نتایج جستجو برای: hereditary thrombophilia

تعداد نتایج: 87725  

Journal: :Thrombosis and haemostasis 2004
Gili Kenet Dalia Waldman Aharon Lubetsky Nurit Kornbrut Abdalla Khalil Ariel Koren Baruch Wolach Aviva Fattal Joseph Kapelushnik Hannah Tamary Joanne Yacobovitch Eyal Raveh Shoshana Revel-Vilk Amos Toren Benjamin Brenner

The etiology and pathophysiology of cerebral sinus venous thrombosis (CSVT) in the paediatric population is still poorly understood, and the role of thrombophilic risk factors remains to be elucidated. In our multi-center case-controlled study we studied 46 patients with CSVT diagnosed from April 1996 to December 2003, consecutively referred for thrombophilia work-up. The results of thrombophil...

Journal: :Lancet 1996
F E Preston F R Rosendaal I D Walker E Briët E Berntorp J Conard J Fontcuberta M Makris G Mariani W Noteboom I Pabinger C Legnani I Scharrer S Schulman F J van der Meer

BACKGROUND A successful outcome of pregnancy requires an efficient uteroplacental vascular system. Since this system may be compromised by disorders of haemostasis associated with a prothrombotic state, we postulated that maternal thrombophilia might be a risk factor for fetal loss. We studied the relation between heritable thrombophilic defects and fetal loss in a cohort of women with factor V...

Journal: :Circulation 2004
J Ernesto Molina

BACKGROUND One third of cases of upper-extremity deep vein thrombosis (DVT) are primary, ie, they occur in the absence of central venous catheters or cancer. Risk factors for primary upper-extremity DVT are not well established, and the recurrence rate is unknown. METHODS AND RESULTS We studied 115 primary upper-extremity DVT patients and 797 healthy controls for the presence of thrombophilia...

2004
Ida Martinelli Serena Maria Passamonti

Background—One third of cases of upper-extremity deep vein thrombosis (DVT) are primary, ie, they occur in the absence of central venous catheters or cancer. Risk factors for primary upper-extremity DVT are not well established, and the recurrence rate is unknown. Methods and Results—We studied 115 primary upper-extremity DVT patients and 797 healthy controls for the presence of thrombophilia d...

2016
Nada Aracic Damir Roje Ivana Alujevic Jakus Marinela Bakotin Vedran Stefanovic

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 inherited thrombophilias and adverse pregnancy outcome (APO) in previous pregnancies. We particularly investigated the impact of LMWH on reducing the...

Journal: :The Netherlands journal of medicine 2004
P W Kamphuisen F R Rosendaal

In the last ten years, several risk factors that increase the risk of venous thrombosis have been discovered. Venous thrombosis is a multicausal disease in which several risk factors, both genetic and acquired, have to occur simultaneously to cause thrombosis. This means that most individuals with single thrombophilia are asymptomatic. Although testing thrombosis patients and their relatives fo...

Journal: :Thrombosis research 2009
Federico Lussana Francesco Dentali Rosanna Abbate Ernesto d'Aloja Armando D'Angelo Valerio De Stefano Elena M Faioni Elvira Grandone Cristina Legnani Ida Martinelli Paolo Simioni Daniela Tormene

The term thrombophilia describes an increased tendency to develop thrombosis and many laboratory markers with different strengths of association with thrombosis have been identified. The main causes of maternal mortality and morbidity in developed countries is venous thromboembolism (VTE) and obstetric complications. During pregnancy and puerperium the risk for VTE increases due to hemostatic i...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1987
G Romeo H J Hassan S Staempfli L Roncuzzi L Cianetti A Leonardi V Vicente P M Mannucci R Bertina C Peschle

The structure of the gene for protein C, an anticoagulant serine protease, was analyzed in 29 unrelated patients with hereditary thrombophilia and protein C deficiency. Gene deletion(s) or gross rearrangement(s) was not demonstrable by Southern blot hybridization to cDNA probes. However, two unrelated patients showed a variant restriction pattern after Pvu II or BamHI digestion, due to mutation...

Journal: :Japanese Journal of Thrombosis and Hemostasis 2006

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید