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The Capital Region of Denmark - a part of Copenhagen University Hospital

Lena Elisabeth Hjermind

(Former)

  1. 2019
  2. Published

    Safety and efficacy of pridopidine in patients with Huntington's disease (PRIDE-HD): a phase 2, randomised, placebo-controlled, multicentre, dose-ranging study

    European Huntington's Disease Network, Vangsted-Hansen, C. & Hjermind, L. E., Feb 2019, In : The Lancet Neurology. 18, 2, p. 165-176 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

    International Frontotemporal Dementia Genomics Consortium, Hjermind, L. E. & Nielsen, J. E., Jan 2019, In : Nature Medicine. 25, 1, p. 152-164 13 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Clinical and genetic characteristics of late-onset Huntington's disease

    REGISTRY investigators of the European Huntington's Disease Network, Oosterloo, M., Bijlsma, E. K., van Kuijk, S. M., Minkels, F., de Die-Smulders, C. E., Hjermind, L. E., Nielsen, J. E., Roos, P., Stokholm, J., Vangsted-Hansen, C., Lindquist, S. G. & Vinther-Jensen, T., 2019, In : Parkinsonism & related disorders. 61, p. 101-105

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Peripheral neuropathy in hereditary spastic paraplegia caused by REEP1 variants

    Toft, A., Birk, S., Ballegaard, M., Dunø, M., Hjermind, L. E., Nielsen, J. E. & Svenstrup, K., 2019, In : Journal of Neurology. 266, 3, p. 735-744 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. 2018
  7. Published

    A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

    International FTD-Genomics Consortium (IFGC) , Zhang, M., Ferrari, R., Tartaglia, M. C., Keith, J., Surace, E. I., Wolf, U., Sato, C., Grinberg, M., Liang, Y., Xi, Z., Dupont, K., McGoldrick, P., Weichert, A., McKeever, P. M., Schneider, R., McCorkindale, M. D., Manzoni, C., Rademakers, R., Graff-Radford, N. R., Dickson, D. W., Parisi, J. E., Boeve, B. F., Petersen, R. C., Miller, B. L., Seeley, W. W., van Swieten, J. C., van Rooij, J., Pijnenburg, Y., van der Zee, J., Van Broeckhoven, C., Le Ber, I., Van Deerlin, V., Suh, E., Rohrer, J. D., Mead, S., Graff, C., Öijerstedt, L., Pickering-Brown, S., Rollinson, S., Rossi, G., Tagliavini, F., Brooks, W. S., Dobson-Stone, C., Halliday, G. M., Hodges, J. R., Piguet, O., Binetti, G., Benussi, L., Ghidoni, R., Nacmias, B., Hjermind, L. E. & Nielsen, J. E., 1 Oct 2018, In : Brain : a journal of neurology. 141, 10, p. 2895-2907 13 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Quantitative Measurements of Motor Function in Alzheimer's Disease, Frontotemporal Dementia, and Dementia with Lewy Bodies: A Proof-of-Concept Study

    Jeppesen Kragh, F., Bruun, M., Budtz-Jørgensen, E., Hjermind, L. E., Schubert, R., Reilmann, R., Nielsen, J. E. & Hasselbalch, S. G., 26 Sep 2018, In : Dementia and Geriatric Cognitive Disorders. 46, 3-4, p. 168-179 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Does arterial hypertension influence the onset of Huntington's disease?

    REGISTRY investigators of the European Huntington’s Disease Network (EHDN), Valcárcel-Ocete, L., Fullaondo, A., Alkorta-Aranburu, G., García-Barcina, M., Roos, R. A. C., Hjermind, L. E., Saft, C., Frontali, M., Reilmann, R., Rickards, H., Zubiaga, A. M. & Aguirre, A., 23 May 2018, In : PLoS One. 13, 5, p. e0197975

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

    International FTD-Genomics Consortium, Taskesen, E., Mishra, A., van der Sluis, S., Ferrari, R., Veldink, J. H., van Es, M. A., Smit, A. B., Posthuma, D., Pijnenburg, Y., Hjermind, L. E. & Nielsen, J. E., 14 May 2018

