C Parker, M Omine, S Richards, J Nishimura, M … - Blood, 2005 - Am Soc Hematology From the Division of Hematology, University of Utah School of Medicine and the
George E. Whalen VA Medical Center, Salt Lake City, UT; the Department of
Medicine, Division of Hematology, Showa University Fujigaoka Hospital, ... Cited by 133 - Related articles - BL Direct - All 6 versions
R Sašo, J Marsh, L Čevreska, J Szer, RP … - Br J Haematol, 1999 - interscience.wiley.com Paroxysmal nocturnal haemoglobinuria (PNH) is a rare clonal haematological
disorder characterized by intravascular haemolysis and increased risk of
thrombosis. PNH is associated with bone marrow failure syndromes including ... Cited by 78 - Related articles - BL Direct - All 4 versions
- ►bloodjournal.org [PDF] JH Antin, D Ginsburg, BR Smith, DG Nathan, … - Blood, 1985 - Am Soc Hematology . Hematology; all rights reserved Copyright 2007 by The American Society of DC
20036. by the American Society of Hematology, 1900 M St, NW, Suite 200,
Washington Blood (print ISSN 0006-4971, online ISSN 1528-0020), is ... Cited by 56 - Related articles - All 5 versions
K Kawahara, RP Witherspoon, R Storb - Am J Hematol, 1992 - interscience.wiley.com Between 1971 and 1990, nine patients ranging in age from 14-38 years received
marrow transplants for paroxysmal nocturnal hemoglobinuria (PNH). Six were
transplanted for aplastic complications of PNH. Four of these were from HLA- ... Cited by 52 - Related articles - All 3 versions
- ►haematologica-thj.org [PDF] AM Raiola, MT Van Lint, T Lamparelli, F … - Haematologica, 2000 - haematologica-thj.org Background and Objectives. Paroxysmal nocturnal hemoglobinuria (PNH) is an
acquired clonal disease of the hemopoietic stem cell (HSC) characterized by
intravascular hemolysis and increased risk of venous thrombosis. There are ... Cited by 37 - Related articles - BL Direct - All 16 versions
HT Greinix, R Storb, JE Sanders, H Joachim … - British journal of haematology, 1993 - interscience.wiley.com Summary. Four patients with Diamond-Blackfan syndrome (congenital hypoplastic
anaemia) whose disease was resistant to corticosteroid treatment and who were
red blood cell transfusion-dependent, were given marrow grafts from ... Cited by 34 - Related articles - BL Direct - All 3 versions
- ►bloodjournal.org K Nafa, M Bessler, HJ Deeg, L Luzzatto - Blood, 1998 - Am Soc Hematology We report a detailed longitudinal study of the first patient to be treated (in
1973) for paroxysmal nocturnal hemoglobinuria (PNH) with syngeneic bone marrow
transplantation (BMT). The patient subsequently relapsed with PNH in 1983, ... Cited by 30 - Related articles - BL Direct - All 5 versions
P Boccuni, L Del Vecchio, R Di Noto, B Rotoli - Critical Reviews in Oncology and Hematology, 2000 - Elsevier Paroxysmal nocturnal hemoglobinuria (PNH) is characterized by the expansion of
one or more clones of stem cells producing a progeny of mature blood cells
deficient in the plasma membrane expression of all glycosyl – ... Cited by 26 - Related articles - All 4 versions
U Hegenbart, D Niederwieser, S Forman, E … - Biology of Blood and Marrow Transplantation, 2003 - Elsevier Paroxysmal nocturnal hemoglobinuria (PNH) is a rare clonal disorder caused by a
somatic mutation of the X-linked phosphatidylinositol glycan class A gene.
Allogeneic hematopoietic cell transplantation (HCT) after high-dose ... Cited by 23 - Related articles - BL Direct - All 8 versions
