Publications by authors named "Anna Majander"

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PREVALENCE AND DEGREE OF RETINAL VASCULATURE ALTERATIONS IN ADULTS BORN PRETERM WITH VERY LOW BIRTH WEIGHT: A Birth Cohort Study.
Maarit K Kulmala, Eero Kajantie, Tora S Morken, Anna Majander

Retina· December 2025

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Visual pathway function in adults born preterm with very low birth weight: a two-country birth cohort study.
Anna P M Jørgensen, Maarit Kulmala, Dordi Austeng, Trond Sand, Arnstein Grøtting, Anna Majander

Doc Ophthalmol· August 2025

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Motor outcomes and visual function in adults born preterm with very low birthweight.
Silje D Benum, Urd E Svennevig, Anna Fivelstad, Anna P M Jørgensen, Maarit Kulmala, Anna Majander

Dev Med Child Neurol· August 2025

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A retrospective longitudinal study of 52 Finnish patients with X-linked retinoschisis.
Mira A Järvinen, Rigmor C Baraas, Anna Majander, Michael P Backlund, Julia Krootila

Acta Ophthalmol· March 2025

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Imprint of preterm birth with very low birth weight on optic disc OCT in adulthood-A two-country birth cohort study.
Maarit K Kulmala, Anna Jørgensen, Dordi Austeng, Kari Anne I Evensen, Eero Kajantie, Anna Majander

Acta Ophthalmol· February 2025

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Foveal thickness and its association with visual acuity in adults born preterm with very low birth weight: A two-country birth cohort study.
Anna P M Jørgensen, Maarit Kulmala, Dordi Austeng, Kari Anne I Evensen, Eero Kajantie, Anna Majander

Acta Ophthalmol· December 2024

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Visual function in adults born preterm with very low birth weight-A two-country birth cohort study.
Maarit Kulmala, Anna Perregaard Munch Jørgensen, Kristina Anna Djupvik Aakvik, Laura Jussinniemi, Silje Dahl Benum, Anna Majander

Acta Ophthalmol· February 2024

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Analysis of glaucoma genes in Finnish patients with juvenile open-angle glaucoma.
Perttu J Liuska, Abdessallam Tadji, Pauliina Repo, Juho Hiltunen, Michael Backlund, Anna Majander

Acta Ophthalmol· November 2023

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Childhood-Onset Leber Hereditary Optic Neuropathy-Clinical and Prognostic Insights.
Piero Barboni, Chiara La Morgia, Maria Lucia Cascavilla, Eun Hee Hong, Marco Battista, Anna Majander

Am J Ophthalmol· May 2023

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Virtual visits at the Helsinki Head and Neck Center during the COVID-19 pandemic: patient safety incidents and the experiences of patients and staff.
Morag Tolvi, Lotta-Maria Oksanen, Lasse Lehtonen, Ahmed Geneid, Pia Männikkö, Anna Majander

BMC Health Serv Res· May 2023

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Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG.
Anna Majander, Eeva-Marja Sankila, Aura Falck, Laura Kristiina Vasara, Sanna Seitsonen

Acta Ophthalmol· March 2023

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WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correlations and Disease Progression.
Anna Majander, Neringa Jurkute, Florence Burté, Kristian Brock, Catarina João

Am J Ophthalmol· September 2022

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Clinical Spectrum and Geographic Distribution of Keratitis Fugax Hereditaria Caused by the Pathogenic Variant c.61G>C in NLRP3.
Annamari T Immonen, Sabita Kawan, Minna Vesaluoma, J Miikael Heiskanen, Claudia Taipale, Anna Majander

Am J Ophthalmol· April 2022

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WFS1 protein expression correlates with clinical progression of optic atrophy in patients with Wolfram syndrome.
Kun Hu, Malgorzata Zatyka, Dewi Astuti, Nicola Beer, Renuka P Dias, Anna Majander

J Med Genet· January 2022

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In Vivo Corneal Confocal Microscopy and Histopathology of Keratitis Fugax Hereditaria From a Pathogenic Variant in NLRP3.
Joni A Turunen, Annamari T Immonen, Reetta-Stiina Järvinen, Sabita Kawan, Pauliina Repo, Anna Majander

Am J Ophthalmol· May 2020

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Clinical utility gene card for: inherited optic neuropathies including next-generation sequencing-based approaches.
Neringa Jurkute, Anna Majander, Richard Bowman, Marcela Votruba, Stephen Abbs

Eur J Hum Genet· March 2019

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Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 (NLRP3) Gene.
Joni A Turunen, Juho Wedenoja, Pauliina Repo, Reetta-Stiina Järvinen, Johannes E Jäntti, Anna Majander

Am J Ophthalmol· April 2018

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Childhood-onset Leber hereditary optic neuropathy.
Anna Majander, Richard Bowman, Joanna Poulton, Richard J Antcliff, M Ashwin Reddy

Br J Ophthalmol· November 2017

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The Pattern of Retinal Ganglion Cell Loss in OPA1-Related Autosomal Dominant Optic Atrophy Inferred From Temporal, Spatial, and Chromatic Sensitivity Losses.
Anna Majander, Catarina João, Andrew T Rider, G Bruce Henning, Marcela Votruba

Invest Ophthalmol Vis Sci· January 2017

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Indications and outcomes of keratoplasties in children during a 40-year period.
Anna Majander, Tero T Kivelä, Kari Krootila

Acta Ophthalmol· September 2016

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Lamination of the Outer Plexiform Layer in Optic Atrophy Caused by Dominant WFS1 Mutations.
Anna Majander, Maria Bitner-Glindzicz, Choi M Chan, Holly J Duncan, Patrick F Chinnery

Ophthalmology· July 2016

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Potential Effect of Tumor Necrosis Factor Inhibitors on Trabeculectomy With Mitomycin C for Patients With Juvenile Idiopathic Arthritis-Related Uveitic Glaucoma: A Retrospective Analysis.
Sanna Leinonen, Kaisu Kotaniemi, Tero Kivelä, Anna Majander

JAMA Ophthalmol· November 2015

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Anterior segment optical coherence tomography in autosomal recessive cornea plana.
Elina Rantala, Anna Majander

Acta Ophthalmol· May 2015

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Anterior segment optical coherence tomography in congenital corneal opacities.
Anna S Majander, Päivi M Lindahl, L Kristiina Vasara, Kari Krootila

Ophthalmology· December 2012

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Refined staging for chorioretinopathy in long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency.
Tiina Tyni, Tuuli Immonen, Päivi Lindahl, Anna Majander, Tero Kivelä

Ophthalmic Res· August 2012

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