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Journal Abstract Search

154 related items for PubMed ID: 175723

  • 21. [Congenital hereditary corneal dystrophy associated with various extraoculary anomalies].
    Scialfa A, Mollica F, Pavone L.
    Ophthalmologica; 1975; 171(6):410-8. PubMed ID: 1080846
    [Abstract] [Full Text] [Related]

  • 22. [Metabolic disorders and corneal changes (author's transl)].
    François J.
    Klin Monbl Augenheilkd; 1981 Jun; 178(6):419-23. PubMed ID: 6973662
    [Abstract] [Full Text] [Related]

  • 23. The clinical spectrum of posterior polymorphous dystrophy.
    Cibis GW, Krachmer JA, Phelps CD, Weingeist TA.
    Arch Ophthalmol; 1977 Sep; 95(9):1529-37. PubMed ID: 302697
    [Abstract] [Full Text] [Related]

  • 24. Quantitative analysis of lipid deposits from Schnyder's corneal dystrophy.
    Yamada M, Mochizuki H, Kamata Y, Nakamura Y, Mashima Y.
    Br J Ophthalmol; 1998 Apr; 82(4):444-7. PubMed ID: 9640198
    [Abstract] [Full Text] [Related]

  • 25. 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; 116(6):1029-37.e1. PubMed ID: 19394700
    [Abstract] [Full Text] [Related]

  • 26. [Contribution to the knowledge of Schnyder's crystalline corneal dystrophy].
    Delogu A.
    Ann Ottalmol Clin Ocul; 1967 Nov; 93(11):1219-25. PubMed ID: 5306656
    [No Abstract] [Full Text] [Related]

  • 27. [Clinical appearance of corneal lattice-type dystrophy (author's transl)].
    Lisch W.
    Klin Monbl Augenheilkd; 1980 Sep; 177(3):284-91. PubMed ID: 7005516
    [Abstract] [Full Text] [Related]

  • 28. 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]

  • 29. 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]

  • 30. Hyperlipidemia in adult, pediatric and diabetic renal transplant recipients.
    Ibels LS, Alfrey AC, Weil R.
    Am J Med; 1978 Apr; 64(4):634-42. PubMed ID: 206137
    [No Abstract] [Full Text] [Related]

  • 31. Cloudy central corneal dystrophy of François. Five cases in the same family.
    Strachan IM.
    Br J Ophthalmol; 1969 Mar; 53(3):192-4. PubMed ID: 5305046
    [No Abstract] [Full Text] [Related]

  • 32. Hyperlipidemia in coronary heart disease. 3. Evaluation of lipoprotein phenotypes of 156 genetically defined survivors of myocardial infarction.
    Hazzard WR, Goldstein JL, Schrott MG, Motulsky AG, Bierman EL.
    J Clin Invest; 1973 Jul; 52(7):1569-77. PubMed ID: 4352458
    [Abstract] [Full Text] [Related]

  • 33. [Current status of linkage studies for gene localization in corneal dystrophies].
    Lisch W, Weidle EG, Emmig CT, Kömpf J, Baur MP.
    Fortschr Ophthalmol; 1991 Jul; 88(2):105-6. PubMed ID: 1855722
    [Abstract] [Full Text] [Related]

  • 34. [Primary hereditary cristalline corneal dystrophy of Schnyder. Histopathology and ultrastructure (author's transl)].
    Pfannkuch F.
    Klin Monbl Augenheilkd; 1978 Sep; 173(3):355-8. PubMed ID: 312360
    [Abstract] [Full Text] [Related]

  • 35. Lattice dystrophy type 1: a report of 8 families.
    Tsubota K, Hida T, Murata H, Akiya S, Shinji T, Kimura W.
    Ophthalmologica; 1987 Sep; 194(2-3):71-6. PubMed ID: 3497371
    [Abstract] [Full Text] [Related]

  • 36. Schnyder's crystalline corneal dystrophy.
    Handa S, Thakur A, Rajneesh D, Kulshrestha A, Gupta A.
    QJM; 2020 Jan 01; 113(1):66. PubMed ID: 31147712
    [No Abstract] [Full Text] [Related]

  • 37. Morphological evaluation of Schnyder's crystalline corneal dystrophy by laser scanning confocal microscopy and Fourier-domain optical coherence tomography.
    Jing Y, Wang L.
    Clin Exp Ophthalmol; 2009 Apr 01; 37(3):308-12. PubMed ID: 19459870
    [Abstract] [Full Text] [Related]

  • 38. [Congenital and familial cases of corneal dystrophy].
    Offret G, Guillaumat L, Campinchi R, Pouliquen Y.
    J Genet Hum; 1966 Apr 01; 15():Suppl:263-9. PubMed ID: 5301275
    [No Abstract] [Full Text] [Related]

  • 39. Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to xp22.3.
    Lisch W, Büttner A, Oeffner F, Böddeker I, Engel H, Lisch C, Ziegler A, Grzeschik K.
    Am J Ophthalmol; 2000 Oct 01; 130(4):461-8. PubMed ID: 11024418
    [Abstract] [Full Text] [Related]

  • 40. Hereditary crystalline corneal dystrophy of Schnyder.
    Ehlers N, Matthiessen ME.
    Acta Ophthalmol (Copenh); 1973 Oct 01; 51(3):316-24. PubMed ID: 4543169
    [No Abstract] [Full Text] [Related]

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