Camiel Boon
Hoogleraar Oogheelkunde, in het bijzonder ziekten van de retina
- Naam
- Prof.dr. C.J.F. Boon
- c.j.f.boon@lumc.nl
Camiel J.F. Boon (1980, ’s-Hertogenbosch) is oogarts en sinds 2019 hoogleraar oogheelkunde in het Leids Universitair Medisch Centrum. Hij is binnen de oogheelkunde in het bijzonder gespecialiseerd in de ziekten van het netvlies (de retina), vitreoretinale chirurgie, en erfelijke netvliesziekten. Hij is sinds 2016 tevens bijzonder hoogleraar Klinische Ophthalmogenetica in de Amsterdam Universitaire Medische Centra / Universiteit van Amsterdam.
Meer informatie over Camiel Boon
Promovendi
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Helena Feenstra, MD. Evidence-based treatment of chronic central serous chorioretinopathy.
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Thanh Nguyen, MD. Clinical and genetic characteristics of retinitis pigmentosa.
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Leo Hahn, MD. Clinical and genetic characteristics of X-linked juvenile retinoschisis
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Joost Brinks, MD. Cell model studies on the pathogenesis of central serous chorioretinopathy.
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Thomas van Rijssen, MD. Evidence-based treatment of chronic central serous chorioretinopathy.
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Mays Talib, MD. Clinical and genetic characteristics of phenotypes associated with mutations in the CRB1 gene, the RPGR gene, and the CHM gene.
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Danial Mohabati, MD. Clinical and genetic studies on the spectrum of central serous chorioretinopathy.
Oogheelkunde
De oogarts heeft als medisch specialist vrijwel alle diagnostiek en behandeling van oogziekten in eigen hand. Het wonderlijke fenomeen van het zien start op het moment dat de lichtgevoelige cellen van de retina (het netvlies) - de fotoreceptoren - een lichtsignaal (foton) omzetten naar een elektrisch signaal. Dit elektrische signaal wordt na een complexe cascade van signaalverwerking uiteindelijk via de oogzenuw doorgegeven naar onze hersenen, waar het verder wordt geconstrueerd tot een betekenisvol beeld met bijbehorende interpretatie en ervaringen.
De ziekten van de retina hebben een belangrijk aandeel in de oogheelkundige praktijk. Deze oogziekten hebben vaak een enorme impact op het zicht, omdat ze het centrum van het netvlies - de macula of gele vlek - kunnen aantasten. Als oogarts maakt Boon gebruik van zeer gedetailleerd onderzoek met scans op micrometer-niveau, waarmee ziektebeelden zeer nauwkeurig in kaart gebracht en behandeld kunnen worden. Doordat het oog ook uitstekend benaderbaar is met microchirurgische technieken, is het ook een aantrekkelijk orgaan voor de toepassing van innovatieve nieuwe behandeltechnieken zoals gen- en stamceltherapie.
Wetenschappelijke carrière
Camiel Boon studeerde magna cum laude af in de geneeskunde aan de Katholieke Universiteit Leuven (België). Vervolgens promoveerde hij in 2009 cum laude aan de Radboud Universiteit Nijmegen, op zijn proefschrift ‘Hereditary retinal disease – Clinical and genetic studies on the role of the peripherin/RDS gene, the BEST1 gene, and the CFH gene’, waarin hij onderzoek deed naar erfelijke netvliesziekten. Voor dit proefschrift, waarin hij meerdere ziektebeelden en hun genetische associaties voor het eerst beschreef, ontving hij diverse prijzen. In 2012 voltooide hij zijn opleiding tot oogarts in het Radboud UMC te Nijmegen. Hij behaalde het predicaat Fellow of the European Board of Ophthalmology summa cum laude. Vervolgens specialiseerde Boon zich verder in de ziekten van de retina, met een fellowship medische retina en vitreoretinale chirurgie in het Oxford Eye Hospital (Oxford, Verenigd Koninkrijk), een observership bij de Vitreous Macula Retina Consultants of New York (VRMNY), gevolgd door een fellowship vitreoretinale chirurgie in Het Oogziekenhuis Rotterdam.
Met zijn onderzoeksgroep concentreert Boon zich op klinisch en genetisch wetenschappelijk onderzoek naar centrale sereuze chorioretinopathie (serosa), erfelijke netvliesziekten (inclusief gen- en stamceltherapie), en leeftijdsgebonden maculadegeneratie. Hij heeft inmiddels ruim 130 artikelen in toonaangevende wetenschappelijke tijdschriften en diverse hoofdstukken in atlassen op zijn naam staan. Prof. Boon is een veelgevraagd spreker op nationale en internationale oogheelkundige bijeenkomsten. Hij is mede-initiatiefnemer en oprichter van YOURS, de Europese vereniging van jonge netvliesspecialisten.
Boon heeft diverse prestigieuze beurzen en subsidies ontvangen, zoals een Niels Stensen Fellowship (2011), het Gisela Thier Fellowship van de Universiteit Leiden (2013), een ZonMw Veni subsidie (2015) en ZonMw Meer Kennis met Minder Dieren subsidie (2018), een ODAS Stichting subsidie (2018), een Euretina Clinical Research Award (2019), het eerste Stichting Blindenhulp Fellowship (2019), evenals meerdere EU Horizon 2020 subsidies.
Als Principal Investigator is Boon betrokken bij diverse innovatieve ‘regeneratieve geneeskunde’ studies op het vlak van nieuwe behandelingen voor netvliesziekten, zoals gentherapie. Hij is hoofdonderzoeker en medisch specialist binnen het NFU Expertisecentrum voor centrale sereuze chorioretinopathie en erfelijke netvliesziekten van het LUMC-AmsterdamUMC, evenals het European Reference Network for Rare Eye Diseases (ERN-EYE). Prof. Boon is voorzitter van de Werkgroep Ophthalmogenetica en secretaris van de Werkgroep Medische Retina van het Nederlands Oogheelkundig Gezelschap (NOG). Daarnaast is hij lid van het Steering Committee van het European Vision Institute (EVI), en lid van de prestigieuze Macula Society.
Op 5 mei 2021 vindt de oratie van Camiel Boon plaats
Hoogleraar Oogheelkunde, in het bijzonder ziekten van de retina
- Faculteit Geneeskunde
- Divisie 3
- Oogheelkunde
- Boon, N.; Lu, X.F.; Andriessen, C.A.; Orlovà, M.; Quinn, P.M.J.; Boon, C.J.F. & Wijnholds, J. (2023), Characterization and AAV-mediated CRB gene augmentation in human-derived CRB1KO and CRB1KOCRB2+/- retinal organoids, Molecular Therapy - Methods and Clinical Development 31.
- Sirks, M.J.; Dijk, E.H.C. van; Pauleikhoff, L.J.B.; Diederen, R.M.H. & Boon, C.J.F. (2023), NOn-Pachychoroid PEripapillary Schisis (NOPPES) of the Retina: A New Phenotype and its Differential Diagnosis, Asia-Pacific Journal of Ophthalmology 12(6): 614-621.
- Guimaraes, T.A.C. de; Georgiou, M.; Robson, A.G.; Fujinami, K.; Vincent, A.; Nasser, F.; Khateb, S.; Mahroo, O.A.; Pontikos, N.; Vargas, M.E.; Thiadens, A.A.H.J.; Carvalho, E.R. de; Nguyen, X.T.A.; Arno, G.; Fujinami-Yokokawa, Y.; Liu, X.; Tsunoda, K.; Hayashi, T.; Jimenez-Rolando, B.; Martin-Merida, M.I.; Avila-Fernandez, A.; Salas, E.C.; Garcia-Sandoval, B.; Ayuso, C.; Sharon, D.; Kohl, S.; Huckfeldt, R.M.; Banin, E.; Pennesi, M.E.; Khan, A.O.; Wissinger, B.; Webster, A.R.; Heon, E.; Boon, C.J.F.; Zrenner, E. & Michaelides, M. (2023), KCNV2-associated retinopathy: genotype-phenotype correlations-KCNV2 study group report 3, British Journal of Ophthalmology.
- Emde, L. von der; Mallwitz, M.; Vaisband, M.; Hasenauer, J.; Sassmannshausen, M.; Terheyden, J.H.; Sloan, K.R.; Schmitz-Valckenberg, S.; Finger, R.P.; Holz, F.G.; Ach, T.; Agostini, H.; Altay, L.; Atia, R.; Bandello, F.; Basile, P.G.; Batuca, J.; Behning, C.; Belmouhand, M.; Berger, M.; Binns, A.; Boon, C.J.F.; Böttger, M.; Bouchet, C.; Brazier, J.E.; Butt, T.; Carapezzi, C.; Carlton, J.; Carneiro, A.; Charil, A.; Coimbra, R.; Cozzi, M.; Crabb, D.P.; Cunha-Vaz, J.; Dahlke, C.; Sisternes, L. de; Dunbar, H.; Finger, R.P.; Fletcher, E.; Floyd, H.; Francisco, C.; Gutfleisch, M.; Hinz, S.; Hogg, R.; Holz, F.G.; Hoyng, C.B.; Kilani, A.; Kratzschmar, J.; Kühlewein, L.; Larsen, M.; Leal, S.; Lechanteur, Y.T.E.; Luhmann, U.F.O.; Lüning, A.; Marques, I.; Martinho, C.; Montesano, G.; Mulyukov, Z.; Paques, M.; Parodi, B.; Parravano, M.; Penas, S.; Peters, T.; Peto, T.; Pfau, M.; Poor, S.; Priglinger, S.; Rowen, D.; Rubin, G.S.; Sahel, J.; Sánchez, C.; Sander, O.; Sassmannshausen, M.; Schmid, M.; Schmitz-Valckenberg, S.; Siedlecki, J.; Silva, R.; Skelly, A.; Souied, E.; Staurenghi, G.; Stöhr, L.; Taylor, D.J.; Terheyden, J.H.; Thiele, S.; Tufail, A.; Varano, M.; Vieweg, L.; Wintergerst, L.; Wolf, A.; Zakaria, N. & MACUSTAR Consortium (2023), Retest variability and patient reliability indices of quantitative fundus autofluorescence in age-related macular degeneration: a MACUSTAR study report, Scientific Reports 13(1).
- Moekotte, L.; Kuiper, J.J.W.; Hiddingh, S.; Nguyen, X.T.A.; Boon, C.J.F.; Born, L.I. van den; Boer, J.H. de & Genderen, M.M. van (2023), CRB1-Associated Retinal Dystrophy Patients Have Expanded Lewis Glycoantigen-Positive T Cells, Investigative Ophthalmology & Visual Science 64(13).
- Moekotte, L.; Kuiper, J.J.W.; Hiddingh, S.; Nguyen, X.T.A.; Boon, C.J.F.; Born, L.I. van den; Boer, J.H. de & Genderen, M.M. van (2023), CRB1-Associated Retinal Dystrophy Patients Have Expanded Lewis Glycoantigen-Positive T Cells, Investigative Ophthalmology & Visual Science 64(13).
- Karuntu, J.S.; Nguyen, X.T.A.; Talib, M.; Schooneveld, M.J. van; Wijnholds, J.; Genderen, M.M. van; Schalij-Delfos, N.E.; Klaver, C.C.W.; Meester-Smoor, M.A.; Born, L.I. van den; Hoyng, C.B.; Thiadens, A.A.H.J.; Bergen, A.A.; Nispen, R.M.A. van & Boon, C.J.F. (2023), Quality of life in patients with CRB1-associated retinal dystrophies: A longitudinal study, Acta Ophthalmologica.
- Buck, T.M.; Quinn, P.M.J.; Pellissier, L.P.; Mulder, A.A.; Jongejan, A.; Lu, X.F.; Boon, N.; Koot, D.; Almushattat, H.; Arendzen, C.H.; Vos, R.M.; Bradley, E.J.; Freund, C.; Mikkers, H.M.M.; Boon, C.J.F.; Moerland, P.D.; Baas, F.; Koster, A.J.; Neefjes, J.; Berlin, I.; Jost, C.R. & Wijnholds, J. (2023), CRB1 is required for recycling by RAB11A+vesicles in human retinal organoids, Stem Cell Reports 18(9): 1793-1810.
