Rapid linear scale-up of a protein separation by centrifugal partition chromatography von Sutherland, I.A., Audo, G., Bourton, E., Couillard, F., Fisher, D., Garrard, I., Hewitson, P., Intes, O.

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Fractionation of UV-B absorbing molecules and of free radical scavenging compounds from Solieria chordalis by using centrifugal partition chromatography von Boulho, R., Le Roux, J., Le Quémener, C., Audo, G., Bourgougnon, N., Bedoux, G.

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Congenital stationary night blindness: An analysis and update of genotype–phenotype correlations and pathogenic mechanisms von Zeitz, Christina, Robson, Anthony G., Audo, Isabelle

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Multiplex PCR for detection of seven virulence factors and K1/K2 capsular serotypes of Klebsiella pneumoniae von Compain, Fabrice, Babosan, Ana, Brisse, Sylvain, Genel, Nathalie, Audo, Jennifer, Ailloud, Florent, Kassis-Chikhani, Najiby, Arlet, Guillaume, Decré, Dominique

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New thylacocephalans from the Cretaceous Lagerstatten of Lebanon von Charbonnier, S, Teruzzi, G, Audo, D, Lasseron, M, Haug, C, Haug, J. T

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Three‐Year Safety Results of SAR422459 (EIAV‐ABCA4) Gene Therapy in Patients With ABCA4‐Associated Stargardt Disease: An Open‐Label Dose‐Escalation Phase I/IIa Clinical Trial, Coho... von Parker, Maria A., Erker, Laura R., Audo, Isabelle, Choi, Dongseok, Mohand-Said, Saddek, Sestakauskas, Kastytis, Benoit, Patrick, Appelqvist, Terence, Krahmer, Melissa, Ségaut-Prévost, Caroline, Lujan, Brandon J., Faridi, Ambar, Chegarnov, Elvira N., Steinkamp, Peter N., Ku, Cristy, da Palma, Mariana Matioli, Barale, Pierre-Olivier, Ayelo-Scheer, Sarah, Lauer, Andreas, Stout, Tim, Wilson, David J., Weleber, Richard G., Pennesi, Mark E., Sahel, José Alain, Yang, Paul

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Reduction of residual excess noise in class-A lasers using two-photon absorption von Audo, Kévin, Amili, Abdelkrim El, Baili, Ghaya, Dolfi, Daniel, Alouini, Mehdi

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Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium von Thompson, Debra A, Ali, Robin R, Banin, Eyal, Branham, Kari E, Flannery, John G, Gamm, David M, Hauswirth, William W, Heckenlively, John R, Iannaccone, Alessandro, Jayasundera, K Thiran, Khan, Naheed W, Molday, Robert S, Pennesi, Mark E, Reh, Thomas A, Weleber, Richard G, Zacks, David N

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Change in Cone Structure Over 24 Months in USH2A-Related Retinal Degeneration von Duncan, Jacque L., Liang, Wendi, Maguire, Maureen G., Porco, Travis C., Wong, Jessica, Audo, Isabelle, Cava, Jenna A., Grieve, Kate, Kalitzeos, Angelos, Kreis, Joseph, Michaelides, Michel, Norberg, Nathaniel, Paques, Michel, Carroll, Joseph

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Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 24-Month Period (ProgStar Report No. 17) von Strauss, Rupert W., Ho, Alexander, Jha, Anamika, Fujinami, Kaoru, Michaelides, Michel, Cideciyan, Artur V., Audo, Isabelle, Birch, David G., Sadda, Srinivas, Ip, Michael, West, Sheila, Schönbach, Etienne M., Kong, Xiangrong, Scholl, Hendrik P.N.

