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A multicenter, randomized, dose-finding study of mechanochemical ablation using ClariVein and liquid polidocanol for great saphenous vein incompetence.
Lam YL, Alozai T, Schreve MA, de Smet AAEA, Vahl AC, Nagtzaam I, Lawson JA, Nieman FHM, Wittens CHA. Lam YL, et al. Among authors: nagtzaam i. J Vasc Surg Venous Lymphat Disord. 2022 Jul;10(4):856-864.e2. doi: 10.1016/j.jvsv.2021.10.016. Epub 2021 Nov 12. J Vasc Surg Venous Lymphat Disord. 2022. PMID: 34781008 Clinical Trial.
Improving the diagnostic yield for filaggrin: Concealed mutations in the Dutch population.
van Leersum FS, Nagtzaam IF, van Oosterhoud CN, Ghesquiere SAI, Brandts RRHFJ, Gostyński A, Steijlen PM, van Geel M. van Leersum FS, et al. Among authors: nagtzaam if. J Allergy Clin Immunol. 2020 Jun;145(6):1704-1706.e2. doi: 10.1016/j.jaci.2020.01.033. Epub 2020 Feb 1. J Allergy Clin Immunol. 2020. PMID: 32018027 No abstract available.
Chanarin-Dorfman syndrome caused by a novel splice site mutation in ABHD5.
Badeloe S, van Geel M, Nagtzaam I, Rubio-Gozalbo ME, Oei RL, Steijlen PM, van Steensel MA. Badeloe S, et al. Among authors: nagtzaam i. Br J Dermatol. 2008 Jun;158(6):1378-80. doi: 10.1111/j.1365-2133.2008.08544.x. Epub 2008 Apr 10. Br J Dermatol. 2008. PMID: 18410411 No abstract available.
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.
Sandilands A, Terron-Kwiatkowski A, Hull PR, O'Regan GM, Clayton TH, Watson RM, Carrick T, Evans AT, Liao H, Zhao Y, Campbell LE, Schmuth M, Gruber R, Janecke AR, Elias PM, van Steensel MA, Nagtzaam I, van Geel M, Steijlen PM, Munro CS, Bradley DG, Palmer CN, Smith FJ, McLean WH, Irvine AD. Sandilands A, et al. Among authors: nagtzaam i. Nat Genet. 2007 May;39(5):650-4. doi: 10.1038/ng2020. Epub 2007 Apr 8. Nat Genet. 2007. PMID: 17417636
A case of Lelis syndrome with hystrix-like ichthyosis.
van Steensel MA, Winnepenninckx V, Nagtzaam IF, Janssens R, De Vos R, Steijlen PM. van Steensel MA, et al. Among authors: nagtzaam if. Am J Med Genet A. 2008 Aug 15;146A(16):2155-8. doi: 10.1002/ajmg.a.32409. Am J Med Genet A. 2008. PMID: 18627052 No abstract available.
15 results