- Ramtohul, P.; Pellegrini, M.; Pichi, F.; Preziosa, C.; Marchese, A.; Cicinelli, M.V.; Miserocchi, E.; Mundae, R.; Mrejen, S.; Rofagha, S.; Mein, C.E.; Mein, L.; Ober, M.D.; Souza, E.C. de; Cohen, S.Y.; Dijk, E.H.C. van; Jampol, L.; Boon, C.J.F. & Freund, K.B. (2023), STELLATE MULTIFORM AMELANOTIC CHOROIDOPATHY Clinical and Multimodal Imaging Features, RETINA: The Journal of Retinal and Vitreous Diseases 43(9): 1448-1461.
- Pauleikhoff, L.J.B.; Diederen, R.M.H.; Feenstra, H.M.A.; Schlingemann, R.O.; Dijk, E.H.C. van & Boon, C.J.F. (2023), SINGLE-SESSION BILATERAL REDUCED-SETTINGS PHOTODYNAMIC THERAPY FOR BILATERAL CHRONIC CENTRAL SEROUS CHORIORETINOPATHY, RETINA: The Journal of Retinal and Vitreous Diseases 43(8): 1356-1363.
- Groot, E.L. de; Norel, J.O.V.; Boer, J.H. de; Hiddingh, S.; Bakker, B.; Huet, R.A.C. van; Dam-Van Loon, N.H. ten; Thiadens, A.A.H.J.; Meester-Smoor, M.A.; Jong-Hesse, Y. de; , L.I. los; Hollander, A.I. den; Boon, C.J.F.; Kiemeney, L.A.; Eijk, K.R. van; Bakker, M.K.; Hoyng, C.B. & Kuiper, J.J.W. (2023), Association of risk variants in the CFH gene with elevated levels of coagulation and complement factors in idiopathic multifocal choroiditis, JAMA Ophthalmology 141(8): 737-745.
- Muijnck, C. de; Brink, J.B. ten; Bergen, A.A.; Boon, C.J.F. & Genderen, M.M. van (2023), Delineating Wolfram-like syndrome: A systematic review and discussion of the WFS1-associated disease spectrum, Survey of Ophthalmology 68(4): 641-654.
- Rämö, J.T.; Abner, E.; Dijk, E.H.C. van; Wang, X.; Brinks, J.; Nikopensius, T.; Noukas, M.; Marjonen, H.; Silander, K.; Jukarainen, S.; Kiiskinen, T.; Choi, S.H.; Kajanne, R.; Mehtonen, J.; Palta, P.; Lubitz, S.A.; Kaarniranta, K.; Sobrin, L.; Kurki, M.; Yzer, S.; Ellinor, P.T.; Esko, T.; Daly, M.J.; Hollander, A.I. den; Palotie, A.; Turunen, J.A.; Boon, C.J.F.; Rossin, E.J.; FinnGen Study & Estonian Biobank Res Team (2023), Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration (vol 141, pg.no 499, 2023), JAMA Ophthalmology.
- Boon, N.; Lu, X.F.; Andriessen, C.A.; Moustakas, I.; Buck, T.M.; Freund, C.; Arendzen, C.H.; Böhringer, S.; Boon, C.J.F.; Mei, H.L. & Wijnholds, J. (2023), AAV-mediated gene augmentation therapy of CRB1 patient-derived retinal organoids restores the histological and transcriptional retinal phenotype, Stem Cell Reports 18(5): 1123-1137.
- Ramo, J.; Abner, E.; Dijk, E.H.C. van; Wang, X.; Brinks, J.; Nikopensius, T.; Noukas, M.; Marjonen, H.; Silander, K.; Jukarainen, S.; Kiiskinen, T.; Choi, S.H.; Kajanne, R.; Mehtonen, J.; Palta, P.; Lubitz, S.A.; Kaarniranta, K.; Sobrin, L.; Kurki, M.; Yzer, S.; Ellinor, P.T.; Esko, T.; Daly, M.J.; Hollander, A.I. den; Palotie, A.; Turunen, J.A.; Boon, C.J.F.; Rossin, E.J. & Estonian Biobank Res Team (2023), Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration, JAMA Ophthalmology 141(5): 449-457.