    Research output: Other contributionResearch

  11. Published

    CXCR4 involvement in neurodegenerative diseases

    International FTD-Genomics Consortium (IFGC) , Bonham, L. W., Karch, C. M., Fan, C. C., Tan, C., Geier, E. G., Wang, Y., Wen, N., Broce, I. J., Li, Y., Barkovich, M. J., Ferrari, R., Hardy, J., Momeni, P., Höglinger, G., Müller, U., Hess, C. P., Sugrue, L. P., Dillon, W. P., Schellenberg, G. D., Miller, B. L., Andreassen, O. A., Dale, A. M., Barkovich, A. J., Yokoyama, J. S., Desikan, R. S., Hjermind, L. E. & Nielsen, J. E., 11 Apr 2018, In : Translational psychiatry. 8, 1, p. 73

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

    International FTD-Genomics Consortium, Broce, I., Karch, C. M., Wen, N., Fan, C. C., Wang, Y., Tan, C. H., Kouri, N., Ross, O. A., Höglinger, G. U., Muller, U., Hardy, J., Momeni, P., Hess, C. P., Dillon, W. P., Miller, Z. A., Bonham, L. W., Rabinovici, G. D., Rosen, H. J., Schellenberg, G. D., Franke, A., Karlsen, T. H., Veldink, J. H., Ferrari, R., Yokoyama, J. S., Miller, B. L., Andreassen, O. A., Dale, A. M., Desikan, R. S., Sugrue, L. P., Hjermind, L. E. & Nielsen, J. E., Jan 2018, In : PLOS Medicine. 15, 1, p. e1002487

    Research output: Contribution to journalJournal articleResearchpeer-review

  13. Published

    Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study

    REGISTRY investigators of the European Huntington's Disease Network, McNulty, P., Pilcher, R., Ramesh, R., Necuiniate, R., Hughes, A., Farewell, D., Holmans, P., Jones, L., Hjermind, L. E., Nielsen, J. E., Vangsted-Hansen, C., Stokholm, J., Lindquist, S. G. & Vinther-Jensen, T., 2018, In : Journal of Huntington's disease. 7, 3, p. 209-222 14 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  14. 2017
  15. Published
  16. Published

    Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

    Hensman Moss, D. J., Pardiñas, A. F., Langbehn, D., Lo, K., Leavitt, B. R., Roos, R., Durr, A., Mead, S., Holmans, P., Jones, L., Tabrizi, S. J., TRACK-HD investigators, Hjermind, L. E. & Nielsen, J. E., Sep 2017, In : The Lancet Neurology. 16, 9, p. 701-711 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  17. Published

    Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases

    Ferrari, R., Wang, Y., Vandrovcova, J., Guelfi, S., Witeolar, A., Karch, C. M., Schork, A. J., Fan, C. C., Brewer, J. B., Momeni, P., Schellenberg, G. D., Dillon, W. P., Sugrue, L. P., Hess, C. P., Yokoyama, J. S., Bonham, L. W., Rabinovici, G. D., Miller, B. L., Andreassen, O. A., Dale, A. M., Hardy, J., Desikan, R. S., International FTD-Genomics Consortium (IFGC), Hjermind, L. E. & Nielsen, J. E., Feb 2017, In : Journal of neurology, neurosurgery, and psychiatry. 88, 2, p. 152-164 13 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  18. Published

    A Novel TTBK2 De Novo Mutation in a Danish Family with Early-Onset Spinocerebellar Ataxia

    Lindquist, S. G., Møller, L. B., Dali, C. I., Marner, L., Kamsteeg, E-J., Nielsen, J. E. & Hjermind, L. E., 2017, In : Cerebellum (London, England). 16, 1, p. 268-71

    Research output: Contribution to journalJournal articleResearchpeer-review

  19. Published

    Medical facts about Huntington's Disease

    Hjermind, L. E., 2017, Touched by Huntington s Disease: Life Stories and Psychological Reflections. Andersen, L. B. (ed.). Frydenlund, p. 15-39

