Ghent University Academic Bibliography

Journal Article
A1
open access

X-linked Retinoschisis : novel clinical observations and genetic spectrum in 340 patients

Leo C. Hahn, Mary J. van Schooneveld, Nieneke L. Wesseling, Ralph J. Florijn, Jacoline B. ten Brink, Birgit I. Lissenberg-Witte, Ine Strubbe, Magda A. Meester-Smoor, Alberta A. Thiadens, Roselie M. Diederen, et al.

(2022) OPHTHALMOLOGY. 129(2). p.191-202

Add to list

Photoreceptor progenitor mRNA analysis reveals exon skipping resulting from the ABCA4 c.5461-10T/C mutation in Stargardt disease

Riccardo Sangermano, Nathalie M Bax, Miriam Bauwens (UGent) , L Ingeborgh Van den Born, Elfride De Baere (UGent) , Alejandro Garanto, Rob WJ Collin, Angelique SA Goercharn-Ramlal, Anke HA den Engelsman-van Dijk, Klaus Rohrschneider, et al.

(2016) OPHTHALMOLOGY. 123(6). p.1375-1385

Add to list

Visual prognosis in USH2A-associated retinitis pigmentosa is worse for patients with Usher syndrome type IIa than for those with nonsyndromic retinitis pigmentosa

Laurence HM Pierrache, Bas P Hartel, Erwin van Wijk, Magda A Meester-Smoor, Frans PM Cremers, Elfride De Baere (UGent) , Julie De Zaeytijd (UGent) , Mary J van Schooneveld, Cor WRJ Cremers, Gislin Dagnelie, et al.

(2016) OPHTHALMOLOGY. 123(5). p.1151-1160

Add to list

Miscellaneous

Retinal development in infants and young children with achromatopsia

Helena Lee, Ravi Purohit, Viral Sheth, Rebecca J McLean, Susanne Kohl, Bart Leroy (UGent) , Venki Sundaram, Michel Michaelides, Frank A Proudlock and Irene Gottlob

(2015) OPHTHALMOLOGY. 122(10). p.2145-2147

Add to list

Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction

Susanne Roosing, L Ingeborgh van den Bon, Carel B Hoyng, Alberta AHJ Thiadeus, Elfride De Baere (UGent) , Rob WJ Collin, Robert K Koenekoop, Bart Leroy (UGent) , Norka van Moll-Ramirez, Hanka Venselaar, et al.

(2013) OPHTHALMOLOGY. 120(6). p.1239-1246

Add to list

Clinical course, genetic etiology, and visual outcome in cone and cone-rod dystrophy

Alberta AHJ Thiadens, T My Lan Phan, Renate C Zekveld-Vroon, Bart Leroy (UGent) , L Ingeborgh van den Born, Crel B Hoyng, Caroline CW Klaver, Susanne Roosing, Jan-Willem R Pott, Mary J van Schooneveld, et al.

(2012) OPHTHALMOLOGY. 119(4). p.819-826

Add to list

Vernal keratoconjunctivitis in school children in Rwanda: clinical presentation, impact on school attendance, and access to medical care

Stefan K De Smedt, John Nkurikiye, Yannick S Fonteyne, Stephen J Tuft, Clare E Gilbert and Philippe Kestelyn (UGent)

(2012) OPHTHALMOLOGY. 119(9). p.1766-1772

Add to list

Evaluation of an Intravitreal Fluocinolone Acetonide Implant versus Standard Systemic Therapy in Noninfectious Posterior Uveitis

Carlos Pavesio, M Zierhut, K Bairi, TL Comstock and DW Usner

(2010) OPHTHALMOLOGY. 117(3). p.567-U194

Add to list

Retinopathy and vision loss in insulin-dependent diabetes in Europe: the EURODIAB IDDM Complications Study

AK Sjolie, J Stephenson, S Aldington, E Kohner, H Janka, L Stevens and J Fuller

(1997) OPHTHALMOLOGY. 104(2). p.252-260

Academic Bibliography

X-linked Retinoschisis : novel clinical observations and genetic spectrum in 340 patients

Photoreceptor progenitor mRNA analysis reveals exon skipping resulting from the ABCA4 c.5461-10T/C mutation in Stargardt disease

Visual prognosis in USH2A-associated retinitis pigmentosa is worse for patients with Usher syndrome type IIa than for those with nonsyndromic retinitis pigmentosa

Retinal development in infants and young children with achromatopsia

Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction

Clinical course, genetic etiology, and visual outcome in cone and cone-rod dystrophy

Vernal keratoconjunctivitis in school children in Rwanda: clinical presentation, impact on school attendance, and access to medical care

Evaluation of an Intravitreal Fluocinolone Acetonide Implant versus Standard Systemic Therapy in Noninfectious Posterior Uveitis

Retinopathy and vision loss in insulin-dependent diabetes in Europe: the EURODIAB IDDM Complications Study

Contents

Support

Contact