Síndromes atáxicos. Ataxias heredodegenerativas y adquiridas.

No abstract is available for this paper.

• Publication year

  2007

• Venue

  Medicine

• Publication date

  2007-03-01

• Fields of study

  Not labeled

• Identifiers
  DOI 10.1016/S0211-3449(07)75443-7
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

• The wide spectrum of spinocerebellar ataxias (SCAs)

  2008cited by this paper
• The pathogenesis of spinocerebellar ataxia

  2008cited by this paper
• Spinocerebellar ataxia with mental retardation (SCA13)

  2008cited by this paper
• SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2.

  2006cited by this paper
• Trastornos del movimiento

  2006cited by this paper
• Spinocerebellar ataxia type 20

  2005cited by this paper
• Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG gene

  2005cited by this paper
• Clinical feature profile of spinocerebellar ataxia type 1–8 predicts genetically defined subtypes

  2005cited by this paper
• Recent Advances in Hereditary Spinocerebellar Ataxias

  2005cited by this paper
• Ataxia espinocerebelosa tipo 7: descripción de una familia mexicana

  2004cited by this paper
• A pathogenetic classification of hereditary ataxias: Is the time ripe?

  2004cited by this paper
• Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3.

  2004cited by this paper
• Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.

  2004cited by this paper
• Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus

  2004cited by this paper
• Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease

  2004cited by this paper
• Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p

  2004cited by this paper
• Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients.

  2004cited by this paper
• Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies.

  2003cited by this paper
• Gluten ataxia in perspective: epidemiology, genetic susceptibility and clinical characteristics.

  2003cited by this paper
• Ataxia-telangiectasia: diagnosis and treatment.

  2003cited by this paper
• Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse

  2003cited by this paper
• Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.

  2002cited by this paper
• A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.

  2002cited by this paper
• Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families.

  2002cited by this paper
• Mutation of TDP1, encoding a topoisomerase I–dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy

  2002cited by this paper
• Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.

  2002cited by this paper
• Friedreich's ataxia: treatment within reach.

  2002cited by this paper
• [Spinocerebellar ataxia type 10 (SCA10): a disease caused by a novel pentanucleotide repeat expansion].

  2001cited by this paper
• ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF

  2000cited by this paper
• Cerebellar and spinocerebellar disorders

  2000cited by this paper
• The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder.

  1999cited by this paper
• Toward cloning of a novel ataxia gene: refined assignment and physical map of the IOSCA locus (SCA8) on 10q24.

  1997cited by this paper
• Principles of Neurology

  1996cited by this paper
• Autoantibodies to glutamate decarboxylase in a patient with cerebellar cortical atrophy, peripheral neuropathy, and slow eye movements.

  1995cited by this paper
• Tratado de neurología

  1981cited by this paper
• Degenerative diseases of the nervous system.

  1961cited by this paper

• Celiac disease and malabsorption: a case report of ataxia secondary to vitamin E deficiency.

  2014cites this paper
• Celiac disease and malabsorption: a case report of ataxia secondary to vitamin E deficiency.

  2014cites this paper