About: Primary hypomagnesaemia, an autosomal recessive inherited disease?

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific article published on 01 April 1983

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 1983 (uk) գիտական հոդված հրատարակված 1983 թվականի ապրիլի 1-ին (hy) im April 1983 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'abril de 1983 (ast) scientific article published on 01 April 1983 (en)
publication date	wds:Q72549338-09EE810F-61FB-431D-9DD8-E5B7F658D81B
publication date	1983-04-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q72549338-FF0C98BA-7A2D-42B7-9375-70771AFEF89E
language of work or name	English
cites work	wds:Q72549338-8820EB1A-8C0F-49E0-B25A-63099D00DBA2
cites work	Pharmacokinetics of a single evening dose of slow release theophylline in patients with chronic lung disease [letter]
author name string	wds:Q72549338-9197C00E-E9DB-43B6-AD5B-4BF8BD09B82D wds:Q72549338-ACB2C5C6-35E6-4CC4-8440-960D1E17EF39
author name string	R C Hennekam R A Donckerwolcke
rdfs:label	Primary hypomagnesaemia, an autosomal recessive inherited disease? (en) Primary hypomagnesaemia, an autosomal recessive inherited disease? (nl)
skos:prefLabel	Primary hypomagnesaemia, an autosomal recessive inherited disease? (en) Primary hypomagnesaemia, an autosomal recessive inherited disease? (nl)
name	Primary hypomagnesaemia, an autosomal recessive inherited disease? (en) Primary hypomagnesaemia, an autosomal recessive inherited disease? (nl)
title	wds:Q72549338-083C6578-43E2-4324-84F3-D42EF4155D10
title	Primary hypomagnesaemia, an autosomal recessive inherited disease? (en)
page(s)	wds:Q72549338-F5FBA1D8-3F8B-4051-9698-034CE3867756
page(s)	927
instance of	wds:Q72549338-B53A93FE-9A7E-410E-8C46-A699074A5008
instance of	scholarly article
PubMed ID	wds:Q72549338-9271C26C-2002-4399-970C-68A020E5C252
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6132241
PubMed ID	6132241
published in	wds:Q72549338-D4173D60-147F-4D6B-9F09-6170854B221B
published in	The Lancet
issue	wds:Q72549338-258A5A33-5E3A-4D30-9499-D91C0A40C845
volume	wds:Q72549338-C489C9FE-8134-4D79-90CD-030346C2B27D
issue	8330
volume	1
DOI	wds:Q72549338-D07404B7-B204-4087-9E89-89F2E2FA50F9
DOI	http://dx.doi.org/10.1016/S0140-6736(83)91352-1
DOI	10.1016/S0140-6736(83)91352-1
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q72549338
is cites work of	Primary hypomagnesaemia. A case report and literature review Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint Clinical presentation and outcome in primary familial hypomagnesaemia Familial hypomagnesaemia with secondary hypocalcaemia--autosomal or X-linked inheritance? Long-term follow-up of a patient with primary hypomagnesaemia and secondary hypocalcaemia due to a novel TRPM6 mutation
is cites work of	wds:Q39774312-37B6B839-C4D0-4B48-BE83-11C6E8E0FA57 wds:Q41469765-FBECAF2E-4EA0-4196-9F25-074AFA19303B wds:Q81441834-1D61D65C-0D2D-4A49-98AC-109D9AFAF25C wds:Q67823212-6256BE6F-9A07-4B6E-B909-F0C5F885DB3E wds:Q35258328-65B7E879-6728-41AC-B6C6-BB74B9C24C40

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