Cargando…

Thrombophilic Genetic Factors PAI-1, MTHFRC677T, V Leiden 506Q, and Prothrombin 20210A in Noncirrhotic Portal Vein Thrombosis and Budd-Chiari Syndrome in a Caucasian Population

Thrombophilic genetic factors PAI-1, MTHFRC677T, V Leiden 506Q, and Prothrombin 20210A were studied as risk factors in 235 Caucasian subjects: 85 patients with abdominal thrombosis (54 with portal vein thrombosis (PVT) and 31 with Budd-Chiari syndrome (BCS) without liver cirrhosis or hepatocellular...

Descripción completa

Detalles Bibliográficos
Autores principales:	D'Amico, Mario, Sammarco, Pietro, Pasta, Linda
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2013
Materias:	Clinical Study
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880691/ https://www.ncbi.nlm.nih.gov/pubmed/24455271 http://dx.doi.org/10.1155/2013/717480

Ejemplares similares

Risk of Budd-Chiari Syndrome Associated with Factor V Leiden and G20210A Prothrombin Mutation: A Meta-Analysis
por: Zhang, Peijin, et al.
Publicado: (2014)

Thrombophilic Risk of Factor V Leiden, Prothrombin G20210A, MTHFR, and Calreticulin Mutations in Essential Thrombocythemia Egyptian Patients
por: El-Ghonemy, Mohamed S., et al.
Publicado: (2020)

The Role of Factor V Leiden, Prothrombin G20210A, and MTHFR C677T Mutations in Neonatal Cerebral Sinovenous Thrombosis
por: Garrido-Barbero, Maria, et al.
Publicado: (2019)

Large‐scale screening for factor V Leiden (G1691A), prothrombin (G20210A), and MTHFR (C677T) mutations in Greek population
por: Raptopoulou, Alkistis, et al.
Publicado: (2022)

Factor V Leiden and Prothrombin 20210A Mutations among Turkish Pediatric Leukemia Patients
por: Akın, Dilara Fatma, et al.
Publicado: (2012)

MTHFR C677T, Prothrombin G20210A, and Factor V Leiden (G1691A) Polymorphism and Beta-Thalassemia Risk: A Meta-Analysis
por: Nigam, Nitu, et al.
Publicado: (2020)

Direct‐to‐consumer genetic testing for factor V Leiden and prothrombin 20210G>A: the consumer experience
por: Elson, Sarah L., et al.
Publicado: (2020)

Factor V Leiden G1691A and Prothrombin Gene G20210A Mutations on Pregnancy Outcome
por: Padda, Jaskamal, et al.
Publicado: (2021)

Acute Myocardial Infarction in Patients with Hereditary Thrombophilia—A Focus on Factor V Leiden and Prothrombin G20210A
por: Badescu, Minerva Codruta, et al.
Publicado: (2023)

The Combined Heterozygosity of Factor V Leiden and G20210A Prothrombin Gene Mutation in a Patient With Venous Thromboembolism
por: Machado, Marcia, et al.
Publicado: (2023)

Association of Factor V Leiden and Prothrombin G20210A Polymorphisms in Women with Recurrent Pregnancy Loss in Isfahan Province, Iran
por: Kardi, Mohammad Taghi, et al.
Publicado: (2018)

Factor V Leiden G1691A and prothrombin G20210A mutations among Palestinian patients with sickle cell disease
por: Samarah, Fekri, et al.
Publicado: (2018)

Factor-V Leiden G1691A and prothrombin G20210A polymorphisms in Sudanese women with preeclampsia, a case -control study
por: Ahmed, Nadir A., et al.
Publicado: (2019)

Effect of MTHFRC677 T Gene Polymorphism on Early Morning Blood Pressure in Elderly Female Patients with H-Type Hypertension
por: Zhang, Chi, et al.
Publicado: (2022)

Exercise Caution with ChAdOx1 COVID-19 Vaccination in Chronic Budd-Chiari Syndrome with a Thrombophilic Genetic Predisposition
por: Kulkarni, Anand V., et al.
Publicado: (2022)

