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Article

Charcot-Marie-Tooth features and maculopathy in a patient with Danon disease.

Neurology - 26 Oct 2004

Laforêt P, Charron P, Maisonobe T, Romero N B, Villard E, Sebillon P, Drouin-Garraud V, Dubourg O, Fardeau M, Komajda M, Eymard B

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Identifiers

PMID: 15505188
DOI: 10.1212/01.wnl.0000141858.80738.aa

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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

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Charcot-Marie-Tooth features and maculopathy in a patient with Danon disease.PMID 15505188Read ↗

Danon disease. A novel mutation in the LAMP-2 gene and ophthalmic abnormality.Semantic proximity Read ↗

Sjögren-larsson syndrome and crystalline maculopathy associated with a novel mutation.Semantic proximity Read ↗

Charcot-Marie-Tooth disease with a mutation in FBLN5 accompanying with the small vasculitis and widespread onion-bulb formations.Semantic proximity Read ↗

Danon disease: further clinical and molecular heterogeneity.Semantic proximity Read ↗

Danon disease: clinical features, evaluation, and management.Semantic proximity Read ↗

Clinical features of Danon disease and insights gained from LAMP-2 deficiency modelsSemantic proximity Read ↗

Danon Disease: Understanding the Role of LAMP2 Variants in Cardiomyopathy and Multisystemic Involvement.Semantic proximity Read ↗

Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations.Semantic proximity Read ↗

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