Croonen EA - 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. 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. Among authors: croonen ea. 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

Electrocardiography in Noonan syndrome PTPN11 gene mutation--phenotype characterization.

Croonen EA, van der Burgt I, Kapusta L, Draaisma JM. Croonen EA, et al. Am J Med Genet A. 2008 Feb 1;146A(3):350-3. doi: 10.1002/ajmg.a.32140. Am J Med Genet A. 2008. PMID: 18203203

4

Perceived motor problems in daily life: Focus group interviews with people with Noonan syndrome and their relatives.

Croonen EA, Harmsen M, Van der Burgt I, Draaisma JM, Noordam K, Essink M, Nijhuis-van der Sanden MW. Croonen EA, et al. Am J Med Genet A. 2016 Sep;170(9):2349-56. doi: 10.1002/ajmg.a.37814. Epub 2016 Jun 24. Am J Med Genet A. 2016. PMID: 27338165

5

Motor performance in children with Noonan syndrome.

Croonen EA, Essink M, van der Burgt I, Draaisma JM, Noordam C, Nijhuis-van der Sanden MWG. Croonen EA, et al. Am J Med Genet A. 2017 Sep;173(9):2335-2345. doi: 10.1002/ajmg.a.38322. Epub 2017 Jun 19. Am J Med Genet A. 2017. PMID: 28627718

6

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.

7

Patient with a neurofibromatosis type 1 mutation but a clinical diagnosis of Noonan syndrome.

Croonen EA, Yntema HG, van Minkelen R, van den Ouweland AMW, van der Burgt I. Croonen EA, et al. Clin Dysmorphol. 2012 Oct;21(4):212-214. doi: 10.1097/MCD.0b013e3283557231. Clin Dysmorphol. 2012. PMID: 22664660 No abstract available.

8

Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings.

Croonen EA, Nillesen WM, Stuurman KE, Oudesluijs G, van de Laar IM, Martens L, Ockeloen C, Mathijssen IB, Schepens M, Ruiterkamp-Versteeg M, Scheffer H, Faas BH, van der Burgt I, Yntema HG. Croonen EA, et al. Eur J Hum Genet. 2013 Sep;21(9):936-42. doi: 10.1038/ejhg.2012.285. Epub 2013 Jan 16. Eur J Hum Genet. 2013. PMID: 23321623 Free PMC article.

9

External ear anomalies and hearing impairment in Noonan Syndrome.

van Trier DC, van Nierop J, Draaisma JMT, van der Burgt I, Kunst H, Croonen EA, Admiraal RJC. van Trier DC, et al. Among authors: croonen ea. Int J Pediatr Otorhinolaryngol. 2015 Jun;79(6):874-878. doi: 10.1016/j.ijporl.2015.03.021. Epub 2015 Apr 1. Int J Pediatr Otorhinolaryngol. 2015. PMID: 25862627

10

It Is Not Just the FEV1 That Matters, but the Personal Goals We Reach Along the Way: Qualitative, Multicenter, Prospective, Observational Study.

Oppelaar MC, van den Wijngaart LS, Merkus PJFM, Croonen EA, Hugen CAC, Brouwer ML, Boehmer ALM, Roukema J. Oppelaar MC, et al. Among authors: croonen ea. J Med Internet Res. 2021 Oct 20;23(10):e29218. doi: 10.2196/29218. J Med Internet Res. 2021. PMID: 34668868 Free PMC article.

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