Lotta Gränse

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2021
Mark Low fraction of fetal haemoglobin is associated with retinopathy of prematurity in the very preterm infant
Hellström, William ; Martinsson, Tobias ; Morsing, Eva ^LU ; Gränse, Lotta ^LU ; Ley, David ^LU and Hellström, Ann ^LU (2021) In British Journal of Ophthalmology
- Contribution to journal › Article
Mark High rate and large intercentre variability in retreatment of retinopathy of prematurity in infants born <24 gestational weeks
Lundgren, Pia ^LU ; Jacobson, Lena ; Hård, Anna Lena ; Al-Hawasi, Abbas ; Larsson, Eva ; Gränse, Lotta ^LU ; Saric, Marie ; Sunnqvist, Birgitta ; Tornqvist, Kristina ^LU and Wallin, Agneta , et al. (2021) In BMJ Open Ophthalmology 6(1).
- Contribution to journal › Article
Mark Association of Docosahexaenoic Acid and Arachidonic Acid Serum Levels with Retinopathy of Prematurity in Preterm Infants
Hellström, Ann ; Pivodic, Aldina ; Gränse, Lotta ^LU ; Lundgren, Pia ; Sjöbom, Ulrika ; Nilsson, Anders K. ; Söderling, Helena ; Hård, Anna Lena ; Smith, Lois E.H. and Löfqvist, Chatarina Alice (2021) In JAMA Network Open 4(10).
- Contribution to journal › Article
Mark Dexamethasone eye-drops for treatment of retinopathy of prematurity
Öhnell, Hanna Maria ^LU ; Andreasson, Sten ^LU and Gränse, Lotta ^LU (2021) In Ophthalmology Retina
- Contribution to journal › Article
2020
Mark New modifications of Swedish ROP guidelines based on 10-year data from the SWEDROP register
Holmström, Gerd ; Hellström, Ann ; Gränse, Lotta ^LU ; Saric, Marie ; Sunnqvist, Birgitta ; Wallin, Agneta ; Tornqvist, Kristina ^LU and Larsson, Eva (2020) In British Journal of Ophthalmology 104(7). p.943-949
- Contribution to journal › Article
Mark Development and validation of a new clinical decision support tool to optimize screening for retinopathy of prematurity
Pivodic, Aldina ; Johansson, Helena ; Smith, Lois E.H. ; Hård, Anna Lena ; Löfqvist, Chatarina ; Yoder, Bradley A. ; Hartnett, M. Elizabeth ; Wu, Carolyn ; Bründer, Marie Christine and Lagrèze, Wolf A. , et al. (2020) In British Journal of Ophthalmology
- Contribution to journal › Article
2019
Mark A novel missense variant in IDH3A causes autosomal recessive retinitis pigmentosa
Peter, Virginie G. ; Nikopoulos, Konstantinos ; Quinodoz, Mathieu ; Granse, Lotta ^LU ; Farinelli, Pietro ^LU ; Superti-Furga, Andrea ; Andréasson, Sten ^LU and Rivolta, Carlo (2019) In Ophthalmic Genetics 40(2). p.177-181
- Contribution to journal › Article
2012
Mark Multifocal Visual Evoked Potentials (mfVEP) in Diabetic Patients with and without Polyneuropathy.
Lövestam Adrian, Monica ^LU ; Gränse, Lotta ^LU ; Andersson, Gert ^LU and Andréasson, Sten ^LU (2012) In Open Ophthalmology Journal 6. p.98-103
- Contribution to journal › Article
2009
Mark Macular Dysfunction and Morphology in Spinocerebellar Ataxia Type 7 (SCA 7)
Hugosson, Therése ^LU ; Gränse, Lotta ^LU ; Ponjavic, Vesna ^LU and Andréasson, Sten ^LU (2009) In Ophthalmic Genetics 30(1). p.1-6
- Contribution to journal › Article
Mark Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa
Friedman, James S. ; Ray, Joseph W. ; Waseem, Naushin ; Johnson, Kory ; Brooks, Matthew J. ; Hugosson, Therése ^LU ; Breuer, Debra ; Branham, Kari E. ; Krauth, Daniel S. and Bowne, Sara J. , et al. (2009) In American Journal of Human Genetics 84(6). p.792-800
- Contribution to journal › Article

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