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

504 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.
Tarpey P, Thomas S, Sarvananthan N, Mallya U, Lisgo S, Talbot CJ, Roberts EO, Awan M, Surendran M, McLean RJ, Reinecke RD, Langmann A, Lindner S, Koch M, Jain S, Woodruff G, Gale RP, Bastawrous A, Degg C, Droutsas K, Asproudis I, Zubcov AA, Pieh C, Veal CD, Machado RD, Backhouse OC, Baumber L, Constantinescu CS, Brodsky MC, Hunter DG, Hertle RW, Read RJ, Edkins S, O'Meara S, Parker A, Stevens C, Teague J, Wooster R, Futreal PA, Trembath RC, Stratton MR, Raymond FL, Gottlob I. Tarpey P, et al. Among authors: lindner s. Nat Genet. 2006 Nov;38(11):1242-4. doi: 10.1038/ng1893. Epub 2006 Oct 1. Nat Genet. 2006. PMID: 17013395 Free PMC article.
Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7.
Thomas S, Proudlock FA, Sarvananthan N, Roberts EO, Awan M, McLean R, Surendran M, Kumar AS, Farooq SJ, Degg C, Gale RP, Reinecke RD, Woodruff G, Langmann A, Lindner S, Jain S, Tarpey P, Raymond FL, Gottlob I. Thomas S, et al. Among authors: lindner s. Brain. 2008 May;131(Pt 5):1259-67. doi: 10.1093/brain/awn046. Epub 2008 Mar 27. Brain. 2008. PMID: 18372314
The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus.
Thomas MG, Crosier M, Lindsay S, Kumar A, Thomas S, Araki M, Talbot CJ, McLean RJ, Surendran M, Taylor K, Leroy BP, Moore AT, Hunter DG, Hertle RW, Tarpey P, Langmann A, Lindner S, Brandner M, Gottlob I. Thomas MG, et al. Among authors: lindner s. Brain. 2011 Mar;134(Pt 3):892-902. doi: 10.1093/brain/awq373. Epub 2011 Feb 8. Brain. 2011. PMID: 21303855 Free PMC article.
Congenital third nerve palsy in septo-optic dysplasia.
Langmann A, Lindner S. Langmann A, et al. Among authors: lindner s. Br J Ophthalmol. 2004 Jul;88(7):969. doi: 10.1136/bjo.2003.034405. Br J Ophthalmol. 2004. PMID: 15205251 Free PMC article. No abstract available.
[A refractory pupil].
Koch M, Lindner S, Langmann A. Koch M, et al. Among authors: lindner s. Ophthalmologe. 2006 Aug;103(8):704-6. doi: 10.1007/s00347-005-1278-3. Ophthalmologe. 2006. PMID: 16283188 German. No abstract available.
[The differential diagnosis of exophthalmos].
Langmann A, Lindner S. Langmann A, et al. Among authors: lindner s. Ophthalmologe. 2004 Feb;101(2):190-2. doi: 10.1007/s00347-003-0889-9. Ophthalmologe. 2004. PMID: 14991318 German. No abstract available.
[Endocrine orbitopathy--eye muscule surgery].
Langmann A, Lindner S. Langmann A, et al. Among authors: lindner s. Acta Med Austriaca. 2001;28(4):108. doi: 10.1046/j.1563-2571.2001.01027.x. Acta Med Austriaca. 2001. PMID: 11593893 German.
[Endocrine orbitopathy--diagnosis].
Langmann A, Lindner S. Langmann A, et al. Among authors: lindner s. Acta Med Austriaca. 2001;28(4):87-8. doi: 10.1046/j.1563-2571.2001.01020.x. Acta Med Austriaca. 2001. PMID: 11593896 German.
504 results