نتایج جستجو برای: family history of hemophilia

تعداد نتایج: 21212455  

پایان نامه :وزارت بهداشت، درمان و آموزش پزشکی - دانشگاه علوم پزشکی و خدمات بهداشتی درمانی استان کرمانشاه 1371

background: organic nitrates relax all kinds of smooth muscle , not only vascular smooth muscle , a fact that has allowed the use of these drugs to treat many different aliments. objective.-the purpuse of this study was to examine prosepectively benefical effects , if any, of sublingual nitroglycerin on the pain of renal colic. design.- prospective , randomised , double blind, placebo- contoled...

Journal: :Blood 2006
Jenny Goudemand Chantal Rothschild Virginie Demiguel Christine Vinciguerrat Thierry Lambert Hervé Chambost Annie Borel-Derlon Ségolène Claeyssens Yves Laurian Thierry Calvez

Inhibitor development is the major treatment complication in children with severe hemophilia A. It is not clear whether the risk of inhibitors is higher with recombinant factor VIII or with plasma-derived factor VIII. We used multivariate analysis to compare 2 cohorts of previously untreated patients (PUPs) with severe hemophilia A: 62 patients treated with the same brand of high-purity plasma-...

Journal: :iranian journal of blood and cancer 0
morteza karimipour sirous zeinali edward graham tuddenham nafiseh nafissi manijeh lak peter green

background: heterogeneous mutations in the human coagulation factor ix gene lead to an x-linked recessive bleeding disorder known as hemophilia b. the disease is distributed worldwide with no ethnic or geographical priority. materials and methods: the aim of this study was to characterize the factor ix gene mutations in 28 unrelated iranian hemophilia b patients. polymerase chain reaction (pcr)...

Journal: :Blood 2006
Iris Plug Eveline P Mauser-Bunschoten Annette H J T Bröcker-Vriends Hans Kristian Ploos van Amstel Johanna G van der Bom Joanna E M van Diemen-Homan José Willemse Frits R Rosendaal

A wide range of factor VIII and IX levels is observed in heterozygous carriers of hemophilia as well as in noncarriers. In female carriers, extreme lyonization may lead to low clotting factor levels. We studied the effect of heterozygous hemophilia carriership on the occurrence of bleeding symptoms. A postal survey was performed among most of the women who were tested for carriership of hemophi...

Journal: :journal of family and reproductive health 0
rezaul karim department of population dynamic, national institute of preventive and social medicine (nipsom), mohakhali, dhaka, bangladesh. nusrat jahan mona bangladesh medical college and hospital, dhanmondi, dhaka, bangladesh.

objective: to identify the proportion and some selected characteristics of juvenile diabetics attending birdem hospital. materials and methods: this was a cross sectional study. the study was conducted in the birdem hospital. all diabetic young aged up to 18 years who visit birdem hospital were included in study population. the sample size was 240. results: it was observed that among the respon...

پایان نامه :0 1391

employees always concern about losing their job , or in other word , losing their income resources. for this purpose, every government requires strong system for covering these concerns. the unemployment insurance (ui) program’s can be used for achieving this goal. in this thesis, we price ui based on the insurance history of employee and the duration of being unemployed. we use the weibull dis...

2004
J. Michael Soucie Christy Cianfrini Robert L. Janco Roshni Kulkarni Julie Hambleton Bruce Evatt Angela Forsyth Sue Geraghty Keith Hoots Tom Abshire Randall Curtis Ann Forsberg Heather Huszti Margaret Wagner

Chronic joint disease from repeated bleeding into joints is a serious complication of hemophilia. To measure the extent of and to identify risk factors for deviations from normal in joint range of motion (ROM), we used crosssectional data collected from 4343 males with hemophilia aged 2 to 19 years who received care at 136 US hemophilia treatment centers (HTCs). Factors examined included age, r...

Journal: :Journal of pediatric psychology 2003
Janice D Bordeaux Katherine A Loveland David Lachar James Stehbens Terece S Bell Sharon Nichols Nancy Amodei Kristin Brelsford Adkins

OBJECTIVE To assess differences in caregiver report of youth and family psychosocial adjustment associated with HIV infection and greater immune compromise in youths with hemophilia. METHODS Caregivers of 162 boys with hemophilia 8 to 20 years old completed three youth and family questionnaires (Personality Inventory for Children, Revised [PIC-R]; Questionnaire on Resources and Stress [QRS]; ...

Edward Graham Tuddenham, Manijeh Lak, Morteza Karimipour, Nafiseh Nafissi, Peter Green, Sirous Zeinali,

Background: Heterogeneous mutations in the human coagulation factor IX gene lead to an X-linked recessive bleeding disorder known as hemophilia B. The disease is distributed worldwide with no ethnic or geographical priority. Materials and Methods: The aim of this study was to characterize the factor IX gene mutations in 28 unrelated Iranian hemophilia B patients. Polymerase chain reaction (PCR)...

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