نتایج جستجو برای: paroxysmal nocturnal hemoglobinuria

تعداد نتایج: 26047  

2012
Antonio M. Risitano

Paroxysmal nocturnal hemoglobinuria (PNH) is a complex hematological disorder resulting in a quite unique clinical syndrome. In fact, the typical clinical presentation encompasses three distinct hematological manifestations, i.e., hemolytic anemia, bone marrow failure and thrombophilia (Dunn et al 2000; Parker & Ware 2003; Notaro & Luzzatto 2003). Thus, the term PNH covers only one feature of t...

Journal: :Haematologica 2010
Lucio Luzzatto Antonio Maria Risitano Rosario Notaro

Journal: :Haematologica 2012
Régis Peffault de Latour Hubert Schrezenmeier Andrea Bacigalupo Didier Blaise Carmino A de Souza Stephane Vigouroux Roelf Willemze Louis Terriou Andre Tichelli Mohamad Mohty Sophie de Guibert Judith C Marsh Jakob Passweg Jean Yves Mary Gerard Socié

BACKGROUND In the era of eculizumab, identifying patients with paroxysmal nocturnal hemoglobinuria who may benefit from allogeneic stem cell transplantation is challenging. DESIGN AND METHODS We describe the characteristics and overall survival of 211 patients transplanted for paroxysmal nocturnal hemoglobinuria in 83 EBMT centers from 1978 to 2007. Next, we conducted a comparison with a coho...

Journal: :Haematologica 2010
Stella Santarone Andrea Bacigalupo Antonio M Risitano Elena Tagliaferri Erminia Di Bartolomeo Anna Paola Iori Alessandro Rambaldi Emanuele Angelucci Alessandra Spagnoli Federico Papineschi Stefania Tamiazzo Marta Di Nicola Paolo Di Bartolomeo

BACKGROUND Paroxysmal nocturnal hemoglobinuria is an acquired clonal disorder of the hemopoietic stem cells for which the only curative treatment is allogeneic hematopoietic stem cell transplantation. DESIGN AND METHODS The aim of this retrospective study was to assess the long-term clinical and hematologic results in 26 paroxysmal nocturnal hemoglobinuria patients who received hematopoietic ...

Journal: :Haematologica 2012
Jeffrey J Pu Rong Hu Galina L Mukhina Hetty E Carraway Michael A McDevitt Robert A Brodsky

BACKGROUND Patients with paroxysmal nocturnal hemoglobinuria harbor clonal glycosylphosphatidylinositol-anchor deficient cells arising from a multipotent hematopoietic stem cell acquiring a PIG-A mutation. Many patients with aplastic anemia and myelodysplastic syndromes also harbor small populations of glycosylphosphatidylinositol-anchor deficient cells. Patients with aplastic anemia often evol...

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