Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

230 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Diagnostic delay in neurofibromatosis type 1.
Cnossen MH, Smit FJ, de Goede-Bolder A, Frets PG, Duivenvoorden HJ, Niermeijer MF. Cnossen MH, et al. Among authors: niermeijer mf. Eur J Pediatr. 1997 Jun;156(6):482-7. doi: 10.1007/s004310050644. Eur J Pediatr. 1997. PMID: 9208248
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. Among authors: niermeijer mf. 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.
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. Among authors: niermeijer mf. 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.
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. Among authors: niermeijer mf. 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
[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: niermeijer mf. Ned Tijdschr Geneeskd. 2001 Sep 8;145(36):1736-8. Ned Tijdschr Geneeskd. 2001. PMID: 11572174 Review. Dutch.
The fragile X syndrome.
de Vries BB, Halley DJ, Oostra BA, Niermeijer MF. de Vries BB, et al. Among authors: niermeijer mf. J Med Genet. 1998 Jul;35(7):579-89. doi: 10.1136/jmg.35.7.579. J Med Genet. 1998. PMID: 9678703 Free PMC article. Review.
230 results