Jørgen Erik Nielsen

Jørgen Erik Nielsen

Clinical Professor

Member of:

  • Neurology


Publication year:
All
1 - 9 out of 9Page size: 10
  1. 2010
  2. Published

    Reduced gluconeogenesis and lactate clearance in Huntington's disease

    Josefsen, K., Nielsen, S. M. B., Campos, A., Seifert, T., Hasholt, Lis Frydenreich, Nielsen, Jørgen Erik, Nørremølle, Anne, Skotte, Niels Henning, Secher, Niels H. & Quistorff, B., 1 Dec 2010, In: Neurobiology of Disease. 40, 3, p. 656-62 7 p.

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

  3. Published

    Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease

    Lesca, G., Boutry-Kryza, N., de Toffol, B., Milh, M., Steschenko, D., Lemesle-Martin, M., Maillard, L., Foletti, G., Rudolf, G., Nielsen, J. E., á Rogvi-Hansen, B., Erdal, J., Mancini, J., Thauvin-Robinet, C., M'Rrabet, A., Ville, D., Szepetowski, P., Raffo, E., Hirsch, E., Ryvlin, P. & 2 others, Calender, A. & Genton, P., 1 Sep 2010, In: Epilepsia. 51, 9, p. 1691-8 8 p.

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

  4. Published

    Proteomic investigations of the ventriculo-lumbar gradient in human CSF

    Simonsen, A. H., Bech, S. B. W., Laursen, I., Salvesen, Lisette, Winge, K., Waldemar, Gunhild, Werdelin, L., Nielsen, Jørgen Erik, McGuire, J. N. & Hjermind, L. E., Aug 2010, In: Journal of Neuroscience Methods. 191, 2, p. 244-8 5 p.

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

  5. Published

    Hereditary spastic paraplegia caused by the PLP1 'rumpshaker mutation'

    Svenstrup, K., Giraud, G., Boespflug-Tanguy, O., Danielsen, E. R., Thomsen, C., Rasmussen, K., Law, I., Vogel, A., Stokholm, J., Crone, C., Hjermind, L. E., Nielsen, J. E., Svenstrup, K., Giraud, G., Boespflug-Tanguy, O., Danielsen, E. R., Thomsen, C., Rasmussen, K., Law, I., Vogel, A. & 4 others, Stokholm, J., Crone, C., Hjermind, L. E. & Nielsen, J. E., 1 Jun 2010, In: Journal of Neurology, Neurosurgery and Psychiatry. 81, 6, p. 666-72 13 p.

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

  6. Published

    Behavioral variant of frontotemporal dementia mimicking Huntington's disease

    Nielsen, T. R., Bruhn, P., Nielsen, Jørgen Erik & Hjermind, L. E., 2010, In: International Psychogeriatrics. 22, 4, p. 674-7 3 p.

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

  7. Published

    Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations

    Urwin, H., Authier, A., Nielsen, Jørgen Erik, Metcalf, D., Powell, C., Froud, K., Malcolm, D. S., Holm, I., Johannsen, P., Brown, J., Fisher, E. M. C., van der Zee, J., Bruyland, M., FReJA Consortium, F. C., Van Broeckhoven, C., Collinge, J., Brandner, S., Futter, C. & Isaacs, A. M., 2010, In: Human Molecular Genetics. 19, 11, p. 2228-38 10 p.

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

  8. Published

    FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration

    Urwin, H., Josephs, K. A., Rohrer, J. D., Mackenzie, I. R., Neumann, M., Authier, A., Seelaar, H., Van Swieten, J. C., Brown, J. M., Johannsen, P., Nielsen, J. E., Holm, I. E., FReJA Consortium, Dickson, D. W., Rademakers, R., Graff-Radford, N. R., Parisi, J. E., Petersen, R. C., Hatanpaa, K. J., White, C. L. & 28 others, Weiner, M. F., Geser, F., Van Deerlin, V. M., Trojanowski, J. Q., Miller, B. L., Seeley, W. W., van der Zee, J., Kumar-Singh, S., Engelborghs, S., De Deyn, P. P., Van Broeckhoven, C., Bigio, E. H., Deng, H., Halliday, G. M., Kril, J. J., Munoz, D. G., Mann, D. M., Pickering-Brown, S. M., Doodeman, V., Adamson, G., Ghazi-Noori, S., Fisher, E. M. C., Holton, J. L., Revesz, T., Rossor, M. N., Collinge, J., Mead, S. & Isaacs, A. M., 2010, In: Acta Neuropathologica. 120, 1, p. 33-41 8 p.

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

  9. Published

    Huntington's disease-like and ataxia syndromes: identification of a family with a de novo SCA17/TBP mutation

    Bech, S., Petersen, T., Nørremølle, Anne, Gjedde, Albert, Ehlers, L., Eiberg, Hans Rudolf Lytchoff, Hjermind, L. E., Hasholt, Lis Frydenreich, Lundorf, E. & Nielsen, Jørgen Erik, 2010, In: Parkinsonism & Related Disorders. 16, 1, p. 12-5 3 p.

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

  10. Published

    Transthyretin as a potential CSF biomarker for Alzheimer's disease and dementia with Lewy bodies: effects of treatment with cholinesterase inhibitors

    Schultz, K., Nilsson, K., Nielsen, Jørgen Erik, Lindquist, Suzanne Granhøj, Hjermind, L. E., Andersen, B. B., Wallin, A., Nilsson, C. & Petersén, A., 2010, In: European Journal of Neurology. 17, 3, p. 456-60 4 p.

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

ID: 9689629