Birgitte Rahbek Kornum

Birgitte Rahbek Kornum

Associate Professor, Visiting researcher

ORCID: 0000-0002-2515-9451

Publication year:
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1 - 4 out of 4Page size: 10
  1. 2012
  2. Published

    Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy

    Winkelmann, J., Lin, L., Schormair, B., Kornum, Birgitte Rahbek, Faraco, J., Plazzi, G., Melberg, A., Cornelio, F., Urban, A. E., Pizza, F., Poli, F., Grubert, F., Wieland, T., Graf, E., Hallmayer, J., Strom, T. M. & Mignot, E., 15 May 2012, In: Human Molecular Genetics. 21, 10, p. 2205-10 6 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  3. Published

    DQB1*06:02 allele-specific expression varies by allelic dosage, not narcolepsy status

    Weiner Lachmi, K., Lin, L., Kornum, Birgitte Rahbek, Rico, T., Lo, B., Aran, A. & Mignot, E., Apr 2012, In: Human Immunology. 73, 4, p. 405-10 6 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  4. Published

    Early IVIg treatment has no effect on post-H1N1 narcolepsy phenotype or hypocretin deficiency

    Knudsen, S., Biering-Sørensen, B., Kornum, Birgitte Rahbek, Petersen, E., Ibsen, J. D., Gammeltoft, S., Mignot, E. & Jennum, Poul, 2012, In: Neurology. 79, 1, p. 102-3 2 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  5. Published

    Predictors of hypocretin (orexin) deficiency in narcolepsy without cataplexy

    Andlauer, O., Moore, H., Hong, S., Dauvilliers, Y., Kanbayashi, T., Nishino, S., Han, F., Silber, M. H., Rico, T., Einen, M., Kornum, Birgitte Rahbek, Jennum, Poul, Knudsen, S., Nevsimalova, S., Poli, F., Plazzi, G. & Mignot, E., 2012, In: Sleep. 35, 9, p. 1247-55F

    Research output: Contribution to journal › Journal article › Research › peer-review

ID: 143987587