About: Homozygous protein S deficiency in an infant with purpura fulminans

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scientific article published on 01 November 1990

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 1990 (uk) im November 1990 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en payares de 1990 (ast) scientific article published on 01 November 1990 (en)
publication date	wds:Q68588889-8ED0E927-B0A6-4406-AEB9-45D6740AB173
publication date	1990-11-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q68588889-6E05118B-09F3-456A-B1C5-A847C3EC5F85
language of work or name	English
cites work	wds:Q68588889-1313DB5F-B599-4D0F-9CE4-A2D2853040D5 wds:Q68588889-6D613D56-C146-4C99-916E-07EA260ADF80 wds:Q68588889-A691EC7A-3F8C-40F4-ACBC-170842186684 wds:Q68588889-B0DD6C73-E1B2-4D55-9620-E5AEA371E7A9 wds:Q68588889-EDF9BF23-D779-49C2-BBD3-79B7E2E88D01 wds:Q68588889-FF150F9F-517C-4F17-A337-B7E982A39D24
cites work	Deficiency of protein C in congenital thrombotic disease Inherited protein C deficiency and coumarin-responsive chronic relapsing purpura fulminans in a newborn infant Severe protein C deficiency in newborn infants Homozygous protein C deficiency manifested by massive venous thrombosis in the newborn Familial protein S deficiency is associated with recurrent thrombosis Neonatal purpura fulminans associated with homozygous protein S deficiency
author name string	wds:Q68588889-0CF79821-1B49-4D77-8E70-9F3E999004F5 wds:Q68588889-22C509F1-E80D-4029-8006-BD2CB1395170 wds:Q68588889-255B0EC0-58F7-4023-99E8-E3D96B02B0AC wds:Q68588889-39AACD23-97D0-4FB0-8387-3997DACAF7A4 wds:Q68588889-7930D603-0A30-4AEB-85BC-C75F7DE3E442 wds:Q68588889-9C709C0A-92FD-44EA-99B4-233C8F45E070 wds:Q68588889-A63B265E-5339-4A0F-AC75-0811A93813CD
author name string	R A Marlar M J Manco-Johnson A Chuansumrit V Suvatte C Mahasandana W E Hathaway L J Jacobson
rdfs:label	Homozygous protein S deficiency in an infant with purpura fulminans (en) Homozygous protein S deficiency in an infant with purpura fulminans (nl)
skos:prefLabel	Homozygous protein S deficiency in an infant with purpura fulminans (en) Homozygous protein S deficiency in an infant with purpura fulminans (nl)
name	Homozygous protein S deficiency in an infant with purpura fulminans (en) Homozygous protein S deficiency in an infant with purpura fulminans (nl)
title	wds:Q68588889-3BE88C26-4A02-4CD7-B08C-0DAA9E57E2F2
title	Homozygous protein S deficiency in an infant with purpura fulminans (en)
page(s)	wds:Q68588889-A4E8C276-B87F-4701-82C9-DA6FA54B45CD
page(s)	750-753
instance of	wds:Q68588889-AC3BBB39-55F0-4876-9B9A-E6E44ABF8081
instance of	scholarly article
main subject	wds:Q68588889-6D42B589-1411-4E82-A3B5-F4C86FE942FB wds:Q68588889-8686762C-91F4-4670-95B8-8DE3378DC333 wds:Q68588889-DB2DCBB2-35C0-43C9-B68D-4E47218B000E
main subject	protein S deficiency purpura fulminans homozygosity
PubMed ID	wds:Q68588889-35428B33-9B75-4332-9481-49F9CDD17216
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2231208
PubMed ID	2231208
published in	wds:Q68588889-305BDCF7-B136-4D2B-9404-76ADF112A7B8
published in	The Journal of Pediatrics
issue	wds:Q68588889-7C8E8422-7168-4D63-92F2-61F597AE634F
volume	wds:Q68588889-EB845A52-5624-426F-8111-52704245E4F6
issue	5
volume	117
DOI	wds:Q68588889-BB6FB88E-E0E0-4545-B242-250B78CF2003
DOI	http://dx.doi.org/10.1016/S0022-3476(05)83335-9
DOI	10.1016/S0022-3476(05)83335-9
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q68588889
is cites work of	Venous thrombosis: a multicausal disease Antithrombotic therapy in neonates and children: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines. Evaluation and treatment of thrombosis in the neonatal intensive care unit Purpura in infants and children The genetics of venous and arterial thromboembolism Use of prothrombin complex concentrates for prophylaxis and treatment of bleeding episodes in patients with hereditary deficiency of prothrombin, factor VII, factor X, protein C protein S, or protein Z A pilot study of the possible role of familial defects in anticoagulation as a cause for terminal limb reduction malformations Blood component therapy in neonatal hemostatic disorders Risk factors of venous thromboembolism in thai patients Venous thrombosis in pediatric cardiac surgery Inherited resistance to activated protein C in a boy with multiple thromboses in early infancy. Inherited Thrombophilia in Pediatric Venous Thromboembolic Disease: Why and Who to Test Cardiopulmonary bypass and activation of antithrombotic plasma protein C.
is cites work of	wds:Q34207412-999287D9-594E-4374-9EB6-68C0E9CF0803 wds:Q40406587-2B864AFE-E7DD-4F6E-A338-4F5719C20E7C wds:Q28145121-67CE991C-F095-4CB4-BEDC-47DED441DB78 wds:Q54176993-83131806-F60B-4F71-9060-314F214814AC wds:Q34032605-2003F2AC-62C2-4347-A7E5-9E65DC90B5F0 wds:Q33597786-C01FF8A7-30FC-4991-AC37-20678C16879E wds:Q54080510-584A662B-BAEA-439D-9CCD-4E65CDE377B7 wds:Q35752608-30E7ECD8-0E59-4B52-83A7-68D34B3822B4 wds:Q80485832-D5F32B4C-2E90-44FE-9FD1-70414040136B wds:Q73715641-7480F8B2-50C9-4B70-9B6A-98DD3104F584 wds:Q37697342-72412ED1-0471-47F5-BEC7-47716C6FC441 wds:Q41641122-F475A1C2-3493-44A8-8F81-38EDAC1DF233 wds:Q41669537-D2F28E27-F374-406C-81E2-7C99EA21E149

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