Emil Ygland Rödström

affiliated with the university, MD
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  1. 2019
  2. Low prevalence of known pathogenic mutations in dominant PD genes: A Swedish multicenter study

    Puschmann, A., Jiménez-Ferrer, I., Lundblad-Andersson, E., Mårtensson, E., Hansson, O., Odin, P., Widner, H., Brolin, K., Mzezewa, R., Kristensen, J., Soller, M., Rödström, E. Y., Ross, O. A., Toft, M., Breedveld, G. J., Bonifati, V., Brodin, L., Zettergren, A., Sydow, O., Linder, J. & 6 others, Wirdefeldt, K., Svenningsson, P., Nissbrandt, H., Belin, A. C., Forsgren, L. & Maria Swanberg, 2019, In : Parkinsonism and Related Disorders. 66, p. 158-165

    Research output: Contribution to journalArticle

  3. Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?

    Sorina Gorcenco, Vaz, F. M., Tracewska-Siemiatkowska, A., Tranebjærg, L., Cremers, F. P. M., Emil Ygland, Kicsi, J., Rendtorff, N. D., Möller, C., Kjellström, U., Sten Andréasson & Andreas Puschmann, 2019, In : Parkinsonism & Related Disorders. 61, p. 245-247 3 p.

    Research output: Contribution to journalLetter

  4. 2018
  5. Will FTLD-tau work for all when FTDP-17 retires?

    Emil Ygland, Maria Landqvist Waldö, Elisabet Englund, Andreas Puschmann & Nilsson, C., 2018, In : Brain : a journal of neurology. 141, 8, p. e62

    Research output: Contribution to journalArticle

  6. 2016
  7. Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden

    Ran, C., Brodin, L., Forsgren, L., Westerlund, M., Ramezani, M., Gellhaar, S., Xiang, F., Fardell, C., Nissbrandt, H., Söderkvist, P., Andreas Puschmann, Emil Ygland, Olson, L., Willows, T., Johansson, A., Sydow, O., Wirdefeldt, K., Galter, D., Svenningsson, P. & Belin, A. C., 2016 Sep, In : Neurobiology of Aging. 45, p. 212.e5-212e.11

    Research output: Contribution to journalArticle

  8. 2014
  9. Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosis.

    EMIL YGLAND, Taroni, F., Gellera, C., Caldarazzo, S., Duno, M., Soller, M. & Andreas Puschmann, 2014, In : Parkinsonism & Related Disorders. 20, 8, p. 919-923

    Research output: Contribution to journalArticle

  10. 2012
  11. Friedreich's ataxia in patients with FXN p.R165P point mutation

    E. Ygland, Taroni, F., Gellera, C., Duno, M., Johnels, P., Soller, M. & A. Puschmann, 2012 Sep 1, In : European Journal of Neurology. 19, Suppl 1, p. 727 1 p.

    Research output: Contribution to journalPublished meeting abstract

  12. 2011