My NCBI | Sign In
RSS Settings
  • Search:

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

    Results: 1 to 20 of 200

    1.

    Pellucid marginal degeneration coexistent with cornea plana in one member of a family exhibiting a novel KERA mutation.

    Khan AO, Aldahmesh M, Al-Saif A, Meyer B.

    Br J Ophthalmol. 2005 Nov;89(11):1538-40. No abstract available. PMID: 16234475 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Clinical and molecular characterization of a family with autosomal recessive cornea plana.

    Ebenezer ND, Patel CB, Hariprasad SM, Chen LL, Patel RJ, Hardcastle AJ, Allen RC.

    Arch Ophthalmol. 2005 Sep;123(9):1248-53.PMID: 16157807 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2.

    Aldave AJ, Sonmez B, Bourla N, Schultz G, Papp JC, Salem AK, Rayner SA, Yellore VS.

    Ophthalmic Genet. 2007 Jun;28(2):57-67.PMID: 17558846 [PubMed - indexed for MEDLINE]Related articles

    4.

    A novel KERA mutation associated with autosomal recessive cornea plana.

    Khan A, Al-Saif A, Kambouris M.

    Ophthalmic Genet. 2004 Jun;25(2):147-52. Erratum in: Ophthalmic Genet. 2004 Dec;25(4):289. Ophthalmic Genet. 2005 Dec;26(4):195. PMID: 15370545 [PubMed - indexed for MEDLINE]Related articles

    5.

    Mutations in KERA, encoding keratocan, cause cornea plana.

    Pellegata NS, Dieguez-Lucena JL, Joensuu T, Lau S, Montgomery KT, Krahe R, Kivelä T, Kucherlapati R, Forsius H, de la Chapelle A.

    Nat Genet. 2000 May;25(1):91-5.PMID: 10802664 [PubMed - indexed for MEDLINE]Related articles

    6.

    Recessive cornea plana in the Kingdom of Saudi Arabia.

    Khan AO, Aldahmesh M, Meyer B.

    Ophthalmology. 2006 Oct;113(10):1773-8.PMID: 17011957 [PubMed - indexed for MEDLINE]Related articles

    7.

    A novel keratocan mutation causing autosomal recessive cornea plana.

    Lehmann OJ, El-ashry MF, Ebenezer ND, Ocaka L, Francis PJ, Wilkie SE, Patel RJ, Ficker L, Jordan T, Khaw PT, Bhattacharya SS.

    Invest Ophthalmol Vis Sci. 2001 Dec;42(13):3118-22.PMID: 11726611 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Corneal ectasia and hydrops in a patient with autosomal recessive cornea plana.

    Khan AO, Aldahmesh M, Meyer B.

    Ophthalmic Genet. 2006 Sep;27(3):99-101.PMID: 17050286 [PubMed - indexed for MEDLINE]Related articles

    9.

    Study of p.N247S KERA mutation in a British family with cornea plana.

    Liskova P, Hysi PG, Williams D, Ainsworth JR, Shah S, de la Chapelle A, Tuft SJ, Bhattacharya SS.

    Mol Vis. 2007 Jul 27;13:1339-47.PMID: 17679937 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Further information regarding KERA and recessive cornea plana.

    Khan AO.

    Arch Ophthalmol. 2006 Sep;124(9):1371-2; author reply 1372. No abstract available. PMID: 16966646 [PubMed - indexed for MEDLINE]Related articles

    11.

    Focus on molecules: keratocan (KERA).

    Chakravarti S.

    Exp Eye Res. 2006 Feb;82(2):183-4. Epub 2005 Dec 19. No abstract available. PMID: 16360151 [PubMed - indexed for MEDLINE]Related articles

    12.

    Corneal topography in asymptomatic family members of a patient with pellucid marginal degeneration.

    Santo RM, Bechara SJ, Kara-José N.

    Am J Ophthalmol. 1999 Feb;127(2):205-7.PMID: 10030565 [PubMed - indexed for MEDLINE]Related articles

    13.

    Autosomal dominant cornea plana: clinical findings in a Cuban family and a review of the literature.

    Sigler-Villanueva A, Tahvanainen E, Lindh S, Dieguez-Lucena J, Forsius H.

    Ophthalmic Genet. 1997 Jun;18(2):55-62. Review.PMID: 9228241 [PubMed - indexed for MEDLINE]Related articles

    14.

    Clinical manifestation of a novel PAX6 mutation Arg128Pro.

    Bredrup C, Knappskog PM, Rødahl E, Boman H.

    Arch Ophthalmol. 2008 Mar;126(3):428-30. No abstract available. PMID: 18332330 [PubMed - indexed for MEDLINE]Related articles

    15.

    Hereditary sclerocornea.

    Elliott JH, Feman SS, O'Day DM, Garber M.

    Arch Ophthalmol. 1985 May;103(5):676-9.PMID: 3994576 [PubMed - indexed for MEDLINE]Related articles

    16.

    Colobomatous macrophthalmia with microcornea.

    Bateman JB, Maumenee IH.

    Ophthalmic Paediatr Genet. 1984 Aug;4(2):59-66.PMID: 6545385 [PubMed - indexed for MEDLINE]Related articles

    17.

    Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8.

    Hansen L, Yao W, Eiberg H, Kjaer KW, Baggesen K, Hejtmancik JF, Rosenberg T.

    Invest Ophthalmol Vis Sci. 2007 Sep;48(9):3937-44.PMID: 17724170 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    [Cornea plana congenita]

    Forsius H, Eriksson AW.

    Duodecim. 1972;88(1):52-9. Finnish. No abstract available. PMID: 5013578 [PubMed - indexed for MEDLINE]Related articles

    19.

    Vertical corneal striae in families with autosomal dominant hearing loss: DFNA9/COCH.

    Bischoff AM, Pauw RJ, Huygen PL, Aandekerk AL, Kremer H, Cremers CW, Cruysberg JR.

    Am J Ophthalmol. 2007 May;143(5):847-852. Epub 2007 Mar 19.PMID: 17368553 [PubMed - indexed for MEDLINE]Related articles

    20.

    Inflammatory Terrien's marginal corneal disease.

    Austin P, Brown SI.

    Am J Ophthalmol. 1981 Aug;92(2):189-92.PMID: 7270631 [PubMed - indexed for MEDLINE]Related articles

    Supplemental Content

    Filter your results:

    Find related data

    Recent activity