van Haeringen A - Search Results

1

Familial adenomatous polyposis and its clinical surveillance.

Vasen HF, Griffioen G, Tops CM, van Haeringen A, Nagengast FM, van Leeuwen-Cornelisse IS, Khan PM, van Slooten EA. Vasen HF, et al. Among authors: van haeringen a, van slooten ea, van leeuwen cornelisse is. Neth J Med. 1993 Apr;42(3-4):105-8. Neth J Med. 1993. PMID: 8391128 Review. No abstract available.

2

The familial dysplastic nevus syndrome. Natural history and the impact of screening on prognosis. A study of nine families in the Netherlands.

Vasen HF, Bergman W, van Haeringen A, Scheffer E, van Slooten EA. Vasen HF, et al. Among authors: van haeringen a, van slooten ea. Eur J Cancer Clin Oncol. 1989 Feb;25(2):337-41. doi: 10.1016/0277-5379(89)90027-8. Eur J Cancer Clin Oncol. 1989. PMID: 2702987

3

Further evidence for localization of the gene of erythrokeratodermia variabilis.

van der Schroeff JG, van Leeuwen-Cornelisse I, van Haeringen A, Went LN. van der Schroeff JG, et al. Among authors: van leeuwen cornelisse i, van haeringen a. Hum Genet. 1988 Sep;80(1):97-8. doi: 10.1007/BF00451466. Hum Genet. 1988. PMID: 3417312

4

Exclusion of the dysplastic nevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in Dutch families.

van Haeringen A, Bergman W, Nelen MR, van der Kooij-Meijs E, Hendrikse I, Wijnen JT, Khan PM, Klasen EC, Frants RR. van Haeringen A, et al. Among authors: van der kooij meijs e. Genomics. 1989 Jul;5(1):61-4. doi: 10.1016/0888-7543(89)90086-4. Genomics. 1989. PMID: 2504660

5

[Familial dysplastic nevus syndrome in the Netherlands; various clinical and genetic aspects].

Bergman W, Palan A, van Haeringen A, van Leeuwen-Cornelisse I, Went LN. Bergman W, et al. Among authors: van leeuwen cornelisse i, van haeringen a. Ned Tijdschr Geneeskd. 1987 Jun 6;131(23):994-6. Ned Tijdschr Geneeskd. 1987. PMID: 3600841 Dutch. No abstract available.

6

Genetic testing in familial melanoma: uptake and implications.

de Snoo FA, Riedijk SR, van Mil AM, Bergman W, ter Huurne JA, Timman R, Bertina W, Gruis NA, Vasen HF, van Haeringen A, Breuning MH, Tibben A. de Snoo FA, et al. Among authors: van mil am, van haeringen a. Psychooncology. 2008 Aug;17(8):790-6. doi: 10.1002/pon.1377. Psychooncology. 2008. PMID: 18613292

7

Autosomal dominant epidermolysis bullosa dystrophica: are the Cockayne-Touraine, the Pasini and the Bart-types different expressions of the same mutant gene?

Bouwes Bavinck JN, van Haeringen A, Ruiter D, van der Schroeff JG. Bouwes Bavinck JN, et al. Among authors: van haeringen a, van der schroeff jg. Clin Genet. 1987 Jun;31(6):416-24. doi: 10.1111/j.1399-0004.1987.tb02836.x. Clin Genet. 1987. PMID: 3621647

8

Acromesomelic dysplasia Maroteaux type maps to human chromosome 9.

Kant SG, Polinkovsky A, Mundlos S, Zabel B, Thomeer RT, Zonderland HM, Shih L, van Haeringen A, Warman ML. Kant SG, et al. Among authors: van haeringen a. Am J Hum Genet. 1998 Jul;63(1):155-62. doi: 10.1086/301917. Am J Hum Genet. 1998. PMID: 9634515 Free PMC article.

9

Hereditary melanoma and predictive genetic testing: why not?

Riedijk SR, de Snoo FA, van Dijk S, Bergman W, van Haeringen A, Silberg S, van Elderen TM, Tibben A. Riedijk SR, et al. Among authors: van haeringen a, van dijk s, van elderen tm. Psychooncology. 2005 Sep;14(9):738-45. doi: 10.1002/pon.901. Psychooncology. 2005. PMID: 15744786

10

Multiple agminate Spitz naevi.

Hulshof MM, van Haeringen A, Gruis NA, Snels DC, Bergman W. Hulshof MM, et al. Among authors: van haeringen a. Melanoma Res. 1998 Apr;8(2):156-60. doi: 10.1097/00008390-199804000-00009. Melanoma Res. 1998. PMID: 9610869

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