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- 2023
-
Mark
Analysis of age at detection and outcomes of dense unilateral congenital cataract surgery for children on the paediatric cataract register
- Contribution to journal › Article
-
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
-
Mark
Performance of a [18F]Flortaucipir PET Visual Read Method Across the Alzheimer Disease Continuum and in Dementia with Lewy Bodies
- Contribution to journal › Article
-
Mark
Early findings in a prospective randomised study on three cross-linking treatment protocols : Interruption of the iontophoresis treatment protocol
Gustafsson, Ingemar LU
; Ivarsen, Anders
and Hjortdal, Jesper
(2023)
In BMJ Open Ophthalmology
8(1).
- Contribution to journal › Article
-
Mark
Prognostic Value of Parenteral Nutrition Duration on Risk of Retinopathy of Prematurity : Development and Validation of the Revised DIGIROP Clinical Decision Support Tool
Pivodic, Aldina ; Holmström, Gerd ; Smith, Lois E.H. ; Hård, Anna Lena ; Löfqvist, Chatarina ; Al-Hawasi, Abbas ; Larsson, Eva ; Lundgren, Pia ; Gränse, Lotta LU
and Tornqvist, Kristina
LU
, et al.
(2023)
In JAMA Ophthalmology
141(8).
p.716-724
- Contribution to journal › Article
-
Mark
Cone dystrophy associated with autoimmune polyglandular syndrome type 1
Badawi, Abdulrahman ; Magliyah, Moustafa ; Alabbasi, Omar ; AlAbdi, Lama ; Alkuraya, Fowzan S. ; Schatz, Patrik LU
; ALBalawi, Hani Basher
and Mura, Marco
(2023)
In Scientific Reports
13(1).
- Contribution to journal › Article
-
Mark
Two point four million cataract surgeries : 30 years with the Swedish National Cataract Register, 1992-2021
- Contribution to journal › Scientific review
-
Mark
A Description of the Yield of Genetic Reinvestigation in Patients with Inherited Retinal Dystrophies and Previous Inconclusive Genetic Testing
Areblom, Maria LU ; Kjellström, Sten LU ; Andréasson, Sten LU ; Öhberg, Anders ; Gränse, Lotta LU
and Kjellström, Ulrika
LU
(2023)
In Genes
14(7).
- Contribution to journal › Article
- 2022
-
Mark
A novel phenotype associated with the R162W variant in the KCNJ13 gene
Schroeder, Marion LU ; Peter, Virginie G. ; Gränse, Lotta LU
; Andréasson, Sten
LU
; Rivolta, Carlo
and Kjellström, Ulrika
LU
(2022)
In Ophthalmic Genetics
43(4).
p.500-507
- Contribution to journal › Article
-
Mark
First-Onset Dacryocystitis : Characterization, Treatment, and Prognosis
- Contribution to journal › Article