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Forte de plus de 10 ans d'exp\u00e9rience en ophtalmologie p\u00e9diatrique, elle se consacre chaque jour au d\u00e9veloppement visuel des enfants et \u00e0 l'accompagnement des familles.\r\n\r\nLe Dr Balikova est sp\u00e9cialis\u00e9e en ophtalmologie p\u00e9diatrique, en strabisme, en amblyopie (\u0153il paresseux), en maladies oculaires h\u00e9r\u00e9ditaires et en ophtalmog\u00e9n\u00e9tique. Elle traite aussi bien les probl\u00e8mes oculaires courants chez les enfants que les maladies g\u00e9n\u00e9tiques rares pouvant affecter la vision. Elle pratique \u00e9galement la chirurgie du strabisme chez les enfants et les adultes.\r\n\r\nSa formation comprend une sp\u00e9cialisation en ophtalmologie \u00e0 l\u2019Universit\u00e9 Libre de Bruxelles, un doctorat (PhD) \u00e0 la KU Leuven et une sous-sp\u00e9cialisation en ophtalmologie p\u00e9diatrique et strabisme acquise dans le cadre de formations internationales, notamment le dipl\u00f4me universitaire (DIU) d\u2019ophtalmologie p\u00e9diatrique et de strabisme \u00e0 Paris et le dipl\u00f4me europ\u00e9en d\u2019ophtalmologie p\u00e9diatrique et de strabisme (EBO - EPOS).\r\n\r\nLe Dr Balikova combine ses activit\u00e9s cliniques avec un engagement scientifique fort.\r\n\r\nPour le Dr Balikova, ce n\u2019est pas seulement le diagnostic qui est au centre de ses pr\u00e9occupations, mais aussi le bien-\u00eatre de l\u2019enfant et le soutien \u00e0 la famille. Elle estime qu\u2019un bon traitement commence par une communication claire et la confiance.","behandelingen_aandoeningen":[{"naam":"Amblyopie"},{"naam":"Strabisme"},{"naam":"Myopia"},{"naam":"Orientations vers Kind en Gezin\/CLB"},{"naam":"Maladies oculaires h\u00e9r\u00e9ditaires"},{"naam":"Examen g\u00e9n\u00e9ral"}],"talen":[{"taal":"Fran\u00e7ais","niveau":""},{"taal":"N\u00e9erlandais","niveau":""},{"taal":"Anglais","niveau":""},{"taal":"Russe","niveau":""},{"taal":"Bulgare","niveau":""}],"locaties":[{"praktijk":"Brussels Eye Doctors","straat_nummer":" Sint-Michielslaan 12-16","gemeente":"Sint-Pieters-Woluwe","maps_link":"https:\/\/www.google.com\/maps\/place\/Brussels+Eye+Doctors+%7C+J.C.+Vryghem\/@50.8361443,4.4025654,17z\/data=!3m1!4b1!4m6!3m5!1s0x47c3db52b07b7119:0x21eda2609d17852d!8m2!3d50.8361444!4d4.4074363!16s%2Fg%2F1tt1gcy7?entry=ttu"}]},"carriere":{"tijdslijn":[{"tijdspanne":"2005 - 2007","studie":"Programme de pr\u00e9-doctorat et stage clinique au Centre de g\u00e9n\u00e9tique humaine,","locatie":"H\u00f4pital universitaire de Gasthuisberg, KU Leuven, Belgique","extra_notitie":"Sujet : Le r\u00f4le des variations du nombre de copies dans l'\u00e9tiologie des anomalies oculaires cong\u00e9nitales (Directeur de th\u00e8se : Prof. JP Fryns, Centre de g\u00e9n\u00e9tique humaine, Louvain)"},{"tijdspanne":"2007 - 2009","studie":"Doctorat en m\u00e9decine","locatie":"D\u00e9partement des sciences biom\u00e9dicales, KU Leuven, Belgique","extra_notitie":""},{"tijdspanne":"2008 - 2009","studie":"Cours de g\u00e9n\u00e9tique humaine","locatie":"BESHG, Belgi\u00eb","extra_notitie":""},{"tijdspanne":"2010 - 2014","studie":"Formation en ophtalmologie","locatie":"Universit\u00e9 libre de Bruxelles (ULB), Belgique","extra_notitie":"distinction prestigieuse"},{"tijdspanne":"2012","studie":"Cours d'ophtalmologie p\u00e9diatrique et de strabisme","locatie":"Londres, UK","extra_notitie":""},{"tijdspanne":"2012","studie":"Cours d'\u00e9lectrophysiologie","locatie":"Moorfields Eye