Ghent University Academic Bibliography

Your filters: cql: jcr.category exact "OPHTHALMOLOGY"

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Bio-interface electro-active sensing platform for intraocular pressure monitoring in real-time

Pablo Perez Merino (UGent) , Andrés Felipe Vasquez Quintero (UGent) and Jan Vanfleteren (UGent)

(2024) ARVO Annual Meeting Abstract. In Investigative Ophthalmology & Visual Science 65(7).
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Spiroplasma infection as a cause of severe congenital keratouveitis, cataract and glaucoma

Helena Van Haecke, Dimitri Roels (UGent) , Fanny Nerinckx (UGent) , Heidi Schaballie (UGent) , Petra Schelstraete (UGent) , Linos Vandekerckhove (UGent) , Jolien Van Cleemput (UGent) , Wim Van Den Broeck (UGent) , Liesbeth Couck (UGent) , Hannelore Hamerlinck (UGent) , et al.

(2024) BMC OPHTHALMOLOGY. 24(1).
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Levamisole-adulterated cocaine-induced mucous membrane pemphigoid : case reports and literature review

Elke Thijs, Daire Hurley, Brendan Cummings, Dirk Elewaut (UGent) , Nick Verougstraete (UGent) , Ilse Claerhout, Conor C. Murphy, William Power and Dimitri Roels (UGent)

(2024) CORNEA. 43(8). p.1053-1057
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Anterior scleral thickness in Marfan syndrome : a quantitative analysis

Lien Alluyn (UGent) , Laure Dequeker, Siska Dhaese, Alejandra Consejo, Julie De Zaeytijd (UGent) , Bart Leroy (UGent) , Julie De Backer (UGent) and Elke O. Kreps (UGent)

(2024) ACTA OPHTHALMOLOGICA. 102(7). p.e1050-e1056
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The first step in developing an International Classification of Functioning, Disability and Health Core Set for vision loss : a systematic review

Lorenzo Billiet (UGent) , Ruth MA Van Nispen, Stijn De Baets (UGent) , Dominique Van de Velde (UGent) and Hilde Van der Aa

(2024) OPHTHALMIC AND PHYSIOLOGICAL OPTICS. 44(2). p.413-425
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Single domain antibodies to tackle autosomal dominant retinitis pigmentosa caused by NR2E3 mutation G56R

Edith De Bruycker (UGent) , Olivier Zwaenepoel (UGent) , Frauke Coppieters (UGent) , Jan Gettemans (UGent) and Elfride De Baere (UGent)

(2024) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 65(7).
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Genetic testing of patients with inherited retinal diseases in the European countries : an international survey by the European Vision Institute

Giacomo Calzetti, Kerstin Schwarzwalder, Giorgia Ottonelli, Karolina Kaminska, Rupert Wolfgang Strauss, Elfride De Baere (UGent) , Bart Leroy (UGent) , Isabelle Audo, Christina Zeitz, Claus Cursiefen, et al.

(2024) OPHTHALMIC RESEARCH. 67(1). p.448-457
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Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR mutation in the RDH12 gene

Manon Bouckaert (UGent) , Kyana Van Acker (UGent) , Maria Georgiou, Filip Van Den Broeck (UGent) , Edith De Bruycker (UGent) , Alfredo Dueñas Rey, Emma Delanote (UGent) , Hanne Lenaerts (UGent) , Melita Kaltak, Elfride De Baere (UGent) , et al.

(2024) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 65(7).
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Diagnostic yield of an inherited retinal disease gene panel in retinopathy of unknown origin

Stéphane Abramowicz (UGent) , Audrey Meunier, Laurence Postelmans, Laure Caspers, Francis Corazza, Marieke De Bruyne (UGent) , Stijn Van de Sompele (UGent) , Elfride De Baere (UGent) , Bart Leroy (UGent) , François Willermain, et al.

(2024) RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES. 44(9). p.1597-1607
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Comprehensive tissue specificity analysis identifies (novel) retinaspecific, long non-coding RNAs

Emma Delanote (UGent) , Alfredo Dueñas Rey, Karla Ruiz, Victor Lopez Soriano, Manon Bouckaert (UGent) , Kelly Lemeire (UGent) , Jasper Verwilt, Hanne Lenaerts (UGent) , Sarah De Keulenaer (UGent) , Filip Van Nieuwerburgh (UGent) , et al.

(2024) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 65(7).

Academic Bibliography

Bio-interface electro-active sensing platform for intraocular pressure monitoring in real-time

Spiroplasma infection as a cause of severe congenital keratouveitis, cataract and glaucoma

Levamisole-adulterated cocaine-induced mucous membrane pemphigoid : case reports and literature review

Anterior scleral thickness in Marfan syndrome : a quantitative analysis

The first step in developing an International Classification of Functioning, Disability and Health Core Set for vision loss : a systematic review

Single domain antibodies to tackle autosomal dominant retinitis pigmentosa caused by NR2E3 mutation G56R

Genetic testing of patients with inherited retinal diseases in the European countries : an international survey by the European Vision Institute

Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR mutation in the RDH12 gene

Diagnostic yield of an inherited retinal disease gene panel in retinopathy of unknown origin

Comprehensive tissue specificity analysis identifies (novel) retinaspecific, long non-coding RNAs

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