Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.
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Inactivation of the gene for anticoagulant protein C causes lethal perinatal consumptive coagulopathy in miceThe 2.8 A crystal structure of Gla-domainless activated protein CEndothelium-specific loss of murine thrombomodulin disrupts the protein C anticoagulant pathway and causes juvenile-onset thrombosisProtein S controls hypoxic/ischemic blood-brain barrier disruption through the TAM receptor Tyro3 and sphingosine 1-phosphate receptor.Neonatal thrombosisProtein S as an in vivo cofactor to activated protein C in prevention of microarterial thrombosis in rabbits.An accompanying genetic severe deficiency of tissue factor protects mice with a protein C deficiency from lethal endotoxemia.Antithrombotic therapy in neonates and children: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines.Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein CThrombophilia - how far and how much to investigate?Successful pregnancy outcome in a case of protein s deficiencyCombined factor VII/protein C deficiency results in intrauterine coagulopathy in mice.Purpura Fulminans Associated with Hemiparesis Following Measles Infection in a Nigerian Girl: A Case Report.Molecular genetics of venous thromboembolism.Purpura fulminans and late onset group B streptococcal sepsis in a premature twin.Lack of protein S in mice causes embryonic lethal coagulopathy and vascular dysgenesisAn endogenous vitamin K-dependent mechanism regulates cell proliferation in the brain subventricular stem cell niche.Skin Necrosis and Purpura Fulminans in Children With and Without Thrombophilia--A Tertiary Center's Experience.The role of TAM family receptors and ligands in the nervous system: From development to pathobiology.Postinfection purpura fulminans in a patient heterozygous for prothrombin G20210A and acquired protein S resistance.Rare presentation of rickettsial infection as purpura fulminans: a case report.
P2860
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P2860
Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on October 1990
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
@cs
name
Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.
@en
Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.
@nl
type
label
Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.
@en
Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.
@nl
prefLabel
Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.
@en
Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.
@nl
P356
P1476
Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.
@en
P2093
P304
P356
10.1055/S-2007-1002683
P577
1990-10-01T00:00:00Z