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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

2,950 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF.
Filges I, Bruder E, Brandal K, Meier S, Undlien DE, Waage TR, Hoesli I, Schubach M, de Beer T, Sheng Y, Hoeller S, Schulzke S, Røsby O, Miny P, Tercanli S, Oppedal T, Meyer P, Selmer KK, Strømme P. Filges I, et al. Among authors: meyer p. Hum Mutat. 2016 Apr;37(4):359-63. doi: 10.1002/humu.22960. Epub 2016 Feb 9. Hum Mutat. 2016. PMID: 26820108
The spectrum of WRN mutations in Werner syndrome patients.
Huang S, Lee L, Hanson NB, Lenaerts C, Hoehn H, Poot M, Rubin CD, Chen DF, Yang CC, Juch H, Dorn T, Spiegel R, Oral EA, Abid M, Battisti C, Lucci-Cordisco E, Neri G, Steed EH, Kidd A, Isley W, Showalter D, Vittone JL, Konstantinow A, Ring J, Meyer P, Wenger SL, von Herbay A, Wollina U, Schuelke M, Huizenga CR, Leistritz DF, Martin GM, Mian IS, Oshima J. Huang S, et al. Among authors: meyer p. Hum Mutat. 2006 Jun;27(6):558-67. doi: 10.1002/humu.20337. Hum Mutat. 2006. PMID: 16673358 Free PMC article.
[Heterotopic glioneuronal brain tissue in the orbit: case report].
Meyer P, Arnold Wörner N, Goldblum D, Bruder E. Meyer P, et al. Klin Monbl Augenheilkd. 2013 Aug;230(8):829-31. doi: 10.1055/s-0032-1328640. Epub 2013 Jul 10. Klin Monbl Augenheilkd. 2013. PMID: 23842870 German. No abstract available.
Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF.
Filges I, Bruder E, Brandal K, Meier S, Undlien DE, Waage TR, Hoesli I, Schubach M, de Beer T, Sheng Y, Hoeller S, Schulzke S, Røsby O, Miny P, Tercanli S, Oppedal T, Meyer P, Selmer KK, Strømme P. Filges I, et al. Among authors: meyer p. Hum Mutat. 2016 Jul;37(7):711. doi: 10.1002/humu.22997. Epub 2016 Apr 15. Hum Mutat. 2016. PMID: 27300082 No abstract available.
Congenital orbital teratoma: A clinicopathologic case report.
Reinhold A, Meyer P, Bruder E, Soleman J, von der Weid N, Mueller AA, Savic M. Reinhold A, et al. Among authors: meyer p. Am J Ophthalmol Case Rep. 2022 Feb 11;26:101420. doi: 10.1016/j.ajoc.2022.101420. eCollection 2022 Jun. Am J Ophthalmol Case Rep. 2022. PMID: 35243160 Free PMC article.
An Unusual Case of "Red Eye".
Janeschitz-Kriegl L, Meyer P, Scholl HP, Della Volpe Waizel M. Janeschitz-Kriegl L, et al. Among authors: meyer p. Klin Monbl Augenheilkd. 2019 Apr;236(4):377-378. doi: 10.1055/a-0795-3136. Epub 2019 Jan 7. Klin Monbl Augenheilkd. 2019. PMID: 30616282 English. No abstract available.
2,950 results