Niermeijer MF - Search Results

1

Preparing for presymptomatic DNA testing for early onset Alzheimer's disease/cerebral haemorrhage and hereditary Pick disease.

Tibben A, Stevens M, de Wert GM, Niermeijer MF, van Duijn CM, van Swieten JC. Tibben A, et al. Among authors: niermeijer mf. J Med Genet. 1997 Jan;34(1):63-72. doi: 10.1136/jmg.34.1.63. J Med Genet. 1997. PMID: 9032652 Free PMC article.

2

Presymptomatic DNA testing for Huntington disease: identifying the need for psychological intervention.

Tibben A, Duivenvoorden HJ, Vegter-van der Vlis M, Niermeijer MF, Frets PG, van de Kamp JJ, Roos RA, Rooijmans HG, Verhage F. Tibben A, et al. Among authors: niermeijer mf. Am J Med Genet. 1993 Oct 15;48(3):137-44. doi: 10.1002/ajmg.1320480305. Am J Med Genet. 1993. PMID: 8291567

3

Presymptomatic DNA-testing for Huntington disease: pretest attitudes and expectations of applicants and their partners in the Dutch program.

Tibben A, Frets PG, van de Kamp JJ, Niermeijer MF, Vegter-van der Vlis M, Roos RA, van Ommen GJ, Duivenvoorden HJ, Verhage F. Tibben A, et al. Among authors: niermeijer mf. Am J Med Genet. 1993 May 1;48(1):10-6. doi: 10.1002/ajmg.1320480105. Am J Med Genet. 1993. PMID: 8357031

4

On attitudes and appreciation 6 months after predictive DNA testing for Huntington disease in the Dutch program.

Tibben A, Frets PG, van de Kamp JJ, Niermeijer MF, Vegtervan der Vlis M, Roos RA, Rooymans HG, van Ommen GJ, Verhage F. Tibben A, et al. Among authors: niermeijer mf. Am J Med Genet. 1993 Jul 15;48(2):103-11. doi: 10.1002/ajmg.1320480209. Am J Med Genet. 1993. PMID: 8362926

5

Attitudes of Dutch general practitioners towards presymptomatic DNA-testing for Huntington disease.

Thomassen R, Tibben A, Niermeijer MF, van der Does E, van de Kamp JJ, Verhage F. Thomassen R, et al. Among authors: niermeijer mf. Clin Genet. 1993 Feb;43(2):63-8. doi: 10.1111/j.1399-0004.1993.tb04428.x. Clin Genet. 1993. PMID: 8448902

6

Psychological distress in applicants for predictive DNA testing for autosomal dominant, heritable, late onset disorders. The Rotterdam/Leiden Genetics Workgroup.

DudokdeWit AC, Tibben A, Duivenvoorden HJ, Frets PG, Zoeteweij MW, Losekoot M, van Haeringen A, Niermeijer MF, Passchier J. DudokdeWit AC, et al. Among authors: niermeijer mf. J Med Genet. 1997 May;34(5):382-90. doi: 10.1136/jmg.34.5.382. J Med Genet. 1997. PMID: 9152835 Free PMC article.

7

DNA testing for fragile X syndrome: implications for parents and family.

van Rijn MA, de Vries BB, Tibben A, van den Ouweland AM, Halley DJ, Niermeijer MF. van Rijn MA, et al. Among authors: niermeijer mf. J Med Genet. 1997 Nov;34(11):907-11. doi: 10.1136/jmg.34.11.907. J Med Genet. 1997. PMID: 9391884 Free PMC article.

8

Distress in individuals facing predictive DNA testing for autosomal dominant late-onset disorders: comparing questionnaire results with in-depth interviews. Rotterdam/Leiden Genetics Workgroup.

DudokdeWit AC, Tibben A, Duivenvoorden HJ, Niermeijer MF, Passchier J, Trijsburg RW. DudokdeWit AC, et al. Among authors: niermeijer mf. Am J Med Genet. 1998 Jan 6;75(1):62-74. doi: 10.1002/(sici)1096-8628(19980106)75:1<62::aid-ajmg14>3.0.co;2-q. Am J Med Genet. 1998. PMID: 9450860 Review.

9

Predicting adaptation to presymptomatic DNA testing for late onset disorders: who will experience distress? Rotterdam Leiden Genetics Workgroup.

DudokdeWit AC, Tibben A, Duivenvoorden HJ, Niermeijer MF, Passchier J. DudokdeWit AC, et al. Among authors: niermeijer mf. J Med Genet. 1998 Sep;35(9):745-54. doi: 10.1136/jmg.35.9.745. J Med Genet. 1998. PMID: 9733033 Free PMC article.

10

Dilemmas in counselling females with the fragile X syndrome.

de Vries BB, van den Boer-van den Berg HM, Niermeijer MF, Tibben A. de Vries BB, et al. Among authors: niermeijer mf. J Med Genet. 1999 Feb;36(2):167-70. J Med Genet. 1999. PMID: 10051021 Free PMC article.

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