نتایج جستجو برای: hemophilic patients

تعداد نتایج: 2085548  

Journal: :مجله دانشگاه علوم پزشکی کرمانشاه 0
mehri sirous . assistant professor of radiology, isfahan university of medical sciences mohammad javdan assistant professor of orthopedics, isfahan university of medical sciences hamid esfahani orthopedis gholamreza mohseni anesthetist

introduction: hemophilia is a hereditary disease with intraarticular hemorrhage as the most common manifestation of it. having taken into consideration the progressive articular degeneration, individual dysfunction, need for medical and surgical treatment, great cost to the patients, and also legal problems brought about by hemophilia patients’ dysfunction, this study examines the relationship ...

2015
Jiliang Zhai Xisheng Weng Baozhong Zhang Hui-ming Peng Yan-yan Bian Lei Zhou

Hemophilic pseudotumor gradually erodes bone and induces fracture or deformity, causing joint dysfunction or destructive osteoarthropathy. Reports about surgery for hemophilic pseudotumor complicated by destructive osteoarthropathy are scarce. The object of this study was to evaluate the results and complications of surgical management for patients of pseudotumor complicated by destructive oste...

Journal: :The Journal of clinical investigation 1969
S S Shapiro J Martinez

The metabolism of human prothrombin labeled with radioactive iodine was studied in seven normal subjects and four hemophilic patients. Results in the normal subjects were: plasma volume, 37.6+/-3.8 ml/kg; plasma prothrombin concentration, 303+/-40 U/ml (0.153+/-0.02 mg/ml); prothrombin half-life, 2.81+/-0.51 days; total plasma prothrombin pool, 5.72+/-0.62 mg/kg, representing 64.1+/-9.1% of tot...

2017
Annette von Drygalski Katherine C Rappazzo Richard F W Barnes Eric Y Chang

Hemophilic arthropathy is a progressive, disabling condition with poorly understood pathobiology. Since there is an emerging interest to study the role of intra-articular fat pad size and biology in arthritic conditions, we explored fat pad volume changes in hemophilic arthropathy and to what extent they differed from osteoarthritis. We matched a cohort of 13 adult patients with hemophilic arth...

Journal: :The Journal of clinical investigation 1973
B Bennett W B Forman O D Ratnoff

Normal human antihemophilic factor (AHF, factor VIII) and the protein antigenically related to it in hemophilic plasma both appeared in the void volume of columns of agarose (Sepharose 4B) during purification of these agents. On ultracentrifugation upon sucrose gradients, both agents had sedimentation characteristics similar to those of an S30 marker. After reduction, the polypeptide chains of ...

Journal: :Journal of thrombosis and haemostasis : JTH 2010
L A Valentino

Arthropathy is a frequent and serious complication of repeated joint bleeding in patients with hemophilia, resulting in pain, deformity, and disability. Although the pathogenesis of hemophilic arthropathy has not been fully elucidated, it appears to have similarities with the degenerative joint damage that occurs in osteoarthritis and the inflammatory processes associated with rheumatoid arthri...

Journal: :The Journal of Experimental Medicine 1957
John B. Graham Emily M. Barrow

It has been possible to duplicate in the hemophilic dog four of the major experiments which have suggested in humans an "anticephalin" hypothesis for the pathogenesis of hemophilia. The experiments in the dog have been considerably extended, as compared with the human experiments, by a variety of techniques. I. Asbestos was placed in contact with hemophilic dog plasma, and the clotting time bec...

2014
Zehra Özcan

UNLABELLED Radisosynovectomy (RS) is a local form of radionuclide therapy used in various forms of arthritis characterized by synovitis. In hemophilic arthropathy, RS provides removal of inflamed synovium and prevents further joint damage. This review focuses on the practical aspects of radionuclide synovectomy in hemophilic patients and describes the issues both related to the methodology and ...

Abdolah Gorgi F, Abed-Saeedi J, Alavi S, Eshghi P, Farahani H, Habib- Panah B, Khanali L, Taslimi S, Tehrani Tarighat S,

Background: Treating a chronic disease such as hemophilia is to improve the symptoms and quality of life (QOL) of the patients. This study aimed to study the quality of life among hemophilic children and compare the quality of life between patients receiving prophylactic or on demand treatments. Materials and Methods: In this descriptive-comparative study, we enrolled 60 patients from three ...

احمدی متمایل, فاطمه, هادیان, نگین,

Introduction: Platelets and clotting factors dysfunction lead to hereditary hemorrhagic disease. In according to the importance of these diseases, the aim of this study was the evaluation of oral health and bleeding management of the patients with congenital bleeding disorders in Tehran city in 2015. Methods: In this case-control study, 68 hemophilic patients  as case group were compare...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید