Search Results - "Gire, Anisa I"

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

“…A complex relationship between Graves' ophthalmopathy (GO) and dry eye syndrome exists. New research brings more insight into the association between these two…”
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Prevalence of Disease-Causing Mutations in Families with Autosomal Dominant Retinitis Pigmentosa: A Screen of Known Genes in 200 Families by Sullivan, Lori S, Bowne, Sara J, Birch, David G, Hughbanks-Wheaton, Dianna, Heckenlively, John R, Lewis, Richard Alan, Garcia, Charles A, Ruiz, Richard S, Blanton, Susan H, Northrup, Hope, Gire, Anisa I, Seaman, Robyn, Duzkale, Hatice, Spellicy, Catherine J, Zhu, Jingya, Shankar, Suma P, Daiger, Stephen P

“…To survey families with clinical evidence of autosomal dominant retinitis pigmentosa (adRP) for mutations in genes known to cause adRP. Two hundred adRP…”
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Frequent Dosing of Topical Cyclosporine A for Severe Ocular Surface Disease by Gire, Anisa I, Karakus, Sezen, Ingrodi, Shanna M, Akpek, Esen Karamursel

“…To study the systemic safety and patient tolerability of frequent dosing of cyclosporine A (CsA) 0.05% eyedrops in the treatment of ocular surface disease…”
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Spectrum and Frequency of Mutations in IMPDH1 Associated with Autosomal Dominant Retinitis Pigmentosa and Leber Congenital Amaurosis by Bowne, Sara J, Sullivan, Lori S, Mortimer, Sarah E, Hedstrom, Lizbeth, Zhu, Jingya, Spellicy, Catherine J, Gire, Anisa I, Hughbanks-Wheaton, Dianna, Birch, David G, Lewis, Richard A, Heckenlively, John R, Daiger, Stephen P

“…The purpose of this study was to determine the frequency and spectrum of inosine monophosphate dehydrogenase type I (IMPDH1) mutations associated with…”
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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

“…Mutations in the orphan nuclear receptor gene NR2E3 have been found to cause both recessive and dominant retinopathies. The purpose of this study was to…”
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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

“…The purpose of this project was to determine if mutations, including large insertions or deletions, in the recently identified RP31 gene topoisomerase…”
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Mutations in known genes account for 58% of autosomal dominant retinitis pigmentosa (adRP) by Daiger, Stephen P, Sullivan, Lori S, Gire, Anisa I, Birch, David G, Heckenlively, John R, Bowne, Sara J

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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

“…Abstract Background The environment preferred by Acanthamoeba trophozoites and the mechanism by which the amebae enters the cornea are not yet fully…”
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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.

“…To evaluate the clinical features associated with the RP10 form of autosomal-dominant retinitis pigmentosa in 11 affected members of various ages from one…”
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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

“…Purpose To evaluate the clinical features associated with the RP10 form of autosomal-dominant retinitis pigmentosa in 11 affected members of various ages from…”
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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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