K C Gilmour
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Explore the profile of K C Gilmour including associated specialties, affiliations and a list of published articles.
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20
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1296
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Recent Articles
1.
Johnson S, Standing J, Klein N, Irwin A, Shingadia D, Lonsdale D, et al.
HIV Med
. 2019 Jan;
20(4):e8-e9.
PMID: 30693658
No abstract available.
2.
Adams S, Kricke S, Ralph E, Gilmour N, Gilmour K
Clin Exp Immunol
. 2017 Oct;
191(2):198-202.
PMID: 28976005
Assessment of thymic output by measurement of naive T cells is carried out routinely in clinical diagnostic laboratories, predominantly using flow cytometry with a suitable panel of antibodies. Naive T...
3.
Kiani-Alikhan S, Yong P, Gilmour K, Grosse-Kreul D, Davies E, Ibrahim M
J Clin Immunol
. 2011 Oct;
32(1):70-7.
PMID: 22009004
We describe a family with the rare mutation R11X that leads to a truncated CD40 ligand (CD40L) missing the intracellular domain. The index case had detectable CD40L expression and presented...
4.
Gholam C, Grigoriadou S, Gilmour K, Gaspar H
Clin Exp Immunol
. 2011 Feb;
163(3):271-83.
PMID: 21303357
Familial haemophagocytic lymphohistiocytosis (FHL) is a rare autosomal recessive disorder of immune dysregulation associated with uncontrolled T cell and macrophage activation and hypercytokinaemia. The incidence of FHL is 0·12/100·000 children...
5.
Sharpe L, Ancliff P, Amrolia P, Gilmour K, Vellodi A
J Inherit Metab Dis
. 2009 Mar;
32 Suppl 1:S107-10.
PMID: 19267217
Haemophagocytic lymphohistiocytosis (HLH) is a rare and rapidly progressive disease which, untreated, invariably leads to death. Gaucher disease is a rare lysosomal storage disorder. The acute neuronopathic variant; type II,...
6.
Yong P, Post F, Gilmour K, Grosse-Kreul D, King A, Easterbrook P, et al.
J Clin Pathol
. 2008 Oct;
61(11):1220-2.
PMID: 18955577
Cerebral toxoplasmosis can occur outside the setting of advanced HIV immunodeficiency or drug-induced immunosuppression. A case of cerebral toxoplasmosis is reported in a previously healthy 41-year-old man who was found...
7.
Eastwood D, Gilmour K, Nistala K, Meaney C, Chapel H, Sherrell Z, et al.
Clin Exp Immunol
. 2004 Aug;
137(3):584-8.
PMID: 15320910
The molecular basis of common variable immunodeficiency (CVID) is undefined, and diagnosis requires exclusion of other diseases including X-linked lymphoproliferative disease (XLP). This rare disorder of immunedysregulation presents typically after...
8.
Gilmour K, Walshe D, Heath S, Monaghan G, Loughlin S, Lester T, et al.
Mol Pathol
. 2003 Sep;
56(5):256-62.
PMID: 14514918
Background: X linked hyper-IgM (XHIM) is a primary immunodeficiency caused by mutations in the tumour necrosis factor superfamily 5 gene, TNFSF5, also known as the CD40 ligand (CD40L) gene. Patients...
9.
Nistala K, Gilmour K, Cranston T, Davies E, Goldblatt D, Gaspar H, et al.
Clin Exp Immunol
. 2001 Oct;
126(1):126-30.
PMID: 11678908
Common variable immunodeficiency (CVID) is the most frequently occurring primary immunodeficiency in both children and adults. The molecular basis of CVID has not been defined, and diagnosis involves exclusion of...
10.
Gilmour K, Fujii H, Cranston T, Davies E, Kinnon C, Gaspar H
Blood
. 2001 Jul;
98(3):877-9.
PMID: 11468191
Development of T and natural killer (NK) cells is critically dependent on cytokine signaling, and defects in cytokine receptor complex subunits have been shown to result in severe combined immunodeficiency...