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Journal Articles

Allogeneic stem cell transplantation compared to conservative management in adults with inborn errors of immunity

Blood (2023) 141 (1): 60–71.

https://doi.org/10.1182/blood.2022015482

Published: 2023

Includes: Supplemental data

Journal Articles

Hematopoietic stem cell transplantation for adolescents and adults with inborn errors of immunity: an EBMT IEWP study

Blood (2022) 140 (14): 1635–1649.

https://doi.org/10.1182/blood.2022015506

Published: 2022

Includes: Supplemental data

Journal Articles

How I use allogeneic HSCT for adults with inborn errors of immunity

Siobhan O. Burns, Emma C. Morris

Blood (2021) 138 (18): 1666–1676.

https://doi.org/10.1182/blood.2020008187

Published: 2021

Includes: Supplemental data

Journal Articles

Key diagnostic markers for autoimmune lymphoproliferative syndrome with molecular genetic diagnosis

Emese Molnár, Nesrine Radwan, Gábor Kovács, Hajnalka Andrikovics, Frances Henriquez, Anton Zarafov, Matthew Hayman, Daniela Linzner, Adrian J. Thrasher, Matthew Buckland, Siobhan O. Burns, Kimberly C. Gilmour

Blood (2020) 136 (17): 1933–1945.

https://doi.org/10.1182/blood.2020005486

Published: 2020

Includes: Supplemental data

Journal Articles

Topoisomerase 2β mutation impairs early B-cell development

Olivier Papapietro, Anita Chandra, Davide Eletto, Sarah Inglott, Vincent Plagnol, James Curtis, Mailis Maes, Ali Alisaac, Adriana S. Albuquerque, Eugenie Basseres, Olivier Hermine, Capucine Picard, Alain Fischer, Anne Durandy, Sven Kracker, Siobhan O. Burns, Delphine Cuchet-Lourenco, Klaus Okkenhaug, Sergey Nejentsev

Blood (2020) 135 (17): 1497–1501.

https://doi.org/10.1182/blood.2019003299

Published: 2020

Includes: Supplemental data

Journal Articles

Gene therapy for Wiskott-Aldrich syndrome in a severely affected adult

Blood (2017) 130 (11): 1327–1335.

https://doi.org/10.1182/blood-2017-04-777136

Published: 2017

Includes: Supplemental data

Journal Articles

Identifying functional defects in patients with immune dysregulation due to LRBA and CTLA-4 mutations

Blood (2017) 129 (11): 1458–1468.

https://doi.org/10.1182/blood-2016-10-745174

Published: 2017

Journal Articles

Immunodeficiency and severe susceptibility to bacterial infection associated with a loss-of-function homozygous mutation of MKL1

Julien Record, Dessislava Malinova, Helen L. Zenner, Vincent Plagnol, Karolin Nowak, Farhatullah Syed, Gerben Bouma, James Curtis, Kimberly Gilmour, Catherine Cale, Scott Hackett, Guillaume Charras, Dale Moulding, Sergey Nejentsev, Adrian J. Thrasher, Siobhan O. Burns

Blood (2015) 126 (13): 1527–1535.

https://doi.org/10.1182/blood-2014-12-611012

Published: 2015

Includes: Multimedia, Supplemental data

Journal Articles

Disease-associated missense mutations in the EVH1 domain disrupt intrinsic WASp function causing dysregulated actin dynamics and impaired dendritic cell migration

Austen J. J. Worth, Joao Metelo, Gerben Bouma, Dale Moulding, Marco Fritzsche, Bertrand Vernay, Guillaume Charras, Giles O. C. Cory, Adrian J. Thrasher, Siobhan O. Burns

Blood (2013) 121 (1): 72–84.

https://doi.org/10.1182/blood-2012-01-403857

Published: 2013

Includes: Supplemental data

Journal Articles

B cell–intrinsic deficiency of the Wiskott-Aldrich syndrome protein (WASp) causes severe abnormalities of the peripheral B-cell compartment in mice

Blood (2012) 119 (12): 2819–2828.

https://doi.org/10.1182/blood-2011-09-379412

Published: 2012

Includes: Supplemental data

Journal Articles

Cytoskeletal remodeling mediated by WASp in dendritic cells is necessary for normal immune synapse formation and T-cell priming

Gerben Bouma, Ariadna Mendoza-Naranjo, Michael P. Blundell, Elena de Falco, Kathryn L. Parsley, Siobhan O. Burns, Adrian J. Thrasher

Blood (2011) 118 (9): 2492–2501.

https://doi.org/10.1182/blood-2011-03-340265

Published: 2011

Includes: Multimedia, Supplemental data

Journal Articles

A congenital activating mutant of WASp causes altered plasma membrane topography and adhesion under flow in lymphocytes

Siobhan O. Burns, David J. Killock, Dale A. Moulding, Joao Metelo, Joao Nunes, Ruth R. Taylor, Andrew Forge, Adrian J. Thrasher, Aleksandar Ivetic

Blood (2010) 115 (26): 5355–5365.

https://doi.org/10.1182/blood-2009-08-236174

Published: 2010

Includes: Multimedia, Supplemental data

NARROW

Allogeneic stem cell transplantation compared to conservative management in adults with inborn errors of immunity

Hematopoietic stem cell transplantation for adolescents and adults with inborn errors of immunity: an EBMT IEWP study

How I use allogeneic HSCT for adults with inborn errors of immunity

Key diagnostic markers for autoimmune lymphoproliferative syndrome with molecular genetic diagnosis

Topoisomerase 2β mutation impairs early B-cell development

Gene therapy for Wiskott-Aldrich syndrome in a severely affected adult

Identifying functional defects in patients with immune dysregulation due to LRBA and CTLA-4 mutations

Immunodeficiency and severe susceptibility to bacterial infection associated with a loss-of-function homozygous mutation of MKL1

Disease-associated missense mutations in the EVH1 domain disrupt intrinsic WASp function causing dysregulated actin dynamics and impaired dendritic cell migration

B cell–intrinsic deficiency of the Wiskott-Aldrich syndrome protein (WASp) causes severe abnormalities of the peripheral B-cell compartment in mice

Cytoskeletal remodeling mediated by WASp in dendritic cells is necessary for normal immune synapse formation and T-cell priming

A congenital activating mutant of WASp causes altered plasma membrane topography and adhesion under flow in lymphocytes

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American Society of Hematology

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ASH Publications

American Society of Hematology

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