About: The beta fibrinogen gene G-455-A polymorphism is a risk factor for Legg-Perthes disease

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rdf:type	Item
description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 2003 (uk) مقالة علمية تنشرت ف 1 نونمبر 2003 (ary) im November 2003 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q64134027-2068F696-52F2-47CD-A4C8-2069B110EF7F
publication date	2003-11-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q64134027-0CD5326F-A278-4718-82BF-9DB351C643D2
language of work or name	English
cites work	wds:Q64134027-216B81A8-E877-44CC-A489-4C6476D99076 wds:Q64134027-8EF5FCF4-EFAE-4E1D-A3FA-615BA6FCDA6B wds:Q64134027-9276946A-5937-483C-B5F5-3A03969EDA2B wds:Q64134027-942E2C21-A7E7-45FC-867A-8F0D5BD52741 wds:Q64134027-9E9756EF-D723-4893-8927-1905BAFA7696 wds:Q64134027-B305C18E-6E61-4CCD-8607-259ED037F7E4 wds:Q64134027-BDFBBFFD-BB14-4DED-A753-311C68925D16 wds:Q64134027-E146AE5F-A041-4F97-8035-D74F2EAFA5C4 wds:Q64134027-F002C797-9963-4B5F-9AA5-99686190466B
cites work	Beta fibrinogen gene polymorphisms are associated with plasma fibrinogen and coronary artery disease in patients with myocardial infarction. The ECTIM Study. Etude Cas-Temoins sur l'Infarctus du Myocarde Haemostatic function and ischaemic heart disease: principal results of the Northwick Park Heart Study Effects of changes in smoking and other characteristics on clotting factors and the risk of ischaemic heart disease Perthes' disease and the relevance of thrombophilia The role of protein C, protein S, and resistance to activated protein C in Legg-Perthes disease. Legg-Calvé-Perthes disease and passive smoking Coagulation and fibrinolysis in smoking and nonsmoking pregnant women Thyropathic endemic dystrophy in an area of the Argeş Valley Fibrinogen genotype and risk of peripheral atherosclerosis
author name string	wds:Q64134027-2D3DFC64-D527-41D8-AEBA-61F1496F4B68 wds:Q64134027-32FD42EC-77DA-445A-9D59-033CD4E52E46 wds:Q64134027-4FFCA8A5-48DB-4953-97AD-DEBF71127B8E wds:Q64134027-6D658822-4728-40BB-9D4F-3E001FB02A9E wds:Q64134027-C5C84A84-A278-4062-A528-017C42E55ABF wds:Q64134027-C60FB87C-1A4D-463B-AF98-BE94430EBD44 wds:Q64134027-EA6EB02F-EAB4-43E4-9426-B26DFEDBEC58
author name string	W C Hooper B Evatt H Austin J Eldridge M Stokes A Dilley M Jamil
rdfs:label	The beta fibrinogen gene G-455-A polymorphism is a risk factor for Legg-Perthes disease (en) The beta fibrinogen gene G-455-A polymorphism is a risk factor for Legg-Perthes disease (nl)
skos:prefLabel	The beta fibrinogen gene G-455-A polymorphism is a risk factor for Legg-Perthes disease (en) The beta fibrinogen gene G-455-A polymorphism is a risk factor for Legg-Perthes disease (nl)
name	The beta fibrinogen gene G-455-A polymorphism is a risk factor for Legg-Perthes disease (en) The beta fibrinogen gene G-455-A polymorphism is a risk factor for Legg-Perthes disease (nl)
author	wds:Q64134027-14B376E8-E635-49E4-B022-7698DC14FB9E
author	Connie H. Miller
title	wds:Q64134027-015198DD-7553-45C2-8E87-04FB0F61F531
title	The beta fibrinogen gene G-455-A polymorphism is a risk factor for Legg-Perthes disease (en)
page(s)	wds:Q64134027-8F7E79E7-B91B-4809-BD5F-C7507498125F
page(s)	2317-2321
instance of	wds:Q64134027-6B5A3FE9-FF55-4580-9CA3-CE3CD8EA2A57
instance of	scholarly article
PubMed ID	wds:Q64134027-6CC15653-097F-43DA-9E89-5603927608B3
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/14629463
PubMed ID	14629463
published in	wds:Q64134027-A911CDD7-B09C-4DC2-9F7C-AE4F07F84249
published in	Journal of Thrombosis and Haemostasis
issue	wds:Q64134027-9936521F-9D9A-4ED9-8607-5FE5A769B926
volume	wds:Q64134027-8936DC59-74D0-40FE-9BF6-FB413C294F27
issue	11
volume	1
DOI	wds:Q64134027-C328E9CF-8779-42B7-B7A8-4AE1E8C9C4C5
DOI	http://dx.doi.org/10.1046/J.1538-7836.2003.00416.X
DOI	10.1046/J.1538-7836.2003.00416.X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q64134027
is cites work of	Genetic association studies in osteonecrosis of the femoral head: mini review of the literature The physiopathology of avascular necrosis of the femoral head: an update A recurrent mutation in type II collagen gene causes Legg-Calvé-Perthes disease in a Japanese family. The epidemiology and demographics of legg-calvé-perthes' disease Legg-Calvé-Perthes syndrome (LCPS): an up-to-date critical review Charles W. Goff, MD CORR 1962;22:93-107. The time of the insult/triggering event in Legg-Calvé-Perthes' disease determined by incubation period modeling and the age distribution of children with Perthes'.
is cites work of	wds:Q36982436-C8C5861C-597B-43F9-BEF3-0B751DAF2362 wds:Q39063584-37E8C106-0DB9-44FF-B45D-3162E82A9417 wds:Q33776437-69F8B610-476C-4616-AFE4-5B79C50EB301 wds:Q38027058-17FF3F17-26D6-49B4-B754-98D216614F80 wds:Q55043682-D1471820-938C-47A2-896A-FD918D2CFB04 wds:Q43183499-328108F1-920F-4ABC-BAD7-3FC2EEBDA8F1

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