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

  20. Published
  21. 2016
  22. Published
  23. Published

    Generation of a gene-corrected isogenic control hiPSC line derived from a familial Alzheimer's disease patient carrying a L150P mutation in presenilin 1

    Poon, A., Schmid, B., Pires, C., Nielsen, T. T., Hjermind, L. E., Nielsen, J. E., Holst, B., Hyttel, P. & Freude, K. K., 24 Sep 2016, In : Stem Cell Research. 17, 3, p. 466-469 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  24. Published

    Generation of a gene-corrected isogenic control cell line from an Alzheimer's disease patient iPSC line carrying a A79V mutation in PSEN1

    Pires, C., Schmid, B., Petræus, C., Poon, A., Nimsanor, N., Nielsen, T. T., Waldemar, G., Hjermind, L. E., Nielsen, J. E., Hyttel, P. & Freude, K. K., Sep 2016, In : Stem Cell Research. 17, 2, p. 285-288 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  25. Published

    Clinical manifestations of intermediate allele carriers in Huntington disease

    Cubo, E., Ramos-Arroyo, M. A., Martinez-Horta, S., Martínez-Descalls, A., Calvo, S., Gil-Polo, C., European HD Network (Lena Elisabeth Hjermind, Jørgen E Nielsen members), Hjermind, L. E. & Nielsen, J. E., 9 Aug 2016, In : Neurology. 87, 6, p. 571-8 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  26. Published

    Liver function in Huntington's disease assessed by blood biochemical analyses in a clinical setting

    Nielsen, S. M. B., Vinther-Jensen, T., Nielsen, J. E., Nørremølle, A., Hasholt, L., Hjermind, L. E. & Josefsen, K., 15 Mar 2016, In : Journal of the Neurological Sciences. 362, p. 326-32 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  27. Published

    Generation of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying a M146I mutation in PSEN1

    Li, T., Pires, C., Nielsen, T. T., Waldemar, G., Hjermind, L. E., Nielsen, J. E., Dinnyes, A., Holst, B., Hyttel, P. & Freude, K. K., Mar 2016, In : Stem Cell Research. 16, 2, p. 334-7 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  28. Published

    Generation of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying an A79V mutation in PSEN1

    Li, T., Pires, C., Nielsen, T. T., Waldemar, G., Hjermind, L. E., Nielsen, J. E., Dinnyes, A., Hyttel, P. & Freude, K. K., Mar 2016, In : Stem Cell Research. 16, 2, p. 229-32 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  29. Published

    Generation of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying a L150P mutation in PSEN-1

    Tubsuwan, A., Pires, C., Rasmussen, M. A., Schmid, B., Nielsen, J. E., Hjermind, L. E., Hall, V., Nielsen, T. T., Waldemar, G., Hyttel, P., Clausen, C., Kitiyanant, N., Freude, K. K. & Holst, B., Jan 2016, In : Stem Cell Research. 16, 1, p. 110-2 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  30. Published

    Induced pluripotent stem cells (iPSCs) derived from a patient with frontotemporal dementia caused by a P301L mutation in microtubule-associated protein tau (MAPT)

    Rasmussen, M. A., Hjermind, L. E., Hasholt, L. F., Waldemar, G., Nielsen, J. E., Clausen, C., Hyttel, P. & Holst, B., Jan 2016, In : Stem Cell Research. 16, 1, p. 70-4 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  31. Published

    Induced pluripotent stem cells (iPSCs) derived from a patient with frontotemporal dementia caused by a R406W mutation in microtubule-associated protein tau (MAPT)

    Rasmussen, M. A., Hjermind, L. E., Hasholt, L. F., Waldemar, G., Nielsen, J. E., Clausen, C., Hyttel, P. & Holst, B., Jan 2016, In : Stem Cell Research. 16, 1, p. 75-8 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  32. Published

    Induced pluripotent stem cells (iPSCs) derived from a pre-symptomatic carrier of a R406W mutation in microtubule-associated protein tau (MAPT) causing frontotemporal dementia

