Search Results - "Razeen, Moataz M"

Assessing Photoreceptor Structure in Retinitis Pigmentosa and Usher Syndrome by Sun, Lynn W, Johnson, Ryan D, Langlo, Christopher S, Cooper, Robert F, Razeen, Moataz M, Russillo, Madia C, Dubra, Alfredo, Connor, Jr, Thomas B, Han, Dennis P, Pennesi, Mark E, Kay, Christine N, Weinberg, David V, Stepien, Kimberly E, Carroll, Joseph

“…The purpose of this study was to examine cone photoreceptor structure in retinitis pigmentosa (RP) and Usher syndrome using confocal and nonconfocal…”
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Correlating Photoreceptor Mosaic Structure to Clinical Findings in Stargardt Disease by Razeen, Moataz M, Cooper, Robert F, Langlo, Christopher S, Goldberg, Mara R, Wilk, Melissa A, Han, Dennis P, Connor, Jr, Thomas B, Fishman, Gerald A, Collison, Frederick T, Sulai, Yusufu N, Dubra, Alfredo, Carroll, Joseph, Stepien, Kimberly E

“…To demonstrate a method for correlating photoreceptor mosaic structure with optical coherence tomography (OCT) and microperimetry findings in patients with…”
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Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia by Langlo, Christopher S, Patterson, Emily J, Higgins, Brian P, Summerfelt, Phyllis, Razeen, Moataz M, Erker, Laura R, Parker, Maria, Collison, Frederick T, Fishman, Gerald A, Kay, Christine N, Zhang, Jing, Weleber, Richard G, Yang, Paul, Wilson, David J, Pennesi, Mark E, Lam, Byron L, Chiang, John, Chulay, Jeffrey D, Dubra, Alfredo, Hauswirth, William W, Carroll, Joseph

“…Congenital achromatopsia (ACHM) is an autosomal recessive disorder in which cone function is absent or severely reduced. Gene therapy in animal models of ACHM…”
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REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA by Langlo, Christopher S, Erker, Laura R, Parker, Maria, Patterson, Emily J, Higgins, Brian P, Summerfelt, Phyllis, Razeen, Moataz M, Collison, Frederick T, Fishman, Gerald A, Kay, Christine N, Zhang, Jing, Weleber, Richard G, Yang, Paul, Pennesi, Mark E, Lam, Byron L, Chulay, Jeffrey D, Dubra, Alfredo, Hauswirth, William W, Wilson, David J, Carroll, Joseph

“…Congenital achromatopsia is an autosomal recessive disease causing substantial reduction or complete absence of cone function. Although believed to be a…”
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Residual Foveal Cone Structure in CNGB3 -Associated Achromatopsia by Langlo, Christopher S., Patterson, Emily J., Higgins, Brian P., Summerfelt, Phyllis, Razeen, Moataz M., Erker, Laura R., Parker, Maria, Collison, Frederick T., Fishman, Gerald A., Kay, Christine N., Zhang, Jing, Weleber, Richard G., Yang, Paul, Wilson, David J., Pennesi, Mark E., Lam, Byron L., Chiang, John, Chulay, Jeffrey D., Dubra, Alfredo, Hauswirth, William W., Carroll, Joseph

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Reflectance adaptive optics findings in a patient with Vogt-Koyanagi-Harada disease by Pham, Aarin Thuan, Onghanseng, Neil, Halim, Muhammad Sohail, Ormaechea, Maria Soledad, Hassan, Muhammad, Akhavanrezayat, Amir, Uludag, Gunay, Tran, Anh NT, Razeen, Moataz M., Sredar, Nripun, Dubra, Alfredo, Nguyen, Quan Dong

“…To describe the reflectance adaptive optics scanning laser ophthalmoscopy (AOSLO) findings in different stages of Vogt-Koyanagi-Harada (VKH) disease and…”
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Correlating Photoreceptor Mosaic Structure to Clinical Findings in Stargardt Disease by Razeen, Moataz M., Cooper, Robert F., Langlo, Christopher S., Goldberg, Mara R., Wilk, Melissa A., Han, Dennis P., Connor, Thomas B., Fishman, Gerald A., Collison, Frederick T., Sulai, Yusufu N., Dubra, Alfredo, Carroll, Joseph, Stepien, Kimberly E.

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Reflectance adaptive optics findings in a patient with Vogt-Koyanagi-Harada disease by Pham, Aarin Thuan, Onghanseng, Neil, Halim, Muhammad Sohail, Ormaechea, Maria Soledad, Hassan, Muhammad, Akhavanrezayat, Amir, Uludag, Gunay, Tran, Anh Nt, Razeen, Moataz M, Sredar, Nripun, Dubra, Alfredo, Nguyen, Quan Dong

“…PurposeTo describe the reflectance adaptive optics scanning laser ophthalmoscopy (AOSLO) findings in different stages of Vogt-Koyanagi-Harada (VKH) disease and…”
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