نتایج جستجو برای: hemoglobinuria

تعداد نتایج: 2365  

2013
Tommaso Rondelli Antonio M. Risitano Régis Peffault de Latour Michela Sica Benedetta Peruzzi Patrizia Ricci Wilma Barcellini Anna Paola Iori Carla Boschetti Veronica Valle Veronique Frémeaux-Bacchi Maria De Angioletti Gérard Socié Lucio Luzzatto Rosario Notaro Gerard Socie

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...

2003
Minoru Takahashi Junji Takeda Shinichi Hirose Robert Hyman Norimitsu Inoue Toshio Miyata Etsuko Ueda Teruo Kitani M. Edward Medof Taroh Kinoshita

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...

Journal: :Blood 1976
J Whang-Peng T Knutsen E C Lee B Leventhal

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.

2003
Minoru Takahashi Junji Takeda Shinichi Hirose Robert Hyman Norimitsu Inoue Toshio Miyata Etsuko Ueda Teruo Kitani M. Edward Medof Taroh Kinoshita

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...

Journal: :International journal of medical science and clinical research studies 2022

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...

Journal: :Genitourinary medicine 1993
N D Kumar S Sethi R K Pandhi

2005

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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