    Rasmussen, M. A., Hjermind, L. E., Hasholt, L. F., Waldemar, G., Nielsen, J. E., Clausen, C., Hyttel, P. & Holst, B., Jan 2016, In : Stem Cell Research. 16, 1, p. 105-9 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  33. Published

    A germline chromothripsis event stably segregating in 11 individuals through three generations

    Bertelsen, B., Nazaryan, L., Sun, W., Mehrjouy, M. M., Xie, G., Chen, W., Hjermind, L. E., Taschner, P. E. M. & Tümer, Z., 2016, In : Genetics in medicine : official journal of the American College of Medical Genetics. 18, p. 494–500

    Research output: Contribution to journalJournal articleResearchpeer-review

  34. Published

    Berørt af Huntingtons sygdom

    Hjermind, L. E., 2016, Medicinske fakta om Huntingtons sygdom. Andersen, L. B. & Bekke-Hansen, S. (eds.). 1 ed. Frydenlund, p. 13-33

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

  35. Published

    Psychiatric and cognitive symptoms in Huntington's disease are modified by polymorphisms in catecholamine regulating enzyme genes

    Vinther-Jensen, T., Nielsen, T. T., Budtz-Jørgensen, E., Larsen, I. U., Hansen, M. M., Hasholt, L., Hjermind, L. E., Nielsen, J. E. & Nørremølle, A., 2016, In : Clinical Genetics. 89, 3, p. 320-7

    Research output: Contribution to journalJournal articleResearchpeer-review

  36. 2015
  37. Published

    Ubiquitin: a potential cerebrospinal fluid progression marker in Huntington's disease

    Vinther-Jensen, T., Simonsen, A. H., Budtz-Jørgensen, E., Hjermind, L. E. & Nielsen, J. E., Oct 2015, In : European Journal of Neurology. 22, 10, p. 1378-84 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  38. Published
  39. Published

    Diagnostic genetic testing for Huntington's disease

    Craufurd, D., MacLeod, R., Frontali, M., Quarrell, O., Bijlsma, E. K., Davis, M., Hjermind, L. E., Lahiri, N., Mandich, P., Martinez, A., Tibben, A., Roos, R. A. & Working Group on Genetic Counselling and Testing of the European Huntington's Disease Network (EHDN), Feb 2015, In : Practical Neurology. 15, 1, p. 80-4 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  40. 2014
  41. Published

    YKL-40 in cerebrospinal fluid in Huntington's disease - A role in pathology or a nonspecific response to inflammation?

    Vinther-Jensen, T., Budtz-Jørgensen, E., Simonsen, A. H., Nielsen, J. E. & Hjermind, L. E., Nov 2014, In : Parkinsonism & related disorders. 20, 11, p. 1301-3 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  42. Published

    A clinical classification acknowledging neuropsychiatric and cognitive impairment in Huntington¿s disease

    Vinther-Jensen, T., Larsen, I. U., Hjermind, L. E., Budtz-Jørgensen, E., Nielsen, T. T., Nørremølle, A., Nielsen, J. E. & Vogel, A., 17 Jul 2014, In : Orphanet Journal of Rare Diseases. 9, 1, p. 114

    Research output: Contribution to journalJournal articleResearchpeer-review

  43. Published

    Missense dopamine transporter mutations associate with adult parkinsonism and ADHD

    Hansen, F. H., Skjørringe, T., Yasmeen, S., Arends, N. V., Sahai, M. A., Erreger, K., Andreassen, T. F., Holy, M., Hamilton, P. J., Neergheen, V., Karlsborg, M., Newman, A. H., Pope, S., Heales, S. J. R., Friberg, L., Law, I., Pinborg, L. H., Sitte, H. H., Loland, C., Shi, L., Weinstein, H., Galli, A., Hjermind, L. E., Møller, L. B. & Gether, U., 1 Jul 2014, In : The Journal of clinical investigation. 124, 7, p. 3107-20 14 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  44. Published

