Rana Soylu Kucharz

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  1. 2019
  2. 2017
  3. Neurofilament light protein in CSF and blood is associated with neurodegeneration and disease severity in Huntington's disease

    Rana Soylu-Kucharz, Sandelius, Å., Marie Sjögren, Blennow, K., Wild, E. J., Zetterberg, H. & Maria Björkqvist, 2017 Dec 1, In : Scientific Reports. 7, 1, 14114.

    Research output: Contribution to journalArticle

  4. 2016
  5. Hypothalamic and Metabolic Dysfunction in Genetic Models of Huntington’s Disease

    Rana Soylu Kucharz, 2016, Lund: Lund University, Faculty of Medicine. 92 p.

    Research output: ThesisDoctoral Thesis (compilation)

  6. 2015
  7. Low dietary protein content alleviates motor symptoms in mice with mutant dynactin/dynein-mediated neurodegeneration.

    Wiesner, D., Sinniger, J., Henriques, A., Dieterlé, S., Müller, H-P., Rasche, V., Ferger, B., Dirrig-Grosch, S., Rana Soylu, Åsa Petersén, Walther, P., Linkus, B., Kassubek, J., Wong, P. C., Ludolph, A. C. & Dupuis, L., 2015, In : Human Molecular Genetics. 24, 8, p. 2228-2240

    Research output: Contribution to journalArticle

  8. 2013
  9. 2012
  10. 2011
  11. Increased numbers of orexin/hypocretin neurons in a genetic rat depression model.

    Mikrouli, E., Wörtwein, G., Rana Soylu, Mathe, A. A. & Åsa Petersén, 2011, In : Neuropeptides. 45, p. 401-406

    Research output: Contribution to journalArticle

  12. Mutant huntingtin causes metabolic imbalance by disruption of hypothalamic neurocircuits.

    Hult Lundh, S., Rana Soylu, Tomas Björklund, Belgardt, B. F., Mauer, J., Brüning, J. C., Deniz Kirik & Åsa Petersén, 2011, In : Cell Metabolism. 13, 4, p. 428-439

    Research output: Contribution to journalArticle

  13. 2010
  14. A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons

    Braunstein, K. E., Eschbach, J., Rona-Voeroes, K., Soylu, R., Mikrouli, E., Larmet, Y., Rene, F., De Aguilar, J-L. G., Loeffler, J-P., Mueller, H-P., Bucher, S., Kaulisch, T., Niessen, H. G., Tillmanns, J., Fischer, K., Schwalenstoecker, B., Kassubek, J., Pichler, B., Stiller, D., Petersén, Å. & 2 othersLudolph, A. C. & Dupuis, L., 2010, In : Human Molecular Genetics. 19, 22, p. 4385-4398

    Research output: Contribution to journalArticle

  15. Hypothalamic and Neuroendocrine Changes in Huntington's Disease.

    Hult Lundh, S., Schultz, K., Rana Soylu & Åsa Petersén, 2010, In : Current drug targets. 11, p. 1237-1249

    Research output: Contribution to journalArticle