- Mohabati, D.; Boon, C.J.F.; Hoyng, C.B.; Purtskhvanidze, K.; Roider, J. & Dijk, E.H.C. van (2023), Fundus autofluorescence abnormalities can predict fluorescein angiography abnormalities in patients with chronic central serous chorioretinopathy, Graefe's Archive for Clinical and Experimental Ophthalmology 261(9): 2489-2495.
- Nguyen, X.T.A.; Moekotte, L.; Plomp, A.S.; Bergen, A.A.; Genderen, M.M. van & Boon, C.J.F. (2023), Retinitis Pigmentosa: Current Clinical Management and Emerging Therapies, International Journal of Molecular Sciences 24(8).
- Garzone, D.; Terheyden, J.H.; Morelle, O.; Wintergerst, M.W.M.; Sassmannshausen, M.; Schmitz-Valckenberg, S.; Pfau, M.; Thiele, S.; Poor, S.; Leal, S.; Holz, F.G.; Finger, R.P.; Agostini, H.; Altay, L.; Atia, R.; Bandello, F.; Basile, P.G.; Behning, C.; Belmouhand, M.; Berger, M.; Binns, A.; Boon, C.J.F.; Böttger, M.; Bouchet, C.; Brazier, J.E.; Butt, T.; Carapezzi, C.; Carlton, J.; Carneiro, A.; Charil, A.; Coimbra, R.; Cozzi, M.; Crabb, D.P.; Cunha-Vaz, J.; Dahlke, C.; Sisternes, L. de; Dunbar, H.; Fletcher, E.; Francisco, C.; Gutfleisch, M.; Hogg, R.; Hoyng, C.B.; Kilani, A.; Krätzschmar, J.; Kühlewein, L.; Larsen, M.; Lechanteur, Y.T.E.; Luhmann, U.F.O.; Lüning, A.; Marques, I.; Martinho, C.; Montesano, G.; Mulyukov, Z.; Paques, M.; Parodi, B.; Parravano, M.; Penas, S.; Peters, T.; Peto, T.; Priglinger, S.; Rowen, D.; Rubin, G.S.; Sahel, J.; Sánchez, C.; Sander, O.; Schmid, M.; Schrinner-Fenske, H.; Siedlecki, J.; Silva, R.; Skelly, A.; Souied, E.; Staurenghi, G.; Stöhr, L.; Taylor, D.J.; Tufail, A.; Varano, M.; Vieweg, L.; Wintergerst, L.; Wolf, A.; Zakaria, N. & MACUSTAR Consortium (2023), Author Correction: Comparability of automated drusen volume measurements in age-related macular degeneration: a MACUSTAR study report (vol 12, 21911, 2022), Scientific Reports 13(1).
- Feenstra, H.M.A.; Diederen, R.M.H.; Lamme, M.J.C.M.; Tsonaka, R.; Fauser, S.; Yzer, S.; Rijssen, T. van; Gkika, T.; Downes, S.M.; Schlingemann, R.O.; Hoyng, C.B.; Dijk, E.H.C. van & Boon, C.J.F. (2023), INCREASING EVIDENCE FOR THE SAFETY OF FOVEA-INVOLVING HALF-DOSE PHOTODYNAMIC THERAPY FOR CHRONIC CENTRAL SEROUS CHORIORETINOPATHY, RETINA: The Journal of Retinal and Vitreous Diseases 43(3): 379-388.
- Romano, F.; Cozzi, M.; Monteduro, D.; Oldani, M.; Boon, C.J.F.; Staurenghi, G. & Salvetti, A.P. (2023), NATURAL COURSE AND CLASSIFICATION OF EXTENSIVE MACULAR ATROPHY WITH PSEUDODRUSEN-LIKE APPEARANCE, RETINA: The Journal of Retinal and Vitreous Diseases 43(3): 402-411.
