نتایج جستجو برای: factor x deficiency

تعداد نتایج: 1537001  

2015
Andrea Bon Massimo Morfini Alessandro Dini Francesca Mori Simona Barni Sottilotta Gianluca Maurizio de Martino Elio Novembre

Hemophilia B is a rare X-linked recessive disorder with plasma factor IX (FIX) deficiency. 1-3% of patients treated with exogenous FIX-containing products develop inhibitors (i.e. polyclonal high affinity immunoglobulins) that neutralize the procoagulant activity of a specific coagulation factor. Although the incidence of inhibitors in hemophilia B patients is low, most are "high titer" and fre...

ژورنال: پژوهش در پزشکی 2006
دکتر امیر هوشنگ محمد علیزاده, , دکتر سید محسن موسوی, , دکتر فرحناز فلاحیان, , دکتر محمد رضا زالی, , دکتر محمد عباسی, , دکتر مهرداد حاجیلویی, , دکتر میترا رنجبر, , دکترمهدی رضازاده, ,

Abstract: Background: Hemophilia is a x-linked deficiency of factor VIII. The aim of the present study was to determine the frequencies of hepatitis B and C infections, markers of inflammation and liver function tests and also to assess the possible association between factor VIII inhibitor and hepatitis B and C infections in hemophiliacs of Hamedan Province of Iran. Materials and methods: Si...

2007
Xian Zhang Kun Zhou Ruishan Wang Jiankun Cui Stuart A. Lipton Francesca-Fang Liao Huaxi Xu Yun-wu Zhang

Xian Zhang, Kun Zhou, Ruishan Wang, Jiankun Cui, Stuart A. Lipton, Francesca-Fang Liao, Huaxi Xu, and Yun-wu Zhang From the Institute for Biomedical Research and School of Life Sciences, Xiamen University, Xiamen 361005, China, the Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences and Shanghai Jiao Tong University School of Medicine, Shanghai...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2007
Jecko Thachil D K Watson P J T Drew

The association between nephrotic syndrome (NS) and intravascular coagulation is well known, and thromboembolic disease is a relatively common complication of the condition. The association of NS with anticoagulant activity is less well recognized. Factor X deficiency, and sometimes Factor IX and Factor II deficiency, can rarely complicate AL amyloidosis, which may present with a NS. The mechan...

2018
Dosuke Iwadate Eiko Hasegawa Junichi Hoshino Noriko Hayami Keiichi Sumida Masayuki Yamanouchi Akinari Sekine Masahiro Kawada Rikako Hiramatsu Tatsuya Suwabe Naoki Sawa Mitsuhiro Yuasa Atsushi Wake Takeshi Fujii Kenichi Ohashi Kenmei Takaichi Yoshifumi Ubara

A 55-year-old man was admitted to our institute to undergo evaluation for proteinuria (5.4 g/day) with lambda-type Bence-Jones protein (BJP). Primary amyloid light chain (AL) amyloidosis and acquired factor X deficiency were diagnosed. High-dose melphalan combined with autologous stem cell transplantation was performed. After three years, the patient's proteinuria normalized, he was negative fo...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1998
H Böhrer R Waldherr E Martin R P Linke J Lin R Ziegler E Ritz P P Nawroth

The clinical signs of amyloidosis are dependent on the organ systems involved [I]. A common finding is renal involvement which manifests as nephrotic syndrome. Cardiac involvement may result in congestive cardiomyopathy with conduction defects and arrhythm ias. Amyloid deposits especially in the spleen may bind clotting factors , which can lead to coagulation abnormaliti es. Factor X deficiency...

Akbar Dorgalaleh, Farhad Zaker, Hasan Mollanoori, Hojat Shahraki, Majid Fathi, Maryam Daneshi, Omolbanin Sargazi-Aval, Shadi Tabibian, Shahram Teimourian,

Background: Congenital factor XIII (FXIII) deficiency is one of the rarest bleeding disorders with a prevalence of one per 2 million in the general population. The disorder is accompanied by a high rate of life-threatening bleeding. Due to normal results of routine coagulation tests, diagnosis of the disorder is challenging, but molecular methods can be used for precise diagnosis. Direct mutati...

Journal: :Archives of medical case reports and case study 2022

Hemophilia A is an X-linked recessive hereditary bleeding illness that manifests as increased after moderate trauma and spontaneous bleeding. It caused by a deficiency of the clotting factor VIII (FVIII). We report video assisted-thoracoscopy in 48-year-old patient with A. shouldn't be barrier to invasive surgery, but there are few conditions must met ensure straightforward intraoperative posto...

Journal: :Blood 1988
H J Weiss B Lages

The activation of platelets and the coagulation mechanism was studied by collecting blood from a standard bleeding time incision at 30-second intervals and measuring the plasma concentrations of fibrinopeptide A (FPA), platelet factor 4 (PF4), and thromboxane B2 (TxB2). FPA was observed in the first samples (30 to 60 seconds) obtained, increased progressively until cessation of bleeding, and wa...

2005
Robin A. Pixley Marc Schapira Robert W. Colman

Human antithrombin Ill (ATIII) is a plasma inhibitor of several serine proteases of the blood coagulation system. Previous investigations have reported that the presence of heparin has a multifold accelerating effect on the inhibition of factor Xlla and Xllf, the active species derived from factor XII. Recent studies from our laboratories have confirmed that ATIII inactivates factor XIla and fa...

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