Résultats de la recherche - Tom Missotten
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Retinal pigment epithelium and choroid translocation in patients with exudative age-related macular degeneration: long-term results par Kristel Maaijwee, Heinrich Heimann, Tom Missotten, Paul Mulder, Antonia M. Joussen, Jan van Meurs
Publié 2007Artigo -
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Uveitis-like syndrome and iris transillumination after the use of oral moxifloxacin par Marijke Wefers Bettink‐Remeijer, Koos Brouwers, L Van Langenhove, Peter W.T. de Waard, Tom Missotten, José P. Martinez Ciriano, Elisabeth Van Aken
Publié 2009Artigo -
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Clinical characteristics and long-term visual outcome of severe phenotypes of chronic central serous chorioretinopathy par Danial Mohabati, Thomas J. van Rijssen, Elon Van Dijk, Gregorius P. M. Luyten, Tom Missotten, Carel C B Hoyng, Suzanne Yzer, Camiel J. F. Boon
Publié 2018Artigo -
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Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis par Jonas J. W. Kuiper, Jessica van Setten, Matthew Devall, Mircea Cretu-Stancu, Sanne Hiddingh, Roel A. Ophoff, Tom Missotten, Michelle Helena van Velthoven, Anneke I. den Hollander, Carel B. Hoyng, Edward James, Emma Reeves, Miguel Cordero‐Coma, Alejandro Fonollosa, Alfredo Adán, Javier Martı́n, Bobby P. C. Koeleman, Joke H. de Boer, Sara L. Pulit, Ana Márquez, Timothy R. D. J. Radstake
Publié 2018Revisão -
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Treatment Strategies in Primary Vitreoretinal Lymphoma par Anjo Riemens, Jacoline E. C. Bromberg, Valérie Touitou, Bianka Sobolewska, Tom Missotten, Seerp Baarsma, Carel B. Hoyng, Miguel Cordero‐Coma, Oren Tomkins‐Netzer, Anna Rozalski, İlknur Tuğal-Tutkun, Yan Guex‐Crosier, Leonoor I. Los, Jan Geert Bollemeijer, Andrew Nolan, Joya Pawade, François Willermain, Bahram Bodaghi, Ninette ten Dam‐van Loon, Andrew D. Dick, Manfred Zierhut, Susan Lightman, Friederike Mackensen, Alexandre Moulin, Roel J. Erckens, Barbara Wensing, P. Le Hoang, Henk M. Lokhorst, Aniki Rothová
Publié 2014Artigo -
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A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy par Jonas J. W. Kuiper, Jessica van Setten, Stephan Ripke, Ruben van ‘t Slot, Flip Mulder, Tom Missotten, G. S. Baarsma, Laurent C. Francioli, Sara L. Pulit, Carolien G. F. de Kovel, Ninette ten Dam‐van Loon, Anneke I. den Hollander, Paulien Huis in het Veld, Carel B. Hoyng, Miguel Cordero‐Coma, Javier Martı́n, Víctor Llorenç, Bharti Arya, Dhanes Thomas, Steven C. Bakker, Roel A. Ophoff, Aniki Rothová, Paul I. W. de Bakker, Tuna Mutis, Bobby P. C. Koeleman
Publié 2014Artigo -
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ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder par Lewis Williams, Asif Javed, Amin Sabri, Denise J. Morgan, Chad Huff, John Grigg, Xiu Ting Heng, Alexis Jiaying Khng, Iris H.I.M. Hollink, Margaux A. Morrison, Leah A. Owen, Katherine Anderson, Krista Kinard, Rebecca Greenlees, Danica Novacic, Sen Hou, Wadih M. Zein, George M. Rodgers, Albert T. Vitale, Neena B. Haider, Axel M. Hillmer, Pauline C. Ng, Shankaracharya, Anson Cheng, Linda Zheng, Mark C. Gillies, Marjon van Slegtenhorst, P. Martin van Hagen, Tom Missotten, Gary L. Farley, Michael Polo, J. Jeffrey Malatack, Julie Curtin, Frank Martin, Susan Arbuckle, Stephen I. Alexander, Megan Chircop, Sonia Dávila, Kathleen B. Digre, Robyn V. Jamieson, Margaret M. DeAngelis
Publié 2019Artigo -
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Development of a Genotype Assay for Age-Related Macular Degeneration par Anita de Breuk, İlhan E. Acar, Eveline Kersten, Mascha M.V.A.P. Schijvenaars, Johanna M. Colijn, Lonneke Haer‐Wigman, Bjorn Bakker, Sarah de Jong, Magda A. Meester‐Smoor, Timo Verzijden, Tom Missotten, Jordi Monés, Marc Biarnés, Daniel Pauleikhoff, Hans W. Hense, Rufino Silva, Sandrina Nunes, Joana Barbosa Melo, Sascha Fauser, Carel B. Hoyng, Marius Ueffing, Marieke J. H. Coenen, Caroline C. W. Klaver, Anneke I. den Hollander, Soufiane Ajana, Audrey Cougnard‐Grégoire, Cécile Delcourt, Bénédicte M. J. Merle, Blanca Arango‐González, Sascha Dammeier, Sigrid Diether, Sabina Honisch, Ellen Kilger, Marius Ueffing, Tanja Endermann, Markus Zumbansen, Franz Badura, Berta de la Cerda, Marc Biarnés, Anna Borrell, Lucia L. Ferraro, Míriam Garcia, Jordi Monés, Eduardo Rodríguez, Johanna M. Colijn, M. Arfan Ikram, Caroline C. W. Klaver, Magda A. Meester‐Smoor, Timo Verzijden, Johannes Vingerling, Anneke I. den Hollander, Thomas J. Heesterbeek, Caroline C. W. Klaver, Eveline Kersten, Eiko K. de Jong, İlhan E. Acar, Anita de Breuk, Eszter Emri, Imre Lengyel, Hanno Langen, Everson Nogoceke, Tünde Pető, Philip J. Luthert, Frances M. Pool
Publié 2020Artigo
Outils de recherche:
Sujets similaires
Medicine
Internal medicine
Biology
Ophthalmology
Uveitis
Gene
Genetics
Immunology
Disease
Surgery
Visual acuity
Allele
Antigen
Cohort
Dermatology
Fluorescein angiography
Genotype
Haplotype
Human leukocyte antigen
MHC class I
Macular degeneration
Major histocompatibility complex
Odds ratio
Pathology
Phenotype
Retinal
Retinal pigment epithelium
Retrospective cohort study
Single-nucleotide polymorphism
ABCA4