Jørgen Erik Nielsen

Jørgen Erik Nielsen

Clinical Professor

Member of:

  • Neurology


  1. 2011
  2. Published

    Personality disintegration - it runs in the family

    Stokholm, J., Johannsen, P., Nielsen, Jørgen Erik & Gade, A., 2011, Case studies in Dementia: Common and uncommon presentations. Gautier, S. & Rosa-Neto, P. (eds.). Cambridge University Press, p. 115-123 9 p. (Case Studies in Neurology ).

    Research output: Chapter in Book/Report/Conference proceedingBook chapterCommunication

  3. Published

    NIPA1 mutation in complex hereditary spastic paraplegia with epilepsy

    Svenstrup, K., Møller, R. S., Christensen, J., Budtz-Joergensen, Esben, Nielsen, M. G. & Nielsen, Jørgen Erik, 1 Sep 2011, In: European journal of neurology : the official journal of the European Federation of Neurological Societies. 18, 9, p. 1197-9 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. 2012
  5. Published

    Amyloid-related biomarkers and axonal damage proteins in parkinsonian syndromes

    Bech, S., Hjermind, L. E., Salvesen, Lisette, Nielsen, Jørgen Erik, Heegaard, N. H. H., Jørgensen, Henrik Løvendahl, Rosengren, L., Blennow, K., Zetterberg, H. & Winge, K., 2012, In: Parkinsonism & Related Disorders. 18, 1, p. 69-72 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9)

    Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Korbo, L., Nielsen, I., Svenstrup, K., Bech, S., Pinborg, L., Friberg, L., Hjermind, L., Olsen, O. & Nielsen, Jørgen Erik, Nov 2012, In: Clinical Genetics. 82, 3, p. 256-63 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Intravenous immunoglobulin treatment in a patient with adrenomyeloneuropathy

    Jønch, A. E., Danielsen, E. R., Thomsen, C., Meden, Per, Svenstrup, K. & Nielsen, Jørgen Erik, 26 Sep 2012, In: B M C Neurology. 12, 108, 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion

    Lee, J-M., Ramos, E. M., Lee, J-H., Gillis, T., Mysore, J. S., Hayden, M. R., Warby, S. C., Morrison, P., Nance, M., Ross, C. A., Margolis, R. L., Squitieri, F., Orobello, S., Di Donato, S., Gomez-Tortosa, E., Ayuso, C., Suchowersky, O., Trent, R. J. A., McCusker, E., Novelletto, A. & 22 others, Frontali, M., Jones, R., Ashizawa, T., Frank, S., Saint-Hilaire, M. H., Hersch, S. M., Rosas, H. D., Lucente, D., Harrison, M. B., Zanko, A., Abramson, R. K., Marder, K., Sequeiros, J., Paulsen, J. S., Landwehrmeyer, G. B., Myers, R. H., MacDonald, M. E., Gusella, J. F., Hasholt, Lis Frydenreich, Nørremølle, Anne, Nielsen, Jørgen Erik & PREDICT-HD study of the Huntington Study Group (HSG), P. S. O. T. H. S. G. (., Mar 2012, In: Neurology. 78, 10, p. 690-5 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Presymptomatic cerebral blood flow changes in CHMP2B mutation carriers of familial frontotemporal dementia (FTD-3), measured with MRI

    Lunau, L. A., Mouridsen, K., Rodell, A., Ostergaard, L., Nielsen, Jørgen Erik, Isaacs, A., Johannsen, P. & The FReJA Consortium, T. F. C., Mar 2012, In: BMJ Open. 2, 2

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    ATXN2 with intermediate-length CAG/CAA repeats does not seem to be a risk factor in hereditary spastic paraplegia

    Nielsen, T. T., Svenstrup, K., Budtz-Joergensen, Esben, Eiberg, Hans Rudolf Lytchoff, Hasholt, Lis Frydenreich & Nielsen, Jørgen Erik, Oct 2012, In: Journal of the Neurological Sciences. 321, 1-2, p. 100-2 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    Reversal of pathology in CHMP2B-mediated frontotemporal dementia patient cells using RNA interference

    Nielsen, T. T., Mizielinska, S., Hasholt, Lis Frydenreich, Isaacs, A. M., Nielsen, Jørgen Erik & the FReJA Consortium, T. F. C., Aug 2012, In: Journal of Gene Medicine. 14, 8, p. 521-529 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    Severe and rapidly progressing cognitive phenotype in a SCA17-family with only marginally expanded CAG/CAA repeats in the TATA-box binding protein gene: A case report

    Nielsen, T. T., Mardosiene, S., Løkkegaard, Annemette, Stokholm, J., Ehrenfels, S., Bech, S., Friberg, L., Nielsen, J. K. & Nielsen, Jørgen Erik, Aug 2012, In: B M C Neurology. 12, p. 73

    Research output: Contribution to journalJournal articleResearchpeer-review

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