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Article

Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A.

Journal of neurology, neurosurgery, and psychiatry - 1 Nov 1996

Chapon F, Diraison P, Lechevalier B, Chazot G, Viader F, Bonnebouche C, Vandenberghe A, Timmerman V, Van Broeckhoven C, Vandenberghe A

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Identifiers

PMID: 8937360
DOI: 10.1136/jnnp.61.5.535
PMCID: PMC1074063

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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.

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Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A.PMID 8937360Read ↗

PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies.Semantic proximity Read ↗

Deletion of the PMP22 gene and hereditary neuropathy with liability to pressure palsies.Semantic proximity Read ↗

[Hereditary neuropathy with liability to pressure palsies: study of six Spanish families].Semantic proximity Read ↗

Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation.Semantic proximity Read ↗

Peripheral myelin protein-22 gene deletion in two unrelated Japanese pedigrees with hereditary neuropathy with liability to pressure palsies.Semantic proximity Read ↗

[Molecular genetic diagnosis and clinical features of hereditary neuropathy with liability to pressure palsies in Belarusian patients].Semantic proximity Read ↗

Electrodiagnostic Characterization of Hereditary Neuropathy With Liability to Pressure Palsies.Semantic proximity Read ↗

ALS in a patient with hereditary neuropathy with liability to pressure palsy.Semantic proximity Read ↗

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[A rare form of demyelinating polyneuropathy: hereditary neuropathy with predisposition to pressure palsies].Semantic proximity Read ↗

Clinical, electrophysiological and magnetic resonance findings in a family with hereditary neuropathy with liability to pressure palsies caused by a novel PMP22 mutation.Semantic proximity Read ↗

Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion.Semantic proximity Read ↗

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