Assessment of Visual Function with Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa in the Randomized XIRIUS Phase 2/3 Study von Lam, Byron L., Pennesi, Mark E., Kay, Christine N., Panda, Sushil, Gow, James A., Zhao, Guolin, MacLaren, Robert E., MacLaren, Robert, Aleman, Tomas, Birch, David, Jalil, Assad, Lotery, Andrew, Lam, Byron, Pennesi, Mark, Kay, Christine N., Yusuf, Imram H., Cehajic Kapetanovic, Jasmina, Jolly, Jasleen K., Josan, Amandeep S., Taylor, Laura J., Xue, Kanmin, Nanda, Anika, Buckley, Thomas, Salvetti, Anna Paola, Thulasidharan, Suresh, Kurc, Miguel, Khandhadia, Samir, Dias, Karla Orsine Murta, Baltmr, Abeir, Mandal, Nakul, Tsokolas, Georgios, Ivanova, Tsveta, EL-Faouri, Muhannd, Shaarawy, Sherif, Black, Graeme, Davis, Janet L., Gregori, Ninel Z., Mendoza-Santiesteban, Carlos E., Lauer, Andreas K., Yang, Paul, Bailey, Steven, Spencer, Rand, Fish, Gary E., Wang, Robert, Chong, Deborah, Abbey, Ashkan, Anand, Rajiv, MaGuire, Albert A., Roseman, Robert L., Hazariwala, Kaushik M., Parrott, Brandon

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Randomized Trial of Ciliary Neurotrophic Factor Delivered by Encapsulated Cell Intraocular Implants for Retinitis Pigmentosa von Birch, David G, Weleber, Richard G, Duncan, Jacque L, Jaffe, Glenn J, Tao, Weng

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Diabetes Eye Screening in Urban Settings Serving Minority Populations: Detection of Diabetic Retinopathy and Other Ocular Findings Using Telemedicine von Owsley, Cynthia, McGwin, Gerald, Lee, David J, Lam, Byron L, Friedman, David S, Gower, Emily W, Haller, Julia A, Hark, Lisa A, Saaddine, Jinan

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SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia von Srivastava, Siddharth, Shaked, Hagar Mor, Gable, Kenneth, Gupta, Sita D, Pan, Xueyang, Somashekarappa, Niranjanakumari, Han, Gongshe, Mohassel, Payam, Gotkine, Marc, Doney, Elizabeth, Goldenberg, Paula, Tan, Queenie K G, Gong, Yi, Kleinstiver, Benjamin, Wishart, Brian, Cope, Heidi, Pires, Claudia Brito, Stutzman, Hannah, Spillmann, Rebecca C, Sadjadi, Reza, Elpeleg, Orly, Lee, Chia-Hsueh, Bellen, Hugo J, Edvardson, Simon, Eichler, Florian, Dunn, Teresa M

