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GMS Ophthalmology Cases
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December 6, 2019
Ophthalmological and electrophysiological findings in monozygotic twin sisters with phosphomannomutase 2 deficiency (PMM2-CDG) over a period of 37 years
Ines Van Hees, Jaak Jaeken, Wouter Meersseman, et al.
European Journal of Pediatrics
|
August 21, 2007
Ocular findings in children with a microdeletion in chromosome 22q11.2
Ingele Casteels, Patricia Casaer, Marc Gewillig, et al.
Cornea
|
January 24, 2002
Report of a new family with dominant congenital heredity stromal dystrophy of the cornea
Rita Van Ginderdeuren, Rita De Vos, Ingele Casteels, et al.
Case Reports in Ophthalmology
|
May 18, 2017
Optical Coherence Tomography Angiography of Retinal Microvascular Changes Overlying Choroidal Nodules in Neurofibromatosis Type 1
Catherine Cassiman, Ingele Casteels, Peter Stalmans, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
September 20, 2024
Validation of the eye screening tool GoCheck Kids for the detection of amblyopia risk factors in toddlers in Flanders
Hanne Otto, Maaike Deschoemaeker, Bart Van Overmeire, et al.
Ophthalmology and Therapy
|
August 31, 2025
Cystadrops<sup>®</sup> Eye Drops for the Management of Ocular Cystinosis in Patients Aged 6 Months to < 2 Years
Susmito Biswas, Ingele Casteels, Dominique Bremond-Gignac, et al.
Acta Ophthalmologica
|
November 20, 2015
Non-organic visual loss in children: prospective and retrospective analysis of associated psychosocial problems and stress factors
Alix Somers, Kristina Casteels, Elke Van Roie, et al.
Journal of Pediatric Ophthalmology and Strabismus
|
January 20, 2011
Diffuse choroidal atrophy in a boy with Klinefelter syndrome
Sofie Verstraeten, Nele Jaenen, Werner Spileers, et al.
Strabismus
|
October 28, 2021
Extraocular muscle hypoplasia associated with Axenfeld-Rieger syndrome
Milo De Decker, Catherine Cassiman, Ingele Casteels, et al.
Ophthalmic Genetics
|
October 9, 2012
Peculiar fundus abnormalities and pathognomonic electrophysiological findings in a 14-month-old boy with NR2E3 mutations
Catherine Cassiman, Werner Spileers, Elfride De Baere, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 85) with videos related to
Sort By:
Page
of 9
GMS Ophthalmology Cases
|
December 6, 2019
Ophthalmological and electrophysiological findings in monozygotic twin sisters with phosphomannomutase 2 deficiency (PMM2-CDG) over a period of 37 years
Ines Van Hees, Jaak Jaeken, Wouter Meersseman, et al.
European Journal of Pediatrics
|
August 21, 2007
Ocular findings in children with a microdeletion in chromosome 22q11.2
Ingele Casteels, Patricia Casaer, Marc Gewillig, et al.
Cornea
|
January 24, 2002
Report of a new family with dominant congenital heredity stromal dystrophy of the cornea
Rita Van Ginderdeuren, Rita De Vos, Ingele Casteels, et al.
Case Reports in Ophthalmology
|
May 18, 2017
Optical Coherence Tomography Angiography of Retinal Microvascular Changes Overlying Choroidal Nodules in Neurofibromatosis Type 1
Catherine Cassiman, Ingele Casteels, Peter Stalmans, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
September 20, 2024
Validation of the eye screening tool GoCheck Kids for the detection of amblyopia risk factors in toddlers in Flanders
Hanne Otto, Maaike Deschoemaeker, Bart Van Overmeire, et al.
Ophthalmology and Therapy
|
August 31, 2025
Cystadrops<sup>®</sup> Eye Drops for the Management of Ocular Cystinosis in Patients Aged 6 Months to < 2 Years
Susmito Biswas, Ingele Casteels, Dominique Bremond-Gignac, et al.
Acta Ophthalmologica
|
November 20, 2015
Non-organic visual loss in children: prospective and retrospective analysis of associated psychosocial problems and stress factors
Alix Somers, Kristina Casteels, Elke Van Roie, et al.
Journal of Pediatric Ophthalmology and Strabismus
|
January 20, 2011
Diffuse choroidal atrophy in a boy with Klinefelter syndrome
Sofie Verstraeten, Nele Jaenen, Werner Spileers, et al.
Strabismus
|
October 28, 2021
Extraocular muscle hypoplasia associated with Axenfeld-Rieger syndrome
Milo De Decker, Catherine Cassiman, Ingele Casteels, et al.
Ophthalmic Genetics
|
October 9, 2012
Peculiar fundus abnormalities and pathognomonic electrophysiological findings in a 14-month-old boy with NR2E3 mutations
Catherine Cassiman, Werner Spileers, Elfride De Baere, et al.
Page
of 9