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Austen Worth
Austen Worth
Great Ormonds Street Hospital, London
Verified email at gosh.nhs.uk
Title
Cited by
Cited by
Year
The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency
L Gámez-Díaz, D August, P Stepensky, S Revel-Vilk, MG Seidel, M Noriko, ...
Journal of Allergy and Clinical Immunology 137 (1), 223-230, 2016
2912016
Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia
PJ Ancliff, MP Blundell, GO Cory, Y Calle, A Worth, H Kempski, S Burns, ...
Blood 108 (7), 2182-2189, 2006
2582006
Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: an international multicenter retrospective study
F Barzaghi, LCA Hernandez, B Neven, S Ricci, ZY Kucuk, JJ Bleesing, ...
Journal of Allergy and Clinical Immunology 141 (3), 1036-1049. e5, 2018
2532018
Autoimmune lymphoproliferative syndrome: molecular basis of disease and clinical phenotype
A Worth, AJ Thrasher, H Bobby Gaspar
British journal of haematology 133 (2), 124-140, 2006
2192006
Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans
P Tuijnenburg, HL Allen, SO Burns, D Greene, MH Jansen, E Staples, ...
Journal of allergy and clinical immunology 142 (4), 1285-1296, 2018
2072018
Whole-genome sequencing of a sporadic primary immunodeficiency cohort
JED Thaventhiran, H Lango Allen, OS Burren, W Rae, D Greene, ...
Nature 583 (7814), 90-95, 2020
1612020
WIP regulates the stability and localization of WASP to podosomes in migrating dendritic cells
HC Chou, IM Antón, MR Holt, C Curcio, S Lanzardo, A Worth, S Burns, ...
Current Biology 16 (23), 2337-2344, 2006
1502006
The Wiskott-Aldrich syndrome: the actin cytoskeleton and immune cell function
MP Blundell, A Worth, G Bouma, AJ Thrasher
Disease markers 29 (3-4), 157-175, 2010
1432010
Human cytomegalovirus haplotype reconstruction reveals high diversity due to superinfection and evidence of within-host recombination
J Cudini, S Roy, CJ Houldcroft, JM Bryant, DP Depledge, H Tutill, P Veys, ...
Proceedings of the National Academy of Sciences 116 (12), 5693-5698, 2019
1422019
T-cell receptor αβ+ and CD19+ cell–depleted haploidentical and mismatched hematopoietic stem cell transplantation in primary immune deficiency
RM Shah, R Elfeky, Z Nademi, W Qasim, P Amrolia, R Chiesa, K Rao, ...
Journal of Allergy and Clinical Immunology 141 (4), 1417-1426. e1, 2018
1382018
Omission of in vivo T‐cell depletion promotes rapid expansion of naïve CD4+ cord blood lymphocytes and restores adaptive immunity within 2 months after …
R Chiesa, K Gilmour, W Qasim, S Adams, AJJ Worth, H Zhan, ...
British journal of haematology 156 (5), 656-666, 2012
1372012
Phage Therapy of Mycobacterium Infections: Compassionate Use of Phages in 20 Patients With Drug-Resistant Mycobacterial Disease
RM Dedrick, BE Smith, M Cristinziano, KG Freeman, D Jacobs-Sera, ...
Clinical infectious diseases 76 (1), 103-112, 2023
1342023
Thymus transplantation for complete DiGeorge syndrome: European experience
EG Davies, M Cheung, K Gilmour, J Maimaris, J Curry, A Furmanski, ...
Journal of Allergy and Clinical Immunology 140 (6), 1660-1670. e16, 2017
1262017
Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score
VK Tesch, H Abolhassani, B Shadur, J Zobel, Y Mareika, S Sharapova, ...
Journal of Allergy and Clinical Immunology 145 (5), 1452-1463, 2020
1232020
Risk factors predisposing to the development of hypogammaglobulinemia and infections post-Rituximab
EAA Christou, G Giardino, A Worth, F Ladomenou
International Reviews of Immunology 36 (6), 352-359, 2017
1152017
Inherited p40phox deficiency differs from classic chronic granulomatous disease
A Van De Geer, A Nieto-Patlán, DB Kuhns, ATJ Tool, AA Arias, M Bouaziz, ...
The Journal of clinical investigation 128 (9), 3957-3975, 2018
1112018
Identifying functional defects in patients with immune dysregulation due to LRBA and CTLA-4 mutations
TZ Hou, N Verma, J Wanders, A Kennedy, B Soskic, D Janman, ...
Blood, The Journal of the American Society of Hematology 129 (11), 1458-1468, 2017
1072017
Pre‐emptive rituximab based on viraemia and T cell reconstitution: a highly effective strategy for the prevention of Epstein–Barr virus‐associated lymphoproliferative disease …
A Worth, R Conyers, J Cohen, M Jagani, R Chiesa, K Rao, N Goulden, ...
British journal of haematology 155 (3), 377-385, 2011
1012011
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations
T Lorenzini, M Fliegauf, N Klammer, N Frede, M Proietti, A Bulashevska, ...
Journal of Allergy and Clinical Immunology 146 (4), 901-911, 2020
962020
The United Kingdom primary immune deficiency (UKPID) registry 2012 to 2017
B Shillitoe, C Bangs, D Guzman, AR Gennery, HJ Longhurst, M Slatter, ...
Clinical & Experimental Immunology 192 (3), 284-291, 2018
932018
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