Jørgen Erik Nielsen

Jørgen Erik Nielsen

Clinical Professor


  1. 1996
  2. Published

    Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation Danish family. / Nielsen, Jørgen Erik; Sørensen, Sven Asger; Hasholt, Lis Frydenreich; Nørremølle, Anne.

    In: Movement Disorders, Vol. 11, No. 5, 1996, p. 533-541.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. 2002
  4. Published

    Possible autocrine loop of the epidermal growth factor system in patients with benign prostatic hyperplasia treated with finasteride: a placebo-controlled randomized study. / Tørring, Niels; Jensen, Klaus Møller-Ernst; Lund, L; Nielsen, J E; Djurhuus, Jens Christian; Poulsen, S S; Nexø, Ebba; Poulsen, Steen Seier.

    In: B J U International (Print), Vol. 89, No. 6, 01.04.2002, p. 583-90.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. 2004
  6. Published

    Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation. / Nielsen, Jørgen Erik; Johnson, B; Koefoed, Pernille; Scheuer, K.H.; Grønbech-Jensen, M.; Law, I.; Krabbe, K.; Nørremølle, Anne; Eiberg, Hans Rudolf Lytchoff; Søndergård, H.; Dam, M.; Rehfeld, J.F.; Krarup, C.; Paulson, O.B.; Hasholt, Lis Frydenreich; Sørensen, Sven Asger.

    In: European Journal of Neurology, Vol. 11, No. 12, 2004, p. 817-824.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG4) using direct mutation detection. / Nielsen, Jørgen E; Koefoed, Pernille; Kjaergaard, Susanne; Jensen, Lisa Neerup; Nørremølle, Anne; Hasholt, Lis.

    In: Prenatal Diagnosis, Vol. 24, No. 5, 2004, p. 363-6.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. 2005
  9. Published

    Reduced regional cerebral blood flow in SPG4-linked hereditary spastic paraplegia. / Scheuer, Kristin H; Nielsen, Jørgen E; Krabbe, Katja; Simonsen, Carina; Koefoed, Pernille; Sørensen, Sven A; Gade, Anders; Paulson, Olaf B; Law, Ian.

    In: Journal of the Neurological Sciences, Vol. 235, No. 1-2, 2005, p. 23-32.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. 2008
  11. Published

    Cortical volumes and atrophy rates in FTD-3 CHMP2B mutation carriers and related non-carriers. / Eskildsen, Simon F; Østergaard, Lasse R; Rodell, Anders B; Østergaard, Leif; Nielsen, Jørgen E; Isaacs, Adrian M; Johannsen, Peter.

    In: NeuroImage, Vol. 45, No. 3, 2008, p. 713-21.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    [Hereditary Parkinson disease. The Danish Society of Movement Disorders]. / Hjermind, L.E.; Nielsen, Jørgen Erik.

    In: Ugeskrift for læger, Vol. 170, No. 12, 2008, p. 1016-.

    Research output: Contribution to journalJournal articleResearchpeer-review

  13. 2009
  14. Published

    4p16.3 haplotype modifying age at onset of Huntington disease. / Nørremølle, A; Budtz-Jørgensen, E; Fenger, K; Nielsen, Jørgen Erik; Sørensen, S A; Hasholt, L.

    In: Clinical Genetics, Vol. 75, No. 3, 2009, p. 244-50.

    Research output: Contribution to journalJournal articleResearchpeer-review

  15. Published

    A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunction. / Puschmann, Andreas; Ross, Owen A; Vilariño-Güell, Carles; Lincoln, Sarah J; Kachergus, Jennifer M; Cobb, Stephanie A; Lindquist, Suzanne G; Nielsen, Jørgen Erik; Wszolek, Zbigniew K; Farrer, Matthew; Widner, Håkan; van Westen, Danielle; Hägerström, Douglas; Markopoulou, Katerina; Chase, Bruce A; Nilsson, Karin; Reimer, Jan; Nilsson, Christer.

    In: Parkinsonism & Related Disorders, Vol. 15, No. 9, 2009, p. 627-32.

    Research output: Contribution to journalJournal articleResearchpeer-review

  16. Published

    Genetic testing in familial AD and FTD: mutation and phenotype spectrum in a Danish cohort. / Lindquist, S G; Schwartz, M; Batbayli, M; Waldemar, G; Nielsen, Jørgen Erik.

    In: Clinical Genetics, Vol. 76, No. 2, 2009, p. 205-9.

    Research output: Contribution to journalJournal articleResearchpeer-review

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ID: 9689629