- Dhooge, P.P.A.; Möller, P.T.; Meland, N.; Stingl, K.; Boon, C.J.F.; Lotery, A.J.; Parodi, M.B.; Herrmann, P.; Klein, W.; Fsadni, M.G.; Wheeler-Schilling, T.H.; Holz, F.G.; Hoyng, C.B.; Schmitz-Valckenberg, S. & Soraprazan Consortium (2023), Repeatability of Quantitative Autofluorescence Imaging in a Multicenter Study Involving Patients With Recessive Stargardt Disease 1, Translational Vision Science & Technology 12(2).
- Sirks, M.J.; Feenstra, H.M.A.; Vries, F.R. de; Dijkman, G.; Boon, C.J.F. & Dijk, E.H.C. van (2022), Argon laser photocoagulation in polypoidal choroidal vasculopathy, Clinical & Experimental Ophthalmology.
- Bakker, R.; Wagstaff, E.L.; Kruijt, C.C.; Emri, E.; Karnebeek, C.D.M. van; Hoffmann, M.B.; Brooks, B.P.; Boon, C.J.F.; Montoliu, L.; Genderen, M.M. van & Bergen, A.A. (2022), The retinal pigmentation pathway in human albinism: Not so black and white, Progress in Retinal and Eye Research 91.
- Bakker, R.; Wagstaff, E.L.; Kruijt, C.C.; Emri, E.; Karnebeek, C.D.M. van; Hoffmann, M.B.; Brooks, B.P.; Boon, C.J.F.; Montoliu, L.; Genderen, M.M. van & Bergen, A.A. (2022), The retinal pigmentation pathway in human albinism: Not so black and white, Progress in Retinal and Eye Research 91.
- Bakker, R.; Wagstaff, P.E.; Kruijt, C.C.; Emri, E.; Karnebeek, C.D.M. van; Hoffmann, M.B.; Brooks, B.P.; Boon, C.J.F.; Montoliu, L.; Genderen, M.M. van & Bergen, A.A. (2022), The retinal pigmentation pathway in human albinism: Not so black and white, Progress in Retinal and Eye Research 91.
- Sompele, S. van de; Small, K.W.; Cicekdal, M.B.; Soriano, V.L.; D'haene, E.; Shaya, F.S.; Agemy, S.; Snickt, T. van der; Rey, A.D.; Rosseel, T.; Heetvelde, M. van; Vergult, S.; Balikova, I.; Bergen, A.A.; Boon, C.J.F.; Zaeytijd, J. de; Inglehearn, C.F.; Kousal, B.; Leroy, B.P.; Rivolta, C.; Vaclavik, V.; Ende, J. van den; Schooneveld, M.J. van; Gómez-Skarmeta, J.L.; Tena, J.J.; Martinez-Morales, J.R.; Liskova, P.; Vleminckx, K. & Baere, E. de (2022), Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy, American Journal of Human Genetics 109(11): 2029-2048.
- Feenstra, H.M.A.; Dijk, E.H.C. van; Rijssen, T.J. van; Tsonaka, R.; Diederen, R.M.H.; Hoyng, C.B.; Schlingemann, R.O. & Boon, C.J.F. (2022), Long-term follow-up of chronic central serous chorioretinopathy patients after primary treatment of oral eplerenone or half-dose photodynamic therapy and crossover treatment, Graefe's Archive for Clinical and Experimental Ophthalmology 261.
- Feenstra, H.M.A.; Dijk, E.H.C. van; Rijssen, T.J. van; Tsonaka, R.; Diederen, R.M.H.; Schlingemann, R.O.; Hoyng, C.B. & Boon, C.J.F. (2022), Crossover to half-dose photodynamic therapy or eplerenone in chronic central serous chorioretinopathy patients, Ophthalmology Retina 6(10): 930-938.
- Scholz, P.; Altay, L.; Sitnilska, V.; Dijk, E.H.C. van; Pereira, A.M.; Haalen, F.M. van; Akhtar, I.; Boon, C.J.F. & Fauser, S. (2022), Reply.
- Dijk, E.H.C. van; Feenstra, H.M.A.; Bjerager, J.; Grauslund, J.; Boon, C.J.F. & Subhi, Y. (2023), Comparative efficacy of treatments for chronic central serous chorioretinopathy: A systematic review with network meta-analyses, Acta Ophthalmologica 101(2): 140-159.
