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Ingele Casteels

Showing results (31-40 of 85) with videos related to

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Ophthalmic Genetics|May 6, 2021
Two siblings with Heimler syndrome caused by PEX1 variants: follow-up of ophthalmologic findingsDorien Herijgers, Ellen Denayer, Irina Balikova, et al.
Journal of Clinical Medicine|February 25, 2022
Management of Childhood Glaucoma Following Cataract SurgeryAnne-Sophie Simons, Ingele Casteels, John Grigg, et al.
Journal of Pediatric Ophthalmology and Strabismus|July 21, 2021
Two Cases Presenting With Unilateral Adduction Deficit Associated With Human Adenosine Deaminase 2 DeficiencyEline Veryser, Isabelle Meyts, Ingele Casteels, et al.
Ophthalmic Genetics|December 23, 2010
Juvenile xanthogranuloma of the corneoscleral limbus: report of two casesChristophe De Keyser, Prabhat Maudgal, Eric Legius, et al.
Acta Ophthalmologica|September 28, 2018
Ophthalmological examination in neurofibromatosis type 1: a long-term retrospective analysisCatherine Cassiman, Annouschka Laenen, Sandra Jacobs, et al.
Developmental Medicine and Child Neurology|December 17, 2011
Integrity of the inferior longitudinal fasciculus and impaired object recognition in children: a diffusion tensor imaging studyEls Ortibus, Judith Verhoeven, Stefan Sunaert, et al.
Journal of Glaucoma|August 10, 2020
A Retrospective Case Series of Uveal Effusion SyndromeEmilie Claeys, Peter Stalmans, Joachim Van Calster, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|April 12, 2003
Perinatal growth characteristics and associated risk of developing threshold retinopathy of prematurityKarel Allegaert, Christine Vanhole, Ingele Casteels, et al.
Cornea|March 15, 2018
Use of the Masquerade Flap in Ablepharon-Macrostomia Syndrome: A Case ReportKarolien Hollanders, Ingele Casteels, Sylvie Vandelanotte, et al.
Case Reports in Ophthalmology|October 30, 2023
Unilateral Melanoma-Associated Retinopathy Case ReportReinout Peeters, Freya Peeters, Julie Jacob, et al.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
Ophthalmic Genetics|May 6, 2021
Two siblings with Heimler syndrome caused by PEX1 variants: follow-up of ophthalmologic findingsDorien Herijgers, Ellen Denayer, Irina Balikova, et al.
Journal of Clinical Medicine|February 25, 2022
Management of Childhood Glaucoma Following Cataract SurgeryAnne-Sophie Simons, Ingele Casteels, John Grigg, et al.
Journal of Pediatric Ophthalmology and Strabismus|July 21, 2021
Two Cases Presenting With Unilateral Adduction Deficit Associated With Human Adenosine Deaminase 2 DeficiencyEline Veryser, Isabelle Meyts, Ingele Casteels, et al.
Ophthalmic Genetics|December 23, 2010
Juvenile xanthogranuloma of the corneoscleral limbus: report of two casesChristophe De Keyser, Prabhat Maudgal, Eric Legius, et al.
Acta Ophthalmologica|September 28, 2018
Ophthalmological examination in neurofibromatosis type 1: a long-term retrospective analysisCatherine Cassiman, Annouschka Laenen, Sandra Jacobs, et al.
Developmental Medicine and Child Neurology|December 17, 2011
Integrity of the inferior longitudinal fasciculus and impaired object recognition in children: a diffusion tensor imaging studyEls Ortibus, Judith Verhoeven, Stefan Sunaert, et al.
Journal of Glaucoma|August 10, 2020
A Retrospective Case Series of Uveal Effusion SyndromeEmilie Claeys, Peter Stalmans, Joachim Van Calster, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|April 12, 2003
Perinatal growth characteristics and associated risk of developing threshold retinopathy of prematurityKarel Allegaert, Christine Vanhole, Ingele Casteels, et al.
Cornea|March 15, 2018
Use of the Masquerade Flap in Ablepharon-Macrostomia Syndrome: A Case ReportKarolien Hollanders, Ingele Casteels, Sylvie Vandelanotte, et al.
Case Reports in Ophthalmology|October 30, 2023
Unilateral Melanoma-Associated Retinopathy Case ReportReinout Peeters, Freya Peeters, Julie Jacob, et al.
Pageof 9