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Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 5741 - 5741
Abstract Bacterial contamination of haematopoietic stem cell products (HSCP) during collection and processing is a potential risk and has been described as... 
Journal Article
American Journal of Hematology, ISSN 0361-8609, 11/2016, Volume 91, Issue 11, pp. 1160 - 1160
Journal Article
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 2679 - 2679
Abstract Haemopoietic stem cell transplantation (HSCT) is able to achieve normal haemopoiesis in patients with Diamond Blackfan anaemia. However, historically... 
Journal Article
Blood, ISSN 0006-4971, 12/2014, Volume 124, Issue 21, pp. 4082 - 4082
Abstract Introduction Acute chest syndrome (ACS) is a severe complication of sickle cell disease (SCD) and a leading cause of hospitalisation and mortality.... 
Journal Article
Blood, ISSN 0006-4971, 11/2013, Volume 122, Issue 21, pp. 4693 - 4693
Nocturnal enuresis and albuminuria or proteinuria are markers of renal damage in sickle cell disease (SCD) and commonly develop early on in life. Proteinuria... 
Journal Article
Blood, ISSN 0006-4971, 11/2013, Volume 122, Issue 21, pp. 1229 - 1229
Abstract Diamond Blackfan anaemia (DBA) is an inherited bone marrow failure syndrome most commonly presenting as a red cell aplasia in infancy. It is... 
Journal Article
Blood, ISSN 0006-4971, 11/2012, Volume 120, Issue 21, pp. 1268 - 1268
Abstract Abstract 1268 Fifty nine patients with clinical and laboratory features consistent with Diamond Blackfan anaemia attend the DBA clinic at St. Mary's... 
Journal Article
Blood, ISSN 0006-4971, 11/2012, Volume 120, Issue 21, pp. 3037 - 3037
Abstract Abstract 3037 Bone marrow transplantation (BMT) is currently the only cure for thalassaemia major (TM) and sickle cell disease (SCD). Due to the... 
Journal Article
Blood, ISSN 0006-4971, 11/2011, Volume 118, Issue 21, pp. 4919 - 4919
Abstract Abstract 4919 Hermansky Pudlak Syndrome (HPS) is a genetically heterogeneous group of rare disorders that are classified as ‘lysosome biogenesis... 
Journal Article
Blood, ISSN 0006-4971, 11/2012, Volume 120, Issue 21, pp. 997 - 997
Abstract Abstract 997 Diamond Blackfan anaemia is an inherited bone marrow failure syndrome with haematological and systemic manifestations. The classical... 
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 05/2015, Volume 125, Issue 5, pp. 2151 - 2160
Journal Article
Blood, ISSN 0006-4971, 11/2019, Volume 134, Issue Supplement_1, pp. 2277 - 2277
Background: Children and adolescents with sickle cell disease (SCD) are at significant risk for cerebral infarction and neurocognitive deficits. In a... 
Journal Article
Blood, ISSN 0006-4971, 11/2016, Volume 128, Issue 21, pp. 2486 - 2488
In this issue of Blood, the first prospective trial of unrelated donor bone marrow transplantation (BMT) in children with sickle cell disease (SCD), reported... 
HEMATOLOGY | TRANSPLANTATION | CHILDREN
Journal Article
by Gluckman, Eliane and Cappelli, Barbara and Bernaudin, Francoise and Labopin, Myriam and Volt, Fernanda and Carreras, Jeanette and Simões, Belinda Pinto and Ferster, Alina and Dupont, Sophie and De La Fuente, Josu and Dalle, Jean-Hugues and Zecca, Marco and Walters, Mark C and Krishnamurti, Lakshmanan and Bhatia, Monica and Leung, Kathryn and Yanik, Gregory and Kurtzberg, Joanne and Dhedin, Nathalie and Kuentz, Mathieu and Michel, Gerard and Apperley, Jane and Lutz, Patrick and Neven, Bénédicte and Bertrand, Yves and Vannier, Jean Pierre and Ayas, Mouhab and Cavazzana, Marina and Matthes-Martin, Susanne and Rocha, Vanderson and Elayoubi, Hanadi and Kenzey, Chantal and Bader, Peter and Locatelli, Franco and Ruggeri, Annalisa and Eapen, Mary and Bordon, Victoria and Labarque, Veerle and Pereira, Maguy and Bittencourt, Henrique and Petersen, Heidi and Deconninck, Eric and Jubert, Charlotte and Perrin, Jean and Cahn, Jean Yves and Bruno, Bénédicte and Bordigoni, Pierre and Mechinaud, Francoise and Vernant, Jean Paul and Stephan, Jean Luis and Suttorp, Meinolf and Strahm, Brigitte and Da Cunha, Claudia Bettoni and Garwer, Birgit and Rothmayer, Margarete and Wendelin, Knut and Graphakos, Stelios and Tbakhi, Abdelghani and Naeimi, Nooshin and Zuckerman, Tsila and Sharon, Pantel Bakst and Yaniv, Isaac and Amos, Toren and Prete, Arcangelo and Lo Nigro, Luca and Lanino, Edoardo and Faraci, Maura and Ciceri, Fabio and Marktel, Sarah and De Simone, Giusy and Messina, Chiara and Bartolomeo, Paolo D.I and Santarone, Stella and Vallisa, Daniele and Bertaina, Alice and Arcese, William and Foa, Roberto and Berger, Massimo and Maximova, Natalia and Wallet, Sylwia and Bazuaye, G.N and Maschan, Alexei and De Heredia, Cristina Diaz and Bieler, C. Belendez and Pato, Julia Ruiz and Heras, Inmaculata and Trevor, Reyhana and Abayomi, Kym and Thomson, Jackie and Fasth, Anders and Frödin, Ulla and Ljugman, Per and Ansari, Marc and Güngör, Tayfun and Unal, Emel and Pehlivan, Mustafa and Anak, Sema and Ozturk, Gulyuz and Unal, Ali and Lawson, Sarah and ... and European Soc Blood Marrow Transpla and Ctr Int Blood Marrow Transplant Re and Eurocord and Eurocord, the Pediatric Working Party of the European Society for Blood and Marrow Transplantation, and the Center for International Blood and Marrow Transplant Research
Blood, ISSN 0006-4971, 03/2017, Volume 129, Issue 11, pp. 1548 - 1556
Journal Article
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 2468 - 2468
Abstract Related haemopoietic stem cell transplantation is a well-established treatment modality for haemoglobinopathies, but it is limited by the availability... 
Journal Article
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 5801 - 5801
Abstract Sickle cell disease and b-Thalassaemia major comprise the most prevalent haemoglobinopathies in the world. Despite significant advances in the... 
Journal Article
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