نتایج جستجو برای: family history of hemophilia

تعداد نتایج: 21212455  

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...

Journal: :journal of research in medical sciences 0
roya kelishadi ali akbar haghdoost mahmood moosazadeh mojtaba keikha maryam aliramezany

background: different viewpoints exist about lipid screening in all children or only in children with positive family history (fh)of premature cardiovascular diseases (cvds) or hypercholesterolemia. this systematic review and meta-analysis aim to assess the effectiveness of lipid screening in children and adolescents according to the existence of positive fh of cvd risk factors.materials and me...

2014
SHU-KAI QIAO HAN-YUN REN JIN-HAI REN XIAO-NAN GUO

Hemophilia A (HA) in females is rare. Female HA cases are often misdiagnosed as acquired HA (AHA) or as von Willebrand disease type 2N (vWD-2N). Here, we report the case of a 37-year-old female HA patient with a moderate factor VIII (FVIII) deficiency. The patient had no personal or family history of bleeding disorders, but presented with heavy uterine bleeding following surgery to remove an in...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه بوعلی سینا - دانشکده علوم کشاورزی 1391

طی بررسی هائی که جهت جمع آوری و شناسائی فون کنه های باغات میوه در شهرستان نجف آباد در سال های 1391-1390 انجام شد مجموعا، 17 گونه متعلق به 14 جنس و 8 خانواده جمع آوری و شناسائی شد که 1 گونه برای اولین بار از ایران معرفی گردید که با (*) مشخص شد، و تعداد 2 گونه برای اولین بار در دنیا شناسائی و توصیف گردید که با علامت (**) مشخص شده-اند. لیست گونه های گزارش شده بر اساس طبقه بندی راسته و خانواده به ...

Journal: :iranian journal of public health 0
d.d. farhud

a group of iranian patients suffering from factor viii deficiency (hemophilia a) and treated with contaminated coagulation factor (imported), became seropositive as determined by elisa method. sixty of these individuals, which were available, were studied for abo distribution. the b blood group in anti hiv pos. individuals (13.33%) shows a significant decrease in comparison with the total (1504...

پایان نامه :دانشگاه تربیت معلم - تبریز - دانشکده ادبیات 1389

الملخّص الحنین إلی الوطن، کان من الموضوعات الأساسیّه منذ أزمنه قدیمه فی الأدب العربی. فی العصور الماضیه کان یبین الشعراء تذکاراتهم الجیّده، و الحنین إلی الحبیبه ، و القبیله، و الأطلال و الدمن بتحسّر فی أشعارهم. توجد نماذج منها فی أشعار إمرء القیس و عنتره و... . راج هذا النوع من الحنین فی أشعار الشعراء فی العصر الأموی و العباسی کثیراً بسبب الفتوحات و الهجره. نحن شاهدنا آثاراَ کثیره کـ«الحنین إلی الأو...

2014
Dolores Malaspina Roberta Dracxler Julie Walsh-Messinger Susan Harlap Raymond R Goetz David Keefe Mary C Perrin

Leukocyte telomere length (LTL) is longer in association with advanced paternal age, but this association has not been examined along with family history (FH) in schizophrenia. LTL was measured by PCR and compared across cases and controls as part of a study to examine the characteristics of paternal age related schizophrenia. The 53 schizophrenia cases had similar mean LTL as 20 controls, alth...

2017
Christine L Kempton Michael Wang Michael Recht Anne Neff Amy D Shapiro Amit Soni Roshni Kulkarni Tyler W Buckner Katharine Batt Neeraj N Iyer David L Cooper

BACKGROUND Hemophilia is marked by frequent joint bleeding, resulting in pain and functional impairment. OBJECTIVE This study aimed to assess the reliability of five patient-reported outcome (PRO) instruments in people with hemophilia (PWH) in a non-bleeding state. METHODS Adult male PWH of any severity and inhibitor status, with a history of joint pain or bleeding, completed a pain history...

2012
Hussain I Saba Duc Quang Tran

In the past, patients with severe hemophilia have suffered a substantially reduced quality of life with frequent bleeding episodes, disabling arthropathy, and shorter life expectancy. In addition, methods of treatment and management have been costly and time-consuming, and have placed a considerable burden on patients' physical and psychological well-being. With the advent of the on-demand ther...

2016
Yuting Guan Yanlin Ma Qi Li Zhenliang Sun Lie Ma Lijuan Wu Liren Wang Li Zeng Yanjiao Shao Yuting Chen Ning Ma Wenqing Lu Kewen Hu Honghui Han Yanhong Yu Yuanhua Huang Mingyao Liu Dali Li

The X-linked genetic bleeding disorder caused by deficiency of coagulator factor IX, hemophilia B, is a disease ideally suited for gene therapy with genome editing technology. Here, we identify a family with hemophilia B carrying a novel mutation, Y371D, in the human F9 gene. The CRISPR/Cas9 system was used to generate distinct genetically modified mouse models and confirmed that the novel Y371...

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