Cnossen MH - Search Results

1

Endocrinologic disorders and optic pathway gliomas in children with neurofibromatosis type 1.

Cnossen MH, Stam EN, Cooiman LC, Simonsz HJ, Stroink H, Oranje AP, Halley DJ, de Goede-Bolder A, Niermeijer MF, de Muinck Keizer-Schrama SM. Cnossen MH, et al. Pediatrics. 1997 Oct;100(4):667-70. doi: 10.1542/peds.100.4.667. Pediatrics. 1997. PMID: 9310522 Free article. Review.

2

Deletions spanning the neurofibromatosis type 1 gene: implications for genotype-phenotype correlations in neurofibromatosis type 1?

Cnossen MH, van der Est MN, Breuning MH, van Asperen CJ, Breslau-Siderius EJ, van der Ploeg AT, de Goede-Bolder A, van den Ouweland AM, Halley DJ, Niermeijer MF. Cnossen MH, et al. Hum Mutat. 1997;9(5):458-64. doi: 10.1002/(SICI)1098-1004(1997)9:5<458::AID-HUMU13>3.0.CO;2-1. Hum Mutat. 1997. PMID: 9143927

3

Diagnostic delay in neurofibromatosis type 1.

Cnossen MH, Smit FJ, de Goede-Bolder A, Frets PG, Duivenvoorden HJ, Niermeijer MF. Cnossen MH, et al. Eur J Pediatr. 1997 Jun;156(6):482-7. doi: 10.1007/s004310050644. Eur J Pediatr. 1997. PMID: 9208248

4

A prospective 10 year follow up study of patients with neurofibromatosis type 1.

Cnossen MH, de Goede-Bolder A, van den Broek KM, Waasdorp CM, Oranje AP, Stroink H, Simonsz HJ, van den Ouweland AM, Halley DJ, Niermeijer MF. Cnossen MH, et al. Arch Dis Child. 1998 May;78(5):408-12. doi: 10.1136/adc.78.5.408. Arch Dis Child. 1998. PMID: 9659085 Free PMC article.

5

Minor disease features in neurofibromatosis type 1 (NF1) and their possible value in diagnosis of NF1 in children < or = 6 years and clinically suspected of having NF1. Neurofibromatosis team of Sophia Children's Hospital.

Cnossen MH, Moons KG, Garssen MP, Pasmans NM, de Goede-Bolder A, Niermeijer MF, Grobbee DE. Cnossen MH, et al. J Med Genet. 1998 Aug;35(8):624-7. doi: 10.1136/jmg.35.8.624. J Med Genet. 1998. PMID: 9719365 Free PMC article.

6

[From gene to disease; neurofibromatosis type 1].

de Goede-Bolder A, Cnossen MH, Dooijes D, van den Ouweland AM, Niermeijer MF. de Goede-Bolder A, et al. Among authors: cnossen mh. Ned Tijdschr Geneeskd. 2001 Sep 8;145(36):1736-8. Ned Tijdschr Geneeskd. 2001. PMID: 11572174 Review. Dutch.

7

The group medical appointment (GMA) in haemophilia and von Willebrand's disease: a new development in outpatient paediatric care.

Lock J, De Bruin A, Scholten M, Joosten M, Seesing FM, Beishuizen A, De Goede-Bolder A, Cnossen MH. Lock J, et al. Among authors: cnossen mh. Haemophilia. 2012 Sep;18(5):766-72. doi: 10.1111/j.1365-2516.2012.02783.x. Epub 2012 Mar 28. Haemophilia. 2012. PMID: 22458923

8

Silent cerebral infarcts in patients with sickle cell disease: a systematic review and meta-analysis.

Houwing ME, Grohssteiner RL, Dremmen MHG, Atiq F, Bramer WM, de Pagter APJ, Zwaan CM, White TJH, Vernooij MW, Cnossen MH. Houwing ME, et al. Among authors: cnossen mh. BMC Med. 2020 Dec 22;18(1):393. doi: 10.1186/s12916-020-01864-8. BMC Med. 2020. PMID: 33349253 Free PMC article.

9

Familial neurofibromatosis type 1 associated with an overgrowth syndrome resembling Weaver syndrome.

van Asperen CJ, Overweg-Plandsoen WC, Cnossen MH, van Tijn DA, Hennekam RC. van Asperen CJ, et al. Among authors: cnossen mh. J Med Genet. 1998 Apr;35(4):323-7. doi: 10.1136/jmg.35.4.323. J Med Genet. 1998. PMID: 9598729 Free PMC article.

10

Paediatric arterial ischaemic stroke: functional outcome and risk factors.

Cnossen MH, Aarsen FK, Akker SLj, Danen R, Appel IM, Steyerberg EW, Catsman-Berrevoets CE. Cnossen MH, et al. Dev Med Child Neurol. 2010 Apr;52(4):394-9. doi: 10.1111/j.1469-8749.2009.03580.x. Epub 2010 Jan 18. Dev Med Child Neurol. 2010. PMID: 20089051 Free article.

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