Onderzoeker
Caroline Van Cauwenbergh
- Disciplines:Dermatologie
Affiliaties
- Vakgroep Hoofd en Huid (Departement)
Lid
Vanaf1 okt 2018 → 31 dec 2023 - Vakgroep Oogheelkunde (Departement)
Lid
Vanaf1 mei 2017 → 30 sep 2018 - Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf1 jan 2010 → 24 sep 2017
Publicaties
1 - 10 van 14
- Outcome of cataract surgery in patients with retinitis pigmentosa(2023)
Auteurs: Xuan-Thanh-An Nguyen, Alberta A.H.J. Thiadens, Marta Fiocco, Weijen Tan, Martin McKibbin, Caroline C.W. Klaver, Magda A. Meester-Smoor, Caroline Van Cauwenbergh, Ine Strubbe, Andrea Vergaro, et al.
Pagina's: 1 - 9 - Restoration of cone sensitivity to individuals with congenital photoreceptor blindness within the phase 1/2 sepofarsen trial(2022)
Auteurs: Artur V. Cideciyan, Samuel G. Jacobson, Allen C. Ho, Arun K. Krishnan, Alejandro J. Roman, Alexandra V. Garafalo, Vivian Wu, Malgorzata Swider, Alexander Sumaroka, Caroline Van Cauwenbergh, et al.
- Evaluation of visual outcome following cataract surgery in patients with retinitis pigmentosa(2022)Volume: 100
Auteurs: Xuan-Thanh-An Nguyen, Alberta A. H. J Thiadens, Marta Fiocco, Weijen Tan, Martin McKibbin, Caroline C. W Klaver, Magda A Meester-Smoor, Caroline Van Cauwenbergh, Ine Strubbe, Andrea Vergaro, et al.
Pagina's: 21 - 21 - Comparative natural history of visual function from patients with biallelic variants in BBS1 and BBS10(2021)
Auteurs: Monika K. Grudzinska Pechhacker, Samuel G. Jacobson, V Drack, Arlene, Matteo Di Scipio, Ine Strubbe, Wanda Pfeifer, Jacque L. Duncan, Helene Dollfus, Nathalie Goetz, Jean Muller, et al.
- The need for widely available genomic testing in rare eye diseases : an ERN-EYE position statement(2021)
Auteurs: Graeme C. Black, [missing] ERN-EYE study group, Panagiotis Sergouniotis, Andrea Sodi, Bart Leroy, Caroline Van Cauwenbergh, Petra Liskova, Karen Grønskov, Artur Klett, Susanne Kohl, et al.
- Longitudinal phenotypic study of late-onset retinal degeneration due to a founder variant c.562C > A p.(Pro188Thr) in the C1QTNF5 gene(2021)
Auteurs: Julie De Zaeytijd, Frauke Coppieters, Marieke De Bruyne, Jasper Van Royen, Dimitri Roels, Rani Six, Caroline Van Cauwenbergh, Elfride De Baere, Bart Leroy
Pagina's: 521 - 532 - Expanded phenotypic spectrum of retinopathies associated with autosomal recessive and dominant mutations in PROM1(2019)
Auteurs: Marta Del Pozo-Valero, Inmaculada Martin-Merida, Belen Jimenez-Rolando, Ana Arteche, Almudena Avila-Fernandez, Fiona Blanco-Kelly, Rosa Riveiro-Alvarez, Caroline Van Cauwenbergh, Elfride De Baere, Carlo Rivolta, et al.
Pagina's: 204 - 214 - Long-term follow-up of retinal degenerations associated with LRAT mutations and their comparability to phenotypes associated with RPE65 mutations(2019)
Auteurs: Mays Talib, Mary J. van Schooneveld, Roos J. G. van Duuren, Caroline Van Cauwenbergh, Jacoline B. ten Brink, Elfride De Baere, Ralph J. Florijn, Nicoline E. Schalij-Delfos, Bart Leroy, Arthur A. Bergen, et al.
- CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients(2017)
Auteurs: Anja K Mayer, Caroline Van Cauwenbergh, Christine Rother, Britta Baumann, Peggy Reuter, Elfride De Baere, Bernd Wissinger, Susanne Kohl
Pagina's: 1579 - 1591 - SF3B2, a novel candidate gene for autosomal dominant retinitis pigmentosa, encodes a component of the U2 small nuclear ribonucleoprotein(2015)Volume: 56
Auteurs: Caroline Van Cauwenbergh, Kris Vleminckx, Frauke Coppieters, Marcus Karlstetter, Thomas Langmann, Gael Manes, Christian P Hamel, Bart Leroy, Elfride De Baere
Aantal pagina's: 1