Bilaketaren emaitzak - Missotten, Tom

SF-6D utility values for the better- and worse-seeing eye for health states based on the Snellen equivalent in patients with age-related macular degeneration nork Visser, Martijn S., Amarakoon, Sankha, Missotten, Tom, Timman, Reinier, Busschbach, Jan J.

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Polymorphisms of chemokine and chemokine receptor genes in idiopathic immune-mediated posterior segment uveitis nork Ahad, Muhammad A., Missotten, Tom, Abdallah, Atiyeh, Lympany, Penny A., Lightman, Susan

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Six and eight weeks injection frequencies of bevacizumab are non-inferior to the current four weeks injection frequency for quality of life in neovascular age-related macular degen... nork Visser, Martijn S., Amarakoon, Sankha, Missotten, Tom, Timman, Reinier, Busschbach, Jan J. V.

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Case series: rituximab in the treatment of refractory sight-threatening scleritis nork van Bilsen, Kiki, van Hagen, P Martin, Missotten, Tom, Baarsma, Seerp G, Kuijpers, Robert W, van Laar, Jan AM

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Parafoveal Microvascular Alterations in Ocular and Non-Ocular Behҫet's Disease Evaluated With Optical Coherence Tomography Angiography nork Smid, Lisette M., Vermeer, Koenraad A., Missotten, Tom O. A. R., van Laar, Jan A. M., van Velthoven, Mirjam E. J.

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Diagnosis and treatment of uveitis; not restricted to the ophthalmologist nork van Laar, Jan A. M., Rothova, Aniki, Missotten, Tom, Kuijpers, Robert W. A. M., van Hagen, P. Martin, van Velthoven, Mirjam E. J.

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Outcomes in patients with chronic uveitis: which factors matter to patients? A qualitative study nork Stolk-Vos, Aline C., Kasigar, Hamasa, Nijmeijer, Karlijn J., Missotten, Tom O., Busschbach, Jan J., van de Klundert, Joris J., Kranenburg, Leonieke W.

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Clinical characteristics and long-term visual outcome of severe phenotypes of chronic central serous chorioretinopathy nork Mohabati, Danial, van Rijssen, Thomas J, van Dijk, Elon HC, Luyten, Gregorius PM, Missotten, Tom O, Hoyng, Carel B, Yzer, Suzanne, Boon, Camiel JF

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Treatment Effects in Retinal Angiomatous Proliferation Imaged with OCT Angiography nork de Jong, Jan H., Braaf, Boy, Amarakoon, Sankha, Gräfe, Maximilian, Yzer, Suzanne, Vermeer, Koenraad A., Missotten, Tom, de Boer, Johannes F., van Velthoven, Mirjam E.J.

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Aberrant leukocyte telomere length in Birdshot Uveitis nork Vazirpanah, Nadia, Verhagen, Fleurieke H., Rothova, Anna, Missotten, Tom O. A. R., van Velthoven, Mirjam, Den Hollander, Anneke I., Hoyng, Carel B., Radstake, Timothy.R. D. J., Broen, Jasper C. A., Kuiper, Jonas J. W.

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Vitreous proteomics, a gateway to improved understanding and stratification of diverse uveitis aetiologies nork Schrijver, Benjamin, Kolijn, P. Martijn, ten Berge, Josianne C.E.M., Nagtzaam, Nicole M.A., van Rijswijk, Angelique L.C.T., Swagemakers, Sigrid M.A., van der Spek, Peter J., Missotten, Tom O.A.R., van Velthoven, Mirjam E.J., de Hoog, Joeri, van Hagen, P. Martin, Langerak, Anton W., Dik, Willem A.

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Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis nork Kuiper, Jonas J W, van Setten, Jessica, Devall, Matthew, Cretu-Stancu, Mircea, Hiddingh, Sanne, Ophoff, Roel A, Missotten, Tom O A R, van Velthoven, Mirjam, Den Hollander, Anneke I, Hoyng, Carel B, James, Edward, Reeves, Emma, Cordero-Coma, Miguel, Fonollosa, Alejandro, Adán, Alfredo, Martín, Javier, Koeleman, Bobby P C, de Boer, Joke H, Pulit, Sara L, Márquez, Ana, Radstake, Timothy R D J

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A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy nork Kuiper, Jonas J.W., Van Setten, Jessica, Ripke, Stephan, Van ‘T Slot, Ruben, Mulder, Flip, Missotten, Tom, Baarsma, G. Seerp, Francioli, Laurent C., Pulit, Sara L., De Kovel, Carolien G.F., Ten Dam-Van Loon, Ninette, Den Hollander, Anneke I., Huis in het Veld, Paulien, Hoyng, Carel B., Cordero-Coma, Miguel, Martín, Javier, Llorenç, Victor, Arya, Bharti, Thomas, Dhanes, Bakker, Steven C., Ophoff, Roel A., Rothova, Aniki, De Bakker, Paul I.W., Mutis, Tuna, Koeleman, Bobby P.C.

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ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder nork Williams, Lloyd B., Javed, Asif, Sabri, Amin, Morgan, Denise J., Huff, Chad D., Grigg, John R., Heng, Xiu Ting, Khng, Alexis J., Hollink, Iris H. I. M., Morrison, Margaux A., Owen, Leah A., Anderson, Katherine, Kinard, Krista, Greenlees, Rebecca, Novacic, Danica, Nida Sen, H., Zein, Wadih M., Rodgers, George M., Vitale, Albert T., Haider, Neena B., Hillmer, Axel M., Ng, Pauline C., Shankaracharya, Cheng, Anson, Zheng, Linda, Gillies, Mark C., van Slegtenhorst, Marjon, van Hagen, P. Martin, Missotten, Tom O. A. R., Farley, Gary L., Polo, Michael, Malatack, James, Curtin, Julie, Martin, Frank, Arbuckle, Susan, Alexander, Stephen I., Chircop, Megan, Davila, Sonia, Digre, Kathleen B., Jamieson, Robyn V., DeAngelis, Margaret M.

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