Draaisma JMT - Search Results

1

First-year growth in children with Noonan syndrome: Associated with feeding problems?

Croonen EA, Draaisma JMT, van der Burgt I, Roeleveld N, Noordam C. Croonen EA, et al. Among authors: draaisma jmt. Am J Med Genet A. 2018 Apr;176(4):951-958. doi: 10.1002/ajmg.a.38649. Am J Med Genet A. 2018. PMID: 29575624

2

Are ECG abnormalities in Noonan syndrome characteristic for the syndrome?

Raaijmakers R, Noordam C, Noonan JA, Croonen EA, van der Burgt CJ, Draaisma JM. Raaijmakers R, et al. Eur J Pediatr. 2008 Dec;167(12):1363-7. doi: 10.1007/s00431-008-0670-9. Epub 2008 Feb 13. Eur J Pediatr. 2008. PMID: 18270737

3

Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype.

Swinkels ME, Simons A, Smeets DF, Vissers LE, Veltman JA, Pfundt R, de Vries BB, Faas BH, Schrander-Stumpel CT, McCann E, Sweeney E, May P, Draaisma JM, Knoers NV, van Kessel AG, van Ravenswaaij-Arts CM. Swinkels ME, et al. Am J Med Genet A. 2008 Jun 1;146A(11):1430-8. doi: 10.1002/ajmg.a.32310. Am J Med Genet A. 2008. PMID: 18452192

4

[Clinical reasoning and decision making in clinical practice: a boy with fatigue and abdominal pain].

van Os E, Noordam C, Hart W, Draaisma JM. van Os E, et al. Ned Tijdschr Geneeskd. 2009 May 23;153(21):1018-23. Ned Tijdschr Geneeskd. 2009. PMID: 19757756 Dutch. No abstract available.

5

[Clinical reasoning and decision making in clinical practice: a boy with fatigue and abdominal pain].

van Os E, Noordam C, Hart WP, Draaisma JM. van Os E, et al. Ned Tijdschr Geneeskd. 2009;153:B87. Ned Tijdschr Geneeskd. 2009. PMID: 19785903 Dutch.

6

Phenotypic spectrum of 20 novel patients with molecularly defined supernumerary marker chromosomes 15 and a review of the literature.

Kleefstra T, de Leeuw N, Wolf R, Nillesen WM, Schobers G, Mieloo H, Willemsen M, Perrotta CS, Poddighe PJ, Feenstra I, Draaisma J, van Ravenswaaij-Arts CM. Kleefstra T, et al. Am J Med Genet A. 2010 Sep;152A(9):2221-9. doi: 10.1002/ajmg.a.33529. Am J Med Genet A. 2010. PMID: 20683990 Review.

7

Noonan syndrome: comparing mutation-positive with mutation-negative dutch patients.

Croonen EA, Nillesen W, Schrander C, Jongmans M, Scheffer H, Noordam C, Draaisma JM, van der Burgt I, Yntema HG. Croonen EA, et al. Mol Syndromol. 2013 Jun;4(5):227-34. doi: 10.1159/000350686. Epub 2013 May 8. Mol Syndromol. 2013. PMID: 23885229 Free PMC article.

8

Cochlear implantation and clinical features in patients with Noonan syndrome and Noonan syndrome with multiple lentigines caused by a mutation in PTPN11.

van Nierop JWI, van Trier DC, van der Burgt I, Draaisma JMT, Mylanus EAM, Snik AF, Admiraal RJC, Kunst HPM. van Nierop JWI, et al. Among authors: draaisma jmt. Int J Pediatr Otorhinolaryngol. 2017 Jun;97:228-234. doi: 10.1016/j.ijporl.2017.04.024. Epub 2017 Apr 17. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28483241

9

Young children with Noonan syndrome: evaluation of feeding problems.

Draaisma JMT, Drossaers J, van den Engel-Hoek L, Leenders E, Geelen J. Draaisma JMT, et al. Eur J Pediatr. 2020 Nov;179(11):1683-1688. doi: 10.1007/s00431-020-03664-x. Epub 2020 May 11. Eur J Pediatr. 2020. PMID: 32394265 Free PMC article.

10

The added value of the electrocardiogram in Noonan syndrome.

Vos E, Leenders E, Werkman SR, Udink Ten Cate FEA, Draaisma JMT. Vos E, et al. Among authors: draaisma jmt. Cardiol Young. 2022 Jun;32(6):936-943. doi: 10.1017/S1047951121003310. Epub 2021 Aug 12. Cardiol Young. 2022. PMID: 34382536

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