Whole genome sequencing unveils genetic heterogeneity in optic nerve hypoplasia von Dahl, Sara, Pettersson, Maria, Eisfeldt, Jesper, Schroder, Anna Katharina, Wickstrom, Ronny, Fahnehjelm, Kristina Tear, Anderlid, Britt-Marie, Lindstrand, Anna

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Ophthalmological outcome of 6.5 years children treated for retinopathy of prematurity: a Swedish register study von Larsson, Eva, Hellström, Ann, Tornqvist, Kristina, Wallin, Agneta, Sunnqvist, Birgitta, Hochhard, Karin Sandgren, Lundgren, Pia, Al-Hawasi, Abbas, Fahnehjelm, Kristina Teär, Gränse, Lotta, Holmstrom, Gerd

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Treatment for retinopathy of prematurity in Sweden 2008–2021: Reduced gestational age of treated infants and remaining differences in treatment type and recurrence rates between ho... von Holmström, Gerd, Hellström, Ann, Teär Fahnehjelm, Kristina, Gränse, Lotta, Sandgren Hochhard, Karin, Sunnqvist, Birgitta, Tornqvist, Kristina, Tsamadou, Despoina, Wallin, Agneta, Larsson, Eva

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Outcomes of keratoplasty in the mucopolysaccharidoses: an international perspective von Ohden, Kaitlyn L, Pitz, Susanne, Ashworth, Jane, Magalhães, Augusto, Marinho, Diane R, Lindahl, Päivi, Teär Fahnehjelm, Kristina, Summers, C Gail

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Sex differences and risk factors for bleeding in Alagille syndrome von Hankeova, Simona, Van Hul, Noemi, Laznovsky, Jakub, Verboven, Elisabeth, Mangold, Katrin, Hensens, Naomi, Adori, Csaba, Verhoef, Elvira, Zikmund, Tomas, Dawit, Feven, Kavkova, Michaela, Salplachta, Jakub, Sjöqvist, Marika, Johansson, Bengt R, Hassan, Mohamed G, Fredriksson, Linda, Baumgärtel, Karsten, Bryja, Vitezslav, Lendahl, Urban, Jheon, Andrew, Alten, Florian, Fahnehjelm, Kristina Teär, Fischler, Björn, Kaiser, Jozef, Andersson, Emma R

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The new Swedish report on Shaken Baby Syndrome is misleading von Hellgren, Kerstin, Hellström, Ann, Hård, Anna‐Lena, Jacobson, Lena, Lidén, Ulrika, Löfgren, Stefan, Fahnehjelm, Kristina Teär, Ygge, Jan

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Most patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency develop pathological or subnormal retinal function von Fahnehjelm, Kristina Teär, Liu, Ying, Olsson, David, Amrén, Urban, Haglind, Charlotte Bieneck, Holmström, Gerd, Halldin, Maria, Andreasson, Sten, Nordenström, Anna

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Decade-long analysis of postoperative endophthalmitis in Sweden: Insights from insurance and national quality registers von Merkland, Dalia, Viberg, Andreas, Nilsson, Mattias, Gustafson, Pelle, Teär Fahnehjelm, Kristina

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Characteristic deviations of the optic disc and macula in optic nerve hypoplasia based on OCT von Skriapa‐Manta, Athanasia, Venkataraman, Abinaya Priya, Olsson, Monica, Nilsson, Maria, Teär Fahnehjelm, Kristina

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Optic Disc Coloboma in children – prevalence, clinical characteristics and associated morbidity von Skriapa Manta, Athanasia, Olsson, Monica, Ek, Ulla, Wickström, Ronny, Teär Fahnehjelm, Kristina

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Impaired balance and neurodevelopmental disabilities among children with congenital cytomegalovirus infection von Karltorp, Eva, Löfkvist, Ulrika, Lewensohn-Fuchs, Ilona, Lindström, Katarina, Eriksson Westblad, Mimmi, Teär Fahnehjelm, Kristina, Verrecchia, Luca, Engman, Mona-Lisa

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Optical Coherence Tomography Can Predict Visual Acuity in Children with Optic Nerve Hypoplasia von Skriapa-Manta, Athanasia, Nilsson, Mattias, Svoboda, Jan, Olsson, Monica, Nilsson, Maria, Fahnehjelm, Kristina Tear

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Morning Glory Disc Anomaly in childhood – a population‐based study von Ceynowa, Dylan J, Wickström, Ronny, Olsson, Monica, Ek, Ulla, Eriksson, Urban, Wiberg, Maria Kristoffersen, Fahnehjelm, Kristina Teär

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Optic nerve hypoplasia in children and adolescents; prevalence, ocular characteristics and behavioural problems von Teär Fahnehjelm, Kristina, Dahl, Sara, Martin, Lene, Ek, Ulla

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Children with optic nerve hypoplasia face a high risk of neurodevelopmental disorders von Dahl, Sara, Wickström, Ronny, Ek, Ulla, Teär Fahnehjelm, Kristina

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Visual perceptual skills and visual motor integration in children and adolescents after allogeneic hematopoietic stem cell transplantation von Fahnehjelm, Kristina Teär, Törnquist, Alba Lucia, Olsson, Monica, Winiarski, Jacek, Ek, Ulla

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High prevalence of pituitary hormone deficiency in both unilateral and bilateral optic nerve hypoplasia von Dahl, Sara, Kristoffersen Wiberg, Maria, Teär Fahnehjelm, Kristina, Sävendahl, Lars, Wickström, Ronny

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Children with mucopolysaccharidosis risk progressive visual dysfunction despite haematopoietic stem cell transplants von Teär Fahnehjelm, Kristina, Olsson, Monica, Chen, Enping, Hengstler, Jürg, Naess, Karin, Winiarski, Jacek

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Chorioretinal scars and visual deprivation are common in children with cochlear implants after congenital cytomegalovirus infection von Teär Fahnehjelm, Kristina, Olsson, Monica, Fahnehjelm, Cecilia, Lewensohn-Fuchs, Ilona, Karltorp, Eva

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Diagnosis and management of ophthalmological features in patients with mucopolysaccharidosis von Ferrari, Stefano, Ponzin, Diego, Ashworth, Jane L, Fahnehjelm, Kristina Teär, Summers, C Gail, Harmatz, Paul R, Scarpa, Maurizio

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