van Kempen C[au] - Search Results

Year	Number of Results
1967	2
1968	1
1977	1
1996	1
2012	2
2017	3
2022	1
2024	0

1

A retrospective cohort study exploring the association between different mitochondrial diseases and hearing loss.

van Kempen CMA, Beynon AJ, Smits JJ, Janssen MCH. van Kempen CMA, et al. Mol Genet Metab. 2022 Apr;135(4):333-341. doi: 10.1016/j.ymgme.2022.02.003. Epub 2022 Feb 15. Mol Genet Metab. 2022. PMID: 35190254 Free article.

2

[Caries in deprived areas 1. Adults].

Verrips GH, Vermaire JH, van Houtem CM, van Kempen CP, Schuller AA. Verrips GH, et al. Among authors: van kempen cp. Ned Tijdschr Tandheelkd. 2017 Mar;124(3):143-147. doi: 10.5177/ntvt.2017.03.16187. Ned Tijdschr Tandheelkd. 2017. PMID: 28272586 Dutch.

3

[Caries in deprived areas 2. Youngsters].

Verrips GHW, Vermaire JH, van Houtem CMHH, van Kempen CPF, Schuller AA. Verrips GHW, et al. Among authors: van kempen cpf. Ned Tijdschr Tandheelkd. 2017 May;124(5):273-278. doi: 10.5177/ntvt.2017.05.16215. Ned Tijdschr Tandheelkd. 2017. PMID: 28501882 Dutch.

4

[DSQ-13-youth: measuring instrument for patient satisfaction with dental attendance among adolescents, young adults and parents of young children].

van Houtem CMHH, Schuller AA, Vermaire JH, van Kempen CPF, Verrips GHW. van Houtem CMHH, et al. Among authors: van kempen cpf. Ned Tijdschr Tandheelkd. 2017 Dec;124(12):625-633. doi: 10.5177/ntvt.2017.12.16225. Ned Tijdschr Tandheelkd. 2017. PMID: 29257835 Dutch.

5

A 600 kb triplication in the cat eye syndrome critical region causes anorectal, renal and preauricular anomalies in a three-generation family.

Knijnenburg J, van Bever Y, Hulsman LO, van Kempen CA, Bolman GM, van Loon RL, Beverloo HB, van Zutven LJ. Knijnenburg J, et al. Among authors: van kempen ca. Eur J Hum Genet. 2012 Sep;20(9):986-9. doi: 10.1038/ejhg.2012.43. Epub 2012 Mar 7. Eur J Hum Genet. 2012. PMID: 22395867 Free PMC article.

6

Multiplex ligation-dependent probe amplification equals fluorescence in-situ hybridization for the identification of patients at risk for metastatic disease in uveal melanoma.

Vaarwater J, van den Bosch T, Mensink HW, van Kempen C, Verdijk RM, Naus NC, Paridaens D, Brüggenwirth HT, Kiliç E, de Klein A. Vaarwater J, et al. Among authors: van kempen c. Melanoma Res. 2012 Feb;22(1):30-7. doi: 10.1097/CMR.0b013e32834e6a67. Melanoma Res. 2012. PMID: 22157614

7

Ring chromosome 8 in a boy with multiple congenital abnormalities and mental retardation.

Hamers AJ, van Kempen C. Hamers AJ, et al. Among authors: van kempen c. J Med Genet. 1977 Dec;14(6):451-5. doi: 10.1136/jmg.14.6.451. J Med Genet. 1977. PMID: 604497 Free PMC article.

8

Dermatoglyphics in partial C trisomies.

Jongbloet PH, van Kempen C. Jongbloet PH, et al. Among authors: van kempen c. Lancet. 1968 Jun 29;1(7557):1428. doi: 10.1016/s0140-6736(68)92005-9. Lancet. 1968. PMID: 4173012 No abstract available.

9

Low serum cholesterol and serotonin metabolism. Results may have been affected by confounding.

Pijl H, Toornvliet AC, Meinders AE, Leuven JA, Van Kempen CM. Pijl H, et al. Among authors: van kempen cm. BMJ. 1996 May 18;312(7041):1298; author reply 1299. doi: 10.1136/bmj.312.7041.1298b. BMJ. 1996. PMID: 8634629 Free PMC article. No abstract available.

10

A mentally retarded boy with multiple congenital anomalies and aberrant morphology in a no. 18 chromosome.

Van Kempen C. Van Kempen C. Dev Med Child Neurol. 1967 Oct;9(5):617-24. doi: 10.1111/j.1469-8749.1967.tb02333.x. Dev Med Child Neurol. 1967. PMID: 6066027 No abstract available.

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