Hospital, UK","extra_notitie":""},{"tijdspanne":"2012","studie":"SFO DIU \"Inflammations et infections oculaires\"","locatie":"Paris, France","extra_notitie":""},{"tijdspanne":"2012","studie":"Stage en ophtalmog\u00e9n\u00e9tique","locatie":"Moorfields Eye Hospital, Londen, UK","extra_notitie":""},{"tijdspanne":"2013","studie":"Cours sur les techniques de microchirurgie","locatie":"Londres, UK","extra_notitie":""},{"tijdspanne":"2013","studie":"Dipl\u00f4me du Conseil europ\u00e9en d'ophtalmologie","locatie":"","extra_notitie":""},{"tijdspanne":"2013","studie":"Formation ISGEDR","locatie":"Gand, Belgique","extra_notitie":""},{"tijdspanne":"2013","studie":"\u00c9lectrophysiologie, Metrovision","locatie":"Lille, France","extra_notitie":""},{"tijdspanne":"2015","studie":"Cours de l'ESHG sur l'ophtalmog\u00e9n\u00e9tique","locatie":"Bertinoro, Italie","extra_notitie":""},{"tijdspanne":"2007 - 2009","studie":"Assistant de recherche","locatie":"Centre de g\u00e9n\u00e9tique humaine, H\u00f4pital universitaire de Gasthuisberg, KU Leuven, Belgique","extra_notitie":""},{"tijdspanne":"2010 - 2014 ","studie":"Assistant en ophtalmologie","locatie":"Universit\u00e9 libre de Bruxelles (ULB), Belgique","extra_notitie":"distinction prestigieuse"},{"tijdspanne":"2014 - 2019","studie":"Sp\u00e9cialiste en ophtalmologie p\u00e9diatrique et en ophtalmog\u00e9n\u00e9tique","locatie":"H\u00f4pitaux universitaires Reine Fabiola, Erasme et Brugmann, Bruxelles ","extra_notitie":""},{"tijdspanne":"2018 - 2019","studie":"SFO DIU Ophtalmologie p\u00e9diatrique et strabisme","locatie":"","extra_notitie":""},{"tijdspanne":"2016 - 2019 ","studie":"Ophtalmologue (ophtalmologie p\u00e9diatrique, \u00e9lectrophysiologie, ophtalmog\u00e9n\u00e9tique)","locatie":"H\u00f4pital universitaire de Gand","extra_notitie":""},{"tijdspanne":"2019","studie":"Reconnaissance de la double sp\u00e9cialisation en ophtalmog\u00e9n\u00e9tique   ","locatie":"","extra_notitie":""},{"tijdspanne":"2020 - 2023","studie":"Ophtalmologue (ophtalmologie p\u00e9diatrique, \u00e9lectrophysiologie, ophtalmog\u00e9n\u00e9tique)","locatie":"H\u00f4pital universitaire de Louvain","extra_notitie":"Projets : ERG sous s\u00e9dation chez les enfants de moins de 6 mois ; mise en \u0153uvre de la th\u00e9rapie g\u00e9nique Luxturna ; \u00e9tude sur l'\u00e9volution naturelle de la XLRP (Janssens) ; "},{"tijdspanne":"2024","studie":"Dipl\u00f4me en ophtalmologie p\u00e9diatrique et strabisme d\u00e9livr\u00e9 par le Conseil europ\u00e9en d'ophtalmologie ","locatie":"","extra_notitie":""},{"tijdspanne":"2024 - heden","studie":"Ophtalmologue p\u00e9diatrique ind\u00e9pendant ","locatie":"","extra_notitie":"Ophtalmologie p\u00e9diatrique, contr\u00f4le de la myopie, ophtalmog\u00e9n\u00e9tique, strabisme"},{"tijdspanne":"2025","studie":"Examen orthoptique et strabisme vertical \u2013 Visio - Bubo","locatie":"","extra_notitie":""},{"tijdspanne":"2026","studie":"L'IA en m\u00e9decine : fondements et applications dans la pratique m\u00e9dicale et la recherche","locatie":"Harvard Medical School short course","extra_notitie":""}],"diplomas_certificaten":null,"lidmaatschappen":[{"functie":"Boardmember","vereniging":"PEDLOWNOC (Association belge d'ophtalmop\u00e9diatrie)","beschrijving":""},{"functie":"","vereniging":"European Paediatric Ophthalmological Society ","beschrijving":""},{"functie":"","vereniging":"Belgian Myopia Group","beschrijving":""},{"functie":"","vereniging":"Belgian Strabismological