نتایج جستجو برای: protein c s deficiency

تعداد نتایج: 2666311  

Journal: :Indian Journal of Dermatology, Venereology, and Leprology 2012

Journal: :Journal of Nepal Medical Association 2010

Journal: :Haematologica 2008
Begoña Hurtado Xavier Muñoz Maria Carme Mulero Gemma Navarro Pere Domènech Pablo García de Frutos Mercè Pérez-Riba Núria Sala

BACKGROUND The molecular mechanisms by which PROS1 mutations result in protein S deficiency are still unknown for many of the mutations, particularly for those that result in a premature termination codon. The aim of this study was to analyze the functional relevance on mRNA and protein expression of 12 natural PROS1 mutations associated with protein S deficiency. DESIGN AND METHODS Five muta...

Journal: :Actas Dermo-Sifiliográficas (English Edition) 2016

Journal: :Haematologica 2014
Hee-Jin Kim Ja-Young Seo Ki-O Lee Sung-Hwan Bang Seung-Tae Lee Chang-Seok Ki Jong-Won Kim Chul Won Jung Duk-Kyung Kim Sun-Hee Kim

Hereditary natural anticoagulant deficiencies are the major cause of genetic thrombophilia in Asia. Given the growing acknowledgment of the risk of venous thromboembolism in Asian populations, we investigated the frequency and mutation spectrums of natural anticoagulant deficiency in Korea. The group of patients consisted of consecutive patients with venous thromboembolism screened for thrombop...

Journal: :Stroke 1993
H R Martinez R A Rangel-Guerra L J Marfil

BACKGROUND AND PURPOSE Deficiencies in coagulant inhibitors protein C, protein S, and antithrombin III increase the risk of venous thrombosis. We describe 10 young adults with cerebral arterial thrombosis due to deficiencies in these factors. METHODS Sixty patients younger than 45 years were hospitalized because of acute ischemic stroke diagnosed through computed tomography or magnetic resona...

2000
Harry L. A. Janssen Johan R. Meinardi Frank P. Vleggaar Stan H. M. van Uum Elizabeth B. Haagsma Felix J. M. van der Meer Jan van Hattum Robert A. F. M. Chamuleau Rob P. Adang Jan P. Vandenbroucke Bart van Hoek Frits R. Rosendaal

In a collaborative multicenter case-control study, we investigated the effect of factor V Leiden mutation, prothrombin gene mutation, and inherited deficiencies of protein C, protein S, and antithrombin on the risk of Budd-Chiari syndrome (BCS) and portal vein thrombosis (PVT). We compared 43 BCS patients and 92 PVT patients with 474 population-based controls. The relative risk of BCS was 11.3 ...

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