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282 related items for PubMed ID: 15808257

  • 1. Central corneal mosaic opacities in Schnyder's crystalline dystrophy.
    Wu CW, Lin PY, Liu YF, Liu TC, Lin MW, Chen WM, Lee FL, Lee SM, Hsu WM.
    Ophthalmology; 2005 Apr; 112(4):650-3. PubMed ID: 15808257
    [Abstract] [Full Text] [Related]

  • 2. [Schnyder corneal dystrophy and juvenile, systemic hypercholesteremia].
    Kohnen T, Pelton RW, Jones DB.
    Klin Monbl Augenheilkd; 1997 Aug; 211(2):135-7. PubMed ID: 9379642
    [Abstract] [Full Text] [Related]

  • 3. The gene for schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1-p36.
    Shearman AM, Hudson TJ, Andresen JM, Wu X, Sohn RL, Haluska F, Housman DE, Weiss JS.
    Hum Mol Genet; 1996 Oct; 5(10):1667-72. PubMed ID: 8894705
    [Abstract] [Full Text] [Related]

  • 4. [Schnyder's crystalline corneal dystrophy. Further narrowing of the linkage interval at chromosome 1p34.1-p36?].
    Riebeling P, Polz S, Tost F, Weiss JS, Kuivaniemi H, Hoeltzenbein M.
    Ophthalmologe; 2003 Nov; 100(11):979-83. PubMed ID: 14669035
    [Abstract] [Full Text] [Related]

  • 5. Fine mapping of the Schnyder's crystalline corneal dystrophy locus.
    Theendakara V, Tromp G, Kuivaniemi H, White PS, Panchal S, Cox J, Winters RS, Riebeling P, Tost F, Hoeltzenbein M, Tervo TM, Henn W, Denniger E, Krause M, Koksal M, Kargi S, Ugurbas SH, Latvala T, Shearman AM, Weiss JS.
    Hum Genet; 2004 May; 114(6):594-600. PubMed ID: 15034782
    [Abstract] [Full Text] [Related]

  • 6. Analysis of fifteen positional candidate genes for Schnyder crystalline corneal dystrophy.
    Aldave AJ, Rayner SA, Principe AH, Affeldt JA, Katsev D, Yellore VS.
    Mol Vis; 2005 Sep 02; 11():713-6. PubMed ID: 16163269
    [Abstract] [Full Text] [Related]

  • 7. [Schnyder's crystalline-like corneal dystrophy: a case report].
    Brasnu E, Dupas B, Hoang-Xuan T, Baudouin C, Gatinel D.
    J Fr Ophtalmol; 2010 Apr 02; 33(4):264.e1-5. PubMed ID: 20334950
    [Abstract] [Full Text] [Related]

  • 8. In vivo confocal microscopy of a family with Schnyder crystalline corneal dystrophy.
    Vesaluoma MH, Linna TU, Sankila EM, Weiss JS, Tervo TM.
    Ophthalmology; 1999 May 02; 106(5):944-51. PubMed ID: 10328394
    [Abstract] [Full Text] [Related]

  • 9. [Schnyder's crystalline dystrophy. II. Association with genu valgum].
    Hoang-Xuan T, Pouliquen Y, Gasteau J.
    J Fr Ophtalmol; 1985 May 02; 8(11):743-7. PubMed ID: 3879611
    [Abstract] [Full Text] [Related]

  • 10. Schnyder's dystrophy. Progression and metabolism.
    Lisch W, Weidle EG, Lisch C, Rice T, Beck E, Utermann G.
    Ophthalmic Paediatr Genet; 1986 Mar 02; 7(1):45-56. PubMed ID: 3486394
    [Abstract] [Full Text] [Related]

  • 11. Schnyder's dystrophy of the cornea. A Swede-Finn connection.
    Weiss JS.
    Cornea; 1992 Mar 02; 11(2):93-101. PubMed ID: 1582223
    [Abstract] [Full Text] [Related]

  • 12. [Schnyder's corneal dystrophy and hyperlipidemia (author's transl].
    Kaden R, Feurle G.
    Albrecht Von Graefes Arch Klin Exp Ophthalmol; 1976 Feb 04; 198(2):129-38. PubMed ID: 175723
    [Abstract] [Full Text] [Related]

  • 13. Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene.
    Aldave AJ, Gutmark JG, Yellore VS, Affeldt JA, Meallet MA, Udar N, Rao NA, Small KW, Klintworth GK.
    Am J Ophthalmol; 2004 Nov 04; 138(5):772-81. PubMed ID: 15531312
    [Abstract] [Full Text] [Related]

  • 14. In vivo laser confocal microscopy findings and mutational analysis for Schnyder's crystalline corneal dystrophy.
    Kobayashi A, Fujiki K, Murakami A, Sugiyama K.
    Ophthalmology; 2009 Jun 04; 116(6):1029-37.e1. PubMed ID: 19394700
    [Abstract] [Full Text] [Related]

  • 15. Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene.
    Bredrup C, Knappskog PM, Majewski J, Rødahl E, Boman H.
    Invest Ophthalmol Vis Sci; 2005 Feb 04; 46(2):420-6. PubMed ID: 15671264
    [Abstract] [Full Text] [Related]

  • 16. [The different opacity patterns of Lisch corneal dystrophy].
    Butros S, Lang GK, Alvarez de Toledo J, Teimann U, Rohrbach JM, Lisch W.
    Klin Monbl Augenheilkd; 2006 Oct 04; 223(10):837-40. PubMed ID: 17063428
    [Abstract] [Full Text] [Related]

  • 17. [Schnyder's crystalline dystrophy. I. Study of a case by light and electron microscopy].
    Hoang-Xuan T, Pouliquen Y, Savoldelli M, Gasteau J.
    J Fr Ophtalmol; 1985 Oct 04; 8(11):735-42. PubMed ID: 3914502
    [Abstract] [Full Text] [Related]

  • 18. [Crystalline corneal dystrophy (Schnyder) in the presence of familial type IIa hyperlipoproteinaemia (author's transl)].
    Thiel HJ, Voigt GJ, Parwaresch MR.
    Klin Monbl Augenheilkd; 1977 Nov 04; 171(5):678-84. PubMed ID: 202777
    [Abstract] [Full Text] [Related]

  • 19. Spontaneous and inheritable R555Q mutation in the TGFBI/BIGH3 gene in two unrelated families exhibiting Bowman's layer corneal dystrophy.
    Zhao XC, Nakamura H, Subramanyam S, Stock LE, Gillette TE, Yoshikawa S, Ma X, Yee RW.
    Ophthalmology; 2007 Nov 04; 114(11):e39-46. PubMed ID: 17980739
    [Abstract] [Full Text] [Related]

  • 20. Inherited corneal opacifications with an unusual distribution.
    Fagerholm P, Dellby A, Bäckman L.
    Acta Ophthalmol Scand; 2007 Feb 04; 85(1):103-5. PubMed ID: 17244220
    [Abstract] [Full Text] [Related]


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