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Clinical and laboratory features of seventy‐eight UK patients with Good’s syndrome (thymoma and hypogammaglobulinaemia)

Abstract:

Good’s syndrome (thymoma and hypogammaglobulinaemia) is a rare secondary immunodeficiency disease, previously reported in the published literature as mainly individual cases or small case series. We use the national UK‐Primary Immune Deficiency (UKPID) registry to identify a large cohort of patients in the UK with this PID to review its clinical course, natural history and prognosis. Clinical information, laboratory data, treatment and outcome were collated and analysed. Seventy‐eight patient...

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Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1111/cei.13216

Authors


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Role:
Author
ORCID:
0000-0002-5646-4707
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Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
NDM Experimental Medicine
Role:
Author
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Name:
National Institute for Health Research
Publisher:
Wiley
Journal:
Clinical and Experimental Immunology More from this journal
Volume:
195
Pages:
132-138
Publication date:
2018-09-14
Acceptance date:
2018-08-07
DOI:
EISSN:
1365-2249
ISSN:
0009-9104
Pmid:
30216434
Language:
English
Keywords:
Pubs id:
pubs:920586
UUID:
uuid:a7d48618-045f-4338-8a0a-7ddaf3023204
Local pid:
pubs:920586
Source identifiers:
920586
Deposit date:
2019-09-09

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