Association","beschrijving":""}],"prijzen_grants":[{"titel":"FEBS grant ","beschrijving":"1999"},{"titel":"Bulgarian Ministry of Science grant ","beschrijving":"2003"},{"titel":"KU Leuven doctoral grant for East European countries","beschrijving":"2007"},{"titel":"Brugmann foundation grant","beschrijving":"2013"},{"titel":"IRIS network grant","beschrijving":"2016"}]},"publicaties":{"peer-reviewed_publicaties":"","internationale_presentaties":"","boekhoofdstukken":"","onderzoeksgebieden":{"labels":null,"intro":"<ul class=\"ul1\">\r\n \t<li class=\"li1\">Auteur et coauteur de 51 publications scientifiques dans les domaines de l'ophtalmologie p\u00e9diatrique, de l'ophtalmog\u00e9n\u00e9tique et des maladies h\u00e9r\u00e9ditaires de la r\u00e9tine.<\/li>\r\n \t<li class=\"li1\">R\u00e9viseur r\u00e9gulier pour des revues scientifiques et participant \u00e0 des congr\u00e8s et formations internationaux.<\/li>\r\n<\/ul>"},"publicaties_preview":[{"jaartal":"2005","beschrijving":"Acrofacial dysostosis type Rodr\u00edguez.","verschenen_in":""},{"jaartal":"2005","beschrijving":"The acrofacial dysostoses--a wide spectrum of overlapping phenotypes.","verschenen_in":""},{"jaartal":"2006","beschrijving":"Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports.","verschenen_in":""},{"jaartal":"2006","beschrijving":"olecular karyotyping of patients with MCA\/MR: the blurred boundary between normal and pathogenic variation.","verschenen_in":""},{"jaartal":"2007","beschrijving":"Subtelomeric imbalances in phenotypically normal individuals.","verschenen_in":""},{"jaartal":"2008","beschrijving":"Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16.","verschenen_in":""},{"jaartal":"2008","beschrijving":"Lobar holoprosencephaly in 18pter deletion resulting from the karyotype 45,X,-18,der(8;18)t(8; 18)(pter;p11.21).","verschenen_in":""},{"jaartal":"2009","beschrijving":"Bronchiectasis and immune deficiency in an adult patient with deletion 2q37 due to an unbalanced translocation t(2;10).","verschenen_in":""},{"jaartal":"2009","beschrijving":"Another patient with a de novo deletion further delineates the 2q33.1 microdeletion syndrome.","verschenen_in":""},{"jaartal":"2009","beschrijving":"\"Opitz C syndrome and pseudohypoaldosteronism\" is caused by a chromosome 4q deletion.","verschenen_in":""},{"jaartal":"2009","beschrijving":"Deletions in the VPS13B (COH1) gene as a cause of Cohen syndrome.","verschenen_in":""},{"jaartal":"2010","beschrijving":"FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish.","verschenen_in":""},{"jaartal":"2011","beschrijving":"2q31.1 microdeletion syndrome: redefining the associated clinical phenotype.","verschenen_in":""},{"jaartal":"2011","beschrijving":"The power of high-resolution non-targeted array-CGH in identifying intragenic rearrangements responsible for Cohen syndrome.","verschenen_in":""},{"jaartal":"2011","beschrijving":"High frequency of submicroscopic chromosomal deletions in patients with idiopathic congenital eye malformations.","verschenen_in":""},{"jaartal":"2011","beschrijving":"The causality of de novo copy number variants is overestimated.","verschenen_in":""},{"jaartal":"2011","beschrijving":"High frequency of submicroscopic chromosomal deletions in patients with idiopathic congenital eye malformations.","verschenen_in":"Am J Ophthalmol"},{"jaartal":"2015","beschrijving":"Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations in KIF11.","verschenen_in":"Acta Ophthalmol"},{"jaartal":"2015","beschrijving":"No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.","verschenen_in":""},{"jaartal":"2016","beschrijving":"Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations in KIF11.","verschenen_in":""},{"jaartal":"2018","beschrijving":"Analysis of KERA in four families with cornea plana identifies two novel mutations.","verschenen_in":""},{"jaartal":"2019","beschrijving":"ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants.","verschenen_in":"Genet Med."