Results 121 to 130 of about 306,744 (280)

Inherited thrombophilias [PDF]

QJM, 1997
M A, Laffan, E G, Tuddenham
openaire   +2 more sources

Thrombophilia work-up and clinical outcomes in Indian patients with unprovoked venous and arterial thrombosis aged 18-50 years

Bleeding, Thrombosis and Vascular Biology
Background: The prevalence of thrombophilia in patients with unprovoked thrombotic events varies across populations, justifying the need for region-specific data to guide appropriate testing strategies.
Monisha Harimadhavan, Bharath Ram, Karthick R G, Devi Prasad Shetty, Shilpa Prabhu, Nataraj K S, Akshatha Nayak, Sharat Damodar   +7 more
doaj   +1 more source

Effect of platelet glycoprotein IIb/IIIa PLA2 polymorphism on severity of pulmonary thromboembolism [PDF]

, 2014
Background: Pulmonary thromboembolism (PTE) is among the leading causes of death following surgery and/or hospital admission. Role of thrombophilic risk factors in the etiology of PTE is well known; But not much data is available on their role in ...
Deris, Fatemeh., Hasheminia, Alimohammad., Pourgheysari, Batoul., Rouhi Boroujeni, Hamid., Rouhi Boroujeni, Parnia.   +4 more
core   +1 more source

The Impact of Inherited Thrombophilia Types and Low Molecular Weight Heparin Treatment on Pregnancy Complications in Women with Previous Adverse Outcome

Yonsei medical journal, 2016
Purpose To assess the distribution of births and spontaneous abortions, first-trimester abortion (FTA) and mid-trimester abortion (MTA), in untreated (n=128) and low molecular weight heparin (LMWH) treated pregnancies (n=50) of the same women with ...
Nađa Aračić, D. Roje, I. Jakus, Marinela Bakotin, V. Stefanovic   +4 more
semanticscholar   +1 more source

Antiphosphatidylserine antibody as a cause of multiple dural venous sinus thromboses and ST-elevation myocardial infarction [PDF]

, 2018
Objective: Rare disease Background: Antiphospholipid syndrome (APS) is an autoimmune disease characterized by antibodies directed against phos-pholipids on plasma membranes. Through unclear mechanisms, APS confers hypercoagulability.
Marquardt, Caillin W., Pickens, Peter V., Varner, Chelsea K.   +2 more
core   +1 more source

Transient Focal Neurological Deficits During Pregnancy in Carriers of Inherited Thrombophilia [PDF]

, 2000
Michael J. Kupferminc, Yair Daniel, Natan M. Bornstein, Joseph B. Lessing, Amiram Eldor   +4 more
openalex   +1 more source

Marcadores séricos de trombofilias hereditárias e anticorpos antifosfolípides em gestantes com antecedentes de pré-eclâmpsia grave Serum markers of inherited thrombophilia and antiphospholipid antibodies in pregnant women with previous history of severe pre-eclampsia

Revista Brasileira de Ginecologia e Obstetrícia, 2012
OBJETIVO: Verificar a frequência e a associação de marcadores séricos para trombofilias hereditárias e adquiridas em gestantes com histórico de pré-eclâmpsia grave em gestação anterior.
Ernesto Antonio Figueiró-Filho, Vanessa Marcon de Oliveira, Lílian Rezende Coelho, Ili Breda   +3 more
doaj   +1 more source

Inherited thrombophilia in children with venous thromboembolism and the familial risk of thromboembolism: an observational study [PDF]

, 2012
Susanne Holzhauer, Neil A. Goldenberg, Ralf Junker, Christine Heller, Monika Stoll, Daniela Manner, Rolf M. Mesters, Anne Krümpel, Michael Stach, Ulrike Nowak‐Göttl   +9 more
openalex   +1 more source

[Inherited thrombophilia].

Acta haematologica Polonica, 1995
The prevalence of inherited thrombophilia in the general population (1 in 2,500) is higher than that of hemophilia and related bleeding disorders. Well established causes of thrombophilia include deficiencies of natural coagulation inhibitors: antithrombin III, protein C and protein S.
openaire   +1 more source

Thrombosis at unusual sites in reproductive age group-a case series [PDF]

, 2016
Thrombosis is one of the causes of morbidity and mortality in women of reproductive age group. Thrombosis at unusual sites may pose diagnostic and management dilemma for health care personnel.
Khalid, Bahariah, Md Noor, Sabariah, Mohd Tohit, Eusni Rahayu, Seman, Zainina   +3 more
core   +1 more source