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Kaposiform hemangioendothelioma and tufted angioma - (epi)genetic analysis including genome-wide methylation profiling.
Ten Broek RW, Koelsche C, Eijkelenboom A, Mentzel T, Creytens D, Vokuhl C, van Gorp JM, Versleijen-Jonkers YM, van der Vleuten CJ, Kemmeren P, van de Geer E, von Deimling A, Flucke U. Ten Broek RW, et al. Among authors: eijkelenboom a. Ann Diagn Pathol. 2020 Feb;44:151434. doi: 10.1016/j.anndiagpath.2019.151434. Epub 2019 Dec 10. Ann Diagn Pathol. 2020. PMID: 31887709 Free article.
Mutational analysis using Sanger and next generation sequencing in sporadic spindle cell hemangiomas: A study of 19 cases.
Ten Broek RW, Bekers EM, de Leng WWJ, Strengman E, Tops BBJ, Kutzner H, Leeuwis JW, van Gorp JM, Creytens DH, Mentzel T, van Diest PJ, Eijkelenboom A, Flucke U. Ten Broek RW, et al. Among authors: eijkelenboom a. Genes Chromosomes Cancer. 2017 Dec;56(12):855-860. doi: 10.1002/gcc.22501. Epub 2017 Sep 23. Genes Chromosomes Cancer. 2017. PMID: 28845532
Myositis ossificans - Another condition with USP6 rearrangement, providing evidence of a relationship with nodular fasciitis and aneurysmal bone cyst.
Bekers EM, Eijkelenboom A, Grünberg K, Roverts RC, de Rooy JWJ, van der Geest ICM, van Gorp JM, Creytens D, Flucke U. Bekers EM, et al. Among authors: eijkelenboom a. Ann Diagn Pathol. 2018 Jun;34:56-59. doi: 10.1016/j.anndiagpath.2018.01.006. Epub 2018 Jan 12. Ann Diagn Pathol. 2018. PMID: 29661729 Free article.
Multifocal occurrence of extra-abdominal desmoid type fibromatosis - A rare manifestation. A clinicopathological study of 6 sporadic cases and 1 hereditary case.
Bekers EM, van Broekhoven DLM, van Dalen T, Bonenkamp JJ, van der Geest ICM, de Rooy JWJ, van Gorp JM, Creytens DH, de Leng WWJ, Scheijen B, Eijkelenboom A, Flucke U. Bekers EM, et al. Among authors: eijkelenboom a. Ann Diagn Pathol. 2018 Aug;35:38-41. doi: 10.1016/j.anndiagpath.2018.04.001. Epub 2018 Apr 21. Ann Diagn Pathol. 2018. PMID: 29705714 Free article.
Comprehensive molecular and clinicopathological analysis of vascular malformations: A study of 319 cases.
Ten Broek RW, Eijkelenboom A, van der Vleuten CJM, Kamping EJ, Kets M, Verhoeven BH, Grünberg K, Schultze Kool LJ, Tops BBJ, Ligtenberg MJL, Flucke U. Ten Broek RW, et al. Among authors: eijkelenboom a. Genes Chromosomes Cancer. 2019 Aug;58(8):541-550. doi: 10.1002/gcc.22739. Epub 2019 Feb 11. Genes Chromosomes Cancer. 2019. PMID: 30677207 Free PMC article.
GNA11-mutated Sturge-Weber syndrome has distinct neurological and dermatological features.
Dompmartin A, van der Vleuten CJM, Dekeuleneer V, Duprez T, Revencu N, Désir J, Te Loo DMWM, Flucke U, Eijkelenboom A, Schultze Kool L, Vikkula M, Boon L. Dompmartin A, et al. Among authors: eijkelenboom a. Eur J Neurol. 2022 Oct;29(10):3061-3070. doi: 10.1111/ene.15452. Epub 2022 Jul 13. Eur J Neurol. 2022. PMID: 35715928
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