Jørgen Erik Nielsen

Jørgen Erik Nielsen

Clinical Professor


  1. Published
  2. Published

    Sporadic Creutzfeldt-Jakob Disease in a Woman Married Into a Gerstmann-Sträussler-Scheinker Family : An Investigation of Prions Transmission via Microchimerism. / Areškeviciute, Aušrine; Melchior, Linea Cecilie; Broholm, Helle; Krarup, Lars-Henrik; Lindquist, Suzanne Granhøj; Johansen, Peter; McKenzie, Neil; Green, Alison; Nielsen, Jørgen Erik; Laursen, Henning; Lund, Eva Løbner.

    In: Journal of Neuropathology and Experimental Neurology, Vol. 77, No. 8, 2018, p. 673-684.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders. / Bech, Sara; Nørremølle, Anne; Winge, Kristian; Hasholt, Lis; Tommerup, Niels; Svenstrup, Kirsten; Nielsen, Jørgen E; Hjermind, Lena E.

    In: Parkinsonism & Related Disorders, Vol. 17, No. 5, 01.06.2011, p. 398-9.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Huntington's disease-like and ataxia syndromes: identification of a family with a de novo SCA17/TBP mutation. / Bech, Sara; Petersen, Thor; Nørremølle, Anne; Gjedde, Albert; Ehlers, Lise; Eiberg, Hans; Hjermind, Lena E; Hasholt, Lis; Lundorf, Erik; Nielsen, Jørgen E.

    In: Parkinsonism & Related Disorders, Vol. 16, No. 1, 2010, p. 12-5.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Amyloid-related biomarkers and axonal damage proteins in parkinsonian syndromes. / Bech, Sara; Hjermind, Lena E; Salvesen, Lisette; Nielsen, Jørgen E; Heegaard, Niels H H; Jørgensen, Henrik L; Rosengren, Lars; Blennow, Kaj; Zetterberg, Henrik; Winge, Kristian.

    In: Parkinsonism & Related Disorders, Vol. 18, No. 1, 2012, p. 69-72.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Huntington's disease does not appear to increase the risk of diabetes mellitus. / Boesgaard, T W; Nielsen, Troels Tolstrup; Josefsen, Knud Elnegaard; Hansen, T; Jørgensen, T; Pedersen, O; Nørremølle, A; Nielsen, Jørgen Erik; Hasholt, L.

    In: Journal of Neuroendocrinology, Vol. 21, No. 9, 2009, p. 770-6.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia. / Nielsen, J.E.; International FTD-Genomics Consortium (IFGC).

    In: Scientific Reports, Vol. 9, No. 1, 10854, 2019.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Immune-related genetic enrichment in frontotemporal dementia : An analysis of genome-wide association studies. / Broce, Iris; Karch, Celeste M.; Wen, Natalie; Fan, Chun C.; Wang, Yunpeng; Hong Tan, Chin; Kouri, Naomi; Ross, Owen A.; Höglinger, Günter U.; Muller, Ulrich; Hardy, John; Momeni, Parastoo; Hess, Christopher P.; Dillon, William P.; Miller, Zachary A.; Bonham, Luke W.; Rabinovici, Gil D.; Rosen, Howard J.; Schellenberg, Gerard D.; Franke, Andre; Karlsen, Tom H.; Veldink, Jan H.; Ferrari, Raffaele; Yokoyama, Jennifer S.; Miller, Bruce L.; Andreassen, Ole A.; Dale, Anders M.; Desikan, Rahul S.; Sugrue, Leo P.; Ferrari, Raffaele; Hernandez, Dena G.; Nalls, Michael A.; Rohrer, Jonathan D.; Ramasamy, Adaikalavan; Kwok, John B.J.; Dobson-Stone, Carol; Brooks, William S.; Schofield, Peter R.; Halliday, Glenda M.; Hodges, John R.; Piguet, Olivier; Bartley, Lauren; Thompson, Elizabeth; Haan, Eric; Hernández, Isabel; Ruiz, Agustín; Boada, Mercè; Rowe, James B.; Nielsen, Jørgen E.; Hjermind, Lena E.; International FTD-Genomics Consortium.

    In: PLoS Medicine, Vol. 15, No. 1, e1002487, 2018.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14. / Chelban, Viorica; Wiethoff, Sarah; Fabian-Jessing, Bjørn K; Haridy, Nourelhoda A; Khan, Alaa; Efthymiou, Stephanie; Becker, Esther B E; O'Connor, Emer; Hersheson, Joshua; Newland, Katrina; Hojland, Allan Thomas; Gregersen, Pernille A; Lindquist, Suzanne G.; Petersen, Michael B.; Nielsen, Jørgen E.; Nielsen, Michael; Wood, Nicholas W; Giunti, Paola; Houlden, Henry.

    In: Movement Disorders, Vol. 33, No. 7, 2018, p. 1119-1129.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Frontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathology. / Clayton, Emma L.; Mizielinska, Sarah; Edgar, James R.; Nielsen, Troels Tolstrup; Marshall, Sarah; Norona, Frances E.; Robbins, Miranda; Damirji, Hana; Holm, Ida E.; Johannsen, Peter; Nielsen, Jorgen E.; Asante, Emmanuel A.; Collinge, John; Isaacs, Adrian M.

    In: Acta Neuropathologica, Vol. 130, No. 4, 10.2015, p. 511-523.

    Research output: Contribution to journalJournal articleResearchpeer-review

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ID: 9689629