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Article

SPECT study of a German CADASIL family: a phenotype with migraine and progressive dementia only.

Neurology - 1 Jun 1998

Mellies J K, Bäumer T, Müller J A, Tournier-Lasserve E, Chabriat H, Knobloch O, Hackelöer H J, Goebel H H, Wetzig L, Haller P

Abstract excerpt

OBJECTIVE: We describe the clinical, molecular, genetic, MRI, and SPECT features of a German family with autosomal dominant migraine and dementia, mapping to the cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) locus. We studied the correlation of cerebral blood flow, MRI, and cognitive function. BACKGROUND: CADASIL is a small-vessel disease of the brain mapped...

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Identifiers

PMID: 9633716
DOI: 10.1212/wnl.50.6.1715

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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