Cale CM - Search Results

1

Immunological and genetic analysis of 65 patients with a clinical suspicion of X linked hyper-IgM.

Gilmour KC, Walshe D, Heath S, Monaghan G, Loughlin S, Lester T, Norbury G, Cale CM. Gilmour KC, et al. Among authors: cale cm. Mol Pathol. 2003 Oct;56(5):256-62. doi: 10.1136/mp.56.5.256. Mol Pathol. 2003. PMID: 14514918 Free PMC article.

2

The many faces of Artemis-deficient combined immunodeficiency - Two patients with DCLRE1C mutations and a systematic literature review of genotype-phenotype correlation.

Lee PP, Woodbine L, Gilmour KC, Bibi S, Cale CM, Amrolia PJ, Veys PA, Davies EG, Jeggo PA, Jones A. Lee PP, et al. Among authors: cale cm. Clin Immunol. 2013 Dec;149(3):464-74. doi: 10.1016/j.clim.2013.08.006. Epub 2013 Aug 27. Clin Immunol. 2013. PMID: 24230999 Review.

3

Improved outcome for children with disseminated adenoviral infection following allogeneic stem cell transplantation.

Kampmann B, Cubitt D, Walls T, Naik P, Depala M, Samarasinghe S, Robson D, Hassan A, Rao K, Gaspar H, Davies G, Jones A, Cale C, Gilmour K, Real M, Foo M, Bennett-Rees N, Hewitt A, Amrolia P, Veys P. Kampmann B, et al. Br J Haematol. 2005 Aug;130(4):595-603. doi: 10.1111/j.1365-2141.2005.05649.x. Br J Haematol. 2005. PMID: 16098075 Free article.

4

Signal transducer and activator of transcription 5 tyrosine phosphorylation for the diagnosis and monitoring of patients with severe combined immunodeficiency.

Walshe D, Gaspar HB, Thrasher AJ, Cale CM, Gilmour KC. Walshe D, et al. Among authors: cale cm. J Allergy Clin Immunol. 2009 Feb;123(2):505-8. doi: 10.1016/j.jaci.2008.11.041. J Allergy Clin Immunol. 2009. PMID: 19203666 No abstract available.

5

Signal transducer and activator of transcription 2 deficiency is a novel disorder of mitochondrial fission.

Shahni R, Cale CM, Anderson G, Osellame LD, Hambleton S, Jacques TS, Wedatilake Y, Taanman JW, Chan E, Qasim W, Plagnol V, Chalasani A, Duchen MR, Gilmour KC, Rahman S. Shahni R, et al. Among authors: cale cm. Brain. 2015 Oct;138(Pt 10):2834-46. doi: 10.1093/brain/awv182. Epub 2015 Jun 29. Brain. 2015. PMID: 26122121 Free PMC article.

6

Impact of viral reactivations in the era of pre-emptive antiviral drug therapy following allogeneic haematopoietic SCT in paediatric recipients.

Hiwarkar P, Gaspar HB, Gilmour K, Jagani M, Chiesa R, Bennett-Rees N, Breuer J, Rao K, Cale C, Goulden N, Davies G, Amrolia P, Veys P, Qasim W. Hiwarkar P, et al. Bone Marrow Transplant. 2013 Jun;48(6):803-8. doi: 10.1038/bmt.2012.221. Epub 2012 Nov 26. Bone Marrow Transplant. 2013. PMID: 23178547

7

Immunodeficiency and severe susceptibility to bacterial infection associated with a loss-of-function homozygous mutation of MKL1.

Record J, Malinova D, Zenner HL, Plagnol V, Nowak K, Syed F, Bouma G, Curtis J, Gilmour K, Cale C, Hackett S, Charras G, Moulding D, Nejentsev S, Thrasher AJ, Burns SO. Record J, et al. Blood. 2015 Sep 24;126(13):1527-35. doi: 10.1182/blood-2014-12-611012. Epub 2015 Jul 29. Blood. 2015. PMID: 26224645 Free PMC article.

8

Omission of in vivo T-cell depletion promotes rapid expansion of naïve CD4+ cord blood lymphocytes and restores adaptive immunity within 2 months after unrelated cord blood transplant.

Chiesa R, Gilmour K, Qasim W, Adams S, Worth AJ, Zhan H, Montiel-Equihua CA, Derniame S, Cale C, Rao K, Hiwarkar P, Hough R, Saudemont A, Fahrenkrog CS, Goulden N, Amrolia PJ, Veys P. Chiesa R, et al. Br J Haematol. 2012 Mar;156(5):656-66. doi: 10.1111/j.1365-2141.2011.08994.x. Epub 2012 Jan 9. Br J Haematol. 2012. PMID: 22224700 Free article.

9

A novel assay for investigation of suspected familial haemophagocytic lymphohistiocytosis.

Wheeler RD, Cale CM, Cetica V, Aricò M, Gilmour KC. Wheeler RD, et al. Among authors: cale cm. Br J Haematol. 2010 Sep;150(6):727-30. doi: 10.1111/j.1365-2141.2010.08289.x. Br J Haematol. 2010. PMID: 20618327 Free article. No abstract available.

10

Immunological abnormalities in CHARGE syndrome.

Writzl K, Cale CM, Pierce CM, Wilson LC, Hennekam RC. Writzl K, et al. Among authors: cale cm. Eur J Med Genet. 2007 Sep-Oct;50(5):338-45. doi: 10.1016/j.ejmg.2007.05.002. Epub 2007 May 27. Eur J Med Genet. 2007. PMID: 17684005 Review.

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