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Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity von Duncan, Jacque L., Liang, Wendi, Maguire, Maureen G., Audo, Isabelle, Ayala, Allison R., Birch, David G., Carroll, Joseph, Cheetham, Janet K., Esposti, Simona Degli, Durham, Todd A., Erker, Laura, Farsiu, Sina, Ferris, Frederick L., Heon, Elise, Hufnagel, Robert B., Iannaccone, Alessandro, Jaffe, Glenn J., Kay, Christine N., Michaelides, Michel, Pennesi, Mark E., Sahel, José-Alain

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The RUSH2A Study: Dark-Adapted Visual Fields in Patients With Retinal Degeneration Associated With Biallelic Variants in the USH2A Gene von Birch, David G, Samarakoon, Lassana, Melia, Michele, Duncan, Jacque L, Ayala, Allison R, Audo, Isabelle, Cheetham, Janet K, Durham, Todd A, Iannaccone, Alessandro, Pennesi, Mark E, Stingl, Katarina

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The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy von Wissinger, Bernd, Baumann, Britta, Buena-Atienza, Elena, Ravesh, Zeinab, Cideciyan, Artur V, Stingl, Katarina, Audo, Isabelle, Meunier, Isabelle, Bocquet, Beatrice, Traboulsi, Elias I, Hardcastle, Alison J, Gardner, Jessica C, Michaelides, Michel, Branham, Kari E, Rosenberg, Thomas, Andreasson, Sten, Dollfus, Hélène, Birch, David, Vincent, Andrea L, Martorell, Loreto, Català Mora, Jaume, Kellner, Ulrich, Rüther, Klaus, Lorenz, Birgit, Preising, Markus N, Manfredini, Emanuela, Zarate, Yuri A, Vijzelaar, Raymon, Zrenner, Eberhart, Jacobson, Samuel G, Kohl, Susanne

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Deep‐intronic variants in CNGB3 cause achromatopsia by pseudoexon activation von Weisschuh, Nicole, Sturm, Marc, Baumann, Britta, Audo, Isabelle, Ayuso, Carmen, Bocquet, Beatrice, Branham, Kari, Brooks, Brian P., Catalá‐Mora, Jaume, Giorda, Roberto, Heckenlively, John R., Hufnagel, Robert B., Jacobson, Samuel G., Kellner, Ulrich, Kitsiou‐Tzeli, Sofia, Matet, Alexandre, Martorell Sampol, Loreto, Meunier, Isabelle, Rudolph, Günther, Sharon, Dror, Stingl, Katarina, Streubel, Berthold, Varsányi, Balázs, Wissinger, Bernd, Kohl, Susanne

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Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene von Felden, Julia, Baumann, Britta, Ali, Manir, Audo, Isabelle, Ayuso, Carmen, Bocquet, Beatrice, Casteels, Ingele, Garcia‐Sandoval, Blanca, Jacobson, Samuel G., Jurklies, Bernhard, Kellner, Ulrich, Kessel, Line, Lorenz, Birgit, McKibbin, Martin, Meunier, Isabelle, Ravel, Thomy, Rosenberg, Thomas, Rüther, Klaus, Vadala, Maria, Wissinger, Bernd, Stingl, Katarina, Kohl, Susanne

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TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness von Audo, Isabelle, Kohl, Susanne, Leroy, Bart P., Munier, Francis L., Guillonneau, Xavier, Mohand-Saïd, Saddek, Bujakowska, Kinga, Nandrot, Emeline F., Lorenz, Birgit, Preising, Markus, Kellner, Ulrich, Renner, Agnes B., Bernd, Antje, Antonio, Aline, Moskova-Doumanova, Veselina, Lancelot, Marie-Elise, Poloschek, Charlotte M., Drumare, Isabelle, Defoort-Dhellemmes, Sabine, Wissinger, Bernd, Léveillard, Thierry, Hamel, Christian P., Schorderet, Daniel F., De Baere, Elfride, Berger, Wolfgang, Jacobson, Samuel G., Zrenner, Eberhart, Sahel, José-Alain, Bhattacharya, Shomi S., Zeitz, Christina

