2001057     Document Type: Article

References (9)

1. Ataxias y genética
2. An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
3. Cerebellar and spinocerebellar disorders
4. Hereditary ataxias and paraplegias in Cantabria, Spain. An epidemiological and clinical study
5. Spinocerebellar ataxia type 8. Clinical features in a large family
6. Ataxias heredodegenerativas
7. Spinocerebellar ataxias in Spanish patients: Genetic analysis of familial and sporadic cases
8. Dis tribución de ataxias hereditarias dominantes y ataxia de Friedreich en la población española
9. Ataxia espinocerebelar tipo VII (AEC7). Comunicación de una familia afectada española