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Page 1
Multiple familial trichoepithelioma and familial cylindroma: one cause!
Oranje AP, Halley D, den Hollander JC, Teepe RG, van de Graaf R, van den Ouweland A, Wagner A. Oranje AP, et al. J Eur Acad Dermatol Venereol. 2008 Nov;22(11):1395-6. doi: 10.1111/j.1468-3083.2008.02648.x. Epub 2008 Mar 18. J Eur Acad Dermatol Venereol. 2008. PMID: 18355210 No abstract available.
Rhabdoid tumor mimicking hemangioma.
Assen YJ, Madern GC, de Laat PC, den Hollander JC, Oranje AP. Assen YJ, et al. Among authors: oranje ap. Pediatr Dermatol. 2011 May-Jun;28(3):295-8. doi: 10.1111/j.1525-1470.2010.01248.x. Epub 2010 Sep 1. Pediatr Dermatol. 2011. PMID: 20825569
Mast cell distribution in normal adult skin.
Janssens AS, Heide R, den Hollander JC, Mulder PG, Tank B, Oranje AP. Janssens AS, et al. Among authors: oranje ap. J Clin Pathol. 2005 Mar;58(3):285-9. doi: 10.1136/jcp.2004.017210. J Clin Pathol. 2005. PMID: 15735162 Free PMC article.
Support for the hypoxia theory in the pathogenesis of infantile haemangioma.
Janmohamed SR, Brinkhuizen T, den Hollander JC, Madern GC, de Laat PC, van Steensel MA, Oranje AP. Janmohamed SR, et al. Among authors: oranje ap. Clin Exp Dermatol. 2015 Jun;40(4):431-7. doi: 10.1111/ced.12557. Epub 2014 Dec 16. Clin Exp Dermatol. 2015. PMID: 25511669
Mastocytosis in children: a protocol for management.
Heide R, Beishuizen A, De Groot H, Den Hollander JC, Van Doormaal JJ, De Monchy JG, Pasmans SG, Van Gysel D, Oranje AP; Dutch National Mastocytosis Work Group. Heide R, et al. Among authors: oranje ap. Pediatr Dermatol. 2008 Jul-Aug;25(4):493-500. doi: 10.1111/j.1525-1470.2008.00738.x. Pediatr Dermatol. 2008. PMID: 18789103
A prospective 10 year follow up study of patients with neurofibromatosis type 1.
Cnossen MH, de Goede-Bolder A, van den Broek KM, Waasdorp CM, Oranje AP, Stroink H, Simonsz HJ, van den Ouweland AM, Halley DJ, Niermeijer MF. Cnossen MH, et al. Among authors: oranje ap. Arch Dis Child. 1998 May;78(5):408-12. doi: 10.1136/adc.78.5.408. Arch Dis Child. 1998. PMID: 9659085 Free PMC article.
Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC) patients. Mutations in brief no. 119. Online.
Wang Q, Verhoef S, Tempelaars AM, Bakker PL, Vrtel R, Hesseling-Janssen AL, Nellist M, Oranje AP, Stroink H, Lindhout D, Halley DJ, van den Ouweland AM. Wang Q, et al. Among authors: oranje ap. Hum Mutat. 1998;11(4):331-2. doi: 10.1002/(SICI)1098-1004(1998)11:4<331::AID-HUMU12>3.0.CO;2-3. Hum Mutat. 1998. PMID: 10215407
245 results