},{"jaartal":"2019","beschrijving":"Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders.","verschenen_in":"Hum Mutat"},{"jaartal":"2019","beschrijving":"Truncating RAX Mutations: Anophthalmia, Hypopituitarism, Diabetes Insipidus, and Cleft Palate in Mice and Men.","verschenen_in":""},{"jaartal":"2019","beschrijving":"Genetic biomarkers in the VEGF pathway predicting response to anti-VEGF therapy in age-related macular degeneration.","verschenen_in":""},{"jaartal":"2019","beschrijving":"Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders.","verschenen_in":""},{"jaartal":"2019","beschrijving":"ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants.","verschenen_in":""},{"jaartal":"2019","beschrijving":"Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect.","verschenen_in":""},{"jaartal":"2020","beschrijving":"MULTIMODAL IMAGING IN HELLP-RELATED CHORIORETINOPATHY.","verschenen_in":""},{"jaartal":"2020","beschrijving":"Three cases of molecularly confirmed Knobloch syndrome.","verschenen_in":""},{"jaartal":"2020","beschrijving":"Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertility.","verschenen_in":""},{"jaartal":"2020","beschrijving":"The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56.","verschenen_in":""},{"jaartal":"2020","beschrijving":"Microcoria due to first duplication of 13q32.1 including the GPR180 gene and maternal mosaicism.","verschenen_in":""},{"jaartal":"2021","beschrijving":"Peripheral polypoidal choroidal vasculopathy in Sorsby fundus dystrophy: Report of two cases.","verschenen_in":""},{"jaartal":"2021","beschrijving":"Congenital stationary night blindness in a patient with mild learning disability due to a compound heterozygous microdeletion of 15q13 and a missense mutation in TRPM1.","verschenen_in":"Ophthalmic Genet"},{"jaartal":"2021","beschrijving":"Peripheral polypoidal choroidal vasculopathy in Sorsby fundus dystrophy: Report of two cases.","verschenen_in":"Online ahead of print"},{"jaartal":"2021","beschrijving":"Two siblings with Heimler syndrome caused by PEX1 variants: follow-up of ophthalmologic findings.","verschenen_in":""},{"jaartal":"2021","beschrijving":"Risdiplam-Treated Infants with Type 1 Spinal Muscular Atrophy versus Historical Controls","verschenen_in":""},{"jaartal":"2021","beschrijving":"Risdiplam in Type 1 Spinal Muscular Atrophy.","verschenen_in":"Clinical Trial"},{"jaartal":"2021","beschrijving":"The Retina in Patients With Triple A Syndrome: A Window Into Neurodegeneration?","verschenen_in":""},{"jaartal":"2021","beschrijving":"CLINICAL CHARACTERISTICS AND NATURAL HISTORY OF RHO-ASSOCIATED RETINITIS PIGMENTOSA: A Long-Term Follow-Up Study.","verschenen_in":""},{"jaartal":"2021","beschrijving":"Expanding the clinical spectrum and management of Traboulsi syndrome: report on two siblings homozygous for a novel pathogenic variant in ASPH.","verschenen_in":""},{"jaartal":"2021","beschrijving":"Congenital stationary night blindness in a patient with mild learning disability due to a 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