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Ectodermal dysplasia with immunodeficiency caused by a branch-point mutation in IKBKG/NEMO.
Jørgensen SE, Bøttger P, Kofod-Olsen E, Holm M, Mørk N, Ørntoft TF, Sørensen UBS, Bernth-Jensen JM, Herlin T, Veirum J, Larsen CS, Østergaard L, Hartmann R, Christiansen M, Mogensen TH. Jørgensen SE, et al. Among authors: herlin t. J Allergy Clin Immunol. 2016 Dec;138(6):1706-1709.e4. doi: 10.1016/j.jaci.2016.05.030. Epub 2016 Jun 29. J Allergy Clin Immunol. 2016. PMID: 27477329 No abstract available.
[Hereditary periodical fever syndromes].
Herlin T, Sørensen N, Veirum J. Herlin T, et al. Ugeskr Laeger. 2011 Mar 28;173(13):968-73. Ugeskr Laeger. 2011. PMID: 21453638 Review. Danish.
Idiopathic hypereosinophilic syndrome: A rare diagnosis in children.
Pallesen KAU, Herlin T, Holm M, Høst C, Christiansen M, Ramsing M, Rasmussen MK, Sommerlund M. Pallesen KAU, et al. Among authors: herlin t. Clin Case Rep. 2020 Sep 14;8(10):2013-2016. doi: 10.1002/ccr3.3165. eCollection 2020 Oct. Clin Case Rep. 2020. PMID: 33088541 Free PMC article.
258 results