نتایج جستجو برای: amegakaryocytic thrombocytopenia

تعداد نتایج: 24775  

Journal: :American Journal of Hematology 2006

2005
Alan M. Gewirtz Michelle Keefer Sacchetti Rebecca Bien William E. Barry

Acquired amegakaryocytic thrombocytopenic purpura (AATP) is a disorder of hematopoiesis characterized by severe thrombocytopenia due to a selective reduction or total absence of megakaryocytes in an otherwise normalappearing bone marrow. Although the development of autoantibodies directed against cells in the megakaryocyte progenitor cell pool has been implicated in the pathogenesis of this dis...

2014
Tao Sun Wenbin Gui Zhigang Yu Zhimin Gao

The automatic positioning control of mooring system for deepwater semi-submersible platform has become a key issue in the research and development field of deep-sea resources. The DualStage Actuator (DSA) proposed in this paper can replace the single actuator to achieve the high speed and high precision positioning by cooperative control. The relative model and control algorithm of motion traje...

N Mohammad Pour, Z Eslami, A Hashemi , A PirDehghan, M Noorishadkam , M.H Lookzadeh, R Ghilian ,

Abstract Background Thrombocytopenia is the most common hematological abnormality which is encountered in the neonatal intensive care unit (NICU). The incidence in neonates varies greatly, depending upon the population studies. According to the frequency of thrombocytopenia and its complications and because of lack of such research in Iran, this study was performed on neonates admitted to Sha...

Journal: :Thrombosis and haemostasis 2017
Viola Lorenz Haley Ramsey Zhi-Jian Liu Joseph Italiano Karin Hoffmeister Sihem Bihorel Donald Mager Zhongbo Hu William B Slayton Benjamin T Kile Martha Sola-Visner Francisca Ferrer-Marin

Congenital amegakaryocytic thrombocytopaenia (CAMT) is a disorder caused by c-MPL mutations that impair thrombopoietin (TPO) signalling, resulting in a near absence of megakaryocytes (MKs). While this phenotype is consistent in adults, neonates with CAMT can present with severe thrombocytopaenia despite normal MK numbers. To investigate this, we characterized MKs and platelets in newborn c-MPL ...

Journal: :archives of pediatric infectious diseases 0
ali hosseininasab infectious and tropical diseases research centre, kerman university of medical sciences, kerman, ir iran; infectious and tropical diseases research centre, kerman university of medical sciences, kerman, ir iran. tel: +98-3423222250, fax: +98-3413222763سازمان اصلی تایید شده: دانشگاه علوم پزشکی کرمان (kerman university of medical sciences) zahra farahmandinia kerman university of medical sciences, kerman, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی کرمان (kerman university of medical sciences) mahdieh eslamian kerman university of medical sciences, kerman, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی کرمان (kerman university of medical sciences) pegah arfa kerman university of medical sciences, kerman, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی کرمان (kerman university of medical sciences) motahareh abbaszadeh kerman university of medical sciences, kerman, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی کرمان (kerman university of medical sciences)

conclusions sever thrombocytopenia and bleeding may be the presentation of brucellosis. case presentation we report on an eight-year-old boy who presented epistaxis and gum bleeding. the physical examination revealed petechiae, purpura, ecchymosis, and cervical while inguinal lymphadenopathy and splenomegaly were noted. brucella agglutinin titer was positive. after five days of specific therapy...

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