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98 results

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Page 1
UBIAD1 mutation alters a mitochondrial prenyltransferase to cause Schnyder corneal dystrophy.
Nickerson ML, Kostiha BN, Brandt W, Fredericks W, Xu KP, Yu FS, Gold B, Chodosh J, Goldberg M, Lu DW, Yamada M, Tervo TM, Grutzmacher R, Croasdale C, Hoeltzenbein M, Sutphin J, Malkowicz SB, Wessjohann L, Kruth HS, Dean M, Weiss JS. Nickerson ML, et al. Among authors: sutphin j. PLoS One. 2010 May 21;5(5):e10760. doi: 10.1371/journal.pone.0010760. PLoS One. 2010. PMID: 20505825 Free PMC article.
Genetic analysis of 14 families with Schnyder crystalline corneal dystrophy reveals clues to UBIAD1 protein function.
Weiss JS, Kruth HS, Kuivaniemi H, Tromp G, Karkera J, Mahurkar S, Lisch W, Dupps WJ Jr, White PS, Winters RS, Kim C, Rapuano CJ, Sutphin J, Reidy J, Hu FR, Lu DW, Ebenezer N, Nickerson ML. Weiss JS, et al. Among authors: sutphin j. Am J Med Genet A. 2008 Feb 1;146A(3):271-83. doi: 10.1002/ajmg.a.32201. Am J Med Genet A. 2008. PMID: 18176953
IC3D classification of corneal dystrophies--edition 2.
Weiss JS, Møller HU, Aldave AJ, Seitz B, Bredrup C, Kivelä T, Munier FL, Rapuano CJ, Nischal KK, Kim EK, Sutphin J, Busin M, Labbé A, Kenyon KR, Kinoshita S, Lisch W. Weiss JS, et al. Among authors: sutphin j. Cornea. 2015 Feb;34(2):117-59. doi: 10.1097/ICO.0000000000000307. Cornea. 2015. PMID: 25564336 Free article.
The IC3D classification of the corneal dystrophies.
Weiss JS, Møller HU, Lisch W, Kinoshita S, Aldave AJ, Belin MW, Kivelä T, Busin M, Munier FL, Seitz B, Sutphin J, Bredrup C, Mannis MJ, Rapuano CJ, Van Rij G, Kim EK, Klintworth GK. Weiss JS, et al. Among authors: sutphin j. Cornea. 2008 Dec;27 Suppl 2(Suppl 2):S1-83. doi: 10.1097/ICO.0b013e31817780fb. Cornea. 2008. PMID: 19337156 Free PMC article. Review.
[The IC3D classification of the corneal dystrophies].
Weiss JS, Møller HU, Lisch W, Kinoshita S, Aldave AJ, Belin MW, Kivelä T, Busin M, Munier FL, Seitz B, Sutphin J, Bredrup C, Mannis MJ, Rapuano C, Van Rij G, Kim EK, Klintworth GK. Weiss JS, et al. Among authors: sutphin j. Klin Monbl Augenheilkd. 2011 Jan;228 Suppl 1:S1-39. doi: 10.1055/s-0029-1245895. Epub 2011 Feb 2. Klin Monbl Augenheilkd. 2011. PMID: 21290351 German.
Coexistent Acanthamoeba keratitis and herpetic keratitis.
Mathers WD, Goldberg MA, Sutphin JE, Ditkoff JW, Folberg R. Mathers WD, et al. Among authors: sutphin je. Arch Ophthalmol. 1997 Jun;115(6):714-8. doi: 10.1001/archopht.1997.01100150716002. Arch Ophthalmol. 1997. PMID: 9194720
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.
Biswas S, Munier FL, Yardley J, Hart-Holden N, Perveen R, Cousin P, Sutphin JE, Noble B, Batterbury M, Kielty C, Hackett A, Bonshek R, Ridgway A, McLeod D, Sheffield VC, Stone EM, Schorderet DF, Black GC. Biswas S, et al. Among authors: sutphin je. Hum Mol Genet. 2001 Oct 1;10(21):2415-23. doi: 10.1093/hmg/10.21.2415. Hum Mol Genet. 2001. PMID: 11689488
Donor age and corneal endothelial cell loss 5 years after successful corneal transplantation. Specular microscopy ancillary study results.
Cornea Donor Study Investigator Group; Lass JH, Gal RL, Dontchev M, Beck RW, Kollman C, Dunn SP, Heck E, Holland EJ, Mannis MJ, Montoya MM, Schultze RL, Stulting RD, Sugar A, Sugar J, Tennant B, Verdier DD. Cornea Donor Study Investigator Group, et al. Ophthalmology. 2008 Apr;115(4):627-632.e8. doi: 10.1016/j.ophtha.2008.01.004. Ophthalmology. 2008. PMID: 18387408 Free PMC article. Clinical Trial.
98 results