About: Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study

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scientific article published on 29 March 2014

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 2014 (uk) article scientifique publié en 2014 (fr) im März 2014 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 29 March 2014 (en) artículu científicu espublizáu en marzu de 2014 (ast)
publication date	wds:Q57202331-CB7B313A-15C1-4EBA-A81D-DB0A6423A452
publication date	2014-03-29 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57202331-7D468F7E-4F8C-4706-BD2D-20004D3E85B5
language of work or name	English
cites work	wds:Q57202331-0AC15659-B512-4F71-85D6-6413A019F706 wds:Q57202331-1600D5FE-0752-4697-BABB-FF88B287D61C wds:Q57202331-1AAE995C-47B5-48FC-88FE-42E32A932279 wds:Q57202331-29441098-EFB3-41F3-9043-219FA2FDF4DE wds:Q57202331-2FCACDC4-1FD9-4194-98CB-B34477E2EA5C wds:Q57202331-3CE5F456-6D97-4B64-B34B-51C1D4F7A992 wds:Q57202331-4C987860-8A02-4FDA-A396-6BDCF18AA196 wds:Q57202331-4D314387-377C-423D-AA64-C1D507F9B883 wds:Q57202331-98690729-A0EA-404C-824C-8445CC97DE34 wds:Q57202331-9A92D850-DBF2-41A4-93E1-A865AC22CFF7 wds:Q57202331-C108F50C-12D6-4402-9C7B-73776BED0C3A wds:Q57202331-C336F077-8AE0-434A-AB59-486F89F71983 wds:Q57202331-C43C448E-985E-4306-9657-581F4839B83C wds:Q57202331-C5566DCA-064D-42EB-88A2-E45016A43210 wds:Q57202331-CB7BDED8-5FEF-425D-97F8-BCDD247C173D wds:Q57202331-CF607288-312D-46F9-97EE-DBA26AE3BCB6 wds:Q57202331-DD752A9D-0A55-4A2B-AA99-F4FFCE84922E wds:Q57202331-F00CFEF1-462D-4676-9FF5-02CBA2AC99B9 wds:Q57202331-F2C5438F-77AB-4CF9-8BEF-313F5448CC9B wds:Q57202331-F66BF3A5-14F0-47C8-A47E-14DE5319DF50
cites work	Inherited antithrombin deficiency: a review Abdominal venous thrombosis in neonates and infants: role of prothrombotic risk factors - a multicentre case-control study. For the Childhood Thrombophilia Study Group. Management of patients with hereditary hypercoagulable disorders Misfolded proteins partition between two distinct quality control compartments Role of conformational sampling in computing mutation-induced changes in protein structure and stability Electrostatics of nanosystems: application to microtubules and the ribosome Prevalence of antithrombin deficiency in the healthy population. Inherited antithrombin III deficiency in the neonate Role of genetic prothrombotic risk factors in childhood caval vein thrombosis Risk of venous thromboembolism and clinical manifestations in carriers of antithrombin, protein C, protein S deficiency, or activated protein C resistance: a multicenter collaborative family study Hereditary and acquired antithrombin deficiency: epidemiology, pathogenesis and treatment options. Multicentre evaluation of combined prothrombotic defects associated with thrombophilia in childhood. Childhood Thrombophilia Study Group. Molecular genetics of inherited antithrombin III deficiencies Inherited thrombophilia in children with venous thromboembolism and the familial risk of thromboembolism: an observational study Impact of inherited thrombophilia on venous thromboembolism in children: a systematic review and meta-analysis of observational studies. High prevalence of thrombophilic traits in children with family history of thromboembolism. Regions flanking exon 1 regulate constitutive expression of the human antithrombin gene Mortality in hereditary antithrombin-III deficiency--1830 to 1989. Relationship between an enhancer element in the human antithrombin III gene and an immunoglobulin light-chain gene enhancer Inherited thrombophilia: implications for prevention and treatment of venous thromboembolism
author name string	wds:Q57202331-6BB33A62-78C2-48F7-9EA8-900BDD09B29E wds:Q57202331-BAC35AC2-EF6E-4D17-B8E8-AD3AB494514A wds:Q57202331-D0B42E9D-2657-4F46-A238-6EA51A235E00
author name string	Walter H A Kahr Suzan Williams Jennifer E Dawson
rdfs:label	Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study (en) Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study (nl)
skos:prefLabel	Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study (en) Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study (nl)
name	Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study (en) Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study (nl)
author	wds:Q57202331-4793A1F4-A0C4-4658-A324-C9DFC197DEA9 wds:Q57202331-52320BB5-CF58-4C8E-AC7F-FE52A662B657 wds:Q57202331-66886B0D-BD72-4957-A057-C470BDA5CB17
author	Julie Forman-Kay Anthony K. C. Chan Riten Kumar
title	wds:Q57202331-359C4ADE-2C6A-44E0-956E-8F0A0F030D16
title	Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study (en)
page(s)	wds:Q57202331-B09827D1-F4BE-4B93-87A9-3842C41EC905
page(s)	130-139
instance of	wds:Q57202331-97B3EFBA-B611-4BDF-8CE6-FF65A8BE7C8B
instance of	scholarly article
PubMed ID	wds:Q57202331-14FCF3D6-5C56-40E0-A1C1-51F3F283A9FF
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/24684277
PubMed ID	24684277
published in	wds:Q57202331-51376A60-83A2-458B-B3C8-083A65DD520F
published in	British Journal of Haematology
issue	wds:Q57202331-7696AEF8-C602-4DA7-A130-9F40AE6303B6
volume	wds:Q57202331-06DB5663-DCB0-4358-B5DB-F7E32B309CF3
issue	1
volume	166
DOI	wds:Q57202331-B475C1FE-0B20-42BE-8346-4CEC7328CF5E
DOI	http://dx.doi.org/10.1111/BJH.12842
DOI	10.1111/BJH.12842
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57202331
is cites work of	c.1058C>T variant in theSERPINC1gene is pathogenic for antithrombin deficiency Molecular structural analysis of a novel and de-novo mutation in the SERPINC1 gene associated with type 1 antithrombin deficiency. Randomized Comparison Study of Novel Recombinant Human Antithrombin Gamma and Plasma-Derived Antithrombin in Healthy Volunteers Incidence and features of thrombosis in children with inherited antithrombin deficiency
is cites work of	wds:Q57202325-28BC74F4-BB09-4704-9B9D-D1B76B008057 wds:Q93164442-D1EE4C36-7FCF-4EB4-880A-A67548D615F7 wds:Q52873934-41883B7B-26BE-4030-8179-B53740A02042 wds:Q93040632-8B82E57D-4473-4303-8C2D-122DDE1F6E5E

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