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Article

Neuromuscular implications in CADASIL.

Cerebrovascular diseases (Basel, Switzerland) - 1 Jan 2007

Finsterer Josef

Abstract excerpt

OBJECTIVES: Recent studies indicate that Notch3 gene mutations not only manifest as cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) but also in the peripheral nerves and skeletal muscles. METHODS: A MEDLINE search with appropriate terms was car...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17878719
DOI: 10.1159/000108428

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17878719-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Neuromuscular implications in CADASIL.PMID 17878719Read ↗

Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family.Semantic proximity Read ↗

Peripheral nerve and skeletal muscle involvement in CADASIL.Semantic proximity Read ↗

A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASIL.Semantic proximity Read ↗

A Novel NOTCH3 Frameshift Deletion and Mitochondrial Abnormalities in a Patient With CADASILSemantic proximity Read ↗

Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL.Semantic proximity Read ↗

Mitochondrial DNA m.3243A>G mutation rarely causes CADASIL-like phenotype.Semantic proximity Read ↗

Peripheral neuropathy in CADASIL.Semantic proximity Read ↗

Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL.Semantic proximity Read ↗

Investigation of Mitochondrial Related Variants in a Cerebral Small Vessel Disease Cohort.Semantic proximity Read ↗

CADASIL with cord involvement associated with a novel and atypical NOTCH3 mutationSemantic proximity Read ↗

Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL.Semantic proximity Read ↗

[Clinical, radiological, histopathological and genetic findings in a Danish "CADASIL" family].Semantic proximity Read ↗

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