    Frontotemporal dementia and its subtypes: a genome-wide association study

    Ferrari, R., Hernandez, D. G., Nalls, M. A., Rohrer, J. D., Ramasamy, A., Kwok, J. B. J., Dobson-Stone, C., Brooks, W. S., Schofield, P. R., Halliday, G. M., Hodges, J. R., Piguet, O., Bartley, L., Thompson, E., Haan, E., Hernández, I., Ruiz, A., Boada, M., Borroni, B., Padovani, A., Cruchaga, C., Cairns, N. J., Benussi, L., Binetti, G., Ghidoni, R., Forloni, G., Galimberti, D., Fenoglio, C., Serpente, M., Scarpini, E., Clarimón, J., Lleó, A., Blesa, R., Waldö, M. L., Nilsson, K., Nilsson, C., Mackenzie, I. R. A., Hsiung, G-Y. R., Mann, D. M. A., Grafman, J., Morris, C. M., Attems, J., Griffiths, T. D., McKeith, I. G., Thomas, A. J., Pietrini, P., Huey, E. D., Wassermann, E. M., Baborie, A., Jaros, E., Tierney, M. C., Pastor, P., Razquin, C., Ortega-Cubero, S., Alonso, E., Perneczky, R., Diehl-Schmid, J., Alexopoulos, P., Kurz, A., Rainero, I., Rubino, E., Pinessi, L., Rogaeva, E., St George-Hyslop, P., Rossi, G., Tagliavini, F., Giaccone, G., Rowe, J. B., Schlachetzki, J. C. M., Uphill, J., Collinge, J., Mead, S., Danek, A., Van Deerlin, V. M., Grossman, M., Trojanowski, J. Q., van der Zee, J., Deschamps, W., Van Langenhove, T., Cruts, M., Van Broeckhoven, C., Cappa, S. F., Le Ber, I., Hannequin, D., Golfier, V., Vercelletto, M., Brice, A., Nacmias, B., Sorbi, S., Bagnoli, S., Piaceri, I., Nielsen, J. E., Hjermind, L. E., Riemenschneider, M., Mayhaus, M., Ibach, B., Gasparoni, G., Pichler, S., Gu, W., Rossor, M. N., Fox, N. C., Warren, J. D., Spillantini, M. G., Morris, H. R., Rizzu, P., Heutink, P., Snowden, J. S., Rollinson, S., Richardson, A., Gerhard, A., Bruni, A. C., Maletta, R., Frangipane, F., Cupidi, C., Bernardi, L., Anfossi, M., Gallo, M., Conidi, M. E., Smirne, N., Rademakers, R., Baker, M., Dickson, D. W., Graff-Radford, N. R., Petersen, R. C., Knopman, D., Josephs, K. A., Boeve, B. F., Parisi, J. E., Seeley, W. W., Miller, B. L., Karydas, A. M., Rosen, H., van Swieten, J. C., Dopper, E. G. P., Seelaar, H., Pijnenburg, Y. A. L., Scheltens, P., Logroscino, G., Capozzo, R., Novelli, V., Puca, A. A., Franceschi, M., Postiglione, A., Milan, G., Sorrentino, P., Kristiansen, M., Chiang, H-H., Graff, C., Pasquier, F., Rollin, A., Deramecourt, V., Lebert, F., Kapogiannis, D., Ferrucci, L., Pickering-Brown, S., Singleton, A. B., Hardy, J. & Momeni, P., Jul 2014, In : Lancet neurology. 13, 7, p. 686-99 14 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  45. Published

    Functional Dopamine Missense Dopamine Transporter Mutations Associated with Adult Parkinsonism and ADHD

    Hansen, F. H., Skjørringe, T., Yasmeen, S., Arends, N. V., Sahai, M. A., Erreger, K., Andreassen, T. F., Holy, M., Hamilton, P. J., Neergheen, V., Karlsborg, M., Newman, A. H., Pope, S., Heales, SJ., Friberg, L. A., Law, I., Pinborg, L. H., Sitte, H., Loland, C. J., Shi, L., Weinstein, H., Galli, A., Hjermind, L. E., Møller, L. B. & Gether, U., Jul 2014, In : Journal of Clinical Investigation. p. 3107-20 14 p., jun.

