Search Results - Gire, Anisa I.

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  1. 1
    The relationship between Graves' ophthalmopathy and dry eye syndrome

    The relationship between Graves' ophthalmopathy and dry eye syndrome by Selter, Jessica H, Gire, Anisa I, Sikder, Shameema

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  2. 2
    The Gly56Arg mutation in NR2E3 accounts for 1-2% of autosomal dominant retinitis pigmentosa

    The Gly56Arg mutation in NR2E3 accounts for 1-2% of autosomal dominant retinitis pigmentosa by Gire, Anisa I, Sullivan, Lori S, Bowne, Sara J, Birch, David G, Hughbanks-Wheaton, Dianna, Heckenlively, John R, Daiger, Stephen P

    Published in Molecular vision
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  3. 3
    Mutations in the TOPORS gene cause 1% of autosomal dominant retinitis pigmentosa

    Mutations in the TOPORS gene cause 1% of autosomal dominant retinitis pigmentosa by Bowne, Sara J, Sullivan, Lori S, Gire, Anisa I, Birch, David G, Hughbanks-Wheaton, Dianna, Heckenlively, John R, Daiger, Stephen P

    Published in Molecular vision
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  4. 4
    In vitro effects of medium tonicity, nutrient concentration, and free chlorine content on Acanthamoeba

    In vitro effects of medium tonicity, nutrient concentration, and free chlorine content on Acanthamoeba by Bergmanson, Jan P.G, Wang, Eva, Gire, Anisa I, Osato, Michael S

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  5. 5
    Phenotypic Characterization of a Large Family With RP10 Autosomal-Dominant Retinitis Pigmentosa: An Asp226Asn Mutation in the IMPDH1 Gene

    Phenotypic Characterization of a Large Family With RP10 Autosomal-Dominant Retinitis Pigmentosa: An Asp226Asn Mutation in the IMPDH1 Gene by Kozma, Petra, Hughbanks-Wheaton, Dianna K., Locke, Kirsten G., Fish, Garry E., Gire, Anisa I., Spellicy, Catherine J., Sullivan, Lori S., Bowne, Sara J., Daiger, Stephen P., Birch, David G.

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  6. 6
    Phenotypic Characterization of a Large Family With RP10 Autosomal-Dominant Retinitis Pigmentosa: An Asp226Asn Mutation in theIMPDH1Gene

    Phenotypic Characterization of a Large Family With RP10 Autosomal-Dominant Retinitis Pigmentosa: An Asp226Asn Mutation in theIMPDH1Gene by Kozma, Petra, Hughbanks-Wheaton, Dianna K, Locke, Kirsten G, Fish, Garry E, Gire, Anisa I, Spellicy, Catherine J, Sullivan, Lori S, Bowne, Sara J, Daiger, Stephen P, Birch, David G

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  7. 7
    Phenotypic Characterization of a Large Family With RP10 Autosomal-Dominant Retinitis Pigmentosa: An Asp226Asn Mutation in the

    Phenotypic Characterization of a Large Family With RP10 Autosomal-Dominant Retinitis Pigmentosa: An Asp226Asn Mutation in the by KOZMA, PETRA, HUGHBANKS-WHEATON, DIANNA K., LOCKE, KIRSTEN G., FISH, GARRY E., GIRE, ANISA I., SPELLICY, CATHERINE J., SULLIVAN, LORI S., BOWNE, SARA J., DAIGER, STEPHEN P., BIRCH, DAVID G.

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  8. 8
    Extraglandular ocular involvement and morbidity and mortality in primary Sjögren’s Syndrome

    Extraglandular ocular involvement and morbidity and mortality in primary Sjögren’s Syndrome by Mathews, Priya M., Robinson, Susan A., Gire, Anisa, Baer, Alan N., Akpek, Esen K.

    Published in PloS one
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  9. 9
    The Impact of the Boston Ocular Surface Prosthesis on Wavefront Higher-Order Aberrations

    The Impact of the Boston Ocular Surface Prosthesis on Wavefront Higher-Order Aberrations by Gumus, Koray, Gire, Anisa, Pflugfelder, Stephen C

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  10. 10
    PROSE Therapy Used to Minimize Corneal Trauma in Patients With Corneal Epithelial Defects

    PROSE Therapy Used to Minimize Corneal Trauma in Patients With Corneal Epithelial Defects by Ling, Jeanie D, Gire, Anisa, Pflugfelder, Stephen C

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  11. 11
    Patient ocular conditions and clinical outcomes using a PROSE scleral device

    Patient ocular conditions and clinical outcomes using a PROSE scleral device by Dimit, Ryan, Gire, Anisa, Pflugfelder, Stephen C, Bergmanson, Jan P.G

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