Molecular Vision, 1090-0535

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  1. 2018

  2. Full-field ERG as a predictor of the natural course of ABCA4-associated retinal degenerations

    Marion Schroeder & Kjellström, U., 2018 Jan 4, In : Molecular Vision. 24, p. 1-16 16 p.

    Research output: Contribution to journal › Article

  3. 2017

  4. Heterozygous mutation in OTX2 associated with early-onset retinal dystrophy with atypical maculopathy

    Abdalla-Elsayed, M. E. A., Schatz, P., Neuhaus, C. & Khan, A. O., 2017 Nov 13, In : Molecular Vision. 23, p. 778-784 7 p.

    Research output: Contribution to journal › Article

  5. 2016

  6. Characterization of macular structure and function in two swedish families with genetically identified autosomal dominant retinitis pigmentosa

    Abdulridha-Aboud, W., Kjellström, U., Sten Andréasson & Ponjavic, V., 2016 May 22, In : Molecular Vision. 22, p. 362-373 12 p.

    Research output: Contribution to journal › Article

  7. 2015

  8. Reduced macular function in ABCA4 carriers.

    Kjellström, U., 2015, In : Molecular Vision. 21, p. 767-782

    Research output: Contribution to journal › Article

  9. 2014

  10. Association between genotype and phenotype in families with mutations in the ABCA4 gene.

    Kjellström, U., 2014, In : Molecular Vision. 20, Jan 7, p. 89-104

    Research output: Contribution to journal › Article

  11. Reappearance of the tapetal-like reflex after prolonged dark adaptation in a female carrier of RPGR ORF15 X-linked retinitis pigmentosa.

    Bregnhøj, J., Al-Hamdani, S., Sander, B., Larsen, M. & Schatz, P., 2014, In : Molecular Vision. 20, Jun 19, p. 852-863

    Research output: Contribution to journal › Article

  12. 2013

  13. Phenotypic map of porcine retinal ganglion cells

    Patricia Veiga-Crespo, del Río, P., Blindert, M., Ueffing, M., Hauck, S. M. & Vecino, E., 2013, In : Molecular Vision. 19, p. 904-16 13 p.

    Research output: Contribution to journal › Article

  14. 2012

  15. A tapetal-like fundus reflex in a healthy male: evidence against a role in the pathophysiology of retinal degeneration?

    Schatz, P., Bregnhoj, J., Arvidsson, H., Sharon, D., Mizrahi-Meissonnier, L., Sander, B., Gronskov, K. & Larsen, M., 2012, In : Molecular Vision. 18, 119-20, p. 1147-1155

    Research output: Contribution to journal › Article

  16. 2011

  17. Clinical evaluation of two consanguineous families with homozygous mutations in BEST1

    Pineiro-Gallego, T., Alvarez, M., Pereiro, I., Campos, S., Sharon, D., Schatz, P. & Valverde, D., 2011, In : Molecular Vision. 17, 179, p. 1607-1617

    Research output: Contribution to journal › Article

  18. 2010

  19. Mitogen-activated protein kinases in the porcine retinal arteries and neuroretina following retinal ischemia-reperfusion.

    Bodil Gesslein, Håkansson, G., Carpio, R., Gustafsson, L., Maria Thereza Perez & Malin Malmsjö, 2010, In : Molecular Vision. 16, p. 392-407

    Research output: Contribution to journal › Article

  21. 2009

  22. Protein kinase C in porcine retinal arteries and neuroretina following retinal ischemia-reperfusion.

    Bodil Gesslein, Gustafsson, L., Wackenfors, A., Fredrik Ghosh & Malin Malmsjö, 2009, In : Molecular Vision. 15, Apr 13, p. 737-746

    Research output: Contribution to journal › Article

  23. 2008

  24. Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration

    Ahmed, Z. M., Kjellstrom, S., Haywood-Watson, R. J. L., Bush, R. A., Hampton, L. L., Battey, J. F., Riazuddin, S., Frolenkov, G., Sieving, P. A. & Friedman, T. B., 2008, In : Molecular Vision. 14, p. 2227-36 10 p.

    Research output: Contribution to journal › Article

  25. 2007

  26. Evidence against a blood derived origin for transforming growth factor beta induced protein in corneal disorders caused by mutations in the TGFBI gene

    Karring, H., Valnickova, Z., Thogersen, I. B., Hedegaard, C. J., Moller-Pedersen, T., Kristensen, T., Klintworth, G. K. & Enghild, J. J., 2007, In : Molecular Vision. 13, p. 997

    Research output: Contribution to journal › Article

  27. 2006

  28. The human cornea proteome: bioinformatic analyses indicate import of plasma proteins into the cornea

    Karring, H., Thogersen, I. B., Klintworth, G. K., Moller-Pedersen, T. & Enghild, J. J., 2006, In : Molecular Vision. 12, p. 451-460

    Research output: Contribution to journal › Review article

  29. 2003

  30. Growth of the postnatal rat retina in vitro: Quantitative RT-PCR analyses of mRNA expression for photoreceptor proteins

    Liljekvist Soltic, I., Torngren, M., Magnus Abrahamson & Johansson, K., 2003, In : Molecular Vision. 9, 79, p. 657-664

    Research output: Contribution to journal › Article

  31. Mutation screening of patients with Leber congenital amaurosis or the enhanced S-cone syndrome reveals a lack of sequence variations in the NRL gene

    Acar, C., Mears, A., Yashar, B., Maheshwary, A., Sten Andréasson, Baldi, A., Sieving, P., Iannaccone, A., Musarella, M., Jacobson, S. & Swaroop, A., 2003, In : Molecular Vision. 9, 3-4, p. 14-17

    Research output: Contribution to journal › Article