O-210 Cluster analysis reveals two hidden subgroups among patients with cryptozoospermia von Di Persio, S, Schülke, L, Wistuba, J, Cremers, J.F, Kliesch, S, Neuhaus, N

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The Scyther Tool: Verification, Falsification, and Analysis of Security Protocols: Tool Paper von Cremers, Cas J. F.

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Injective synchronisation: An extension of the authentication hierarchy von Cremers, C.J.F., Mauw, S., de Vink, E.P.

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Session-state Reveal Is Stronger Than Ephemeral Key Reveal: Attacking the NAXOS Authenticated Key Exchange Protocol von Cremers, Cas J. F.

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Checking Secrecy by Means of Partial Order Reduction von Cremers, Cas J. F., Mauw, Sjouke

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Comparing State Spaces in Automatic Security Protocol Analysis von Cremers, Cas J. F., Lafourcade, Pascal, Nadeau, Philippe

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A Syntactic Criterion for Injectivity of Authentication Protocols von Cremers, C.J.F., Mauw, S., de Vink, E.P.

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Clinical and Genetic Characteristics of Late-onset Stargardt's Disease von Westeneng-van Haaften, Sarah C., MD, Boon, Camiel J.F., MD, PhD, Cremers, Frans P.M., PhD, Hoefsloot, Lies H., PhD, den Hollander, Anneke I., PhD, Hoyng, Carel B., MD, PhD

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Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome von Arts, Heleen H, Doherty, Dan, van Beersum, Sylvia E C, Parisi, Melissa A, Letteboer, Stef J F, Gorden, Nicholas T, Peters, Theo A, Märker, Tina, Voesenek, Krysta, Kartono, Aileen, Ozyurek, Hamit, Farin, Federico M, Kroes, Hester Y, Wolfrum, Uwe, Brunner, Han G, Cremers, Frans P M, Glass, Ian A, Knoers, Nine V A M, Roepman, Ronald

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Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice von Boldt, Karsten, Mans, Dorus A, Won, Jungyeon, van Reeuwijk, Jeroen, Vogt, Andreas, Kinkl, Norbert, Letteboer, Stef J F, Hicks, Wanda L, Hurd, Ron E, Naggert, Jürgen K, Texier, Yves, den Hollander, Anneke I, Koenekoop, Robert K, Bennett, Jean, Cremers, Frans P M, Gloeckner, Christian J, Nishina, Patsy M, Roepman, Ronald, Ueffing, Marius

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Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein von van Wijk, Erwin, Kersten, Ferry F.J., Kartono, Aileen, Mans, Dorus A., Brandwijk, Kim, Letteboer, Stef J.F., Peters, Theo A., Märker, Tina, Yan, Xiumin, Cremers, Cor W.R.J., Cremers, Frans P.M., Wolfrum, Uwe, Roepman, Ronald, Kremer, Hannie

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Special Issue Introduction: Inherited Retinal Disease: Novel Candidate Genes, Genotype-Phenotype Correlations, and Inheritance Models von Cremers, Frans P M, Boon, Camiel J F, Bujakowska, Kinga, Zeitz, Christina

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Early-onset stargardt disease: phenotypic and genotypic characteristics von Lambertus, Stanley, van Huet, Ramon A C, Bax, Nathalie M, Hoefsloot, Lies H, Cremers, Frans P M, Boon, Camiel J F, Klevering, B Jeroen, Hoyng, Carel B

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OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin von Coene, Karlien L.M., Roepman, Ronald, Doherty, Dan, Afroze, Bushra, Kroes, Hester Y., Letteboer, Stef J.F., Ngu, Lock H., Budny, Bartlomiej, van Wijk, Erwin, Gorden, Nicholas T., Azhimi, Malika, Thauvin-Robinet, Christel, Veltman, Joris A., Boink, Mireille, Kleefstra, Tjitske, Cremers, Frans P.M., van Bokhoven, Hans, de Brouwer, Arjan P.M.

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The spectrum of retinal dystrophies caused by mutations in the peripherin/RDS gene von Boon, Camiel J.F., den Hollander, Anneke I., Hoyng, Carel B., Cremers, Frans P.M., Klevering, B. Jeroen, Keunen, Jan E.E.

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Genotypic and Phenotypic Characteristics of CRB1-Associated Retinal Dystrophies: A Long-Term Follow-up Study von Talib, Mays, van Schooneveld, Mary J, van Genderen, Maria M, Wijnholds, Jan, Florijn, Ralph J, Ten Brink, Jacoline B, Schalij-Delfos, Nicoline E, Dagnelie, Gislin, Cremers, Frans P M, Wolterbeek, Ron, Fiocco, Marta, Thiadens, Alberta A, Hoyng, Carel B, Klaver, Caroline C, Bergen, Arthur A, Boon, Camiel J F

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Density and duration of experimental human pneumococcal carriage von Gritzfeld, J.F., Cremers, A.J.H., Ferwerda, G., Ferreira, D.M., Kadioglu, A., Hermans, P.W.M., Gordon, S.B.

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The Common ABCA4 Variant p.Asn1868Ile Shows Nonpenetrance and Variable Expression of Stargardt Disease When Present in trans With Severe Variants von Runhart, Esmee H, Sangermano, Riccardo, Cornelis, Stéphanie S, Verheij, Joke B G M, Plomp, Astrid S, Boon, Camiel J F, Lugtenberg, Dorien, Roosing, Susanne, Bax, Nathalie M, Blokland, Ellen A W, Jacobs-Camps, Marlie H M, van der Velde-Visser, Saskia D, Pott, Jan-Willem R, Rohrschneider, Klaus, Thiadens, Alberta A H J, Klaver, Caroline C W, van den Born, L Ingeborgh, Hoyng, Carel B, Cremers, Frans P M

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Central Areolar Choroidal Dystrophy von Boon, Camiel J.F., MD, Klevering, B. Jeroen, MD, PhD, Cremers, Frans P.M., PhD, Zonneveld-Vrieling, Marijke N, Theelen, Thomas, MD, PhD, Den Hollander, Anneke I., PhD, Hoyng, Carel B., MD, PhD

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Mutations in C8orf37, Encoding a Ciliary Protein, are Associated with Autosomal-Recessive Retinal Dystrophies with Early Macular Involvement von Estrada-Cuzcano, Alejandro, Neveling, Kornelia, Kohl, Susanne, Banin, Eyal, Rotenstreich, Ygal, Sharon, Dror, Falik-Zaccai, Tzipora C., Hipp, Stephanie, Roepman, Ronald, Wissinger, Bernd, Letteboer, Stef J.F., Mans, Dorus A., Blokland, Ellen A.W., Kwint, Michael P., Gijsen, Sabine J., van Huet, Ramon A.C., Collin, Rob W.J., Scheffer, H., Veltman, Joris A., Zrenner, Eberhart, den Hollander, Anneke I., Klevering, B. Jeroen, Cremers, Frans P.M.

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