نتایج جستجو برای: sibling donor

تعداد نتایج: 74949  

Journal: :international journal of hematology-oncology and stem cell research 0
mohammadreza ostadali hematology- oncology and stem cell transplantation research center, shariati hospital, tehran univer andisheh ghashghaie hematology- oncology and stem cell transplantation research center, shariati hospital, tehran univer ardeshir ghavamzadeh hematology- oncology and stem cell transplantation research center, shariati hospital, tehran univer

the most important factor in donor-recipient matching for hematopoietic stem cell transplantation is their hla typing. for many patients, we can not find a full-matched donor. in high risk patients, one locus  mismatched related donors are suitable alternatives. (1, 2) since the matching of patients and their siblings usually is based on low resolution hla typing, the matching of one locus mism...

ژورنال: یافته 2011
انتظامی, کبری, شاهسوار, فرهاد, علی مقدم, کامران,

A potential factor influencing hematopoietic stem cells transplantation (HSCT) outcome is the presence of donor-derived alloreactive natural killer (NK) cells. This retrospective analysis studied the impact of NK alloreactivity based on the missing KIR ligand, for acute myeloid leukemia (AML) or acute lymphoblastic leukemia (ALL) patients undergoing non-T-cell depleted HLA-identical sibling HS...

Journal: :Fertility and sterility 2011
Cary L Dicken Athena Zapantis Edward Illions Staci Pollack Harry J Lieman Kris Bevilacqua Sangita K Jindal

OBJECTIVE To report the rare occurrence of full-sibling embryos in unrelated women using independently chosen donor sperm and donor oocytes in two different cycles unintentionally created at our IVF program, and to discuss the concept of disclosure to the patients. DESIGN Case report. SETTING Academic IVF program. PATIENT(S) Two women independently undergoing donor recipient cycles with a...

Journal: :Blood 2001
A H Filipovich J V Stone S C Tomany M Ireland C Kollman C J Pelz J T Casper M J Cowan J R Edwards A Fasth R P Gale A Junker N R Kamani B J Loechelt D W Pietryga O Ringdén M Vowels J Hegland A V Williams J P Klein K A Sobocinski P A Rowlings M M Horowitz

Human leukocyte antigen (HLA)-identical sibling bone marrow transplantation is an effective treatment for Wiskott-Aldrich syndrome. However, most children with this disease lack such donors and many patients receive transplants from alternative donors. This study compared outcomes of HLA-identical sibling, other related donor, and unrelated donor transplantation for Wiskott-Aldrich syndrome. Th...

Journal: :American journal of hematology 2004
Bella Bielorai Mark R Hughes Arleen D Auerbach Arnon Nagler Ron Loewenthal Gideon Rechavi Amos Toren

Fanconi anemia is a rare autosomal recessive disease characterized by bone marrow failure, developmental anomalies, and a high incidence of myelodysplasia and acute myeloid leukemia. Stem cell transplantation is the only curative treatment. In the absence of matched- sibling donor, an alternative mismatched family or matched unrelated donor can be used, but the results are inferior to the match...

Journal: :Haematologica 2015
Andrea Bacigalupo Gerard Socié Rose Marie Hamladji Mahmoud Aljurf Alexei Maschan Slawomira Kyrcz-Krzemien Alicja Cybicka Henrik Sengelov Ali Unal Dietrich Beelen Anna Locasciulli Carlo Dufour Jakob R Passweg Rosi Oneto Alessio Signori Judith C W Marsh

We have analyzed 1448 patients with acquired aplastic anemia grafted between 2005 and 2009, and compared outcome of identical sibling (n=940) versus unrelated donor (n=508) transplants. When compared to the latter, sibling transplants were less likely to be performed beyond 180 days from diagnosis (39% vs. 85%), to have a cytomegalovirus negative donor/recipient status (15% vs. 23%), to receive...

Journal: :Annals of the New York Academy of Sciences 2005
Mark C Walters Lynn Quirolo Elizabeth T Trachtenberg Sandie Edwards Lisa Hale Joanna Lee Joi Morton-Wiley Keith Quirolo Shanda Robertson Julie Saba Bert Lubin

The Sibling Donor Cord Blood (SDCB) Program was initiated in 1998 as a resource to collect, characterize, and release cord blood units (CBUs) from families affected by malignant and nonmalignant disorders for transplantation. Families in the United States were recruited by telephone after referrals by community and academic physicians. Collection kits were mailed to prospective participants and...

Journal: :Blood 2009
Jan J Cornelissen Bronno van der Holt Gregor E G Verhoef Mars B van't Veer Marinus H J van Oers Harry C Schouten Gert Ossenkoppele Pieter Sonneveld Johan Maertens Marinus van Marwijk Kooy Martijn R Schaafsma Pierre W Wijermans Douwe H Biesma Shulamit Wittebol Paul J Voogt Joke W Baars Pierre Zachée Leo F Verdonck Bob Löwenberg Adriaan W Dekker

While commonly accepted in poor-risk acute lymphoblastic leukemia (ALL), the role of allogeneic hematopoietic stem cell transplantation (allo-SCT) is still disputed in adult patients with standard-risk ALL. We evaluated outcome of patients with ALL in first complete remission (CR1), according to a sibling donor versus no-donor comparison. Eligible patients (433) were entered in 2 consecutive, p...

1973
S. D. Nelson H. J. O. White

As experience grew, the survival of transplants between genetically similar pairs (sibling-sibling or Parent-child) was found to be better than when donor ap|d recipient were unrelated (Murray & Barnes 1968, ^ Barnes et al 1971). In the unrelated group there were a proportion of outstandingly successful transplants which might have been due to chance similarity in the antigenic make-up of donor...

Journal: :Blood 2003
William Reed Renée Smith Florinna Dekovic Joanna Y Lee Julie D Saba Elizabeth Trachtenberg Joanna Epstein Steffany Haaz Mark C Walters Bertram H Lubin

Banking of cord blood (CB) for unrelated hematopoietic stem cell (HSC) transplantation is well established. However, directed-donor banking of CB for siblings in a current good tissue practices (cGTP) environment has not previously been investigated. Families were eligible for the present study if they were caring for a child with a disorder treatable by HSC transplantation and expecting the bi...

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