Epidemiology of Prothrombin G20210A Mutation in the Mediterranean Region
por: Jadaon, Mehrez M.
Publicado: (2011)

Examination of in Factor V Leiden and Prothrombin II Thrombophilic Mutations in Czech Young Women Using ddPCR—Prevalence and Cost–Benefit Analysis
por: Riedlova, Petra, et al.
Publicado: (2021)

PlA2 Polymorphism of Platelet Glycoprotein IIb/IIIa and C677T Polymorphism of Methylenetetrahydrofolate Reductase (MTHFR), but Not Factor V Leiden and Prothrombin G20210A Polymorphisms, Are Associated with More Severe Forms of Legg–Calvé–Perthes Disease
por: García-Alfaro, María Dolores, et al.
Publicado: (2021)

The impact of prothrombin (G20210A) gene mutation on stroke in youths
por: Saadatnia, Mohammad, et al.
Publicado: (2012)

Review of Budd-Chiari Syndrome
por: Zu, Maoheng, et al.
Publicado: (2020)

Histopathology of Budd–Chiari Syndrome
por: Quaglia, Alberto
Publicado: (2023)

Different outcome of six homozygotes for prothrombin A20210A gene variant
por: Di Micco, Pierpaolo, et al.
Publicado: (2008)

Prevalence of the prothrombin G20210A mutation among ischemic stroke patients
por: Ahmed, Salar A., et al.
Publicado: (2020)

Budd-Chiari Syndrome: Shunt or Transplant?
por: Orloff, Marshall J.
Publicado: (1998)

Budd-Chiari Syndrome: Shunt or Transplant?
por: McMaster, Paul
Publicado: (1994)

Behcet’s disease in budd-chiari syndrome
por: Desbois, Anne Claire, et al.
Publicado: (2014)

Budd–Chiari Syndrome: an unnoticed diagnosis
por: Falcão, Camila Kruschewsky, et al.
Publicado: (2015)

Diagnosis and therapy of Budd Chiari syndrome
por: Lupasco, Iulianna, et al.
Publicado: (2021)

Budd-Chiari-like pathology in dolphins
por: Fernandez, Antonio, et al.
Publicado: (2022)

Interventional Treatment of Budd–Chiari Syndrome
por: Rössle, Martin
Publicado: (2023)

Mutation in the Prothrombin Gene G20210A as a Cause of Cerebral Venous Thrombosis
por: Arroyave, Jorge A., et al.
Publicado: (2012)

Painless Livedoid Vasculopathy in a Patient with G20210A Prothrombin Gene Mutation
por: Mirrakhimov, Aibek E., et al.
Publicado: (2012)

Pregnancy complications in G20210A mutation carriers associated with high prothrombin activity
por: Nikolaeva, M. G., et al.
Publicado: (2021)

Prevalence of Factor V Leiden G1691A and Prothrombin G20210A Gene Mutation Among Pregnant Women: Experience from a Multi-Center Study in Nigeria
por: John-Olabode, Sarah O, et al.
Publicado: (2021)

Small hepatic veins Budd–Chiari syndrome
por: Riggio, Oliviero, et al.
Publicado: (2013)

Budd-Chiari syndrome mimicking autoimmune hepatitis
por: Bova, Carlo, et al.
Publicado: (2023)

Factor VLeiden and Prothrombin G20210A Gene Polymorphisms in Patients with Coronary Artery Disease
por: Ercan, Bahadır, et al.
Publicado: (2008)

Genetic correlation between Prothrombin G20210A polymorphism and retinal vein occlusion risk
por: Zou, Yuanyuan, et al.
Publicado: (2019)

Prothrombin Gene G20210A Variant in Angiographically Documented Patients with Coronary Artery Stenosis
por: Pourgholi, Leyla, et al.
Publicado: (2019)

Association of G20210A Prothrombin Gene Mutation and Cerebral Ischemic Stroke in Young Patients
por: Poudel, Sujan, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_77eeg20dru19bb3ea2715kaso4