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- 2024
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Mark
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 hospitals
(
- Contribution to journal › Article
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Mark
Ophthalmic manifestations in children with tuberous sclerosis complex
(
- Contribution to journal › Article
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Mark
Ophthalmological outcome of 6.5 years children treated for retinopathy of prematurity : A Swedish register study
(
- Contribution to journal › Article
- 2023
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Mark
A Description of the Yield of Genetic Reinvestigation in Patients with Inherited Retinal Dystrophies and Previous Inconclusive Genetic Testing
(
- Contribution to journal › Article
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Mark
Childhood tuberous sclerosis complex in southern Sweden: A paradigm shift in diagnosis and treatment.
(
- Contribution to journal › Article
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Mark
Prognostic Value of Parenteral Nutrition Duration on Risk of Retinopathy of Prematurity : Development and Validation of the Revised DIGIROP Clinical Decision Support Tool
(
- Contribution to journal › Article
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Mark
Visual outcome at 2.5 years of age in ω-3 and ω-6 long-chain polyunsaturated fatty acid supplemented preterm infants : a follow-up of a randomized controlled trial
(
- Contribution to journal › Article
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Mark
Case report : Bilateral damage to the immature optic radiation and secondary massive loss of retinal ganglion cells causing tunnel vision
(
- Contribution to journal › Article
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Mark
Validation of DIGIROP models and decision support tool for prediction of treatment for retinopathy of prematurity on a contemporary Swedish cohort
(
- Contribution to journal › Article
- 2022
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Mark
Dexamethasone eye-drops for treatment of retinopathy of prematurity
(
- Contribution to journal › Article
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Mark
Low fraction of fetal haemoglobin is associated with retinopathy of prematurity in the very preterm infant
(
- Contribution to journal › Article
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Mark
Development and validation of a new clinical decision support tool to optimize screening for retinopathy of prematurity
(
- Contribution to journal › Article
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Mark
A novel phenotype associated with the R162W variant in the KCNJ13 gene
(
- Contribution to journal › Article
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Mark
Retrospective evaluation of ophthalmological and neurological outcomes for infants born before 24 weeks gestational age in a Swedish cohort
(
- Contribution to journal › Article
- 2021
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Mark
Association of Docosahexaenoic Acid and Arachidonic Acid Serum Levels with Retinopathy of Prematurity in Preterm Infants
(
- Contribution to journal › Article
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Mark
High rate and large intercentre variability in retreatment of retinopathy of prematurity in infants born <24 gestational weeks
(
- Contribution to journal › Article
- 2020
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Mark
New modifications of Swedish ROP guidelines based on 10-year data from the SWEDROP register
(
- Contribution to journal › Article
- 2019
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Mark
A novel missense variant in IDH3A causes autosomal recessive retinitis pigmentosa
(
- Contribution to journal › Article
- 2012
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Mark
Multifocal Visual Evoked Potentials (mfVEP) in Diabetic Patients with and without Polyneuropathy.
(
- Contribution to journal › Article
- 2009
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Mark
Macular Dysfunction and Morphology in Spinocerebellar Ataxia Type 7 (SCA 7)
(
- Contribution to journal › Article
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Mark
Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa
(
- Contribution to journal › Article
- 2006
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Mark
Evaluation of the visual pathway with ERG, mfERG and mfVEP in inherited eye disorders
2006)(
- Thesis › Doctoral thesis (compilation)
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Mark
Alterations in multifocal visual evoked potentials during the acute phase of Leber's hereditary optic neuropathy.
(
- Contribution to journal › Article
- 2004
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Mark
Alterations in electroretinograms and retinal morphology in rabbits treated with vigabatrin
(
- Contribution to journal › Article
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Mark
Full-field ERG, multifocal ERG and multifocal VEP in patients with retinitis pigmentosa and residual central visual fields.
(
- Contribution to journal › Article
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Mark
Reduced full-field electroretinogram (ERG) in a patient treated with methotrexate.
(
- Contribution to journal › Article
- 2003
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Mark
Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 gene
(
- Contribution to journal › Article
- 2002
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Mark
Retinal dysfunction and anterior segment deposits in a patient treated with rifabutin
(
- Contribution to journal › Article
- 2001
-
Mark
Electrophysiologic findings in two young patients with Bothnia dystrophy and a mutation in the RLBP1 gene
(
- Contribution to journal › Article