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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1983 1
1984 1
1988 3
1989 1
1990 1
1991 1
1992 3
1993 1
1994 6
1995 6
1996 6
1997 1
1998 3
1999 8
2000 2
2001 5
2002 5
2003 6
2004 6
2005 4
2006 6
2007 10
2008 5
2009 5
2010 9
2011 8
2012 7
2013 9
2014 12
2015 6
2016 8
2017 2
2018 2
2019 3
2020 2
2021 1
2022 2
2023 4
2024 0

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154 results

Results by year

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Page 1
Birt-Hogg-Dubé syndrome: diagnosis and management.
Menko FH, van Steensel MA, Giraud S, Friis-Hansen L, Richard S, Ungari S, Nordenskjöld M, Hansen TV, Solly J, Maher ER; European BHD Consortium. Menko FH, et al. Lancet Oncol. 2009 Dec;10(12):1199-206. doi: 10.1016/S1470-2045(09)70188-3. Lancet Oncol. 2009. PMID: 19959076 Review.
TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes.
Ruijs MW, Verhoef S, Rookus MA, Pruntel R, van der Hout AH, Hogervorst FB, Kluijt I, Sijmons RH, Aalfs CM, Wagner A, Ausems MG, Hoogerbrugge N, van Asperen CJ, Gomez Garcia EB, Meijers-Heijboer H, Ten Kate LP, Menko FH, van 't Veer LJ. Ruijs MW, et al. Among authors: menko fh. J Med Genet. 2010 Jun;47(6):421-8. doi: 10.1136/jmg.2009.073429. J Med Genet. 2010. PMID: 20522432 Free article.
Update of penetrance estimates in Birt-Hogg-Dubé syndrome.
Bruinsma FJ, Dowty JG, Win AK, Goddard LC, Agrawal P, Attina' D, Bissada N, De Luise M, Eisen DB, Furuya M, Gasparre G, Genuardi M, Gerdes AM, Hansen TVO, Houweling AC, Johannesma PC, Lencastre A, Lim D, Lindor NM, Luzzi V, Lynch M, Maffé A, Menko FH, Michels G, Pulido JS, Ryu JH, Sattler EC, Steinlein OK, Tomassetti S, Tucker K, Turchetti D, van de Beek I, van Riel L, van Steensel M, Zenone T, Zompatori M, Walsh J, Bondavalli D, Maher ER, Winship IM; Genetic Susceptibility Working Group I-CONFIRM. Bruinsma FJ, et al. Among authors: menko fh. J Med Genet. 2023 Apr;60(4):317-326. doi: 10.1136/jmg-2022-109104. Epub 2023 Feb 27. J Med Genet. 2023. PMID: 36849229 Review.
European collaboration on genetic tumour risk syndromes.
Vetti HH, Blanco I, Menko FH. Vetti HH, et al. Among authors: menko fh. Eur J Med Genet. 2023 Feb;66(2):104691. doi: 10.1016/j.ejmg.2022.104691. Epub 2022 Dec 26. Eur J Med Genet. 2023. PMID: 36581153 No abstract available.
[Familial ovarian carcinoma].
Verheijen RH, Menko FH, Kenemans P. Verheijen RH, et al. Among authors: menko fh. Ned Tijdschr Geneeskd. 1994 Jan 8;138(2):63-6. Ned Tijdschr Geneeskd. 1994. PMID: 8107904 Review. Dutch. No abstract available.
Constitutional rearrangements of chromosome 22 as a cause of neurofibromatosis 2.
Tsilchorozidou T, Menko FH, Lalloo F, Kidd A, De Silva R, Thomas H, Smith P, Malcolmson A, Dore J, Madan K, Brown A, Yovos JG, Tsaligopoulos M, Vogiatzis N, Baser ME, Wallace AJ, Evans DG. Tsilchorozidou T, et al. Among authors: menko fh. J Med Genet. 2004 Jul;41(7):529-34. doi: 10.1136/jmg.2003.016774. J Med Genet. 2004. PMID: 15235024 Free PMC article. Review. No abstract available.
154 results