C Bangs
Overview
Explore the profile of C Bangs including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
164
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Recent Articles
1.
Shillitoe B, Bangs C, Guzman D, Gennery A, Longhurst H, Slatter M, et al.
Clin Exp Immunol
. 2018 Jun;
192(3):284-291.
PMID: 29878323
This is the second report of the United Kingdom Primary Immunodeficiency (UKPID) registry. The registry will be a decade old in 2018 and, as of August 2017, had recruited 4758...
2.
Stubbs A, Bangs C, Shillitoe B, Edgar J, Burns S, Thomas M, et al.
Clin Exp Immunol
. 2017 Oct;
191(2):212-219.
PMID: 28990652
Immunoglobulin replacement therapy enhances survival and reduces infection risk in patients with agammaglobulinaemia. We hypothesized that despite regular immunoglobulin therapy, some patients will experience ongoing respiratory infections and develop progressive...
3.
Brent J, Guzman D, Bangs C, Grimbacher B, Fayolle C, Huissoon A, et al.
Clin Exp Immunol
. 2015 Dec;
184(1):73-82.
PMID: 26646609
Idiopathic hypogammaglobulinaemia, including common variable immune deficiency (CVID), has a heterogeneous clinical phenotype. This study used data from the national UK Primary Immune Deficiency (UKPID) registry to examine factors associated...
4.
Helbert M, Bangs C, Bishop M, Molesworth A, Ironside J
Vox Sang
. 2015 Nov;
110(3):282-4.
PMID: 26529032
Surveillance of 75 immunodeficiency patients exposed to UK-sourced immunoglobulin, including batches derived from donors who went on to develop vCJD, has not detected any clinical cases of vCJD, or of...
5.
Turley A, Gathmann B, Bangs C, Bradbury M, Seneviratne S, Gonzalez-Granado L, et al.
J Clin Immunol
. 2015 Feb;
35(2):199-205.
PMID: 25663093
Introduction: Complement immunodeficiencies (excluding hereditary angioedema and mannose binding lectin deficiency) are rare. Published literature consists largely of case reports and small series. We collated data from 18 cities across...
6.
D M Edgar J, Buckland M, Guzman D, Conlon N, Knerr V, Bangs C, et al.
Clin Exp Immunol
. 2013 Jul;
175(1):68-78.
PMID: 23841717
This report summarizes the establishment of the first national online registry of primary immune deficency in the United Kingdom, the United Kingdom Primary Immunodeficiency (UKPID Registry). This UKPID Registry is...
7.
Jolles S, Williams P, Carne E, Mian H, Huissoon A, Wong G, et al.
Clin Exp Immunol
. 2013 Jun;
175(1):59-67.
PMID: 23786259
Hereditary angioedema (HAE) and acquired angioedema (AAE) are rare life-threatening conditions caused by deficiency of C1 inhibitor (C1INH). Both are characterized by recurrent unpredictable episodes of mucosal swelling involving three...
8.
Nagler A, BINET C, MacKichan M, Negrin R, Bangs C, Donlon T, et al.
Blood
. 1990 Oct;
76(7):1299-307.
PMID: 1698477
Marrow cells from 36 patients with myelodysplastic syndromes (MDS) (13 refractory anemia [RA], 14 refractory anemia with excess of blasts [RAEB], 9 RAEB in transformation [RAEB-T]) were evaluated for their...
9.