نتایج جستجو برای: myeloproliferative disorder

تعداد نتایج: 601334  

Journal: :Blood 2004
Geraldine Guasch Bénédicte Delaval Christine Arnoulet Min-Jue Xie Luc Xerri Danielle Sainty Daniel Birnbaum Marie-Joséphe Pébusque

Constitutive activation of aberrant fibroblast growth factor receptor 1 (FGFR1) kinase as a consequence of gene fusion such as FOP-FGFR1 associated with t(6; 8)(q27;p11-12) translocation, is the hallmark of an atypical aggressive stem cell myeloproliferative disorder (MPD) in humans. In this study, we show that expression of FOP-FGFR1 in primary bone marrow cells induced by retroviral transduct...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2008
Nan-Nan Zhang Shu-Hong Shen Lin-Jia Jiang Wu Zhang Hong-Xin Zhang Yue-Ping Sun Xian-Yang Li Qiu-Hua Huang Bao-Xue Ge Sai-Juan Chen Zhu-Gang Wang Zhu Chen Jiang Zhu

RIG-I has been implicated in innate immunity by sensing intracellular viral RNAs and inducing type I IFN production. However, we have found a significant RIG-I induction in a biological setting without active viral infection-namely, during RA-induced terminal granulocytic differentiation of acute myeloid leukemias. Here, we present evidence that a significant Rig-I induction also occurs during ...

2009
Mehmet Sönmez Ümit Çobanoğlu Sevdagül Mungan Bircan Sönmez Rasin Özyavuz

Myeloid sarcoma of the urinary bladder is a rare disorder. We report a 71-year-old man with hematuria who had a diffuse myeloid sarcoma of the bladder. He was also under follow-up for unclassified myeloproliferative/myelodysplastic disorder, diagnosed two months before. Abdominal ultrasonography and computed tomography findings were normal. Diagnostic cystoscopy revealed patchy areas of mucosal...

Journal: :Romanian journal of internal medicine = Revue roumaine de medecine interne 2008
Ana Maria Vlădăreanu Cristina Ciufu H Bumbea Minodora Onisâi S Aramă

The thrombotic and hemorrhagic diathesis represents a frequent complication in myeloproliferative disorders (CMPD). They are correlated with the number of platelets, but also with their qualitative disorders, such as membrane glycoprotein changes. The latter are revealed by many platelet essays including flow-cytometry and include modified activation, secretion and aggregation patterns. The thr...

Journal: :Blood 1978
D L Longo J Whang-Peng E Jaffe T J Triche R C Young

A 45-yr-old female presented with a rapidly enlarging bony tumor that was eventually identified as a Philadelphia chromosome (Ph1)-positive myeloproliferative disorder with extramedullary blastic transformation. This transformation occurred in the absence of demonstrable chronic or acute leukemic phase. She had no history of a chronic or prodromal illness in spite of a bone marrow biopsy showin...

Journal: :Blood 1993
H M Kantarjian A Deisseroth R Kurzrock Z Estrov M Talpaz

HRONIC MYELOGENOUS leukemia (CML) is a C clonal myeloproliferative disorder of the primitive hematopoietic stem cell.’-3 It involves the myeloid, erythroid, megakaryocytic, B-, and sometimes T-lymphoid elements, but not the marrow fibrobla~ts.~,~ CML is characterized by (1) the heterogeneity of the disease among patients, (2) a biphasic or triphasic course, and (3) the presence of a chromosomal...

Journal: :European respiratory review : an official journal of the European Respiratory Society 2010
Y Adir M Humbert

Pulmonary hypertension (PH) is a severe haemodynamic disorder in which the pulmonary artery pressure is persistently elevated, leading to right-sided heart failure and death. Recently, chronic myeloproliferative diseases associated with pulmonary hypertension were included in the group 5 category, corresponding to PH for which the aetiology is unclear and/or multifactorial. In this review we wi...

Journal: :Blood 1984
U Budde G Schaefer N Mueller H Egli J Dent Z Ruggeri T Zimmerman

An acquired hemorrhagic disorder developed in two patients in association with postsplenectomy thrombocytosis and leukocytosis during the course of the myeloproliferative syndrome. The presence of acquired von Willebrand's disease in these individuals was demonstrated by a decrease or absence of the larger von Willebrand factor (vWF) multimers, alteration of the repeating vWF multimeric "triple...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید