Gilmour KC - Search Results

1

Autosomal Dominant STAT6 Gain of Function Causes Severe Atopy Associated with Lymphoma.

Minskaia E, Maimaris J, Jenkins P, Albuquerque AS, Hong Y, Eleftheriou D, Gilmour KC, Grace R, Moreira F, Grimbacher B; NIHR Bioresource-Rare Diseases Consortium; Morris EC, Burns SO. Minskaia E, et al. Among authors: gilmour kc. J Clin Immunol. 2023 Oct;43(7):1611-1622. doi: 10.1007/s10875-023-01530-7. Epub 2023 Jun 14. J Clin Immunol. 2023. PMID: 37316763 Free PMC article.

2

Diagnosis of X-linked lymphoproliferative disease by analysis of SLAM-associated protein expression.

Gilmour KC, Cranston T, Jones A, Davies EG, Goldblatt D, Thrasher A, Kinnon C, Nichols KE, Gaspar HB. Gilmour KC, et al. Eur J Immunol. 2000 Jun;30(6):1691-7. doi: 10.1002/1521-4141(200006)30:6<1691::AID-IMMU1691>3.0.CO;2-K. Eur J Immunol. 2000. PMID: 10898506 Free article.

3

Protein assays for diagnosis of Wiskott-Aldrich syndrome and X-linked thrombocytopenia.

Qasim W, Gilmour KC, Heath S, Ashton E, Cranston T, Thomas A, Finn A, Davies EG, Thrasher AJ, Kinnon C, Jones A, Gaspar HB. Qasim W, et al. Among authors: gilmour kc. Br J Haematol. 2001 Jun;113(4):861-5. doi: 10.1046/j.1365-2141.2001.02832.x. Br J Haematol. 2001. PMID: 11442475 Free article.

4

Development of anti-PAX3 immune responses; a target for cancer immunotherapy.

Himoudi N, Nabarro S, Yan M, Gilmour K, Thrasher AJ, Anderson J. Himoudi N, et al. Cancer Immunol Immunother. 2007 Sep;56(9):1381-95. doi: 10.1007/s00262-007-0294-3. Epub 2007 Feb 23. Cancer Immunol Immunother. 2007. PMID: 17318653 Free PMC article.

5

Cerebral toxoplasmosis in a middle-aged man as first presentation of primary immunodeficiency due to a hypomorphic mutation in the CD40 ligand gene.

Yong PF, Post FA, Gilmour KC, Grosse-Kreul D, King A, Easterbrook P, Ibrahim MA. Yong PF, et al. Among authors: gilmour kc. J Clin Pathol. 2008 Nov;61(11):1220-2. doi: 10.1136/jcp.2008.058362. J Clin Pathol. 2008. PMID: 18955577

6

Familial haemophagocytic lymphohistiocytosis: advances in the genetic basis, diagnosis and management.

Gholam C, Grigoriadou S, Gilmour KC, Gaspar HB. Gholam C, et al. Among authors: gilmour kc. Clin Exp Immunol. 2011 Mar;163(3):271-83. doi: 10.1111/j.1365-2249.2010.04302.x. Clin Exp Immunol. 2011. PMID: 21303357 Free PMC article. Review.

7

Phenotypic heterogeneity in a family with a CD40 ligand intracellular domain mutation.

Kiani-Alikhan S, Yong PF, Gilmour KC, Grosse-Kreul D, Davies EG, Ibrahim MA. Kiani-Alikhan S, et al. Among authors: gilmour kc. J Clin Immunol. 2012 Feb;32(1):70-7. doi: 10.1007/s10875-011-9607-6. Epub 2011 Oct 19. J Clin Immunol. 2012. PMID: 22009004

8

Production and first-in-man use of T cells engineered to express a HSVTK-CD34 sort-suicide gene.

Zhan H, Gilmour K, Chan L, Farzaneh F, McNicol AM, Xu JH, Adams S, Fehse B, Veys P, Thrasher A, Gaspar H, Qasim W. Zhan H, et al. PLoS One. 2013 Oct 21;8(10):e77106. doi: 10.1371/journal.pone.0077106. eCollection 2013. PLoS One. 2013. PMID: 24204746 Free PMC article. Clinical Trial.

9

Patients with T⁺/low NK⁺ IL-2 receptor γ chain deficiency have differentially-impaired cytokine signaling resulting in severe combined immunodeficiency.

Fuchs S, Rensing-Ehl A, Erlacher M, Vraetz T, Hartjes L, Janda A, Rizzi M, Lorenz MR, Gilmour K, de Saint-Basile G, Roifman CM, Cheuk S, Gennery A, Thrasher AJ, Fuchs I, Schwarz K, Speckmann C, Ehl S. Fuchs S, et al. Eur J Immunol. 2014 Oct;44(10):3129-40. doi: 10.1002/eji.201444689. Epub 2014 Aug 28. Eur J Immunol. 2014. PMID: 25042067 Free article.

10

Atypical severe combined immunodeficiency caused by a novel homozygous mutation in Rag1 gene in a girl who presented with pyoderma gangrenosum: a case report and literature review.

Patiroglu T, Akar HH, Gilmour K, Ozdemir MA, Bibi S, Henriquez F, Burns SO, Unal E. Patiroglu T, et al. J Clin Immunol. 2014 Oct;34(7):792-5. doi: 10.1007/s10875-014-0077-5. Epub 2014 Aug 8. J Clin Immunol. 2014. PMID: 25104208 Review.

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