About: Sudden infant death syndrome (SIDS) in a family with myophosphorylase deficiency

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About: Sudden infant death syndrome (SIDS) in a family with myophosphorylase deficiency Goto Sponge NotDistinct Permalink

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scientific article published on 01 March 1997

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 1997 (uk) article scientifique publié en 1997 (fr) im März 1997 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en marzu de 1997 (ast) scientific article published on 01 March 1997 (en)
publication date	wds:Q73298404-79370DAE-72D7-43BD-8CB5-891DA9AF2BD3
publication date	1997-03-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q73298404-08034136-1A1A-4B85-B20C-80A0141B51BB wds:Q73298404-0BAFDF5C-4B40-4461-A0B5-0EB24031499D wds:Q73298404-27CDCD9B-61F4-4024-9C5A-7B17D220A893 wds:Q73298404-2A3C8394-8AB6-446B-A2AE-BB5609EFB476 wds:Q73298404-474A636B-F903-454F-8989-FA8D93B308B1 wds:Q73298404-523EBC48-6619-44B4-A3B5-5B99CF6424C1 wds:Q73298404-6D0A490B-2134-4187-8162-23B54627AF7E wds:Q73298404-850F395A-4B05-4096-A6A5-D8BF2A490132 wds:Q73298404-8749350D-1BB9-4F25-857D-77419C67FB0F wds:Q73298404-983407CE-A2E6-4516-8033-728974EA7905 wds:Q73298404-E6E9A952-0491-4A96-9492-71EEB20F27CD
cites work	Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease) Fatal infantile form of muscle phosphorylase deficiency Phosphorylase isoenzymes in normal and myophosphorylase-deficient human heart Novel mutation in the mitochondrial DNA tRNA glycine gene associated with sudden unexpected death Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in the muscle The molecular genetic basis of myophosphorylase deficiency (McArdle's disease) Double trouble: combined myophosphorylase and AMP deaminase deficiency in a child homozygous for nonsense mutations at both loci Fatal infantile muscle phosphorylase deficiency Congenital myopathy due to phosphorylase deficiency Sudden infant death syndrome and inherited disorders of fatty acid beta-oxidation Myophosphorylase deficiency: an unusually severe form with myoglobinuria
author name string	wds:Q73298404-173FABE2-2C1A-4E55-B5BB-A419782D0071 wds:Q73298404-2BF3F8D2-032E-4005-968F-35B2B0C5E2CC wds:Q73298404-315995E4-0994-40E4-A618-319B1328F613 wds:Q73298404-47ECD394-29BB-4AA0-AA5B-FB98F6CB82BF wds:Q73298404-4A7CA828-DA96-49B7-9869-0FCA66B0BCB2 wds:Q73298404-8D215F9D-C794-463F-8CF5-4E24CF46449B wds:Q73298404-98E674AB-D1F6-4B03-8364-1BF92EC861E6
author name string	C Bruno S DiMauro S Shanske S Tsujino A M Sarrazin M G LeRoux M el-Schahawi
rdfs:label	Sudden infant death syndrome (SIDS) in a family with myophosphorylase deficiency (en) Sudden infant death syndrome (SIDS) in a family with myophosphorylase deficiency (nl)
skos:prefLabel	Sudden infant death syndrome (SIDS) in a family with myophosphorylase deficiency (en) Sudden infant death syndrome (SIDS) in a family with myophosphorylase deficiency (nl)
name	Sudden infant death syndrome (SIDS) in a family with myophosphorylase deficiency (en) Sudden infant death syndrome (SIDS) in a family with myophosphorylase deficiency (nl)
title	wds:Q73298404-FF6AA07A-174B-489C-8D04-B86401491A61
title	Sudden infant death syndrome (SIDS) in a family with myophosphorylase deficiency (en)
page(s)	wds:Q73298404-75F974EC-2BB1-41D5-974E-D6F2D98822E4
page(s)	81-83
instance of	wds:Q73298404-7B07E5E5-B0BD-4FF2-B93C-826D1EDF214A
instance of	scholarly article
main subject	wds:Q73298404-89F358E1-7692-4D8D-B17F-47EEC3AB2CD5
main subject	sudden infant death syndrome
PubMed ID	wds:Q73298404-B3D5C66E-CF06-4CC6-B960-DA994569AF09
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9131647
PubMed ID	9131647
published in	wds:Q73298404-ABB16A9A-B511-4BCB-BBF9-EE2072658991
published in	Neuromuscular Disorders
issue	wds:Q73298404-1814E724-4B8A-48DD-92A7-F1D4511F9D81
volume	wds:Q73298404-6ECA233E-6B96-413A-B0E0-9CB82AE15293
issue	2
volume	7
DOI	wds:Q73298404-22AF0D66-3C6D-4718-B263-237C50DBB173
DOI	http://dx.doi.org/10.1016/S0960-8966(97)00424-0
DOI	10.1016/S0960-8966(97)00424-0
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73298404
is cites work of	Progress and problems in muscle glycogenoses Disorders of carbohydrate metabolism Glycogen storage myopathies Differentiating idiopathic inflammatory myopathies from metabolic myopathies Phrenic nerves and diaphragms in sudden infant death syndrome A Systematic Review of Molecular Autopsy Studies in Sudden Infant Death Cases
is cites work of	wds:Q82029880-DB0E2961-F75E-489D-8FEC-6BE6B03EF25C wds:Q35036173-674F33DE-8363-48B4-B04C-77BF01767919 wds:Q93083911-AB237B69-13F6-4629-871A-68F74BB90777 wds:Q74459308-4B4994DB-C0BE-4613-ADC8-7F11407C5EF5 wds:Q33829454-60485BF8-6BF1-48A3-A8AD-BCAE8E8FC2D8 wds:Q34235074-DC2AD627-6018-4294-A17B-323F18B12708

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