J SZER, HJ DEEG, RP WITHERSPOON, A … - Annals of internal medicine, 1984 - Am Coll Physicians Four patients with paroxysmal nocturnal hemoglobinuria and severe marrow aplasia
were given marrow grafts either from allogeneic
human-leukocyte-antigen-identical siblings (three patients) or from a ... Cited by 27 - Related articles - All 3 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
HJ Kolb, E Holler, C Bender-Götze, U … - Bone marrow transplantation, 1989 - ncbi.nlm.nih.gov Paroxysmal nocturnal haemoglobinuria (PNH) and myelodysplastic syndromes (MDS)
are disorders of pluripotent stem cells resulting in haematopoietic
insufficiency which can be cured by marrow transplantation. The extent of ... Cited by 20 - Related articles
R Storb, RS Evans, ED Thomas, CD Buckner, … - Br J Haematol, 1973 - interscience.wiley.com Summary. A patient with pancytopenia and paroxysmal nocturnal haemoglobinuria
(PNH) following exposure to insecticide spray developed complete marrow failure
after inhalation of vapours containing benzol. There was no sign of ... Cited by 26 - Related articles - All 2 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
A Fefer, H Freeman, R Storb, J Hill, J Singer … - Annals of Internal Medicine, 1976 - Am Coll Physicians An 18-year-old white Canadian male patient with paroxysmal nocturnal
hemoglobinuria and refractory marrow failure received a marrow infusion from his
normal identical twin brother without prior ablation of the patient's ... Cited by 39 - Related articles - All 2 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
- ►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
H Van Kamp, GW Van Imhoff, JTM De Wolf, JW … - British journal of haematology, 1995 - 万方数据资源系统 Four patients with paroxysmal nocturnal haemoglobinuria (PNH) were treated with
cyclosporine. The treatment with cyclosporine was based on the hypothesis that
immune-mediated bone-marrow damage is the common pathogenetic mechanism of ... Cited by 31 - Related articles - BL Direct - All 3 versions
M Bemba, P Guardiola, L Garderet, A … - British journal of haematology, 1999 - interscience.wiley.com Paroxysmal nocturnal haemoglobinuria (PNH) is an acquired clonal disorder of the
haemopoietic stem cells for which the only curative treatment is bone marrow
transplantation. There are few reports on the use of allogeneic ... Cited by 39 - Related articles - BL Direct - All 5 versions
