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2025
Mark Electrophysiological evaluation and morphology of inherited and acquired retinal diseases
Meinert, Monika ^LU (2025) In Lund University, Faculty of Medicine Doctoral Dissertation Series
- Thesis › Doctoral thesis (compilation)
2022
Mark The potential role of retinal cGMP-interaction partners within the degeneration mechanism causing Retinitis Pigmentosa
Rasmussen, Michel ^LU (2022) In Lund University, Faculty of Medicine Doctoral Dissertation Series
- Thesis › Doctoral thesis (compilation)
2021
Mark Clinical spectrum, genetic associations and management outcomes of Coats-like exudative retinal vasculopathy in autosomal recessive retinitis pigmentosa
Magliyah, Moustafa ; Alshamrani, Abdulaziz A. ; Schatz, Patrik ^LU ; Taskintuna, Ibrahim ; Alzahrani, Yahya and Nowilaty, Sawsan R. (2021) In Ophthalmic Genetics 42(2). p.178-185
- Contribution to journal › Article
2020
Mark Severe retinitis pigmentosa phenotype associated with novel CNGB1 variants
Alshamrani, Abdulaziz A. ; Raddadi, Osama ; Schatz, Patrik ^LU ; Lenzner, Steffen ; Neuhaus, Christine ; Azzam, Eman and Abdelkader, Ehab (2020) In American Journal of Ophthalmology Case Reports 19.
- Contribution to journal › Article
Mark Longitudinal changes of macular curvature in patients with retinitis pigmentosa
Meinert, Monika ^LU ; Ueno, Shinji ; Komori, Shiori ; Koyanagi, Yoshito ; Sayo, Akira ; Andreasson, Sten ^LU ; Kominami, Taro ; Ito, Yasuki and Terasaki, Hiroko (2020) In Translational Vision Science and Technology 9(10).
- 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
2018
Mark Severe retinal degeneration at an early age in Usher syndrome type 1B associated with homozygous splice site mutations in MYO7A gene
Abdelkader, Ehab ; Enani, Lama ; Schatz, Patrik ^LU and Safieh, Leen (2018) In Saudi Journal of Ophthalmology 32(2). p.119-125
- Contribution to journal › Article
2016
Mark Characterization of macular structure and function in two swedish families with genetically identified autosomal dominant retinitis pigmentosa
Abdulridha-Aboud, Wissam ^LU ; Kjellström, Ulrika ^LU ; Andréasson, Sten ^LU and Ponjavic, Vesna ^LU (2016) In Molecular Vision 22. p.362-373
- Contribution to journal › Article
2007
Mark Intracellular mechanisms in rd1 mouse retinal degeneration
Johnson, Leif ^LU (2007) In Lund University Faculty of Medicine Doctoral Dissertation Series
- Thesis › Doctoral thesis (compilation)
Mark Calpain activity in retinal degeneration.
Paquet-Durand, Francois ^LU ; Johnson, Leif ^LU and Ekström, Per ^LU (2007) In Journal of Neuroscience Research 85(4). p.693-702
- Contribution to journal › Scientific review

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