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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

BMC health services research, 2023-05, Vol.23 (1), p.483-483, Article 483

2023

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Anterior Segment Optical Coherence Tomography in Congenital Corneal Opacities

Ophthalmology (Rochester, Minn.), 2012-12, Vol.119 (12), p.2450-2457

2012

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Lamination of the Outer Plexiform Layer in Optic Atrophy Caused by Dominant WFS1 Mutations

Ophthalmology (Rochester, Minn.), 2016-07, Vol.123 (7), p.1624-1626

2016

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Anterior segment optical coherence tomography in autosomal recessive cornea plana

Acta ophthalmologica (Oxford, England), 2015-05, Vol.93 (3), p.e232-e233

2015

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Keratitis fugax hereditaria ‐ useful to consider when you have a child with non‐specific corneal findings and symptoms

Acta ophthalmologica (Oxford, England), 2022-12, Vol.100 (S275), p.n/a

2022

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Clinical utility gene card for: inherited optic neuropathies including next-generation sequencing-based approaches

European journal of human genetics : EJHG, 2019-03, Vol.27 (3), p.494-502

2019

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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

Acta ophthalmologica (Oxford, England), 2024-05

2024

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WFS1 protein expression correlates with clinical progression of optic atrophy in patients with Wolfram syndrome

Journal of medical genetics, 2022-01, Vol.59 (1), p.65

2022

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Childhood-Onset Leber Hereditary Optic Neuropathy—Clinical and Prognostic Insights

American journal of ophthalmology, 2023-05, Vol.249, p.99-107

2023

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Childhood-onset Leber hereditary optic neuropathy

British journal of ophthalmology, 2017-11, Vol.101 (11), p.1505

2017

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Clinical spectrum and geographic distribution of keratitis fugax hereditaria caused by the pathogenic variant c.61G>C in NLRP3

Acta ophthalmologica (Oxford, England), 2022-01, Vol.100 (S267), p.n/a

2022

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Visual function in adults born preterm with very low birth weight—A two‐country birth cohort study

Acta ophthalmologica (Oxford, England), 2024-02, Vol.102 (1), p.49-57

2024

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Clinical Spectrum and Geographic Distribution of Keratitis Fugax Hereditaria Caused by the Pathogenic Variant c.61G>C in NLRP3

American journal of ophthalmology, 2022-04, Vol.236, p.309-318

2022

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Analysis of glaucoma genes in Finnish patients with juvenile open‐angle glaucoma

Acta ophthalmologica (Oxford, England), 2022-12, Vol.100 (S275), p.n/a

2022

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Indications and outcomes of keratoplasties in children during a 40‐year period

Acta ophthalmologica (Oxford, England), 2016-09, Vol.94 (6), p.618-624

2016

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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

American journal of ophthalmology, 2018-04, Vol.188, p.41-50

2018

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Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG

Acta ophthalmologica (Oxford, England), 2023-03, Vol.101 (2), p.215-221

2023

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WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correlations and Disease Progression

American journal of ophthalmology, 2022-09, Vol.241, p.9-27

2022

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In Vivo Corneal Confocal Microscopy and Histopathology of Keratitis Fugax Hereditaria From a Pathogenic Variant in NLRP3

American journal of ophthalmology, 2020-05, Vol.213, p.217-225

2020

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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

JAMA ophthalmology, 2015-11, Vol.133 (11), p.1323

2015

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Analysis of glaucoma genes in Finnish patients with juvenile open-angle glaucoma

Acta ophthalmologica (Oxford, England), 2023-11, Vol.101 (7), p.797-806

2023

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In Vivo corneal confocal microscopy study of keratoendotheliitis fugax hereditaria caused by a pathogenic variant in the NLRP3 gene

Acta ophthalmologica (Oxford, England), 2019-12, Vol.97 (S263), p.n/a

2019

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Genetic findings in over 600 individuals with inherited retinal disorders in Finland

Acta ophthalmologica (Oxford, England), 2022-12, Vol.100 (S275), p.n/a

2022

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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

Investigative ophthalmology & visual science, 2017-01, Vol.58 (1), p.502-516

2017

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Neuroradiologic findings in children with mitochondrial disorders

American journal of neuroradiology : AJNR, 1998-02, Vol.19 (2), p.369-377

1998

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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

Anterior Segment Optical Coherence Tomography in Congenital Corneal Opacities

Lamination of the Outer Plexiform Layer in Optic Atrophy Caused by Dominant WFS1 Mutations

Anterior segment optical coherence tomography in autosomal recessive cornea plana

Keratitis fugax hereditaria ‐ useful to consider when you have a child with non‐specific corneal findings and symptoms

Clinical utility gene card for: inherited optic neuropathies including next-generation sequencing-based approaches

Foveal thickness and its association with visual acuity in adults born preterm with very low birth weight: A two-country birth cohort study

WFS1 protein expression correlates with clinical progression of optic atrophy in patients with Wolfram syndrome

Childhood-Onset Leber Hereditary Optic Neuropathy—Clinical and Prognostic Insights

Childhood-onset Leber hereditary optic neuropathy

Clinical spectrum and geographic distribution of keratitis fugax hereditaria caused by the pathogenic variant c.61G>C in NLRP3

Visual function in adults born preterm with very low birth weight—A two‐country birth cohort study

Clinical Spectrum and Geographic Distribution of Keratitis Fugax Hereditaria Caused by the Pathogenic Variant c.61G>C in NLRP3

Analysis of glaucoma genes in Finnish patients with juvenile open‐angle glaucoma

Indications and outcomes of keratoplasties in children during a 40‐year period

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

Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG

WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correlations and Disease Progression

In Vivo Corneal Confocal Microscopy and Histopathology of Keratitis Fugax Hereditaria From a Pathogenic Variant in NLRP3

Potential Effect of Tumor Necrosis Factor Inhibitors on Trabeculectomy With Mitomycin C for Patients With Juvenile Idiopathic Arthritis-Related Uveitic Glaucoma: A Retrospective Analysis

Analysis of glaucoma genes in Finnish patients with juvenile open-angle glaucoma

In Vivo corneal confocal microscopy study of keratoendotheliitis fugax hereditaria caused by a pathogenic variant in the NLRP3 gene

Genetic findings in over 600 individuals with inherited retinal disorders in Finland

The Pattern of Retinal Ganglion Cell Loss in OPA1-Related Autosomal Dominant Optic Atrophy Inferred From Temporal, Spatial, and Chromatic Sensitivity Losses

Neuroradiologic findings in children with mitochondrial disorders

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