- Dijk, E.H.C. van; Feenstra, H.M.A.; Bjerager, J.; Grauslund, J.; Boon, C.J.F. & Subhi, Y. (2022), Comparative efficacy of treatments for chronic central serous chorioretinopathy, Acta Ophthalmologica 101(2).
- Dijk, E.H.C. van; Holtz, J.K.; Sirks, M.J.; Larsson, J.M.E.; Diederen, R.M.H.; Schlingemann, R.O.; Boon, C.J.F. & Subhi, Y. (2022), European prevalence of polypoidal choroidal vasculopathy: a systematic review, meta-analysis, and forecasting study, Journal of Clinical Medicine 11(16).
- Hahn, L.C.; Georgiou, M.; Almushattat, H.; Schooneveld, M.J. van; Carvalho, E.R. de; Wesseling, N.L.; Brink, J.B. ten; Florijn, R.J.; Lissenberg-Witte, B.I.; Strubbe, I.; Cauwenbergh, C. van; Zaeytijd, J. de; Walraedt, S.; Baere, E. de; Mukherjee, R.; McKibbin, M.; Meester-Smoor, M.A.; Thiadens, A.A.H.J.; Al-Khuzaei, S.; Akyol, E.; Lotery, A.J.; Genderen, M.M. van; Ossewaarde-van Norel, J.; Born, L.I. van den; Hoyng, C.B.; Klaver, C.C.W.; Downes, S.M.; Bergen, A.A.; Leroy, B.P.; Michaelides, M. & Boon, C.J.F. (2022), The natural history of Leber congenital amaurosis and cone-rod dystrophy associated with variants in the GUCY2D gene, Ophthalmology Retina 6(8): 711-722.
- Liu, T.Y.A.; Ling, C.; Hahn, L.; Jones, C.K.; Boon, C.J.F. & Singh, M.S. (2022), Prediction of visual impairment in retinitis pigmentosa using deep learning and multimodal fundus images, British Journal of Ophthalmology 107.
- Ferrara, M.; Romano, V.; Iovino, C.; Kadhim, M.R.; Dijk, E.H.C. van; Boon, C.J.F.; Grassi, P.; Demirel, S.; Cartes, C.; Romano, M.R. & E-LOS Study Grp (2022), Tips to optimize digital education in ophthalmology, European Journal of Ophthalmology 33(2).
- Sirks, M.J.; Dijk, E.H.C. van; Rosenberg, N.; Hollak, C.E.M.; Aslanis, S.; Cheung, C.M.G.; Chowers, I.; Eandi, C.M.; Freund, K.B.; Holz, F.G.; Kaiser, P.K.; Lotery, A.J.; Ohno-Matsui, K.; Querques, G.; Subhi, Y.; Tadayoni, R.; Wykoff, C.C.; , D. zur; Diederen, R.M.H.; Boon, C.J.F. & Schlingemann, R.O. (2022), Clinical impact of the worldwide shortage of verteporfin (Visudyne (R)) on ophthalmic care, Acta Ophthalmologica 100(7): E1522-E1532.
- Garanto, A.; Ferreira, C.R.; Boon, C.J.F.; Karnebeek, C.D.M. van & Blau, N. (2022), Clinical and biochemical footprints of inherited metabolic disorders. VII. Ocular phenotypes, Molecular Genetics and Metabolism 135(4): 311-319.
- Feenstra, H.M.A.; Hahn, L.C.; Rijssen, T.J. van; Tsonaka, R.; Breukink, M.B.; Keunen, J.E.E.; Peters, P.J.H.; Dijkman, G.; Souied, E.H.; MacLaren, R.E.; Querques, G.; Downes, S.M.; Fauser, S.; Hoyng, C.B.; Dijk, E.H.C. van & Boon, C.J.F. (2022), Efficacy of half-dose photodynamic therapy versus high-density subthreshold micropulse laser for treating pigment epithelial detachments in chronic central serous chorioretinopathy, RETINA: The Journal of Retinal and Vitreous Diseases 42(4): 721-729.
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