Hakutulokset - Stone, Edwin M

Finding and interpreting genetic variations that are important to ophthalmologists. Tekijä Stone, Edwin M

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Which Leber congenital amaurosis patients are eligible for gene therapy trials? Tekijä Drack, Arlene V., Johnston, Rebecca, Stone, Edwin M.

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From the Laboratory to the Clinic: Molecular Genetic Testing in Pediatric Ophthalmology Tekijä Drack, Arlene V., Lambert, Scott R., Stone, Edwin M.

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Stem cells for investigation and treatment of inherited retinal disease Tekijä Tucker, Budd A., Mullins, Robert F., Stone, Edwin M.

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Autologous cell replacement: a noninvasive AI approach to clinical release testing Tekijä Tucker, Budd A., Mullins, Robert F., Stone, Edwin M.

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Peripapillary Retinal Nerve Fiber Layer Thinning in Patients With Autosomal Recessive Cone-Rod Dystrophy Tekijä PASADHIKA, SIRICHAI, FISHMAN, GERALD A., ALLIKMETS, RANDO, STONE, EDWIN M.

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Treatment of Adult-Onset Acute Macular Retinoschisis in Enhanced-S Cone Syndrome with Oral Acetazolamide Tekijä Iannaccone, Alessandro, Fung, Kenneth H., Eyestone, Mari E., Stone, Edwin M.

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Fibulin-5 Distribution in Human Eyes: Relevance to Age-Related Macular Degeneration Tekijä Mullins, Robert F., Olvera, Marissa A., Clark, Abbot F., Stone, Edwin M.

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BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes Tekijä Zhang, Qihong, Seo, Seongjin, Bugge, Kevin, Stone, Edwin M., Sheffield, Val C.

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Intrinsic Protein-Protein Interaction-mediated and Chaperonin-assisted Sequential Assembly of Stable Bardet-Biedl Syndrome Protein Complex, the BBSome Tekijä Zhang, Qihong, Yu, Dahai, Seo, Seongjin, Stone, Edwin M., Sheffield, Val C.

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Selective Accumulation of the Complement Membrane Attack Complex in Aging Choriocapillaris Tekijä Chirco, Kathleen R., Tucker, Budd A., Stone, Edwin M., Mullins, Robert F.

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Classical and melanopsin photoreception in irradiance detection: negative masking of locomotor activity by light Tekijä Thompson, Stewart, Foster, Russell G., Stone, Edwin M., Sheffield, Val C., Mrosovsky, N.

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Computational Quantification of Complex Fundus Phenotypes in Age-Related Macular Degeneration and Stargardt Disease Tekijä Quellec, Gwenole, Russell, Stephen R., Scheetz, Todd E., Stone, Edwin M., Abràmoff, Michael D.

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Fluocinolone Acetonide Implant Inhibits Neovascularization but not Fibrosis in Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy Tekijä Tlucek, Paul S., Folk, James C., Orien, Jason A., Stone, Edwin M., Mahajan, Vinit B.

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THE VALUE OF RETINAL IMAGING WITH INFRARED SCANNING LASER OPHTHALMOSCOPY IN PATIENTS WITH STARGARDT DISEASE Tekijä Chun, Robert, Fishman, Gerald A., Collison, Frederick T., Stone, Edwin M., Zernant, Jana, Allikmets, Rando

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Basal exon skipping and genetic pleiotropy: A predictive model of disease pathogenesis Tekijä Drivas, Theodore G., Wojno, Adam P., Tucker, Budd A., Stone, Edwin M., Bennett, Jean

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Predicting Progression of ABCA4-Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease Front Tekijä Cideciyan, Artur V., Swider, Malgorzata, Schwartz, Sharon B., Stone, Edwin M., Jacobson, Samuel G.

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Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in Southern India Tekijä Sundaresan, Periasamy, Vijayalakshmi, P., Thompson, Stewart, Ko, Audrey C., Fingert, John H., Stone, Edwin M.

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Complement Component C5a Activates ICAM-1 Expression on Human Choroidal Endothelial Cells Tekijä Skeie, Jessica M., Fingert, John H., Russell, Stephen R., Stone, Edwin M., Mullins, Robert F.

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Residual Electroretinograms in Young Leber Congenital Amaurosis Patients with Mutations of AIPL1 Tekijä Pennesi, Mark E., Stover, Niamh B., Stone, Edwin M., Chiang, Pei-Wen, Weleber, Richard G.

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