Parafoveal Microvascular Alterations in Ocular and Non-Ocular Behҫet's Disease Evaluated With Optical Coherence Tomography Angiography

por Smid, Lisette M., Vermeer, Koenraad A., Missotten, Tom O. A. R., van Laar, Jan A. M., van Velthoven, Mirjam E. J.
Publicado 2021

Outcomes in patients with chronic uveitis: which factors matter to patients? A qualitative study

por Stolk-Vos, Aline C., Kasigar, Hamasa, Nijmeijer, Karlijn J., Missotten, Tom O., Busschbach, Jan J., van de Klundert, Joris J., Kranenburg, Leonieke W.
Publicado 2020

Clinical characteristics and long-term visual outcome of severe phenotypes of chronic central serous chorioretinopathy

por Mohabati, Danial, van Rijssen, Thomas J, van Dijk, Elon HC, Luyten, Gregorius PM, Missotten, Tom O, Hoyng, Carel B, Yzer, Suzanne, Boon, Camiel JF
Publicado 2018

Aberrant leukocyte telomere length in Birdshot Uveitis

por 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.
Publicado 2017

Vitreous proteomics, a gateway to improved understanding and stratification of diverse uveitis aetiologies

por 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.
Publicado 2021

Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis

por 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
Publicado 2018

ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder

por 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.
Publicado 2019