Results 21 to 30 of about 4,535,134 (266)
Methionine synthase reductase A66G polymorphism and ischemic stroke in younger patients
Неврология, нейропсихиатрия, психосоматика, 2021 In the past decade, stroke incidence in younger adults increased. Methionine synthase reductase (MTRR) A66G polymorphism is one of the risk factors for ischemic stroke (IS).
O. V. Tsyganenko +2 more
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Combined Thrombophilia in a Young Male Presenting as Life Threatening Pulmonary Embolism [PDF]
Journal of Clinical and Diagnostic Research, 2017 Combined hereditary thrombophilia is an uncommon entity associated with higher risk of early onset thrombosis. We report a case of 39-year-old male with combined deficiency of natural anticoagulants (protein C, S and anti thrombin) along with hyper ...
Akshyaya Pradhan +4 more
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Clinical and Experimental Obstetrics & Gynecology, 2023 Background: To assess the variations in protein C (PC) activity throughout pregnancy and investigate potential correlations between plasma PC activities and adverse pregnancy outcomes.
Yunxia Wang +4 more
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Indian Journal of Hematology and Blood Transfusion, 2013 This report describes a 4 year old female child who presented with fever, pain and swelling of left leg following a trivial trauma. She was diagnosed as a case of deep vein thrombosis and subsequently found to be due to protein C deficiency.
Arun K, De +3 more
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Regulation and Dysregulation of Thrombin Activity
Southeastern European Medical Journal, 2021 Thrombin is the enzyme of the haemostasis system that stands at the crossroads between the coagulation cascade and coagulation inhibition by protein C, between plasma coagulation factors and cells involved in haemostasis and between haemostasis and the ...
Daria Korolova
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IUBMB Life, 2000 Phosphorylation is a universal language used by cells to relay information between and within cells. One family of kinases that plays a key role in transducing information is the protein kinase C family. Members of this family interpret information from signals that result in phospholipid hydrolysis; they communicate to substrates throughout the cell ...
openaire +2 more sources
Archives of Pathology & Laboratory Medicine, 2019 Protein C (PC) deficiency is a heritable or acquired risk factor for thrombophilia, with presentations varying from asymptomatic to venous thromboembolism to neonatal purpura fulminans, a life-threatening disorder. Hereditary PC deficiency is caused by mutation in the PC (PROC) gene located on chromosome 2q14.3.
Peyman, Dinarvand, Karen A, Moser
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Journal of Biological Chemistry, 2004 C-reactive protein (CRP) is a phylogenetically highly conserved plasma protein, with homologs in vertebrates and many invertebrates, that participates in the systemic response to inflammation. Its plasma concentration increases during inflammatory states, a characteristic that has long been employed for clinical purposes.
Steven, Black +2 more
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Neonatal Purpura Fulminans by an Unusual Pathogen: Elizabethkingia meningoseptica
Indian Pediatrics Case Reports, 2022 Background: Neonatal purpura fulminans (PF) is a rare disorder characterized by the formation of dermal microvascular thrombosis associated with disseminated intravascular coagulation (DIC). It can be caused by inherited protein C or protein S deficiency
Rakesh Kumawat +2 more
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Covid-19 Enfeksiyonunda Anti-Trombin-3, Protein C ve Protein S Düzeylerinin İncelenmesi
Sakarya Tıp Dergisi, 2021 Amaç: SARS-CoV-2 virüsünün etkeni olduğu COVİD-19 enfeksiyonu salgın oluşturan önemli bir hastalıktır. COVİD-19 hastalarının birçoğunda kanama ve pıhtılaşma bozukluklarının geliştiği yapılan çalışmalarla gösterilmiştir.
Gizem Kılıçcıoğlu +11 more
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