Risultati della ricerca - Allikmets, Rando

Further Evidence for an Association of ABCR Alleles with Age-Related Macular Degeneration di Allikmets, Rando

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Simple and Complex ABCR: Genetic Predisposition to Retinal Disease di Allikmets, Rando

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Gene Therapy of ABCA4-Associated Diseases di Auricchio, Alberto, Trapani, Ivana, Allikmets, Rando

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Penetrance of the ABCA4 p.Asn1868Ile Allele in Stargardt Disease di Allikmets, Rando, Zernant, Jana, Lee, Winston

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Reevaluating the Association of Sex With ABCA4 Alleles in Patients With Stargardt Disease di Lee, Winston, Zernant, Jana, Nagasaki, Takayuki, Allikmets, Rando

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Isolation and characterization of a retinal pigment epithelial cell fluorophore: An all-trans-retinal dimer conjugate di Fishkin, Nathan E., Sparrow, Janet R., Allikmets, Rando, Nakanishi, Koji

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

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Preimplantation Genetic Diagnosis for Stargardt Disease di Sohrab, Mahsa A., Allikmets, Rando, Guarnaccia, Michael M., Smith, R. Theodore

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Structural and Genetic Assessment of the ABCA4-Associated Optical Gap Phenotype di Nõupuu, Kalev, Lee, Winston, Zernant, Jana, Tsang, Stephen H., Allikmets, Rando

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Photoreceptor Cells as a Source of Fundus Autofluorescence in Recessive Stargardt Disease di Paavo, Maarjaliis, Lee, Winston, Allikmets, Rando, Tsang, Stephen, Sparrow, Janet R.

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Deep Scleral Exposure: A Degenerative Outcome of End-Stage Stargardt Disease di LEE, WINSTON, ZERNANT, JANA, NAGASAKI, TAKAYUKI, TSANG, STEPHEN H., ALLIKMETS, RANDO

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Disease Progression in Autosomal Dominant Cone-Rod Dystrophy Caused by a Novel Mutation (D100G) in the GUCA1A Gene di Nong, Eva, Lee, Winston, Merriam, Joanna E., Allikmets, Rando, Tsang, Stephen H.

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Generalized Choriocapillaris Dystrophy, a Distinct Phenotype in the Spectrum of ABCA4-Associated Retinopathies di Bertelsen, Mette, Zernant, Jana, Larsen, Michael, Duno, Morten, Allikmets, Rando, Rosenberg, Thomas

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Peripapillary sparing in RDH12-associated Leber congenital amaurosis di Garg, Aakriti, Lee, Winston, Sengillo, Jesse D., Allikmets, Rando, Tsang, Stephen H.

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Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations di Cremers, Frans P.M., Lee, Winston, Collin, Rob W.J., Allikmets, Rando

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Loss of Peripapillary Sparing in non-Group I Stargardt Disease di Burke, Tomas R, Allikmets, Rando, Smith, R. Theodore, Gouras, Peter, Tsang, Stephen H

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Familial discordance in Stargardt disease di Burke, Tomas R., Tsang, Stephen H., Zernant, Jana, Smith, R. Theodore, Allikmets, Rando

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Psychophysical Measurement of Rod and Cone Thresholds in Stargardt Disease with Full-Field Stimuli di Collison, Frederick T., Fishman, Gerald A., McAnany, J. Jason, Zernant, Jana, Allikmets, Rando

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Complement, Age-Related Macular Degeneration and a Vision of the Future di Gehrs, Karen M., Jackson, Jared R., Brown, Eric N., Allikmets, Rando, Hageman, Gregory S.

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Recessive Stargardt Disease Phenocopying Hydroxychloroquine Retinopathy di Noupuu, Kalev, Lee, Winston, Zernant, Jana, Greenstein, Vivienne C., Tsang, Stephen, Allikmets, Rando

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