Experts' opinions on the profile of optimal care for patients with diabetes mellitus type 2 in the Netherlands von VAN DEN AREND, Irma J. M, RUTTEN, Guy E. H. M, SCHRIJVERS, Guus J. P, STOLK, Ronald P

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A human monoclonal antibody targeting the conserved staphylococcal antigen IsaA protects mice against Staphylococcus aureus bacteremia von van den Berg, Sanne, Bonarius, Hendrik P.J, van Kessel, Kok P.M, Elsinga, Goffe S, Kooi, Neeltje, Westra, Hans, Bosma, Tjibbe, van der Kooi-Pol, Magdalena M, Koedijk, Danny G.A.M, Groen, Herman, van Dijl, Jan Maarten, Buist, Girbe, Bakker-Woudenberg, Irma A.J.M

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Mild Staphylococcus aureus Skin Infection Improves the Course of Subsequent Endogenous S. aureus Bacteremia in Mice von van den Berg, Sanne, de Vogel, Corné P, van Belkum, Alex, Bakker-Woudenberg, Irma A J M

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Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype-Phenotype Correlations von Mackay, Donna S., Borman, Arundhati Dev, Sui, Ruifang, van den Born, L. Ingeborgh, Berson, Eliot L., Ocaka, Louise A., Davidson, Alice E., Heckenlively, John R., Branham, Kari, Ren, Huanan, Lopez, Irma, Maria, Maleeha, Azam, Maleeha, Henkes, Arjen, Blokland, Ellen, Andreasson, Sten, de Baere, Elfride, Bennett, Jean, Chader, Gerald J., Berger, Wolfgang, Golovleva, Irina, Greenberg, Jacquie, den Hollander, Anneke I., Klaver, Caroline C.W., Klevering, B. Jeroen, Lorenz, Birgit, Preising, Markus N., Ramesar, Raj, Roberts, Lisa, Roepman, Ronald, Rohrschneider, Klaus, Wissinger], Bernd, Qamar, Raheel, Webster, Andrew R., Cremers, Frans P.M., Moore, Anthony T., Koenekoop, Robert K.

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A multiplex assay for the quantification of antibody responses in Staphylococcus aureus infections in mice von van den Berg, Sanne, Bowden, M. Gabriela, Bosma, Tjibbe, Buist, Girbe, van Dijl, Jan Maarten, van Wamel, Willem J., de Vogel, Corné P., van Belkum, Alex, Bakker-Woudenberg, Irma A.J.M.

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Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements von Wang, Feng, Wang, Hui, Tuan, Han-Fang, Nguyen, Duy H., Sun, Vincent, Keser, Vafa, Bowne, Sara J., Sullivan, Lori S., Luo, Hongrong, Zhao, Ling, Wang, Xia, Zaneveld, Jacques E., Salvo, Jason S., Siddiqui, Sorath, Mao, Louise, Wheaton, Dianna K., Birch, David G., Branham, Kari E., Heckenlively, John R., Wen, Cindy, Flagg, Ken, Ferreyra, Henry, Pei, Jacqueline, Khan, Ayesha, Ren, Huanan, Wang, Keqing, Lopez, Irma, Qamar, Raheel, Zenteno, Juan C., Ayala-Ramirez, Raul, Buentello-Volante, Beatriz, Fu, Qing, Simpson, David A., Li, Yumei, Sui, Ruifang, Silvestri, Giuliana, Daiger, Stephen P., Koenekoop, Robert K., Zhang, Kang, Chen, Rui

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Mutations in SPATA7 Cause Leber Congenital Amaurosis and Juvenile Retinitis Pigmentosa von Wang, Hui, den Hollander, Anneke I., Moayedi, Yalda, Abulimiti, Abuduaini, Li, Yumei, Collin, Rob W.J., Hoyng, Carel B., Lopez, Irma, Bray, Molly, Lewis, Richard Alan, Lupski, James R., Mardon, Graeme, Koenekoop, Robert K., Chen, Rui

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Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing von Wang, Xia, Wang, Hui, Sun, Vincent, Tuan, Han-Fang, Keser, Vafa, Wang, Keqing, Ren, Huanan, Lopez, Irma, Zaneveld, Jacques E, Siddiqui, Sorath, Bowles, Stephanie, Khan, Ayesha, Salvo, Jason, Jacobson, Samuel G, Iannaccone, Alessandro, Wang, Feng, Birch, David, Heckenlively, John R, Fishman, Gerald A, Traboulsi, Elias I, Li, Yumei, Wheaton, Dianna, Koenekoop, Robert K, Chen, Rui

