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  1. 1
    Defective processing of keratan sulfate in macular corneal dystrophy.

    Defective processing of keratan sulfate in macular corneal dystrophy. Yazar: Kiyoshi Nakazawa, John R. Hassell, Vincent Hascall, Stefan Lohmander, D A Newsome, Jay Krachmer

    Baskı/Yayın Bilgisi 1984
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  2. 2
    VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies

    VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies Yazar: Karen L. White, Andreas Marquardt, Bernhard H. F. Weber

    Baskı/Yayın Bilgisi 2000
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  3. 3
    Fundus autofluorescence imaging of retinal dystrophies

    Fundus autofluorescence imaging of retinal dystrophies Yazar: Camiel J.F. Boon, B. Jeroen Klevering, Jan E.E. Keunen, Carel B. Hoyng, Thomas Theelen

    Baskı/Yayın Bilgisi 2008
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  4. 4
    Mutations in MFSD8, Encoding a Lysosomal Membrane Protein, Are Associated with Nonsyndromic Autosomal Recessive Macular Dystrophy

    Mutations in MFSD8, Encoding a Lysosomal Membrane Protein, Are Associated with Nonsyndromic Autosomal Recessive Macular Dystrophy Yazar: Susanne Roosing, L. Ingeborgh van den Born, Riccardo Sangermano, Sandro Banfi, Robert K. Koenekoop, Marijke N. Zonneveld-Vrieling, Caroline C. W. Klaver, Janneke J.C. van Lith-Verhoeven, Frans P.M. Cremers, Anneke I. den Hollander, Carel B. Hoyng

    Baskı/Yayın Bilgisi 2014
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  5. 5
    Deciphering mutant ELOVL4 activity in autosomal-dominant Stargardt macular dystrophy

    Deciphering mutant ELOVL4 activity in autosomal-dominant Stargardt macular dystrophy Yazar: Sreemathi Logan, Martin‐Paul Agbaga, Michael Chan, Nabila Kabir, Nawajes Mandal, Richard S. Brush, Robert E. Anderson

    Baskı/Yayın Bilgisi 2013
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  6. 6
    A New Locus for Autosomal Dominant Stargardt-Like Disease Maps to Chromosome 4

    A New Locus for Autosomal Dominant Stargardt-Like Disease Maps to Chromosome 4 Yazar: Marina Kniazeva, Michael F. Chiang, Basil Morgan, Alfred L. Anduze, Donald J. Zack, Min Han, Kang Zhang

    Baskı/Yayın Bilgisi 1999
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  7. 7
    <i>ABCA4</i>and<i>ROM1:</i>Implications for Modification of the<i>PRPH2</i>-Associated Macular Dystrophy Phenotype

    <i>ABCA4</i>and<i>ROM1:</i>Implications for Modification of the<i>PRPH2</i>-Associated Macular Dystrophy Phenotype Yazar: Charlotte M. Poloschek, Michael Bach, Wolf A. Lagrèze, Esther Glaus, Johannes R. Lemke, Wolfgang Berger, John Neidhardt

    Baskı/Yayın Bilgisi 2010
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  8. 8
    Intravitreal injection of ranibizumab for foveal-macular pattern dystrophy: case report

    Intravitreal injection of ranibizumab for foveal-macular pattern dystrophy: case report Yazar: Alexandre Augusto Cabral de Mello Ventura, Lorna W. Grant, Hajir Dadgostar, Hilel Lewis

    Baskı/Yayın Bilgisi 2011
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  9. 9
    Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies

    Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies Yazar: Jean‐Michel Rozet, S. Gerber, Eric H. Souied, Isabelle Perrault, Sophie Châtelin, Imad Ghazi, Corinne Leowski, Jean‐Louis Dufier, Arnold Munnich, Josseline Kaplan

    Baskı/Yayın Bilgisi 1998
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  10. 10
    Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)

    Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome) Yazar: Klaus Kjaer

    Baskı/Yayın Bilgisi 2005
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  11. 11
    The Effect of Lipid Environment and Retinoids on the ATPase Activity of ABCR, the Photoreceptor ABC Transporter Responsible for Stargardt Macular Dystrophy

    The Effect of Lipid Environment and Retinoids on the ATPase Activity of ABCR, the Photoreceptor ABC Transporter Responsible for Stargardt Macular Dystrophy Yazar: Jinhi Ahn, Jason T. Wong, Robert S. Molday

    Baskı/Yayın Bilgisi 2000
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  12. 12
    Molecular genetics of human retinal dystrophies

    Molecular genetics of human retinal dystrophies Yazar: Chris F. Inglehearn

    Baskı/Yayın Bilgisi 1998
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  13. 13
    Macular dystrophy of the cornea.

    Macular dystrophy of the cornea. Yazar: G Morgan

    Baskı/Yayın Bilgisi 1966
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  14. 14
    The genetics of inherited macular dystrophies

    The genetics of inherited macular dystrophies Yazar: Michel Michaelides, David M. Hunt, A. T. Moore

    Baskı/Yayın Bilgisi 2003
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  15. 15
    Prevalence of Corneal Dystrophies in the United States: Estimates from Claims Data

    Prevalence of Corneal Dystrophies in the United States: Estimates from Claims Data Yazar: David C. Musch, Leslie M. Niziol, Joshua D. Stein, Roheena Kamyar, Alan Sugar

    Baskı/Yayın Bilgisi 2011
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  16. 16
    The<i>PROM1</i>Mutation p.R373C Causes an Autosomal Dominant Bull's Eye Maculopathy Associated with Rod, Rod–Cone, and Macular Dystrophy

    The<i>PROM1</i>Mutation p.R373C Causes an Autosomal Dominant Bull's Eye Maculopathy Associated with Rod, Rod–Cone, and Macular Dystrophy Yazar: Michel Michaelides, Marie‐Claire Gaillard, Pascal Escher, Leila Tiab, Matthew Bedell, François‐Xavier Borruat, Daniel Barthelmes, Ruben Carmona, Kang Zhang, Edward T. White, Michelle E. McClements, Anthony G. Robson, Graham E. Holder, Keith Bradshaw, David M. Hunt, Andrew R. Webster, Anthony T. Moore, Daniel F. Schorderet, Francis L. Munier

    Baskı/Yayın Bilgisi 2010
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  17. 17
    New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups

    New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups Yazar: Mayana Zatz, S. B. Itskan, Ruth Sanger, Oswaldo Frota‐Pessoa, P. H. Saldanha

    Baskı/Yayın Bilgisi 1974
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  18. 18
    Macular dystrophy associated with Kjellin’s syndrome: a case report

    Macular dystrophy associated with Kjellin’s syndrome: a case report Yazar: Vinicius Castro, André Luiz Braga Meirelles, Rafael Saran Arcieri, Katharina Messias, André Messias

    Baskı/Yayın Bilgisi 2015
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  19. 19
    Sorsby's pseudoinflammatory macular dystrophy.

    Sorsby's pseudoinflammatory macular dystrophy. Yazar: Annette K. Hoskin, Kulwant Sehmi, Alan C. Bird

    Baskı/Yayın Bilgisi 1981
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  20. 20
    Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone–rod dystrophy and retinitis pigmentosa

    Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone–rod dystrophy and retinitis pigmentosa Yazar: B. Jeroen Klevering, Suzanne Yzer, Klaus Rohrschneider, Marijke N. Zonneveld, Rando Allikmets, L. Ingeborgh van den Born, Alessandra Maugeri, Carel B. Hoyng, Frans P.M. Cremers

    Baskı/Yayın Bilgisi 2004
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