نتایج جستجو برای: haemophilia a

تعداد نتایج: 13432458  

Journal: :Haemophilia : the official journal of the World Federation of Hemophilia 2017
A Messori F Peyvandi D Mengato P M Mannucci

INTRODUCTION A few studies have been focused on low-titre inhibitors in patients with haemophilia A. Although several putative factors have been implicated in the development of these inhibitors, solid data are still lacking. AIM The aim of this study was to perform a proportion meta-analysis on the incidence of low-titre inhibitors in haemophilia A. METHODS We surveyed the PubMed database ...

Journal: :Journal of medical genetics 1995
P P Deutz-Terlouw M Losekoot R Olmer W C Pieneman S de Vries-v d Weerd E Briët E Bakker

Haemophilia A is an X linked bleeding disorder caused by a heterogeneous spectrum of mutations in the factor VIII gene. It has recently been reported that about 50% of severe haemophilia A cases are the result of an iversion in the factor VIII gene. The inversion results from homologous recombination between the A gene located in intron 22 of the FVIII gene and one of the two distal A genes, th...

Journal: :iranian journal of pediatric hematology and oncology 0
fatemeh sarkargar phd student of biochemistry, department of biology, faculty of science, payamnoor -university, tehran, ira mahta mazaheri associate professor of medical genetics (md-phd), department of genetics, faculty of medicine, shahid sadoughi universiسازمان های دیگر: mother and newborn health research center, shahid sadoughi university of medical science, yazd, iran hossein khodai expert laboratory of genetic, meybod genetic research center, meybod, iranسازمان اصلی تایید شده: دانشگاه پیام نور تهران (payame noor university) razieh sadat tabatabaei assistant professor of gynecology, department of gynecology and obstetrics, faculty of medicine, shahid sadoughi universسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید صدوقی یزد (shahid sadooghi university of medical sciences)

background: haemophilia a (ha) is an x-linked bleeding disorder caused by the absence or reduced activity of coagulation factor viii (fviii). coagulation factors are a group of related proteins that are essential for the formation of blood clots. the aim of this study was to genotype the coagulation factor viii gene mutations using inverse shifting pcr (is-pcr) in an iranian family with severe ...

Journal: :Thrombosis and haemostasis 2010
G Kenet C B Stenmo A Blemings W Wegert J Goudemand M Krause W Schramm C Kirchmaier U Martinowitz

Thromboelastography methods have been used to predict or monitor treatment of haemophilia patients with recombinant activated factor VII (rFVIIa). However, neither of the two thromboelastographic methods (ROTEM and TEG) has as yet been validated. This multi-centre, randomised trial compared both methods in terms of intra- and inter- patient variability following in vivo and ex vivo rFVIIa admin...

Journal: :Haemophilia : the official journal of the World Federation of Hemophilia 2010
J S Stonebraker P H B Bolton-Maggs J Michael Soucie I Walker M Brooker

The objectives of this paper were to study the reported haemophilia A prevalence (per 100 000 males) on a country-by-country basis and address the following: Does the reported prevalence of haemophilia A vary by national economies? We collected prevalence data for 106 countries from the World Federation of Hemophilia (WFH) annual global surveys and the literature. We found that the reported hae...

Journal: :JPMA. The Journal of the Pakistan Medical Association 1999
S Ahmed W Ali M Anwar Y Raashid T Jameel M Ayub T Zafar K A Karamat M Saleem

OBJECTIVE To determine the feasibility of a PCR based strategy for prenatal diagnosis of Haemophilia-A in Pakistani Families. DESIGN Prospective. SETTING Department of Haematology, Armed Forces Institute of Pathology, Rawalpindi. SUBJECTS Five families with at least one child affected with Haemophilia-A. Each family comprised of father, mother, affected child and fetus when present. MAI...

2014
Anita Kar Supriya Phadnis Sumedha Dharmarajan Juhi Nakade

India lacks a national policy on the prevention and control of genetic disorders. Although the haemoglobinopathies have received some attention, there are scarce data on the epidemiology of other genetic disorders in India. Haemophilia, an inherited single gene disorder with an incidence of 1 per 10,000 births, manifests as spontaneous or trauma-induced haemorrhagic episodes in patients, progre...

Journal: :Haemophilia : the official journal of the World Federation of Hemophilia 2008
B T Colvin J Astermark K Fischer A Gringeri R Lassila W Schramm A Thomas J Ingerslev

As the management of haemophilia is complex, it is essential that those with the disorder should have ready access to a range of services provided by a multidisciplinary team of specialists. This document sets out the principles of comprehensive haemophilia care in Europe. Within each country there should be a national organization which oversees the provision of specialist Comprehensive Care C...

Journal: :Haemophilia : the official journal of the World Federation of Hemophilia 2012
K Meijer E B Haagsma

The topic of this monograph is liver cancer associated with chronic HCV infection. We start with some background information on chronic HCV infection and its long-term sequelae, one of which is liver cancer. The rest of the article is concerned with liver cancer or hepatocellular carcinoma (HCC). Epidemiology, risk factors, treatment and outcomes are discussed. We focus on those aspects that ar...

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