نتایج جستجو برای: hemoglobinuria
تعداد نتایج: 2365 فیلتر نتایج به سال:
Citation: Rondelli T, Risitano AM, Peffault de Latour R, Sica M, Peruzzi B, Ricci P, Barcellini W, Iori AP, Boschetti C, Valle V, Frémeaux-Bacchi V, De Angioletti M, Socié G, Luzzatto L, and Notaro R. Polymorphism of the complement receptor 1 gene correlates with hematological response to eculizumab in patients with paroxysmal nocturnal hemoglobinuria. Haematologica. 2013; 98:xxx doi:10.3324/ha...
Deficient Biosynthesis of N-AcetylglucosaminylPhosphatidylinositol, the First hte~iiiediate of Glycosyl Phosphatidylinositol Anchor Biosynthesis, in Cell Lines Established from Patients with Paroxysmal Nocturnal Hemoglobinuria By Minoru Takahashi,* Junji Takeda,* Shinichi Hirose,$ Robert Hyman, ll Norimitsu Inoue,* Toshio Miyata,* Etsuko Ueda,~S Teruo Kitani,~ M. Edward Medof,$ and Taroh Kinosh...
Cytogenetic studies showed both 45XO and 46XY clones in the bone marrow of a 76-yr-old male with a 17-yr history of paroxysmal nocturnal hemoglobinuria (PNH). 55Fe incorporation studies demonstrated that both clones involved the hematopoietic stem cells. The loss of the Y chromosome may reflect an aging phenomenon, rather than be related to the PNH.
Deficient Biosynthesis of N-AcetylglucosaminylPhosphatidylinositol, the First hte~iiiediate of Glycosyl Phosphatidylinositol Anchor Biosynthesis, in Cell Lines Established from Patients with Paroxysmal Nocturnal Hemoglobinuria By Minoru Takahashi,* Junji Takeda,* Shinichi Hirose,$ Robert Hyman, ll Norimitsu Inoue,* Toshio Miyata,* Etsuko Ueda,~S Teruo Kitani,~ M. Edward Medof,$ and Taroh Kinosh...
Splenectomy can treat conditions characterized by hemolysis or thrombocytopenia caused autoantibodies splenic reticuloendothelial function, as well disorders massive splenomegaly and hypersplenism with cytopenias, such hereditary spherocytosis, transfusion-dependent thalassemia, immune thrombocytopenia, autoimmune hemolytic anemia, marginal zone lymph is no longer used for Hodgkin disease stagi...
precursors and progenitors to increase production of fetal hemoglobin. J Clin Invest 75: 547-557, 1985 51. Rosa RM, Bierer BE, Thomas R, Jeffrey BS, Stoff JS, Kruskall M, Robinson S, Bunn HF, Epstein FH: A study of induced hyponatremia in the prevention and treatment of sickle-cell crisis. New Eng J Med303: 1138-1143, 1980 52. Leary M, Abramson N: Induced hyponatremia for sickle-cell crisis. Ne...
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