Blue Cone Monochromacy Caused by the C203R Missense Mutation or Large Deletion Mutations von Sumaroka, Alexander, Garafalo, Alexandra V, Cideciyan, Artur V, Charng, Jason, Roman, Alejandro J, Choi, Windy, Saxena, Supna, Aksianiuk, Valeryia, Kohl, Susanne, Wissinger, Bernd, Jacobson, Samuel G

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Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 Gene von Jacobson, Samuel G, Cideciyan, Artur V, Sumaroka, Alexander, Roman, Alejandro J, Charng, Jason, Lu, Monica, Choi, Windy, Sheplock, Rebecca, Swider, Malgorzata, Kosyk, Mychajlo S, Schwartz, Sharon B, Stone, Edwin M, Fishman, Gerald A

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Cone Vision Changes in the Enhanced S-Cone Syndrome Caused by NR2E3 Gene Mutations von Garafalo, Alexandra V, Calzetti, Giacomo, Cideciyan, Artur V, Roman, Alejandro J, Saxena, Supna, Sumaroka, Alexander, Choi, Windy, Wright, Alan F, Jacobson, Samuel G

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Effectiveness of motivational interviewing on lifestyle modification and health outcomes of clients at risk or diagnosed with cardiovascular diseases: A systematic review von Lee, Windy W.M., Choi, K.C., Yum, Royce W.Y., Yu, Doris S.F., Chair, S.Y.

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Compounds and Compositions as Protein Kinase Inhibitors von GAY NATHANAEL S, LIU YI, YANG KUNYONG, CHOI HA-SOON, SIM TAEBO, HE XIAOHUI, RICHMOND WINDY, HE YUN, GU XIANG-JU, JIANG TOA, WANG ZHICHENG

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