Créton MA - Search Results

1

[Is there more to hypodontia then missing teeth?].

Ross JN, Ruigrok LC, Fennis WMM, Cune MS, Rosenberg AJWP, van Nunen AB, Créton MA, Ploos van Amstel HK, van den Boogaard MJJH. Ross JN, et al. Among authors: creton ma. Ned Tijdschr Tandheelkd. 2023 Jun;130(6):277-286. doi: 10.5177/ntvt.2023.06.22098. Ned Tijdschr Tandheelkd. 2023. PMID: 37279496 Dutch.

2

[An enamel disorder in two siblings].

Créton MA, Cune MS. Créton MA, et al. Ned Tijdschr Tandheelkd. 2004 Oct;111(10):400-2. Ned Tijdschr Tandheelkd. 2004. PMID: 15553370 Dutch.

3

[A description of a population with severe oligodontia].

Créton MA, Cune MS, de Putter C, Verhoeven JW, Meijer GJ. Créton MA, et al. Ned Tijdschr Tandheelkd. 2009 Mar;116(3):119-23. Ned Tijdschr Tandheelkd. 2009. PMID: 19382538 Dutch.

4

Gastrointestinal symptoms in patients with isolated oligodontia and a Wnt gene mutation.

Ross JN, Ruigrok LC, Fennis WMM, Cune MS, Rosenberg AJWP, van Nunen AB, Créton MA, Ploos van Amstel HK, van den Boogaard MJH. Ross JN, et al. Among authors: creton ma. Oral Dis. 2023 Jan;29(1):300-307. doi: 10.1111/odi.13954. Epub 2021 Jul 14. Oral Dis. 2023. PMID: 34228861 Free PMC article.

5

Patterns of missing teeth in a population of oligodontia patients.

Créton MA, Cune MS, Verhoeven W, Meijer GJ. Créton MA, et al. Int J Prosthodont. 2007 Jul-Aug;20(4):409-13. Int J Prosthodont. 2007. PMID: 17695874

6

Dentofacial characteristics of patients with hypodontia.

Créton M, Cune MS, de Putter C, Ruijter JM, Kuijpers-Jagtman AM. Créton M, et al. Clin Oral Investig. 2010 Aug;14(4):467-77. doi: 10.1007/s00784-009-0308-y. Epub 2009 Jul 10. Clin Oral Investig. 2010. PMID: 19590908

7

Mutations in WNT10A are present in more than half of isolated hypodontia cases.

van den Boogaard MJ, Créton M, Bronkhorst Y, van der Hout A, Hennekam E, Lindhout D, Cune M, Ploos van Amstel HK. van den Boogaard MJ, et al. J Med Genet. 2012 May;49(5):327-31. doi: 10.1136/jmedgenet-2012-100750. J Med Genet. 2012. PMID: 22581971 Free article.

8

Concurrent manifestation of oligodontia and thrombocytopenia caused by a contiguous gene deletion in 12p13.2: A three-generation clinical report.

Ross J, Fennis W, de Leeuw N, Cune M, Willemze A, Rosenberg A, Ploos van Amstel HK, Créton M, van den Boogaard MJ. Ross J, et al. Mol Genet Genomic Med. 2019 Jun;7(6):e679. doi: 10.1002/mgg3.679. Epub 2019 Apr 4. Mol Genet Genomic Med. 2019. PMID: 30950205 Free PMC article.

9

Radiographic features of mandibular trabecular bone structure in hypodontia.

Créton M, Geraets W, Verhoeven JW, van der Stelt PF, Verhey H, Cune M. Créton M, et al. Clin Implant Dent Relat Res. 2012 Apr;14(2):241-9. doi: 10.1111/j.1708-8208.2009.00246.x. Epub 2009 Oct 16. Clin Implant Dent Relat Res. 2012. PMID: 19843106

10

The association between WNT10A variants and dental development in patients with isolated oligodontia.

Dhamo B, Fennis W, Créton M, Vucic S, Cune M, Ploos van Amstel HK, Wolvius EB, van den Boogaard MJ, Ongkosuwito EM. Dhamo B, et al. Eur J Hum Genet. 2016 Jan;25(1):59-65. doi: 10.1038/ejhg.2016.117. Epub 2016 Sep 21. Eur J Hum Genet. 2016. PMID: 27650966 Free PMC article.

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