نتایج جستجو برای: refractory anemia

تعداد نتایج: 111788  

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2005
Edvardas Kaminskas Ann Farrell Sophia Abraham Amy Baird Li-Shan Hsieh Shwu-Luan Lee John K Leighton Hasmukh Patel Atiqur Rahman Rajeshwara Sridhara Yong-Cheng Wang Richard Pazdur

PURPOSE This article summarizes data submitted to the U.S. Food and Drug Administration for marketing approval of azacitidine as injectable suspension (Vidaza, Pharmion Corporation, Boulder, CO) for treatment of patients with myelodysplastic syndrome. EXPERIMENTAL DESIGN In one phase 3 controlled trial, 191 study subjects were randomized to treatment with azacitidine or to observation; an add...

Journal: :Canadian Journal of General Internal Medicine 2019

B Abdolkarimi, M Karimi , M Mokhtari, M Shahriari ,

Dear Editors: Adenocarcinoma of colon and rectum is the second most common cancer of the gastrointestinal (GI) tract in children. The development of carcinoma of colon in general appears to be associated with several predisposing factors such as familial polyposis, hereditary non-polyposis syndromes, ulcerative colitis, previous ureterosigmoidostomy or radiation therapy and dietary factors (hig...

Journal: :Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva 2011
Luis Rodrigo Sáez Dolores Fuentes Álvarez Isabel Pérez Martínez Noemí Alvarez Mieres Pilar Niño García Ruth de Francisco García Sabino Riestra Menéndez Santiago Vivas Alegre José Luis Olcoz Goñi

INTRODUCTION refractory iron-deficiency anemia has a multifactorial origin related to various gastrointestinal conditions, with celiac disease plus malabsorption and IBD together with isolated gluten intolerance being most common. OBJECTIVES to determine the prevalence of serum, genetic, and histological markers for gluten intolerance, and to analyze the response to gluten withdrawal from the...

A Fathi M Pedram

Thrombotic thrombocytopenic purpura (TTP) is mostly attributed to the presence of an autoantibody against ADAMTS-13, a metalloprotease that degrades ultralarge von Willebrand protein multimers. Accumulation of vWF multimers and systemic platelet aggregation lead to microangiopathic thrombosis, hemolytic anemia, and end-organ ischemia. Most patients respond to therapeutic plasma exchange (TPE), ...

Journal: :international journal of hematology-oncology and stem cell research 0
behzad nazel khosroshahi emam reza hospital, hamadan university of medical sciences, hamadan, iran ; blood transfusion research center, high institute for research and education in transfusion medicine, tehran, iran. mohammad jafari department of pathology, school of medicine, hamadan university of medical sciences, hamadan, iran. hossein vazini department of nursing, hamedan branch, islamic azad university, hamedan, iran. alireza ahmadi department of hematology and oncology, school of medicine, hamadan university of medical sciences, hamadan, iran. keivan shams department of immunology, school of medicine, shiraz university of medical sciences, shiraz, iran. mahdi kholoujini department of mycology, school of medicine, tarbiat modares university, tehran, iran.

autoimmune hemolytic anemia (aiha) is characterized by shortening of red blood cell (rbc) survival and the presence of autoantibodies directed against autologous rbcs. approximately 20% of autoimmune hemolytic anemia cases are associated with cold-reactive antibody. about half of patients with aiha have no underlying associated disease; these cases are termed primary or idiopathic. secondary ca...

2017
Sarita Pradhan

which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. A 58-year-old man presented with a 1-year history of transfusion-dependent anemia. On examination, he had pallor and his spleen was barely palpable. 9 /L. A blood differential count showed 40% neutrophils, 54% lymphocytes, 2% monocytes, and 3% eosinophils. A...

Journal: :Blood 1988
M Cazzola G Barosi P G Gobbi R Invernizzi A Riccardi E Ascari

We analyzed the natural history of idiopathic refractory sideroblastic anemia (IRSA) in 37 patients studied between 1969 and 1986. Although erythroid abnormalities were prominent in all, 12 patients also showed involvement of the granulocytic and/or megakaryocytic cell lines, and nonrandom chromosomal aberrations were observed in five of 23 patients studied for such defects. Measurements of ery...

Journal: :Blood 2003
Mario Cazzola Rosangela Invernizzi Gaetano Bergamaschi Sonia Levi Barbara Corsi Erica Travaglino Valeria Rolandi Giorgio Biasiotto Jim Drysdale Paolo Arosio

The sideroblastic anemias are characterized by ring sideroblasts, that is, red cell precursors with mitochondrial iron accumulation. We therefore studied the expression of mitochondrial ferritin (MtF) in these conditions. Erythroid cells from 13 patients with refractory anemia with ring sideroblasts (RARS) and 3 patients with X-linked sideroblastic anemia (XLSA) were analyzed for the distributi...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید