Výsledky vyhledávání - 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 Autor 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 Autor 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... Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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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