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Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations von Kurata, Harley T., Jamra, Rami Abou, Alkelai, Anna, Antonarakis, Stylianos E., Bolkier, Yoav, Dickson, Patricia, Donald, Kirsten A., Eliyahu, Aviva, Emrick, Lisa, Odent, Sylvie, Ortiz-Gonzalez, Xilma, Rosenfeld, Jill A., Skraban, Cara, Alejandro, Mercedes E., Azamian, Mahshid S., Chao, Hsiao-Tuan, Dai, Hongzheng, Dhar, Shweta U., Karaviti, Lefkothea, Lee, Brendan H., Rosenfeld, Jill A., Scott, Daryl A., Wangler, Michael F., Eng, Christine M., Sullivan, Kathleen, Goldstein, David B., McConkie-Rosell, Allyn, Schoch, Kelly, Shashi, Vandana, Beggs, Alan H., Cobban, Laurel A., Cooper, Cynthia M., Fieg, Elizabeth L., Korrick, Susan, Loscalzo, Joseph, Maas, Richard L., MacRae, Calum A., Stoler, Joan M., Nagy, Anna, Dasari, Surendra, Lanpher, Brendan C., Bivona, Stephanie, Isasi, Rosario, Levitt, Roy, Tekin, Mustafa, Thorson, Willa, Eckstein, David J., Mamounas, Laura A., D’Souza, Precilla, Ferreira, Carlos, Godfrey, Rena A., Groden, Catherine A., Macnamara, Ellen F., Maduro, Valerie V., Nath, Avi, Baker, Eva, Power, Bradley, Mosbrook-Davis, Deborah, Rossignol, Francis, Yousef, Muhammad, Amendola, Laura, Bamshad, Michael, Beck, Anita, Bennett, Jimmy, Blue, Elizabeth, Chanprasert, Sirisak, Glass, Ian, Jarvik, Gail P., Jarvik, Jeffrey, Mefford, Heather, Merritt, J. Lawrence, Raskind, Wendy, Sybert, Virginia, Wener, Mark, Wenger, Tara, Fisher, Paul G., Reuter, Chloe M., Smith, Kevin S., Zastrow, Diane B., Nakano-Okuno, Mariko, Whitlock, Jordan, Butte, Manish J., Fogel, Brent L., Krakow, Deborah, Lee, Hane, Palmer, Christina G.S., Papp, Jeanette C., Woods, Jeremy D., Andrews, Ashley, Pace, Laura, Viskochil, Dave, Bican, Anna, Kennedy, Jennifer, Cogan, Joy D., Cole, F. Sessions, Kiley, Dana, Sisco, Kathy, Schedl, Timothy, Solnica-Krezel, Lilianna, Pitt, Geoffrey S.

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An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids von Ruiter, Jos P.N., van Lint, Alida E.M., Pras-Raves, Mia, Wever, Eric, Guillen Sacoto, Maria J., Begtrup, Amber, Tarnopolsky, Mark, Sell, Susan L., Nowak, Catherine B., Douglas, Jessica, Perlman, Seth, Martin, Nicole, Brault, Jennifer, Gahl, William A., Alejandro, Mercedes E., Dai, Hongzheng, Dhar, Shweta U., Hanchard, Neil A., Lee, Brendan H., Moretti, Paolo M., Murdock, David R., Nicholas, Sarah K., Potocki, Lorraine, Scott, Daryl A., Eng, Christine M., Deardorff, Matthew, Hassey, Kelly, Sullivan, Kathleen, Tan, Queenie K.-G., Beggs, Alan H., Berry, Gerard T., Cooper, Cynthia M., Pallais, J. Carl, Rodan, Lance H., Kelley, Emily G., Morava, Eva, Forghani, Irman, Lam, Byron, Levitt, Roy, Liu, Xue Zhong, McCauley, Jacob, Tekin, Mustafa, Thorson, Willa, Findley, Laurie C., Krasnewich, Donna M., Manolio, Teri A., Goldrich, Madison P., Draper, David D., Nath, Avi, Pusey, Barbara N., Toro, Camilo, Baker, Eva, Gochuico, Bernadette, Mosbrook-Davis, Deborah, Rossignol, Francis, Adam, Margaret, Amendola, Laura, Cunningham, Michael, Jarvik, Gail P., Jarvik, Jeffrey, Lam, Christina, Raskind, Wendy, Sybert, Virginia, Ashley, Euan A., Coakley, Terra R., Hom, Jason, Majcherska, Marta M., Martin, Beth A., Marwaha, Shruti, Ruzhnikov, Maura, Tabor, Holly K., Tucker, Brianna M., Zastrow, Diane B., Byrd, William E., Dell’Angelica, Esteban C., Douine, Emilie D., Mak, Bryan C., Martin, Martin G., Martínez-Agosto, Julian A., McGee, Elisabeth, Nelson, Stanley F., Parker, Neil H., Sinsheimer, Janet S., Wang, Lee-kai, Perry, Katherine Wesseling, Woods, Jeremy D., Pace, Laura, Marth, Gabor, Viskochil, Dave, Bayrak-Toydemir, Pinar, Duncan, Laura, Robertson, Amy K., Solem, Emily, Schedl, Timothy, Shin, Jimann, Solnica-Krezel, Lilianna, Waisfisz, Quinten, Zwijnenburg, Petra J.G., Wanders, Ronald J.A., Vaz, Frédéric M.

