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1998
Mark Central retinal vein occlusion: Cetrain risk factors, electroretinography and an experimental treatment model.
Larsson, Jörgen ^LU (1998)
- Thesis › Doctoral thesis (compilation)
Mark Phenotype in a Swedish family with X-linked retinitis pigmentosa caused by a novel splice defect in the RPGR gene
Bauer, S ; Fujita, R ; Buraczynska, M ; Abrahamson, Magnus ^LU ; Ehinger, B ; Wu, W ; Falls, TJ ; Andreasson, S and Swaroop, A (1998) In Investigative Ophthalmology & Visual Science 39(12). p.2470-2474
- Contribution to journal › Article
Mark Transplant of full-thickness embryonic rabbit retina using pars plana vitrectomy
Ghosh, F ^LU ; Arnér, K ^LU and Ehinger, B ^LU (1998) In Retina 18(2). p.42-136
- Contribution to journal › Article
Mark Evaluation of a new perimetric threshold strategy, SITA, in patients with manifest and suspect glaucoma
Bengtsson, B ^LU and Heijl, A ^LU (1998) In Acta Ophthalmologica Scandinavica 76(3). p.72-268
- Contribution to journal › Article
Mark Age, gender, IOP, refraction and optic disc topography in normal eyes. A cross-sectional study using raster and scanning laser tomography
Gundersen, Kjell Gunnar ^LU ; Heijl, Anders ^LU and Bengtsson, Bo ^LU (1998) In Acta Ophthalmologica Scandinavica 76(2). p.170-175
- Contribution to journal › Article
1997
Mark Poor metabolic control, early age at onset, and marginal folate deficiency are associated with increasing levels of plasma homocysteine in insulin-dependent diabetes mellitus. A five-year follow-up study
Hultberg, Björn ^LU ; Agardh, Carl-David ^LU ; Agardh, Elisabet ^LU and Lövestam Adrian, Monica ^LU (1997) In Scandinavian Journal of Clinical & Laboratory Investigation 57(7). p.595-600
- Contribution to journal › Article
Mark Retinal examination intervals in diabetic patients on diet treatment only
Hansson-Lundblad, C ; Agardh, Elisabet ^LU and Agardh, Carl-David ^LU (1997) In Acta Ophthalmologica Scandinavica 75(3). p.244-248
- Contribution to journal › Article
Mark A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267–Leu
Ponjavic, Vesna ^LU ; Abrahamson, Magnus ^LU ; Andréasson, Sten ^LU ; Ehinger, Berndt ^LU ; Fex, Göran and Polland, W (1997) In Ophthalmic Genetics 18(2). p.63-70
- Contribution to journal › Article
Mark Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene
Andréasson, Sten ^LU ; Ponjavic, Vesna ^LU ; Abrahamson, Magnus ^LU ; Ehinger, Berndt ^LU ; Wu, W ; Fujita, R ; Buraczynska, M and Swaroop, A (1997) In American Journal of Ophthalmology 124(1). p.95-102
- Contribution to journal › Article
Mark Autosomal dominant retinitis pigmentosa with a rhodopsin mutation (Arg-135–Trp): Disease phenotype in a Swedish family
Ponjavic, Vesna ^LU ; Abrahamson, Magnus ^LU ; Andréasson, Sten ^LU ; Ehinger, Berndt ^LU and Fex, G (1997) In Acta Ophthalmologica Scandinavica 75(2). p.218-223
- Contribution to journal › Article

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