About: Marrow transplantation for thalassaemia

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scientific article published on 01 July 1982

Attributes	Values
rdf:type	Item
description	наукова стаття, опублікована в липні 1982 (uk) im Juli 1982 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 01 July 1982 (en) artículu científicu espublizáu en xunetu de 1982 (ast)
publication date	wds:Q72530538-521415A7-F86A-4C34-95E1-72E97E5F361C
publication date	1982-07-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q72530538-21F599F1-A0DB-4723-94A2-9F62FFF43168
language of work or name	English
cites work	wds:Q72530538-0721FCB6-457C-40EA-BF89-15A9780B4469 wds:Q72530538-08B507AD-4A84-4B0F-AF04-91D02052C31B wds:Q72530538-21217413-C833-407A-9EA6-7D0217E34203 wds:Q72530538-38469299-F0DF-422B-8D5B-C61FE19C1C0C wds:Q72530538-41C23C03-07FB-40B2-977E-214F98AF42F7 wds:Q72530538-641B4104-10CA-4620-A6EA-7C1572403877 wds:Q72530538-785B3F9D-E515-45FA-9BD1-92460061A3BC wds:Q72530538-9107BD4F-7550-488A-B761-2AA7F9A49D4A wds:Q72530538-9B7DB8A9-5F2E-4633-8FA4-64C1C7042230 wds:Q72530538-ABC4BA0B-BD33-412F-9645-0DC89ED0245D wds:Q72530538-C1C98D3D-B625-4EAA-B06F-CA878FE3CD1F wds:Q72530538-C4CA45BF-9F2A-4D04-AE3E-6542B60F7D03 wds:Q72530538-D274767D-C38F-45FC-B6AA-5231266266CB wds:Q72530538-F45628B4-79E4-4EBD-BC0E-08D7770A1539
cites work	Transplantation of marrow from an unrelated donor to a patient with acute leukemia Abnormal human haemoglobins. Separation and characterization of the alpha and beta chains by chromatography, and the determination of two new variants, hb Chesapeak and hb J (Bangkok) Bone-marrow transplantation (first of two parts). Fetal Hb production during acute erythroid expansion. I. Observations in patients with transient erythroblastopenia and post-phlebotomy A randomized study of the prevention of acute graft-versus-host disease Marrow transplantation in thirty "untransfused" patients with severe aplastic anemia Estimation of Small Percentages of Fœtal Hæmoglobin Complete Correction of the Wiskott-Aldrich Syndrome by Allogeneic Bone-Marrow Transplantation Human globin chain separation by isolectric focusing Marrow transplantation from donors other than HLA-identical siblings Correction of infantile agranulocytosis (Kostmann's syndrome) by allogeneic bone marrow transplantation Severe hereditary haemolytic anaemica in dogs treated by marrow trasplantation Marrow transplantation for children with acute nonlymphoblastic leukemia in first remission Mapping of antigenic sites on human haemoglobin by means of monoclonal antibodies and haemoglobin variants
author name string	wds:Q72530538-23102EB8-793F-40FB-A3A1-63D2616473F2 wds:Q72530538-457BAE9F-4C52-4C45-8EA8-FD91DEB3A570 wds:Q72530538-BC0C5E78-2952-445D-9DD0-066BD1564208 wds:Q72530538-C26E6562-441D-43DF-88A3-3C5B2D3C39D0 wds:Q72530538-FDC2071C-B849-4E51-92CE-A53545E7A8D2
author name string	T Papayannopoulou K M Sullivan J E Sanders R A Clift P De Stefano
rdfs:label	Marrow transplantation for thalassaemia (en)
skos:prefLabel	Marrow transplantation for thalassaemia (en)
name	Marrow transplantation for thalassaemia (en)
author	wds:Q72530538-6D7CE5B7-17FA-4FC5-B8ED-A48E17653F9E wds:Q72530538-81ED7A84-DA3C-4925-B6D0-D456C3F04A95 wds:Q72530538-8FC20EAC-2E46-4CEB-BE53-F3D36D5BFD4B wds:Q72530538-9F34513B-9E78-4384-880B-82379282EE7E
author	E. Donnall Thomas Rainer Storb C. Dean Buckner Caterina Borgna-Pignatti
title	wds:Q72530538-47A0F785-867B-4289-9AC4-DE7CA3701E5B
title	Marrow transplantation for thalassaemia (en)
page(s)	wds:Q72530538-A6D5B38F-BFEF-4C55-B5A9-2E854CF2CEB4
page(s)	227-229
instance of	wds:Q72530538-565F9BD2-9952-4E48-839D-480C69B2CF3C
instance of	scholarly article
PubMed ID	wds:Q72530538-AFD383F7-E9DF-4EC5-84D9-34C186B00570
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6124668
PubMed ID	6124668
published in	wds:Q72530538-7C43346D-C18B-4BE3-974D-27751C45D601
published in	The Lancet
issue	wds:Q72530538-9A8A8EE6-25DB-4B7A-95D4-74E8729E0586
volume	wds:Q72530538-363896A8-B11B-4889-A065-32687527FF4C
issue	8292
volume	2
DOI	wds:Q72530538-FD32968F-2E6C-49A2-AFDC-8D328D411B83
DOI	http://dx.doi.org/10.1016/S0140-6736(82)90319-1
DOI	10.1016/S0140-6736(82)90319-1
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q72530538
is cites work of	Bone marrow transplantation from the personal viewpoint Current status of stem cell therapy and prospects for gene therapy for the disorders of globin synthesis Allogeneic cellular gene therapy in hemoglobinopathies--evaluation of hematopoietic SCT in sickle cell anemia. Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel The molecular genetics of human hemoglobin A history of haemopoietic cell transplantation Hematopoietic SCT for the Black African and non-Black African variants of sickle cell anemia. Retrovirus-mediated transfer and expression of drug resistance genes in human haematopoietic progenitor cells Management of Thalassemia Major (Cooley’s Anemia) Future alternative therapies for β-thalassemia Marrow transplantation for nonmalignant disorders Diabetes impairs hematopoietic stem cell mobilization by altering niche function Thalassaemia: the long road from bedside to genome. Bone marrow transplantation: 1982. Allogeneic Bone-Marrow Transplantation Beta thalassemia and heart disease: three decades of gradual progress Improved survival of thalassaemia major in the UK and relation to T2* cardiovascular magnetic resonance Hematopoietic stem cell transplantation for patients with sickle cell disease: progress and future directions Umbilical cord blood stem cells: application for the treatment of patients with hemoglobinopathies Bone marrow transplantation from alternative donors for thalassemia: HLA-phenotypically identical relative and HLA-nonidentical sibling or parent transplants The William Allan Memorial Award address: Thalassemia: molecular mechanism and detection Improved clinical outcomes of high risk β thalassemia major patients undergoing a HLA matched related allogeneic stem cell transplant with a treosulfan based conditioning regimen and peripheral blood stem cell grafts New trends in the treatment of beta-thalassemia

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