EPOS
European Paediatric Ophthalmological Society
Annual Meeting 2008 - Abstracts
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Abstracts of all talks
Aleksandra Starikova: Secondary glaucoma in children with Vogt-Koyanagi-Harada syndrome
Aznauryan Igor: Papain ferment in treatment of ocular developments of systemic inflammatory diseases of the connective tissue
Bainbridge James: Gene therapy for inherited retinal disease
Balikova Irina: Deletions in COH1 as a cause of Cohen syndrome
Becker Matthias: Uveitis / Ocular Inflammation
Berk A. Tulin: Anophthalmia and microphthalmia in pediatric population
Bilkiewicz- Pawelec Anna Maria: Choroidal Neovascularisation in an adolescent previously treated for nasopharyngeal carcinoma
Coppieters Frauke: Genetic testing for Leber Congenital Amaurosis (LCA): a 3-year experience
Creavin Alexandra: Ophthalmic problems in children with Down syndrome: Findings from England
Creavin Alexandra: Ophthalmic problems in children with Down syndrome: A systematic review
croonen danna: Retinal dystrophy due to a vitamin E deficiency
D'haene Barbara: FOXC1/PITX2 mutations and copy number changes in a Belgian-Dutch cohort of patients with anterior segment dysgenesis (ASD)
De Baere Elfride: Disruptions of distant regulatory elements surrounding FOXL2 in the causation of BPES syndrome
de veuster ilse: Myelinated Retinal Nerve Fibers and Amblyopia : 2 case reports.
de Veuster Ilse: Slitlamp-Delivered Laser Photocoagulation Of ROP
Delouvrier Eliane: Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency and retinopathy. A Case report.
Dureau Pascal: Cataract surgery in paediatric uveitis
edelson catherine: Surgical treatment of glaucoma associated with Sturge Weber syndrome
Fomina Natalya: Eye and orbit changes in childhood acute lymphoblastic leukaemia
Friedburg Christoph: Functional impact of retinal cysts on ERG and visual fields in patients with X-linked retinoschisis XLRS
GAMBOA SILVIA: Nutritional Deficit and bilateral hyperopic amblyopia
Gerth Christina: Ocular tilt reaction and internuclear ophthalmoplegia associated with sinus venous thrombosis: an unusual case.
Grünewald Stephanie: Clinical clues to glycosylation disorders
Holmström Gerd: Optical Coherence Tomography (OCT) in the diagnosis of foveal hypoplasia in children
Jarc-Vidmar Martina: Morphology Ana Function Of The Central Retina In Children And Young Adults With Stardgardt Dystrophy
Jensen Hanne: Ophthalmic manifestations in glycosylation disorders
Kim Ungsoo: Change of Visual Field Defect between Short Term Intervals in Child with Migraines
Kim Ungsoo: One brother and sister with mirror image myopic anisometropia
Kirwan Caitriona: Glaucoma in aphakic and pseudophakic eyes following surgery for congenital cataract in the 1st year of life
Knezy Krisztina: Misdiagnosis in connection with Elevated Intracranial Pressure
Leguis Eric: Neurofibromatosis type 1 and related syndromes
LEROY Bart Peter: Leber Congenital Amaurosis Anno 2008 - An Update
Lorenz Birgit: The Spectrum of RPE65 Mutations in Early Onset Severe Retinal Dystrophies (EOSRD)
Ludmila Kogoleva: Long-term clinical and visual results in extremely preterm patients with retinopathy of prematurity
Macarez Remi: Duane’s retraction syndrome associated with mitochondrial DNA mutation.
Maka Erika: Bullous Diseases in Children – Case Reports
Manzotti Francesca: Immunosuppressive drug combination therapy in paediatric autoimmune ocular diseases. Follow-up from 1991.
Moller H U: ICD3 classification of corneal dystrophies, pediatric ophthalmology aspects
Morales Marta: Etiological distribution of paediatric cataracts in Hospital Sant Joan de Déu during the period 1995 to 2007.
Pilling Rachel: Development of a uveitis screening service for Juvenile Idiopathic Arthritis: use of rapid cycle audit
Porro Giorgio: Visual fields in children affected by Periventricular Leukomalacia
Pott Jan Willem: Retinal Dystrophy in CEDNIK-syndrome
Prat Joan: Orbital cellulitis in children: clinical diagnostic criteria
Prat Joan: Differences between complete and partial congenital nasolacrimal duct obstruction.
Preising Markus: Evaluation of Lyonization in cultured Lymphocytes from Carriers of Choroideremia
Ragge Nicola: Anophthalmia and microphthalmia - practical management and emerging genetic syndromes
Ribeiro Lígia: Severe form of tuberous sclerosis in an eight-year-old child
Roulez Françoise: LTBP2 mutation in autosomal recessive microspherophakia with lens luxation and megalocornea
Sauer Arnaud: Ocular features of Lyme borreliosis: an old disease revisited
Schlingemann Reinier: Vascular Endothelial Growth Factors And Angiogenesis In Eye Disease
serra alicia: Retinal haemorrhages in the differential diagnosis of child abuse
Sminia Marije: Eye involvement in lysosomal storage disease;
Stalmans Peter: Pharmacologic vitreolysis: potential application in vitreous surgery in children.
Stellingwerf Catharina: Two halfs fit only half and half
Surachatkumtonekul Thammanoon: Optic disc atrophy in children and neuro-imaging findinds
Taylor David: Inherited Errors of Metabolism IEOMs
Tekavcic Pompe Manca: Optic Neuritis In Children - A Long Term Follow-Up
van den Born L. Ingeborgh: Maculopathies in gyrate atrophy of the choroid and retina
Vanhaesebrouck Sophie: IGF-I and Oxygen-Induced Retinopathy in Mice
Vanhaesebrouck Sophie: Neonatal Insulin Therapy To Drive Normoglycemic Anabolism
Verstraeten Sofie: Bilateral leukokoria in a newborn.
Wenniger-Prick Liesbeth: Eye involvement in children with Peroxisomal Biogenesis disorders(PBD)
Wittebol-Post Dienke: Plasticity of visual functions after brain damage
Wouters Carine: Eye involvement in systemic inflammatory diseases in children
Yzer Suzanne: The ocular and olfactory phenotype of LCA patients with mutations in CEP290
Ziakas Nikolaos: Orbital cellulitis associated with Adamantiades-Behcet disease
Ziakas Nikolaos: Neurofibromatosis type 1 (von Reckinghausen) with glaucoma and sphenoid-orbital dysplasia in a paediatric patient
Ziakas Nikolaos: Congenital simple ectopia lentis with unusual asymmetric bilateral lens displacement in a paediatric patient