van de Kamp JJ - Search Results

1

Identification of a common mutation (R245H) in Sanfilippo A patients from The Netherlands.

Weber B, van de Kamp JJ, Kleijer WJ, Guo XH, Blanch L, van Diggelen OP, Wevers R, Poorthuis BJ, Hopwood JJ. Weber B, et al. Among authors: van de kamp jj. J Inherit Metab Dis. 1998 Jun;21(4):416-22. doi: 10.1023/a:1005362826552. J Inherit Metab Dis. 1998. PMID: 9700599

2

Sanfilippo type B syndrome (mucopolysaccharidosis III B): allelic heterogeneity corresponds to the wide spectrum of clinical phenotypes.

Weber B, Guo XH, Kleijer WJ, van de Kamp JJ, Poorthuis BJ, Hopwood JJ. Weber B, et al. Among authors: van de kamp jj. Eur J Hum Genet. 1999 Jan;7(1):34-44. doi: 10.1038/sj.ejhg.5200242. Eur J Hum Genet. 1999. PMID: 10094189

3

First-trimester diagnosis of mucopolysaccharidosis IIIA (Sanfilippo A disease).

Kleijer WJ, Janse HC, Vosters RP, Niermeijer MF, van de Kamp JJ. Kleijer WJ, et al. Among authors: van de kamp jj. N Engl J Med. 1986 Jan 16;314(3):185-6. doi: 10.1056/NEJM198601163140319. N Engl J Med. 1986. PMID: 3079882 No abstract available.

4

Prenatal monitoring for the Hunter syndrome: the heterozygous female fetus.

Kleijer WJ, Moody PD, Liebaers I, van de Kamp JJ, Niermeijer MF. Kleijer WJ, et al. Among authors: van de kamp jj. Clin Genet. 1979 Feb;15(2):113-7. doi: 10.1111/j.1399-0004.1979.tb01749.x. Clin Genet. 1979. PMID: 153809

5

Genetic heterogeneity and clinical variability in the Sanfilippo syndrome (types A, B, and C).

van de Kamp JJ, Niermeijer MF, von Figura K, Giesberts MA. van de Kamp JJ, et al. Clin Genet. 1981 Aug;20(2):152-60. doi: 10.1111/j.1399-0004.1981.tb01821.x. Clin Genet. 1981. PMID: 6796310

6

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: van de kamp jj, van der does e. Clin Genet. 1993 Feb;43(2):63-8. doi: 10.1111/j.1399-0004.1993.tb04428.x. Clin Genet. 1993. PMID: 8448902

7

Predictive testing for Huntington disease: nonparticipants compared with participants in the Dutch program.

van der Steenstraten IM, Tibben A, Roos RA, van de Kamp JJ, Niermeijer MF. van der Steenstraten IM, et al. Among authors: van de kamp jj. Am J Hum Genet. 1994 Oct;55(4):618-25. Am J Hum Genet. 1994. PMID: 7942839 Free PMC article. Clinical Trial.

8

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: van de kamp jj. Am J Med Genet. 1993 May 1;48(1):10-6. doi: 10.1002/ajmg.1320480105. Am J Med Genet. 1993. PMID: 8357031

9

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: van de kamp jj. Am J Med Genet. 1993 Oct 15;48(3):137-44. doi: 10.1002/ajmg.1320480305. Am J Med Genet. 1993. PMID: 8291567

10

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: van de kamp jj. Am J Med Genet. 1993 Jul 15;48(2):103-11. doi: 10.1002/ajmg.1320480209. Am J Med Genet. 1993. PMID: 8362926

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