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Phenotypic differences in a large family with Kennedy's disease from the Middle Black Sea region of Turkey.

Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases - 1 Jan 2010

Karaer Hatice, Kaplan Yüksel, Kurt Semiha, Gundogdu Asli, Erdoğan Begüm, Başak Nazli A

Abstract excerpt

We report the clinical and electrophysiological features of a large Turkish family with genetically confirmed X-linked spinal and bulbar muscular atrophy (SBMA). Family members were identified by field work. A detailed history was obtained from each subject, and each subject received a detailed n...

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Identifiers

PMID: 20184516
DOI: 10.3109/17482960802445086

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20184516-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Phenotypic differences in a large family with Kennedy's disease from the Middle Black Sea region of Turkey.PMID 20184516Read ↗

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Perspectives of Kennedy's disease.Semantic proximity Read ↗

[Study on clinical manifestation, genotype and genetic characteristics of two Kennedy disease pedigrees].Semantic proximity Read ↗

Spinal and bulbar muscular atrophy: From molecular pathogenesis to pharmacological intervention targeting skeletal muscleSemantic proximity Read ↗

Kennedy's disease: pathogenesis and clinical approaches.Semantic proximity Read ↗

Kennedy disease in two sisters with biallelic CAG expansions of the androgen receptor gene.Semantic proximity Read ↗

A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophy.Semantic proximity Read ↗

CAG repeat size correlates to electrophysiological motor and sensory phenotypes in SBMA.Semantic proximity Read ↗

Molecular analysis of the androgen receptor gene in Kennedy's disease. Report of two families and review of the literature.Semantic proximity Read ↗

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