Results 141 to 150 of about 77,059 (283)

Low prevalence of Factor V Leiden and the prothrombin G20210A mutation in a healthy population from the central-south region of Chile Baixa prevalência do Fator V Leiden e da mutação da protrombina G20210A em uma população sã da região centro-sul do Chile

Revista Brasileira de Hematologia e Hemoterapia, 2009
Thrombosis is a result of the interaction between predisposing genetic polymorphisms and acquired risk factors. The two prothrombotic polymorphisms which are most frequently associated with thrombosis are factor V (FV) Leiden and the prothrombin (PT ...
Iván Palomo, Fabian Segovia, Daniela Parra, Marcelo Alarcón, Edgardo Rojas   +4 more
doaj  

Successful Conservative Treatment of a Complicated Aortic Thrombus in a Woman with Factor V Leiden Mutation. [PDF]

Eur J Case Rep Intern Med, 2021
Frebutte E, Bibombe M, Dumont A, Haxhe M, Reper P.   +4 more
europepmc   +1 more source

Single‐nucleus RNA sequencing reveals ferroptosis as a potential contributor to the pathogenesis of focal cortical dysplasia

Clinical and Translational Medicine, Volume 16, Issue 5, May 2026.
1. A single‐cell analysis was conducted to investigate the transcriptomic changes in cells within focal cortical dysplasia (FCD). 2. Ferroptosis may play a significant role in the pathogenesis of FCD, potentially contributing to cellular damage and epileptogenesis. 3.
Qingyang Zeng, Fengjun Zhu, Dezhi Cao, Yang Sun, Lin Li, Zeshi Tan, Cong Li, Xiaofan Ren, Yidi Liu, Zhiqiang Lin, Dongfang Zou   +10 more
wiley   +1 more source

PO12 | IMPACT OF INHERITED THROMBOPHILIA ON CANCER-ASSOCIATED THROMBOSIS: A SYSTEMATIC REVIEW AND META-ANALYSIS

Bleeding, Thrombosis and Vascular Biology
Introduction. Cancer-associated thrombosis (CAT) is a frequent and clinically relevant complication in patients with malignancy. While inherited thrombophilia is a well-established risk factor for venous thromboembolism in the general population, its ...
Elena Campello
doaj  

Current Knowledge on Factor V Leiden Mutation as a Risk Factor for Recurrent Venous Thromboembolism: A Systematic Review and Meta-Analysis. [PDF]

Front Cardiovasc Med, 2022
Eppenberger D, Nilius H, Anagnostelis B, Huber CA, Nagler M.   +4 more
europepmc   +1 more source

Analysis of the Matrix Metalloproteinases Family Profile in Gastric Cancer Suggests Key Matrix Metalloproteinases for Tumor Development and Their Clinical Impact

Molecular Carcinogenesis, Volume 65, Issue 5, Page 577-588, May 2026.
ABSTRACT Gastric cancer (GC) is the fifth most common type worldwide, representing a public health problem. Among the genes related to this tumorigenesis, the family of matrix metalloproteinases (MMPs), essential regulators of the extracellular matrix (ECM), stand out for their involvement in the development and progression of GC.
Aline Costa Bastos, André Salim Khayat, Emanuele Raimunda Louzada Moraes, Ágatha Tereza Miranda Tavares, Ronald Matheus da Silva Mourão, Fabiano Cordeiro Moreira, Samir Mansour Moraes Casseb, Samia Demachki, Geraldo Ishak, Williams Fernandes Barra, Rommel Mario Rodríguez Burbano, Paulo Pimentel de Assumpção   +11 more
wiley   +1 more source

Arterial Thrombosis Associated with Factor V Leiden Mutation in a Child with Nephrotic Syndrome. [PDF]

Indian J Nephrol, 2021
Nagalla VK, Raju SB, Ramesh Bura NR.
europepmc   +1 more source

Carrier screening in the reproductive setting—Are there medical implications for the heterozygote?—A guide for clinicians

Pregnancy, Volume 2, Issue 3, May 2026.
Abstract Carrier screening for genetic conditions performed preconception or during pregnancy allows identification of fetal risk for inherited autosomal recessive and X‐linked conditions. The goal is to identify at‐risk patients/couples and offer them reproductive options such as preimplantation genetic diagnosis, prenatal testing, or targeted newborn
Emily B. Rosenfeld, Nicole Kasatkin, Bi Liu Yu, Milen Velinov, Justin S. Brandt, Elena Ashkinadze   +5 more
wiley   +1 more source

Cerebral Venous Thrombosis Presenting as a Subacute Headache in a Young Man With Undiagnosed Factor V Leiden Mutation. [PDF]

Cureus, 2021
Patel TH, Bachu R, Naylor JE, Ezell G.
europepmc   +1 more source

Hybrid Horizons: Screening Hybridisation Through Nuclear Environmental DNA

Molecular Ecology Resources, Volume 26, Issue 4, May 2026.
ABSTRACT Effective monitoring of hybrid zones is essential for understanding evolutionary dynamics and mitigating species loss caused by human‐mediated hybridisation. Conventional methods rely on sampling numerous individuals, which is costly, time‐consuming and often impractical for rare or elusive species.
Daniel Zumel, Emilie Didaskalou, Tijana Vučić, Milena Cvijanović, Ana Ivanović, Maja Ajduković, Ben Wielstra, Anagnostis Theodoropoulos, Kathryn Stewart   +8 more
wiley   +1 more source