About: Arthrogryposis multiplex congenita due to congenital myasthenic syndrome

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About: Arthrogryposis multiplex congenita due to congenital myasthenic syndrome Goto Sponge NotDistinct Permalink

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scientific article published on 01 April 1995

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 1995 (uk) artículu científicu espublizáu n'abril de 1995 (ast) scientific article published on 01 April 1995 (en) գիտական հոդված հրատարակված 1995 թվականի ապրիլի 1-ին (hy) im April 1995 veröffentlicher wissenschaftlicher Artikel (de)
publication date	wds:Q71908004-25EC4561-B7B2-494F-B6D0-76B584440420
publication date	1995-04-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q71908004-69777539-F9E2-4518-BB9F-0D1C40F7A6BE wds:Q71908004-6C7700FA-0B94-4DA5-A36A-974AA3F2D046 wds:Q71908004-96388B19-0ED6-4ECE-B6C0-C4400E151116 wds:Q71908004-974B3015-2057-49CD-B6B9-29CE4FA4A557 wds:Q71908004-996E0D38-5ACC-434E-8B99-E14E57A807F1
author name string	L E Becker V Jay J Vajsar D L MacGregor A Sloane
rdfs:label	Arthrogryposis multiplex congenita due to congenital myasthenic syndrome (en) Arthrogryposis multiplex congenita due to congenital myasthenic syndrome (nl)
skos:prefLabel	Arthrogryposis multiplex congenita due to congenital myasthenic syndrome (en) Arthrogryposis multiplex congenita due to congenital myasthenic syndrome (nl)
name	Arthrogryposis multiplex congenita due to congenital myasthenic syndrome (en) Arthrogryposis multiplex congenita due to congenital myasthenic syndrome (nl)
author	wds:Q71908004-ADC1A38A-52E6-4B9B-AF26-150E18E703A9
author	Gabriel M Ronen
title	wds:Q71908004-AA6189FA-21A6-4E25-9C1F-8EE1F59F8FE5
title	Arthrogryposis multiplex congenita due to congenital myasthenic syndrome (en)
page(s)	wds:Q71908004-F2D794C8-D291-4CF8-9FC2-2B4717D3770D
page(s)	237-241
instance of	wds:Q71908004-552A472A-A53E-453E-9FE6-916632521F72
instance of	scholarly article
main subject	wds:Q71908004-9E38AB83-0B6A-4D45-B371-6E1DFF7EFADE
main subject	congenital myasthenic syndrome
PubMed ID	wds:Q71908004-409192B2-9073-4D55-8F3D-0459FA926CF6
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7619191
PubMed ID	7619191
published in	wds:Q71908004-A4FDD644-647C-4447-B4ED-4E51B72510D9
published in	Pediatric Neurology
issue	wds:Q71908004-146E3418-4831-4816-97C2-EC9707FBEB40
volume	wds:Q71908004-65468510-A9DC-4BF3-8030-9E2D85A47D9B
issue	3
volume	12
DOI	wds:Q71908004-3937961A-D453-429E-82F8-B35C59EF77E4
DOI	http://dx.doi.org/10.1016/0887-8994(95)00004-Y
DOI	10.1016/0887-8994(95)00004-Y
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71908004
is cites work of	Arthrogryposis multiplex congenita Neurological disorders caused by inherited ion-channel mutations Acetylcholine receptor delta subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenita Diagnosing arthrogryposis multiplex congenita: a review The natural history and ophthalmic involvement in childhood myasthenia gravis at the hospital for sick children Identification of mutations in the MYO9A gene in patients with congenital myasthenic syndrome Clinical and neurophysiological characteristics of congenital myasthenic syndromes presenting in early infancy AMC: amyoplasia and distal arthrogryposis Arthrogryposis multiplex congenita in Western Australia A case of congenital bilateral absence of elbow flexor muscles: review of differential diagnosis and treatment
is cites work of	wds:Q44732678-F9F8FE79-88A0-4C5C-91FC-FCDBB6631414 wds:Q24671934-758DF252-685E-4709-A256-06F8C88C2C39 wds:Q42044690-00B4A37C-273E-435B-970D-7122C46F554C wds:Q33860068-1CDB0F42-4AEF-4328-BD02-251BE8CFB376 wds:Q77639622-49E13619-C581-4CDE-82CF-917802B30F9F wds:Q24632678-FB23C82B-FB35-45DF-B497-40B1BBA6E972 wds:Q36322704-7BE049B8-862E-491F-8C8D-C66F8707DEA4 wds:Q37263970-D69D26A3-D512-4533-A7A9-58A3EBDCF751 wds:Q35172474-FA93AABF-4D25-4D01-9EF7-23E44DD4A093 wds:Q77936700-25737AF8-C195-4C8C-8250-094806D6FE62

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