Results 131 to 140 of about 306,744 (280)

Inherited thrombophilia is not associated with an increased risk of liver fibrosis [PDF]

, 2023
Iranzu Ezcurra, Ángela Puente, Antonio Cuadrado, Ibai Tamayo, Paula Iruzubieta, M. Arias, Francisco José González, Raúl Pellón, Sara Sánchez, J. Crespo del Pozo, Mercedes Acebo, Marcos López‐Hoyos, Rocío Pérez, Amalia Cuesta, Ángela Antón, V. Rodríguez, Emilio Fábrega, Javier Crespo, José Ignacio Fortea   +18 more
openalex   +1 more source

Whole-exome sequencing in evaluation of patients with venous thromboembolism

Blood Advances, 2017
: Genetics play a significant role in venous thromboembolism (VTE), yet current clinical laboratory-based testing identifies a known heritable thrombophilia (factor V Leiden, prothrombin gene mutation G20210A, or a deficiency of protein C, protein S, or ...
Eun-Ju Lee, Daniel J. Dykas, Andrew D. Leavitt, Rodney M. Camire, Eduard Ebberink, Pablo García de Frutos, Kavitha Gnanasambandan, Sean X. Gu, James A. Huntington, Steven R. Lentz, Koen Mertens, Christopher R. Parish, Alireza R. Rezaie, Peter P. Sayeski, Caroline Cromwell, Noffar Bar, Stephanie Halene, Natalia Neparidze, Terri L. Parker, Adrienne J. Burns, Anne Dumont, Xiaopan Yao, Cassius Iyad Ochoa Chaar, Jean M. Connors, Allen E. Bale, Alfred Ian Lee   +25 more
doaj   +1 more source

Outcomes of Cerebral Venous Thrombosis in Patients With Myeloproliferative Neoplasms from a U.S. Nationwide Hospitalization Study

eJHaem, Volume 7, Issue 1, February 2026.
Nikhil Vojjala, Raj Shah, Viktoriya Gibatova, Lakshmi Kattamuri, Shubham Agrawal, Geetha Krishnamoorthy, Rushad Patell   +6 more
wiley   +1 more source

Combination of factor V Leiden and MTHFR mutations in myocardial infarction

Annals of Saudi Medicine, 2013
Identifying patients who are at high risk of suffering myocardial infarction can be done by determining risk factors or by the adoption of molecular genetic testing for inherited thrombophilia.
Najiba Fekih-Mrissa, Dhouha Berredjeb-Benslama, Abdeddayem Haggui, Habib Haouala, Nasreddine Gritli   +4 more
doaj   +1 more source

Novel mutation in CCBE 1 as a cause of recurrent hydrops fetalis from Hennekam lymphangiectasia-lymphedema syndrome-1. [PDF]

, 2018
Whole exome sequencing (WES) was used to determine the etiology of recurrent hydrops fetalis in this case of Hennekam lymphangiectasia-lymphedema syndrome-1.
Andreasen, Tara S, Lamale-Smith, Leah M, Mao, Rong, Melber, Dora J, Miller, Christine E, Moore, Thomas R, Tvrdik, Tatiana, Woelkers, Douglas A   +7 more
core  

Inherited Thrombophilia and Gestational Venous Thromboembolism

Women's Health, 2003
Thromboembolic disease remains a leading cause of maternal mortality during pregnancy and the puerperium. Rational and risk-adapted administration of heparin prophylaxis depends on the identification of those women who have an increased risk of thrombosis and the accurate quantification of this risk.
Rainer B, Zotz, Andrea, Gerhardt, Rüdiger E, Scharf   +2 more
openaire   +3 more sources

Inherited Thrombophilia and Risk of Thrombosis in Children with Cancer: a Single-center Experience. [PDF]

Acta Med Acad, 2023
Đordević A, Grahovac B, Šegulja S, Bilić Zulle L, Roganović J.   +4 more
europepmc   +1 more source

Association of deficiency of coagulation factors (Prs, Prc, ATIII) and FVL positivity with preeclampsia and/or eclampsia in pregnant women [PDF]

, 2014
Background: Thrombophilia is a pathological state of increased blood coagulability. It causes problems during pregnancy including preeclampsia, stillbirth, repeated abortions, and detached pair.
Al-e-Rasul Dehkordi, Maryam., Al-e-Rasul Dehkordi, Saeid., Haji-Gholami, Ali., Kazemi Vardanjani, Abdolrahim., Soleimani, Akbar.   +4 more
core  

Family History And Inherited Thrombophilia [PDF]

, 1995
Alberto Tosetto, Maurizio Frezzato, Francesco Rodeghiero   +2 more
openalex   +1 more source

Association between non-O blood group and spontaneous abortion in women with inherited thrombophilia [PDF]

, 2021
Anna Poretto, Luca Spiezia, Giacomo Turatti, Michelangelo Marobin, Elisabetta Borella, Elena Campello, Paolo Simioni   +6 more
openalex   +1 more source