About: Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities

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About: Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities Goto Sponge NotDistinct Permalink

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scientific article published on 01 December 1994

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1994 (uk) article scientifique publié en 1994 (fr) im Dezember 1994 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 1994 (ast) scientific article published on 01 December 1994 (en)
publication date	wds:Q72884067-6321DF2F-340A-4D74-9C3C-4839E3F983A5
publication date	1994-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q72884067-C7C0F043-F6B6-43C6-9CA3-59A59DA8ED6A
language of work or name	English
author name string	wds:Q72884067-0D37FA6F-D5DE-43A3-BECE-D4F6850B49F0 wds:Q72884067-17C0BAAB-9D5C-489E-A3C8-8A930FD2A934 wds:Q72884067-31838407-1D9C-48A2-8878-9E0E3E91047B wds:Q72884067-6849BBF3-73FF-4B5F-89B5-D32014B6F96E wds:Q72884067-7577D3C2-E768-41AF-A6BB-8D8CDD9E51D1 wds:Q72884067-8E72593B-54C4-48A0-A914-901349679CBA wds:Q72884067-9BB753F3-D76C-42D3-BD2E-EE5C7133F34A wds:Q72884067-E117A631-ED10-41B5-8488-866514854510 wds:Q72884067-EB1273F8-F1B0-436A-AEBA-8CAA3F8C0638 wds:Q72884067-F8AD2144-54BE-41E6-9B31-F77975841450
author name string	A Brice E LeGuern P Bouche J Weissenbach Y Agid J Emile S Tardieu R Gouider F Cabon M Samid
rdfs:label	Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities (en) Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities (nl)
skos:prefLabel	Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities (en) Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities (nl)
name	Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities (en) Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities (nl)
title	wds:Q72884067-C72E6ED0-E62E-4D86-ACB8-74400E874EE7
title	Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities (en)
page(s)	wds:Q72884067-E6F0B242-C753-4068-A5E3-644F0A8D4EFF
page(s)	2250-2252
instance of	wds:Q72884067-1F5EA861-C6FA-4F3B-B15E-6587A638F964
instance of	scholarly article
main subject	wds:Q72884067-B079D59D-AF07-4F44-8730-E6FA7DCB5FC6 wds:Q72884067-C7DEFD2D-9E40-4D97-8977-A02ECEF5193E
main subject	hereditary neuropathy with liability to pressure palsies Hereditary neuralgic amyotrophy
PubMed ID	wds:Q72884067-00B8D59E-0955-4ADB-AABE-3354B1B07992
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7991107
PubMed ID	7991107
published in	wds:Q72884067-4D285218-2397-4039-873D-CA8819ECBADA
published in	Neurology
issue	wds:Q72884067-0BCC73AE-6A76-41C1-8A3A-3853C33EC880
volume	wds:Q72884067-9735A23F-2B4D-43F3-8AB8-689F4BC6689B
issue	12
volume	44
DOI	wds:Q72884067-600A7076-DB09-4387-920D-4B0F47114563
DOI	http://dx.doi.org/10.1212/WNL.44.12.2250
DOI	10.1212/WNL.44.12.2250
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q72884067
is cites work of	Epidemiology of peripheral neuropathy Tomaculous neuropathy: a clinical and electrophysiological study in patients with and without 1.5-Mb deletions in chromosome 17p11.2. Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsies SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy Clinical and pathophysiological concepts of neuralgic amyotrophy Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection. On behalf of the European CMT Consortium Molecular basis of neuromuscular diseases Charcot-marie-tooth disease: seventeen causative genes Charcot-Marie-Tooth 1A concurrent with schwannomas of the spinal cord and median nerve
is cites work of	wds:Q37873725-83B62810-7154-437F-8951-B768E7F7650A wds:Q30436118-A18507E7-89F8-4FAE-BD8B-BFDEF3526DB6 wds:Q33735651-692C586F-B82C-43E6-8A03-A58B150554F8 wds:Q77810812-C868CC04-FE24-4B08-B133-B6F8803821D3 wds:Q37731961-933121BB-A980-402E-A8A7-7E3AEF0D4C7C wds:Q74342552-94EA285B-3F85-4C07-8860-367936BBD3B6 wds:Q73586503-C8FCFE44-814C-4205-B743-641071C8165E wds:Q37284732-ABEC2ED6-245A-4834-805F-BAE3BAB19E88 wds:Q36507166-0DC9055C-75A8-4F7D-8C4C-788B011B0329 wds:Q70829413-534EDFC8-A99F-4ACE-83AC-4CE0F73DA1DE

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