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Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium von Thompson, Debra A., Iannaccone, Alessandro, Ali, Robin R., Arshavsky, Vadim Y., Audo, Isabelle, Bainbridge, James W. B., Besirli, Cagri G., Birch, David G., Branham, Kari E., Cideciyan, Artur, Daiger, Steven P., Dalkara, Deniz, Duncan, Jacque L., Fahim, Abigail T., Flannery, John G., Gattegna, Roberto, Heckenlively, John R., Heon, Elise, Jayasundera, K. Thiran, Khan, Naheed W., Klassen, Henry, Leroy, Bart P., Molday, Robert S., Musch, David C., Pennesi, Mark E., Petersen-Jones, Simon M., Pierce, Eric A., Rao, Rajesh C., Reh, Thomas A., Sahel, Jose A., Sharon, Dror, Sieving, Paul A., Strettoi, Enrica, Yang, Paul, Zacks, David N.

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Early and mid-term outcomes of 1904 patients undergoing transcatheter balloon-expandable valve implantation in Italy: results from the Italian Transcatheter Balloon-Expandable Valv... von Salizzoni, Stefano, D'Onofrio, Augusto, Agrifoglio, Marco, Colombo, Antonio, Chieffo, Alaide, Cioni, Micaela, Besola, Laura, Regesta, Tommaso, Rapetto, Filippo, Tarantini, Giuseppe, Napodano, Massimo, Gabbieri, Davide, Saia, Francesco, Tamburino, Corrado, Ribichini, Flavio, Cugola, Diego, Aiello, Marco, Sanna, Francesco, Iadanza, Alessandro, Pompei, Esmeralda, Stefàno, Pierluigi, Cappai, Antioco, Minati, Alessandro, Cassese, Mauro, Martinelli, Gian Luca, Agostinelli, Andrea, Fiorilli, Rosario, Casilli, Francesco, Reale, Maurizio, Bedogni, Francesco, Petronio, Anna Sonia, Mozzillo, Rosa Alba, Bonmassari, Roberto, Briguori, Carlo, Liso, Armando, Sardella, Gennaro, Bruschi, Giuseppe, Fiorina, Claudia, Filippini, Claudia, Moretti, Claudio, D'Amico, Maurizio, La Torre, Michele, Conrotto, Federico, Di Bartolomeo, Roberto, Gerosa, Gino, Rinaldi, Mauro

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Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness von Vincent, Ajoy, Audo, Isabelle, Tavares, Erika, Maynes, Jason T., Tumber, Anupreet, Wright, Thomas, Li, Shuning, Michiels, Christelle, Banin, Eyal, Bocquet, Beatrice, De Baere, Elfride, Casteels, Ingele, Defoort-Dhellemmes, Sabine, Drumare, Isabelle, Friedburg, Christoph, Gottlob, Irene, Jacobson, Samuel G., Kellner, Ulrich, Koenekoop, Robert, Kohl, Susanne, Leroy, Bart P., Lorenz, Birgit, McLean, Rebecca, Meire, Francoise, Meunier, Isabelle, Munier, Francis, de Ravel, Thomy, Reiff, Charlotte M., Mohand-Saïd, Saddek, Sharon, Dror, Schorderet, Daniel, Schwartz, Sharon, Zanlonghi, Xavier, Condroyer, Christel, MacDonald, Heather, Verdet, Robert, Sahel, José-Alain, Hamel, Christian P., Zeitz, Christina, Héon, Elise

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The Progression of Stargardt Disease as Determined by Spectral-Domain Optical Coherence Tomography over a 24-Month Period (ProgStar Report No. 18) von Strauss, Rupert Wolfgang, Lang, Lang, Ho, Alexander, Jha, Anamika, Ip, Michael, Bernstein, Paul S, Birch, David G, Cideciyan, Artur V, Michaelides, Michel, Audo, Isabelle, Sunness, Janet S, Traboulsi, Elias I, Zrenner, Eberhart, Sadda, SriniVas R, Janeschitz-Kriegl, Lucas, West, Sheila, Kong, Xiangrong, Scholl, Hendrik P N

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