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Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science von Schoch, Kelly, Esteves, Cecilia, Bican, Anna, Spillmann, Rebecca, Cope, Heidi, McConkie-Rosell, Allyn, Walley, Nicole, Fernandez, Liliana, Kohler, Jennefer N., Bonner, Devon, Reuter, Chloe, Stong, Nicholas, Mulvihill, John J., Novacic, Donna, Wolfe, Lynne, Abdelbaki, Ayat, Toro, Camilo, Tifft, Cyndi, Malicdan, May, Gahl, William, Liu, Pengfei, Newman, John, Goldstein, David B., Hom, Jason, Sampson, Jacinda, Wheeler, Matthew T., Cogan, Joy, Bernstein, Jonathan A., Adams, David R., McCray, Alexa T., Shashi, Vandana

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Structure-Function Modeling of Optical Coherence Tomography and Standard Automated Perimetry in the Retina of Patients with Autosomal Dominant Retinitis Pigmentosa von Smith, Travis B, Parker, Maria, Steinkamp, Peter N, Weleber, Richard G, Smith, Ning, Wilson, David J

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Intravitreal Delivery of rAAV2tYF-CB-hRS1 Vector for Gene Augmentation Therapy in Patients with X-Linked Retinoschisis: 1-Year Clinical Results von Pennesi, Mark Edward, Yang, Paul, Birch, David G, Weng, Christina Y, Moore, Anthony T, Iannaccone, Alessandro, Comander, Jason I, Jayasundera, Thiran, Chulay, Jeffrey

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One is the loneliest number: genotypic matchmaking using the electronic health record von Koziura, Mary E., Phillips, John A., Peterson, Josh F., Newman, John H., Bastarache, Lisa, Bacino, Carlos A., Balasubramanyam, Ashok, Clark, Gary D., Dhar, Shweta U., Jamal, Fariha, Lalani, Seema R., Lewis, Richard A., Orengo, James P., Vogel, Tiphanie P., Wangler, Michael F., Goldstein, David B., Cope, Heidi, Jiang, Yong-hui, Spillmann, Rebecca C., Tan, Queenie K.-G., Walley, Nicole M., Fieg, Elizabeth L., Korrick, Susan, Krier, Joel B., Maas, Richard L., Pallais, J. Carl, Rodan, Lance H., Silverman, Edwin K., Esteves, Cecilia, Kelley, Emily G., Kohane, Isaac S., Bick, David P., Birch, Camille L., Boone, Braden E., Levy, Shawn E., Worthey, Elizabeth A., Oglesbee, Devin, Forghani, Irman, Grajewski, Alana, Isasi, Rosario, McCauley, Jacob, Sacco, Ralph, Thorson, Willa, Colley, Heather A., Krasnewich, Donna M., Mamounas, Laura A., Rowley, Robb K., Tamburro, Cecelia P., Bonnenmann, Carsten, Estwick, Tyra, Ferreira, Carlos, Godfrey, Rena A., Groden, Catherine A., Maduro, Valerie V., Novacic, Donna, Pusey, Barbara N., Sharma, Prashant, Toro, Camilo, Wahl, Colleen E., Yu, Guoyun, Baker, Eva, Adams, David R., Malicdan, May Christine V., Yang, John, Koeller, David M., Kyle, Jennifer E., Webb-Robertson, Bobbie-Jo M., Bernstein, Jonathan A., Bonner, Devon, Fernandez, Liliana, Huang, Yong, Kohler, Jennefer N., Majcherska, Marta M., Reuter, Chloe M., Sampson, Jacinda B., Wheeler, Matthew T., Zastrow, Diane B., Zhao, Chunli, Fresard, Laure, Bejerano, Gill, Butte, Manish J., Dell’Angelica, Esteban C., Dorrani, Naghmeh, Krakow, Deborah, Lee, Hane, Loo, Sandra K., Martin, Martin G., Woods, Jeremy D., Yoon, Amanda J., Botto, Lorenzo, Andrews, Ashley, Carey, John, Quinlan, Aaron, Bayrak-Toydemir, Pinar, Postlethwait, John H., Shakachite, Lisa, Wambach, Jennifer, Wegner, Daniel, Baldridge, Dustin, Solnica-Krezel, Lilianna