    Research output: Contribution to journalJournal articleResearchpeer-review

  46. Published

    Reduction in mitochondrial DNA copy number in peripheral leukocytes after onset of Huntington's disease

    Petersen, M. H., Budtz-Jørgensen, E., Sørensen, S. A., Nielsen, J. E., Hjermind, L. E., Vinther-Jensen, T., Nielsen, S. M. B. & Nørremølle, A., 15 May 2014, In : Mitochondrion. 17C, p. 14-21 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  47. 2013
  48. Published

    A randomized double-blind crossover trial comparing subthalamic and pallidal deep brain stimulation for dystonia

    Schjerling, L., Hjermind, L. E., Jespersen, B., Madsen, F. F., Brennum, J., Jensen, S. R., Løkkegaard, A. & Karlsborg, M., Dec 2013, In : Journal of Neurosurgery. 119, 6, p. 1537-45 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  49. Published
  50. Published

    A randomized, double-blind, placebo-controlled study of latrepirdine in patients with mild to moderate Huntington disease

    HORIZON Investigators of the Huntington Study Group and European Huntington's Disease Network & Hjermind, L. E., Jan 2013, In : JAMA Neurology. 70, 1, p. 25-33 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  51. Published

    Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease

    Lindquist, S. G., Duno, M., Batbayli, M., Puschmann, A., Braendgaard, H., Mardosiene, S., Svenstrup, K., Pinborg, L. H., Vestergaard, K. F., Hjermind, LE., Stokholm, J., Andersen, B. B., Johannsen, P. & Nielsen, J. E., 2013, In : Clinical Genetics. 83, 3, p. 279–283

    Research output: Contribution to journalJournal articleResearchpeer-review

  52. Published

    Germ-line CAG repeat instability causes extreme CAG repeat expansion with infantile-onset spinocerebellar ataxia type 2

    Vinther-Jensen, T., Ek, J., Duno, M., Skovby, F., Hjermind, L. E., Nielsen, J. E. & Nielsen, T. T., 2013, In : European Journal of Human Genetics. 21, p. 626-629

    Research output: Contribution to journalJournal articleResearchpeer-review

  53. 2012
  54. Published

    Amyloid-related biomarkers and axonal damage proteins in parkinsonian syndromes

    Bech, S., Hjermind, L. E., Salvesen, L., Nielsen, J. E., Heegaard, N. H. H., Jørgensen, H. L., 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

  55. 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., Frontali, M., Jones, R. I., Ashizawa, T., Frank, S., Saint-Hilaire, M. H., Hersch, S. M., Rosas, H. D., Lucente, D., Harrison, M., Zanko, A., Abramson, R. K., Marder, K., Sequeiros, J., Paulsen, J. S., Landwehrmeyer, G. B., Myers, R. H., MacDonald, M. E., Gusella, J. F., PREDICT-HD study of the Huntington Study Group (HSG), Hjermind, L. E. & Nielsen, J. E., 2012, In : Neurology. 78, 10, p. 690-5 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  56. Published

    Discrepancies in reporting the CAG repeat lengths for Huntington's disease

    Quarrell, O. W., Handley, O., O'Donovan, K., Dumoulin, C., Ramos-Arroyo, M., Biunno, I., Bauer, P., Kline, M., Landwehrmeyer, G. B., European Huntington’s Disease Network, Hjermind, L. E. & Nielsen, J. E., 2012, In : European Journal of Human Genetics. 20, 1, p. 20-6 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  57. Published

    Kinesogenic and non-kinesogenic dyskenisias, hyperplexia

    Henriksen, T. & Hjermind, L. E., 2012, Borderlands of Epilepsy Revisited. Reuber, M. & Schachter, S. (eds.). New York: Oxford University Press, p. 176-186

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

  58. 2011
  59. Published

    Huntington's disease: effect of memantine on FDG-PET brain metabolism?

    Hjermind, L. E., Law, I., Jønch, A., Stokholm, J. & Nielsen, J. E., 2011, In : Journal of Neuropsychiatry and Clinical Neurosciences. 23, 2, p. 206-10 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

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