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Is tocilizumab a potential therapeutic option for refractory unicentric Castleman disease?
Hematol Oncol. 2018 Feb;36(1):320-323. doi: 10.1002/hon.2420. Epub 2017 Apr 11.
Hematol Oncol. 2018.
PMID: 28401573
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis.
Wen Y, Liu Y, Xu Y, Zhao Y, Hua R, Wang K, Sun M, Li Y, Yang S, Zhang XJ, Kruse R, Cichon S, Betz RC, Nöthen MM, van Steensel MA, van Geel M, Steijlen PM, Hohl D, Huber M, Dunnill GS, Kennedy C, Messenger A, Munro CS, Terrinoni A, Hovnanian A, Bodemer C, de Prost Y, Paller AS, Irvine AD, Sinclair R, Green J, Shang D, Liu Q, Luo Y, Jiang L, Chen HD, Lo WH, McLean WH, He CD, Zhang X.
Wen Y, et al. Among authors: dunnill gs.
Nat Genet. 2009 Feb;41(2):228-33. doi: 10.1038/ng.276. Epub 2009 Jan 4.
Nat Genet. 2009.
PMID: 19122663
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Photoallergic reaction to systemic quinine sulphate.
Hickey JR, Dunnill GS, Sansom JE.
Hickey JR, et al. Among authors: dunnill gs.
Contact Dermatitis. 2007 Dec;57(6):384-6. doi: 10.1111/j.0105-1873.2006.00808.x.
Contact Dermatitis. 2007.
PMID: 17988291
No abstract available.
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A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: prenatal exclusion in a fetus at risk.
McGrath JA, Kivirikko S, Ciatti S, Moss C, Dunnill GS, Eady RA, Rodeck CH, Christiano AM, Uitto J.
McGrath JA, et al. Among authors: dunnill gs.
Genomics. 1995 Sep 1;29(1):282-4. doi: 10.1006/geno.1995.1246.
Genomics. 1995.
PMID: 8530087
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Capillary rarefaction in the forearm skin in essential hypertension.
Prasad A, Dunnill GS, Mortimer PS, MacGregor GA.
Prasad A, et al. Among authors: dunnill gs.
J Hypertens. 1995 Feb;13(2):265-8.
J Hypertens. 1995.
PMID: 7615958
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