Ophthalmology, Lund

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1997
Mark Pre-eclampsia is a potent risk factor for deterioration of retinopathy during pregnancy in Type 1 diabetic patients
Lövestam Adrian, Monica ^LU ; Agardh, Carl-David ^LU ; Åberg, Anders E ^LU and Agardh, Elisabet ^LU (1997) In Diabetic Medicine 14(12). p.1059-1065
- 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 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 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 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
Mark Laurence-Moon-Bardet-Biedl syndrome. Clinical,electrophysiological and genetic aspects.
Riise, Ruth ^LU (1997)
- Thesis › Doctoral thesis (compilation)
Mark Phenotypes and genotypes in families with hereditary tapetoretinal degenerations
Ponjavic, Vesna ^LU (1997)
- Thesis › Doctoral thesis (compilation)
Mark Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: Paucity of mutations in the coding region, but splice defects in two families
Fujita, Ricardo ; Buraczynska, Monika ; Gieser, Linn ; Wu, Weiping ; Forsythe, Patricia ; Abrahamson, Magnus ^LU ; Jacobsson, Samuel G ; Sieving, Paul A ; Andréasson, Sten ^LU and Swaroop, Anand (1997) In American Journal of Human Genetics 61(3). p.571-580
- Contribution to journal › Article
Mark DNA fragmentation characteristic of apoptosis and cell loss induced by kainic acid in rabbit retinas
Perez, M T ^LU ; Arnér, K ^LU and Håkansson, Anders P ^LU (1997) In Neurochemistry International 31(2). p.60-251
- Contribution to journal › Article
Mark Immunocytochemical localisation of neuronal nitric oxide synthase in developing and transplanted rabbit retinas
Sharma, R K ^LU ; Perez, M T ^LU and Ehinger, B ^LU (1997) In Histochemistry and Cell Biology 107(6). p.58-449
- Contribution to journal › Article

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