About: Congenital asplenia and group B streptococcus sepsis in the adult: case report and review of the literature

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About: Congenital asplenia and group B streptococcus sepsis in the adult: case report and review of the literature Goto Sponge NotDistinct Permalink

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scientific article published on 28 July 2008

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2008 (ast) наукова стаття, опублікована в липні 2008 (uk) مقالة علمية نشرت في 28 يوليو 2008 (ar) scientific article published on 28 July 2008 (en)
publication date	wds:Q37194938-FFD6A90A-2D98-44B2-9584-F06BB7D28BA1
publication date	2008-07-28 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37194938-ECEA64CA-98EE-4B05-84F4-7CEEFF3BEB6D
language of work or name	English
cites work	wds:Q37194938-2E219A3B-6DEE-4850-BA3C-63C5E9E2C411 wds:Q37194938-2F111AAA-0084-4032-B79F-5726C6167B5E wds:Q37194938-7BBD0BC2-29A8-4661-8764-5BF2EFF89997 wds:Q37194938-827182C4-B7B6-48F3-BC90-1B7807F1A1B7 wds:Q37194938-82F1BF5C-78F3-4D8E-950D-E9947BBC11F6 wds:Q37194938-97435E24-3BC5-4E54-A23F-4E2FFFE04CB4 wds:Q37194938-A0FDAC40-2874-4830-9342-95C34AD7DF87 wds:Q37194938-A476FAF1-AA38-4AD6-858A-C11DBCD528E8 wds:Q37194938-AC47EFDC-595D-4EEA-9DB4-8BEF89508E33 wds:Q37194938-EF386013-775D-4FAB-ACEA-9E4201951994
cites work	A population-based assessment of invasive disease due to group B Streptococcus in nonpregnant adults Asplenia in ATR-X syndrome: a second report. X-linked situs abnormalities result from mutations in ZIC3 Syndromes of asplenia and polysplenia. A review of cardiac and non-cardiac malformations in 60 cases withspecial reference to diagnosis and prognosis Heterotaxia syndrome and autosomal dominant inheritance. Overwhelming infection in asplenic patients: current best practice preventive measures are not being followed Septicaemia and adrenal haemorrhage in congenital asplenia Group B streptococcal toxic shock syndrome in an asplenic patient: case report and literature review Group B streptococcal toxic shock-like syndrome: report of a case and purification of an associated pyrogenic toxin Familial isolated congenital asplenia: a rare, frequently hereditary dominant condition, often detected too late as a cause of overwhelming pneumococcal sepsis. Report of a new case and review of 31 others
author name string	wds:Q37194938-66B42970-16D7-481B-83A7-9706A76D618B wds:Q37194938-8A9C0573-420D-4ADF-AB8C-78CA08E58809 wds:Q37194938-BFC14E76-F87A-478F-9A79-EDEC99552D65 wds:Q37194938-E533069C-3B99-48BA-B9A7-2262E114D420
author name string	Sanjay Gupta Antonio Privitera Kumaran Thiruppathy Kapila Jain
rdfs:label	Congenital asplenia and group B streptococcus sepsis in the adult: case report and review of the literature (en) Congenital asplenia and group B streptococcus sepsis in the adult: case report and review of the literature (nl) Congenital asplenia and group B streptococcus sepsis in the adult: case report and review of the literature (ast)
skos:prefLabel	Congenital asplenia and group B streptococcus sepsis in the adult: case report and review of the literature (en) Congenital asplenia and group B streptococcus sepsis in the adult: case report and review of the literature (nl) Congenital asplenia and group B streptococcus sepsis in the adult: case report and review of the literature (ast)
name	Congenital asplenia and group B streptococcus sepsis in the adult: case report and review of the literature (en) Congenital asplenia and group B streptococcus sepsis in the adult: case report and review of the literature (nl) Congenital asplenia and group B streptococcus sepsis in the adult: case report and review of the literature (ast)
title	wds:Q37194938-9F5C0004-A466-4C01-848E-915DCA4C7FEE
title	Congenital asplenia and group B streptococcus sepsis in the adult: case report and review of the literature (en)
page(s)	wds:Q37194938-EE7E27EA-BACD-4780-843C-EB9C3A60318F
page(s)	437-439
instance of	wds:Q37194938-1F7B37F1-E4D7-41A4-A753-309503A615DE wds:Q37194938-ccc165ea-7ac5-4382-8959-1168ff6eb058
instance of	review article scholarly article
main subject	wds:Q37194938-148D93A4-65E4-46D8-B196-AEA85086F125 wds:Q37194938-255D45AB-616D-4FB9-80AA-6D21AFDD20CC wds:Q37194938-6BA3B3AF-203B-4290-A80E-07C971CE708E
main subject	sepsis congenital abnormality case report
PubMed ID	wds:Q37194938-239457F5-3E94-4B93-846A-3D681BE944E6
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18564289
PubMed ID	18564289
published in	wds:Q37194938-9CD75561-8747-4D6C-81CC-A8A759FC0297
published in	FEMS Immunology and Medical Microbiology
issue	wds:Q37194938-2F63B72B-FF57-4141-A405-EE30FCD9DFFB
volume	wds:Q37194938-D87FAE70-DAD0-40DB-BD71-B7CC8629DF73
issue	3
volume	53
DOI	wds:Q37194938-F032EA7A-823A-4B50-B8CB-660CF96C63AA
DOI	http://dx.doi.org/10.1111/J.1574-695X.2008.00422.X
DOI	10.1111/J.1574-695X.2008.00422.X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37194938
is cites work of	Persistent thrombocytosis in elderly patients with rare hyposplenias that mimic essential thrombocythemia. Sporadic isolated congenital asplenia with fulminant pneumococcal meningitis: a case report and updated literature review. Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated exons Isolated Congenital Asplenia in an Asymptomatic Patient: A Very Rare Diagnosis Howell-Jolly bodies on peripheral smear leading to the diagnosis of congenital hyposplenism in a patient with septic shock A Rare Association of Congenital Asplenia with Jejunal Arteriovenous Malformation
is cites work of	wds:Q53172692-DFAE719F-609B-4E9A-8BC1-7F0B27824565 wds:Q92067350-1A230F59-A584-4FBD-952F-2E4127460665 wds:Q38578805-F9326817-7AED-4811-9F54-16FF1482FE1E wds:Q47161699-AFCA7197-4355-47A8-AD3E-81141DCA53E5 wds:Q56967318-0D16D369-6881-4458-9781-3A04677BE949 wds:Q42616119-7E4806F5-388F-41F9-80C7-11B1125F44B1

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