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173 results

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Page 1
Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out.
Neumann HP, Erlic Z, Boedeker CC, Rybicki LA, Robledo M, Hermsen M, Schiavi F, Falcioni M, Kwok P, Bauters C, Lampe K, Fischer M, Edelman E, Benn DE, Robinson BG, Wiegand S, Rasp G, Stuck BA, Hoffmann MM, Sullivan M, Sevilla MA, Weiss MM, Peczkowska M, Kubaszek A, Pigny P, Ward RL, Learoyd D, Croxson M, Zabolotny D, Yaremchuk S, Draf W, Muresan M, Lorenz RR, Knipping S, Strohm M, Dyckhoff G, Matthias C, Reisch N, Preuss SF, Esser D, Walter MA, Kaftan H, Stöver T, Fottner C, Gorgulla H, Malekpour M, Zarandy MM, Schipper J, Brase C, Glien A, Kühnemund M, Koscielny S, Schwerdtfeger P, Välimäki M, Szyfter W, Finckh U, Zerres K, Cascon A, Opocher G, Ridder GJ, Januszewicz A, Suarez C, Eng C. Neumann HP, et al. Among authors: weiss mm. Cancer Res. 2009 Apr 15;69(8):3650-6. doi: 10.1158/0008-5472.CAN-08-4057. Epub 2009 Apr 7. Cancer Res. 2009. PMID: 19351833
Chromosomal changes in sporadic and familial head and neck paragangliomas.
Sevilla MA, Hermsen MA, Weiss MM, Grimbergen A, Balbín M, Llorente JL, Rodrigo JP, Suárez C. Sevilla MA, et al. Among authors: weiss mm. Otolaryngol Head Neck Surg. 2009 May;140(5):724-9. doi: 10.1016/j.otohns.2009.01.004. Epub 2009 Mar 9. Otolaryngol Head Neck Surg. 2009. PMID: 19393419
Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma.
Bayley JP, van Minderhout I, Weiss MM, Jansen JC, Oomen PH, Menko FH, Pasini B, Ferrando B, Wong N, Alpert LC, Williams R, Blair E, Devilee P, Taschner PE. Bayley JP, et al. Among authors: weiss mm. BMC Med Genet. 2006 Jan 11;7:1. doi: 10.1186/1471-2350-7-1. BMC Med Genet. 2006. PMID: 16405730 Free PMC article.
The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patients.
Bayley JP, Grimbergen AE, van Bunderen PA, van der Wielen M, Kunst HP, Lenders JW, Jansen JC, Dullaart RP, Devilee P, Corssmit EP, Vriends AH, Losekoot M, Weiss MM. Bayley JP, et al. Among authors: weiss mm. BMC Med Genet. 2009 Apr 15;10:34. doi: 10.1186/1471-2350-10-34. BMC Med Genet. 2009. PMID: 19368708 Free PMC article.
Low penetrance of a SDHB mutation in a large Dutch paraganglioma family.
Hes FJ, Weiss MM, Woortman SA, de Miranda NF, van Bunderen PA, Bonsing BA, Stokkel MP, Morreau H, Romijn JA, Jansen JC, Vriends AH, Bayley JP, Corssmit EP. Hes FJ, et al. Among authors: weiss mm. BMC Med Genet. 2010 Jun 11;11:92. doi: 10.1186/1471-2350-11-92. BMC Med Genet. 2010. PMID: 20540712 Free PMC article.
The natural history of a combined defect in MSH6 and MUTYH in a HNPCC family.
van Puijenbroek M, Nielsen M, Reinards TH, Weiss MM, Wagner A, Hendriks YM, Vasen HF, Tops CM, Wijnen J, van Wezel T, Hes FJ, Morreau H. van Puijenbroek M, et al. Among authors: weiss mm. Fam Cancer. 2007;6(1):43-51. doi: 10.1007/s10689-006-9103-y. Fam Cancer. 2007. PMID: 17039270
173 results