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Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids von Ferdinandusse, Sacha, McWalter, Kirsty, te Brinke, Heleen, IJlst, Lodewijk, Mooijer, Petra M., Ruiter, Jos P. N., van Lint, Alida E. M., Pras-Raves, Mia, Wever, Eric, Millan, Francisca, Guillen Sacoto, Maria J., Begtrup, Amber, Tarnopolsky, Mark, Brady, Lauren, Ladda, Roger L., Sell, Susan L., Nowak, Catherine B., Douglas, Jessica, Tian, Cuixia, Ulm, Elizabeth, Perlman, Seth, Drack, Arlene V., Chong, Karen, Martin, Nicole, Brault, Jennifer, Brokamp, Elly, Toro, Camilo, Gahl, William A., Macnamara, Ellen F., Wolfe, Lynne, Waisfisz, Quinten, Zwijnenburg, Petra J. G., Ziegler, Alban, Barth, Magalie, Smith, Rosemarie, Ellingwood, Sara, Gaebler-Spira, Deborah, Bakhtiari, Somayeh, Kruer, Michael C., van Kampen, Antoine H. C., Wanders, Ronald J. A., Waterham, Hans R., Cassiman, David, Vaz, Frédéric M.

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Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations von Kurata, Harley T., Jamra, Rami Abou, Alkelai, Anna, Antonarakis, Stylianos E., Bolkier, Yoav, Dickson, Patricia, Donald, Kirsten A., Eliyahu, Aviva, Emrick, Lisa, Odent, Sylvie, Ortiz-Gonzalez, Xilma, Rosenfeld, Jill A., Skraban, Cara, Alejandro, Mercedes E., Azamian, Mahshid S., Chao, Hsiao-Tuan, Dai, Hongzheng, Dhar, Shweta U., Karaviti, Lefkothea, Lee, Brendan H., Rosenfeld, Jill A., Scott, Daryl A., Wangler, Michael F., Eng, Christine M., Sullivan, Kathleen, Goldstein, David B., McConkie-Rosell, Allyn, Schoch, Kelly, Shashi, Vandana, Beggs, Alan H., Cobban, Laurel A., Cooper, Cynthia M., Fieg, Elizabeth L., Korrick, Susan, Loscalzo, Joseph, Maas, Richard L., MacRae, Calum A., Stoler, Joan M., Nagy, Anna, Dasari, Surendra, Lanpher, Brendan C., Bivona, Stephanie, Isasi, Rosario, Levitt, Roy, Tekin, Mustafa, Thorson, Willa, Eckstein, David J., Mamounas, Laura A., D’Souza, Precilla, Ferreira, Carlos, Godfrey, Rena A., Groden, Catherine A., Macnamara, Ellen F., Maduro, Valerie V., Nath, Avi, Baker, Eva, Power, Bradley, Mosbrook-Davis, Deborah, Rossignol, Francis, Yousef, Muhammad, Amendola, Laura, Bamshad, Michael, Beck, Anita, Bennett, Jimmy, Blue, Elizabeth, Chanprasert, Sirisak, Glass, Ian, Jarvik, Gail P., Jarvik, Jeffrey, Mefford, Heather, Merritt, J. Lawrence, Raskind, Wendy, Sybert, Virginia, Wener, Mark, Wenger, Tara, Fisher, Paul G., Reuter, Chloe M., Smith, Kevin S., Zastrow, Diane B., Nakano-Okuno, Mariko, Whitlock, Jordan, Butte, Manish J., Fogel, Brent L., Krakow, Deborah, Lee, Hane, Palmer, Christina G.S., Papp, Jeanette C., Woods, Jeremy D., Andrews, Ashley, Pace, Laura, Viskochil, Dave, Bican, Anna, Kennedy, Jennifer, Cogan, Joy D., Cole, F. Sessions, Kiley, Dana, Sisco, Kathy, Schedl, Timothy, Solnica-Krezel, Lilianna, Pitt, Geoffrey S.

