Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Current perspectives in the treatment of Huntington's chorea].

Neurologia i neurochirurgia polska - 1 Jan 2000

Kuran Włodzimierz

Abstract excerpt

Huntington's chorea (HD) is a degenerative condition of the central nervous system of genetic origin, inherited as an autosomal dominant trait. The mechanism of the genetic defect is already known, it is a dynamic mutation in the ITI5 gene situated on chromosome 4 p 16.3 coding the protein huntington. The disease is progressive and leading to lethal outcome and effective treatment is unknown. Methods of treatment...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosomes, Human, Pair 4
Share to Diagnosis, Differential
Share to Genetic Testing

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Huntington Disease

Share to Mutation

Share to Nerve Degeneration

Source

Identifiers

PMID: 12418139

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 10 closest

[Current perspectives in the treatment of Huntington's chorea].PMID 12418139Read ↗

[Huntington chorea: genetics and biochemistry, diagnosis and therapy].Semantic proximity Read ↗

[Disease-modifying treatment approaches in Huntington disease : Past and future].Semantic proximity Read ↗

[Gene silencing approaches for the treatment of Huntington's disease].Semantic proximity Read ↗

[Psychotic syndrome in chorea Huntington].Semantic proximity Read ↗

[Study of the association of genotype and phenotype features of the pathogenesis of Huntington's chorea].Semantic proximity Read ↗

[Huntington chorea: clniical and molecular analysis in Asturian patients].Semantic proximity Read ↗

[Analysis of trinucleotide repeat expansion as a new mechanism of mutation in Huntington's chorea: theoretical and applied aspects].Semantic proximity Read ↗

[A psychodynamic approach in counselling vulnerable persons for Chorea Huntington -- a case report].Semantic proximity Read ↗

[Molecular genetic testing in the diagnosis of sporadic cases of Huntington's chorea].Semantic proximity Read ↗

[The characteristics of the familial polymorphism of Huntington's chorea].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.