Publications by authors named "Moira Thomas"

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Clinical and Molecular Characteristics of X-Linked Agammaglobulinemia Patients 55 Years or Older.
Aaron T Chin, Hans D Ochs, Roger Kobayashi, Hassan Abolhassani, Hana Alachkar, Moira Thomas

J Allergy Clin Immunol Pract· October 2025

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Chronic norovirus infection in immunodeficiency: A UK national case series.
Alexandros Grammatikos, Anisha Mangtani, Mark Ponsford, Stephen Jolles, Elizabeth McDermott, Moira Thomas

J Allergy Clin Immunol Pract· June 2025

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A multi-centre UK-based survey on angioedema secondary to acquired C1 inhibitor deficiency.
Hadeil Morsi, Aarnoud Huissoon, Alexandros Grammatikos, Andrew F Whyte, Ania Manson, Moira Thomas

Clin Exp Immunol· January 2025

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Chronic or recurrent Campylobacter enteritis in primary immunodeficiency: A UK national case-series and review of the literature.
Alexandros Grammatikos, Moira Thomas, Sarah Johnston, Fiona Moghaddas, Mahableshwar Albur

J Allergy Clin Immunol Pract· September 2023

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A National Survey of Hereditary Angioedema and Acquired C1 Inhibitor Deficiency in the United Kingdom.
Patrick F K Yong, Tanya Coulter, Tariq El-Shanawany, Tomaz Garcez, Scott Hackett, Moira Thomas

J Allergy Clin Immunol Pract· August 2023

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Outcomes following SARS-CoV-2 infection in patients with primary and secondary immunodeficiency in the UK.
Adrian M Shields, Ariharan Anantharachagan, Gururaj Arumugakani, Kenneth Baker, Sameer Bahal, Moira Thomas

Clin Exp Immunol· September 2022

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No-biopsy strategy for coeliac disease is applicable in adult patients: a 'real-world' Scottish experience.
Aoisha Hoyle, Peter Gillett, Helen R Gillett, Reuben Borg, Steven Nottley, Moira Thomas

Frontline Gastroenterol· August 2022

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Publisher Correction: Whole-genome sequencing of a sporadic primary immunodeficiency cohort.
James E D Thaventhiran, Hana Lango Allen, Oliver S Burren, William Rae, Daniel Greene, Moira J Thomas

Nature· August 2020

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Whole-genome sequencing of a sporadic primary immunodeficiency cohort.
James E D Thaventhiran, Hana Lango Allen, Oliver S Burren, William Rae, Daniel Greene, Moira J Thomas

Nature· July 2020

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Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans.
Paul Tuijnenburg, Hana Lango Allen, Siobhan O Burns, Daniel Greene, Machiel H Jansen, Moira Thomas

J Allergy Clin Immunol· October 2018

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Clinical associations of the positive anti Ro52 without Ro60 autoantibodies: undifferentiated connective tissue diseases.
Sai H K Murng, Moira Thomas

J Clin Pathol· January 2018

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A low serum sICAM-1 level may assist in the exclusion of neonatal infection.
David Edgar, Vanessa Gabriel, Adam Craig, Darren Wheeler, Moira Thomas

Biol Neonate· June 2002

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