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The Idiopathic Intracranial Hypertension Treatment Trial: Design Considerations and Methods von Friedman, Deborah I, McDermott, Michael P, Kieburtz, Karl, Kupersmith, Mark, Stoutenburg, Ann, Keltner, John L, Feldon, Steven E, Schron, Eleanor, Corbett, James J, Wall, Michael

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Ophthalmic and Systemic Factors of Acute Nonarteritic Anterior Ischemic Optic Neuropathy in the Quark207 Treatment Trial von Kupersmith, Mark J., Fraser, Clare L., Morgenstern, Rachelle, Miller, Neil R., Levin, Leonard A., Jette, Nathalie, Clare, Fraser, Celia, Chen, Neil, Shuey, Stephen, Colley, Wang, Ningli, Dou, Hongliang, Zhong, Yong, Tang, Luosheng, Han, Quanhong, Dirk, Sandner, Maria-Andreea, Gamulescu, Nicole, Eter, Helmut, Wilhelm, Katrin, Lorenz, Santhosh, Krishna G., Ramesh, Kekunnaya, S, Ambika, Kumudini, Sharma, Warkad, Vivekanand Uttamrao, Rohit, Saxena, Mahesh, Kumar S., Dipankar, Das, Atul, Hegade, Shahana, Mazumdar, Sachin, Daighavane, Virender, Sachdeva, Hadas, Kalish, Ainat, Klein, Ruth, Huna-Baron, Hana, Leiba, Nitza, Goldenberg-Cohen, Marina, Shneck, Joshua, Kruger, Pasquale, Ciardella Antonio, Gianni, Virgili, Arturo, Carta, Stefania, Bianchi Marzoli, Tow, Sharon, Fang, Chin Chee, Peter, MacIntosh, Jeffrey, Bennett, Byron, Lam, Bradley, Katz, Zoe, Williams, Michael, Lee, Madhura, Tamhankar, Rudrani, Banik, Michael, Rauser, Marc, Levy, Joyce, Liao Yaping, James, Luu, Michael, Tibbetts, David, Scales, Robert, Lesser, Anil, Patel, Syndee, Givre, Gregory, Van Stavern, Steven, Hamilton, Vivian, Rismondo, Courtney, Francis, Dean, Cestari, Marc, Dinkin, John, Pula, Padmaja, Sudhakar, Steven, Newman, Rosa, Tang, Joseph, Chacko, Sachin, Kedar, Peter, Quiros, Larry, Frohman, Nicholas, Volpe, Patrick, Sibony, John, Chen, Luis, Mejico, Gregory, Kosmorsky, Virgil, Alfaro Daniel, David, Katz, Andrew, Lee, Lindsey, DeLott, Vivek, Patel, Swaraj, Bose, Crandall, Peeler, Bhatti, Tariq

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SYNCHRONOUS MESSAGE MANAGEMENT SYSTEM von WOODS, DONALD R, LAM, BYRON S, ROXBOROUGH, IAN T, DAWES, ADAM S, PETRY, SCOTT M, LUND, PETER K

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Synchronous message management system von WOODS, DONALD R, LAM, BYRON S, ROXBOROUGH, IAN T, DAWES, ADAM S, PETRY, SCOTT M, LUND, PETER K

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SYNCHRONOUS MESSAGE MANAGEMENT SYSTEM von WOODS, DONALD R, LAM, BYRON S, ROXBOROUGH, IAN T, DAWES, ADAM S, PETRY, SCOTT M, LUND, PETER K

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Synchronous message management system von WOODS, DONALD R, LAM, BYRON S, ROXBOROUGH, IAN T, DAWES, ADAM S, PETRY, SCOTT M, LUND, PETER K

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SYNCHRONOUS MESSAGE MANAGEMENT SYSTEM von WOODS, DONALD R, LAM, BYRON S, ROXBOROUGH, IAN T, DAWES, ADAM S, PETRY, SCOTT M, LUND, PETER K

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SYNCHRONOUS MESSAGE MANAGEMENT SYSTEM von WOODS, DONALD R, LAM, BYRON S, ROXBOROUGH, IAN T, DAWES, ADAM S, PETRY, SCOTT M, LUND, PETER K

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