Bergman W - Search Results

1

Promoter hypermethylation: a common cause of reduced p16(INK4a) expression in uveal melanoma.

van der Velden PA, Metzelaar-Blok JA, Bergman W, Monique H, Hurks H, Frants RR, Gruis NA, Jager MJ. van der Velden PA, et al. Among authors: bergman w. Cancer Res. 2001 Jul 1;61(13):5303-6. Cancer Res. 2001. PMID: 11431374

2

Homozygous germline mutation of CDKN2A/p16 and glucose-6-phosphate dehydrogenase deficiency in a multiple melanoma case.

Pavel S, Smit NP, van der Meulen H, Kolb RM, de Groot AJ, van der Velden PA, Gruis NA, Bergman W. Pavel S, et al. Among authors: bergman w. Melanoma Res. 2003 Apr;13(2):171-8. doi: 10.1097/00008390-200304000-00010. Melanoma Res. 2003. PMID: 12690301

3

Familial melanoma: a complex disorder leading to controversy on DNA testing.

de Snoo FA, Bergman W, Gruis NA. de Snoo FA, et al. Among authors: bergman w. Fam Cancer. 2003;2(2):109-16. doi: 10.1023/a:1025758527675. Fam Cancer. 2003. PMID: 14574160 Review.

4

Increased risk of cancer other than melanoma in CDKN2A founder mutation (p16-Leiden)-positive melanoma families.

de Snoo FA, Bishop DT, Bergman W, van Leeuwen I, van der Drift C, van Nieuwpoort FA, Out-Luiting CJ, Vasen HF, ter Huurne JA, Frants RR, Willemze R, Breuning MH, Gruis NA. de Snoo FA, et al. Among authors: bergman w. Clin Cancer Res. 2008 Nov 1;14(21):7151-7. doi: 10.1158/1078-0432.CCR-08-0403. Clin Cancer Res. 2008. PMID: 18981015

5

CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families.

Gruis NA, Sandkuijl LA, van der Velden PA, Bergman W, Frants RR. Gruis NA, et al. Among authors: bergman w. Melanoma Res. 1995 Jun;5(3):169-77. doi: 10.1097/00008390-199506000-00005. Melanoma Res. 1995. PMID: 7640518

6

Genetics of familial atypical multiple mole-melanoma (FAMMM) syndrome in The Netherlands: how far have we come?

Gruis NA, Van der Velden PA, Bergman W, Frants RR. Gruis NA, et al. Among authors: bergman w. Bull Cancer. 1998 Jul;85(7):627-30. Bull Cancer. 1998. PMID: 9752270 Free article.

7

A locus linked to p16 modifies melanoma risk in Dutch familial atypical multiple mole melanoma (FAMMM) syndrome families.

van der Velden PA, Sandkuijl LA, Bergman W, Hille ET, Frants RR, Gruis NA. van der Velden PA, et al. Among authors: bergman w. Genome Res. 1999 Jun;9(6):575-80. Genome Res. 1999. PMID: 10400925 Free PMC article.

8

Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden).

Vasen HF, Gruis NA, Frants RR, van Der Velden PA, Hille ET, Bergman W. Vasen HF, et al. Among authors: bergman w. Int J Cancer. 2000 Sep 15;87(6):809-11. Int J Cancer. 2000. PMID: 10956390

9

[From gene to disease; from p16 to melanoma].

Gruis NA, Bergman W. Gruis NA, et al. Among authors: bergman w. Ned Tijdschr Geneeskd. 2000 Oct 28;144(44):2100-2. Ned Tijdschr Geneeskd. 2000. PMID: 11103670 Review. Dutch.

10

Pancreatic carcinoma in carriers of a specific 19 base pair deletion of CDKN2A/p16 (p16-leiden).

de vos tot Nederveen Cappel WH, Offerhaus GJ, van Puijenbroek M, Caspers E, Gruis NA, De Snoo FA, Lamers CB, Griffioen G, Bergman W, Vasen HF, Morreau H. de vos tot Nederveen Cappel WH, et al. Among authors: bergman w. Clin Cancer Res. 2003 Sep 1;9(10 Pt 1):3598-605. Clin Cancer Res. 2003. PMID: 14506146

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