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Low‐affinity TCR engagement drives IL‐2‐dependent post‐thymic maintenance of naive CD4+ T cells in aged humans von Geest, Kornelis S. M., Abdulahad, Wayel H., Teteloshvili, Nato, Tete, Sarah M., Peters, Jorieke H., Horst, Gerda, Lorencetti, Pedro G., Bos, Nicolaas A., Lambeck, Annechien, Roozendaal, Caroline, Kroesen, Bart‐Jan, Koenen, Hans J. P. M., Joosten, Irma, Brouwer, Elisabeth, Boots, Annemieke M. H.

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Union makes strength: a worldwide collaborative genetic and clinical study to provide a comprehensive survey of RD3 mutations and delineate the associated phenotype von Perrault, Isabelle, Estrada-Cuzcano, Alejandro, Lopez, Irma, Kohl, Susanne, Li, Shiqiang, Testa, Francesco, Zekveld-Vroon, Renate, Wang, Xia, Pomares, Esther, Andorf, Jean, Aboussair, Nisrine, Banfi, Sandro, Delphin, Nathalie, den Hollander, Anneke I, Edelson, Catherine, Florijn, Ralph, Jean-Pierre, Marc, Leowski, Corinne, Megarbane, Andre, Villanueva, Cristina, Flores, Blanca, Munnich, Arnold, Ren, Huanan, Zobor, Ditta, Bergen, Arthur, Chen, Rui, Cremers, Frans P M, Gonzalez-Duarte, Roser, Koenekoop, Robert K, Simonelli, Francesca, Stone, Edwin, Wissinger, Bernd, Zhang, Qingjiong, Kaplan, Josseline, Rozet, Jean-Michel

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Accuracy of the Diagnostic Infant and Preschool Assessment (DIPA) in a Dutch sample von Gigengack, Maj R., Hein, Irma M., van Meijel, Els P.M., Lindeboom, Robert, van Goudoever, Johannes B., Lindauer, Ramón J.L.

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Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons von McEwen, Dyke P, Koenekoop, Robert K, Khanna, Hemant, Jenkins, Paul M, Lopez, Irma, Swaroop, Anand, Martens, Jeffrey R

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A new ocular phenotype associated with an unexpected but known systemic disorder and mutation: novel use of genomic diagnostics and exome sequencing von Majewski, Jacek, Wang, Zibo, Lopez, Irma, Al Humaid, Sulaiman, Ren, Huanan, Racine, Julie, Bazinet, Alex, Mitchel, Grant, Braverman, Nancy, Koenekoop, Robert K

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Finnish mothers’ and fathers’ reports of their boys and girls by using the Brief Infant-Toddler Social and Emotional Assessment (BITSEA) von Alakortes, Jaana, Fyrstén, Jenni, Carter, Alice S., Moilanen, Irma K., Ebeling, Hanna E.

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Exploring Cultural Identity in a Multicultural Context—the Special Case of Luxembourg von Bichler, Samantha, Albert, Isabelle, Barros, Stephanie, Murdock, Elke

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After an initial balance favoring collagen formation and mineralization, bone turnover markers return to pre-treatment levels during long-term TNF-[alpha] inhibition in patients with ankylosing spondylitis von Siderius, Mark, Spoorenberg, Anneke, Kroese, Frans G. M, van der Veer, Eveline, Arends, Suzanne

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Telomere length in Hutchinson-Gilford Progeria Syndrome von Decker, Michelle L., Chavez, Elizabeth, Vulto, Irma, Lansdorp, Peter M.

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Metabolic health of young adults who were born small for gestational age and treated with growth hormone, after cessation of growth hormone treatment: a 5-year longitudinal study von van der Steen, Manouk, Dr, Smeets, Carolina C J, MD, Kerkhof, Gerthe F, PhD, Hokken-Koelega, Anita C S, Prof

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Blockade of gC1qR/p33, a receptor for C1q, inhibits adherence of Staphylococcus aureus to the microvascular endothelium von Sethi, Shneh, Herrmann, Mathias, Roller, Jonas, von Müller, Lutz, Peerschke, Ellinor I., Ghebrehiwet, Berhane, Bajric, Irma, Menger, Michael D., Laschke, Matthias W.

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Progression of Diabetic Capillary Occlusion: A Model von Fu, Xiao, Gens, John Scott, Glazier, James A, Burns, Stephen A, Gast, Thomas J

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