Molecular Vision, 1090-0535

Tidskrift

Fler filtreringsmöjligheter
  1. 2019
  2. Long-term follow-up of retinal function and structure in trpm1-associated complete congenital stationary night blindness

    Haneen Al-Hujaili, Ibrahim Taskintuna, Christine Neuhaus, Carsten Bergmann & Patrik Schatz, 2019, I: Molecular Vision. 25, s. 851-858

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. 2018
  4. Full-field ERG as a predictor of the natural course of ABCA4-associated retinal degenerations

    Marion Schroeder & Ulrika Kjellström, 2018 jan 4, I: Molecular Vision. 24, s. 1-16 16 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. 2017
  6. Heterozygous mutation in OTX2 associated with early-onset retinal dystrophy with atypical maculopathy

    Maram E.A. Abdalla-Elsayed, Patrik Schatz, Christine Neuhaus & Arif O. Khan, 2017 nov 13, I: Molecular Vision. 23, s. 778-784 7 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  7. 2016
  8. Characterization of macular structure and function in two swedish families with genetically identified autosomal dominant retinitis pigmentosa

    Wissam Abdulridha-Aboud, Ulrika Kjellström, Sten Andréasson & Vesna Ponjavic, 2016 maj 22, I: Molecular Vision. 22, s. 362-373 12 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  9. 2015
  10. Reduced macular function in ABCA4 carriers.

    Ulrika Kjellström, 2015, I: Molecular Vision. 21, s. 767-782

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  11. 2014
  12. Association between genotype and phenotype in families with mutations in the ABCA4 gene.

    Ulrika Kjellström, 2014, I: Molecular Vision. 20, Jan 7, s. 89-104

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Jesper Bregnhøj, Sermed Al-Hamdani, Birgit Sander, Michael Larsen & Patrik Schatz, 2014, I: Molecular Vision. 20, Jun 19, s. 852-863

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  14. 2013
  15. Phenotypic map of porcine retinal ganglion cells

    Patricia Veiga-Crespo, Patricia del Río, Marcel Blindert, Marius Ueffing, Stefanie M Hauck & Elena Vecino, 2013, I: Molecular Vision. 19, s. 904-16 13 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  16. 2012
  17. A tapetal-like fundus reflex in a healthy male: evidence against a role in the pathophysiology of retinal degeneration?

    Patrik Schatz, Jesper Bregnhoj, Henrik Arvidsson, Dror Sharon, Liliana Mizrahi-Meissonnier, Birgit Sander, Karen Gronskov & Michael Larsen, 2012, I: Molecular Vision. 18, 119-20, s. 1147-1155

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  18. 2011
  19. Clinical evaluation of two consanguineous families with homozygous mutations in BEST1

    Teresa Pineiro-Gallego, Maria Alvarez, Ines Pereiro, Severiano Campos, Dror Sharon, Patrik Schatz & Diana Valverde, 2011, I: Molecular Vision. 17, 179, s. 1607-1617

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  20. 2010
  21. Mitogen-activated protein kinases in the porcine retinal arteries and neuroretina following retinal ischemia-reperfusion.

    Bodil Gesslein, Gisela Håkansson, Ronald Carpio, Lotta Gustafsson, Maria Thereza Perez & Malin Malmsjö, 2010, I: Molecular Vision. 16, s. 392-407

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  22. 2009
  23. Protein kinase C in porcine retinal arteries and neuroretina following retinal ischemia-reperfusion.

    Bodil Gesslein, Lotta Gustafsson, Angelica Wackenfors, Fredrik Ghosh & Malin Malmsjö, 2009, I: Molecular Vision. 15, Apr 13, s. 737-746

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  24. 2008
  25. Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration

    Zubair M Ahmed, Sten Kjellstrom, Ricky J L Haywood-Watson, Ronald A Bush, Lori L Hampton, James F Battey, Saima Riazuddin, Gregory Frolenkov, Paul A. Sieving & Thomas B Friedman, 2008, I: Molecular Vision. 14, s. 2227-36 10 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  26. 2007
  27. Evidence against a blood derived origin for transforming growth factor beta induced protein in corneal disorders caused by mutations in the TGFBI gene

    Henrik Karring, Zuzana Valnickova, Ida B Thogersen, Chris J Hedegaard, Torben Moller-Pedersen, Torsten Kristensen, Gordon K Klintworth & Jan J Enghild, 2007, I: Molecular Vision. 13, s. 997

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  28. 2006
  29. The human cornea proteome: bioinformatic analyses indicate import of plasma proteins into the cornea

    Henrik Karring, Ida B Thogersen, Gordon K Klintworth, Torben Moller-Pedersen & Jan J Enghild, 2006, I: Molecular Vision. 12, s. 451-460

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

  30. 2003
  31. Growth of the postnatal rat retina in vitro: Quantitative RT-PCR analyses of mRNA expression for photoreceptor proteins

    Ingela Liljekvist Soltic, M Torngren, Magnus Abrahamson & Kjell Johansson, 2003, I: Molecular Vision. 9, 79, s. 657-664

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift