Jørgen Erik Nielsen
Clinical Professor
- 1996
- Published
Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation Danish family.
Nielsen, Jørgen Erik, Sørensen, S. A., Hasholt, Lis Frydenreich & Nørremølle, Anne, 1996, In: Movement Disorders. 11, 5, p. 533-541 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2002
- 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, N., Jensen, K. M., Lund, Line, Nielsen, Jørgen Erik, Djurhuus, J. C., Poulsen, S. S., Nexø, E. & Poulsen, Steen Seier, 1 Apr 2002, In: B J U International (Print). 89, 6, p. 583-90 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2004
- Published
Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.
Nielsen, Jørgen Erik, Johnson, B., Koefoed, P., 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, Olaf B., Hasholt, Lis Frydenreich & Sørensen, S. A., 2004, In: European Journal of Neurology. 11, 12, p. 817-824 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG4) using direct mutation detection
Nielsen, Jørgen Erik, Koefoed, P., Kjaergaard, S., Jensen, L. N., Nørremølle, Anne & Hasholt, Lis Frydenreich, 2004, In: Prenatal Diagnosis. 24, 5, p. 363-6 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2005
- Published
Reduced regional cerebral blood flow in SPG4-linked hereditary spastic paraplegia
Scheuer, K. H., Nielsen, Jørgen Erik, Krabbe, K., Simonsen, C., Koefoed, P., Sørensen, S. A., Gade, A., Paulson, Olaf B. & Law, Ian, 2005, In: Journal of the Neurological Sciences. 235, 1-2, p. 23-32 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2008
- Published
Cortical volumes and atrophy rates in FTD-3 CHMP2B mutation carriers and related non-carriers
Eskildsen, S. F., Østergaard, L. R., Rodell, A. B., Østergaard, L., Nielsen, Jørgen Erik, Isaacs, A. M. & Johannsen, P., 2008, In: NeuroImage. 45, 3, p. 713-21 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
[Hereditary Parkinson disease. The Danish Society of Movement Disorders]
Hjermind, L. E. & Nielsen, Jørgen Erik, 2008, In: Ugeskrift for læger. 170, 12, p. 1016-Research output: Contribution to journal › Journal article › Research › peer-review
- 2009
- Published
4p16.3 haplotype modifying age at onset of Huntington disease
Nørremølle, Anne, Budtz-Joergensen, Esben, Fenger, K., Nielsen, Jørgen Erik, Sørensen, S. A. & Hasholt, Lis Frydenreich, 2009, In: Clinical Genetics. 75, 3, p. 244-50 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunction
Puschmann, A., Ross, O. A., Vilariño-Güell, C., Lincoln, S. J., Kachergus, J. M., Cobb, S. A., Lindquist, Suzanne Granhøj, Nielsen, Jørgen Erik, Wszolek, Z. K., Farrer, M., Widner, H., van Westen, D., Hägerström, D., Markopoulou, K., Chase, B. A., Nilsson, K., Reimer, J. & Nilsson, C., 2009, In: Parkinsonism & Related Disorders. 15, 9, p. 627-32 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genetic testing in familial AD and FTD: mutation and phenotype spectrum in a Danish cohort
Lindquist, Suzanne Granhøj, Schwartz, M., Batbayli, M., Waldemar, Gunhild & Nielsen, Jørgen Erik, 2009, In: Clinical Genetics. 76, 2, p. 205-9 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Huntington's disease does not appear to increase the risk of diabetes mellitus
Boesgaard, T. W., Nielsen, T. T., Josefsen, K. E., Hansen, T., Jørgensen, T., Pedersen, O., Nørremølle, Anne, Nielsen, Jørgen Erik & Hasholt, Lis Frydenreich, 2009, In: Journal of Neuroendocrinology. 21, 9, p. 770-6 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Presymptomatic generalized brain atrophy in frontotemporal dementia caused by CHMP2B mutation
Rohrer, J. D., Ahsan, R. L., Isaacs, A. M., Nielsen, Jørgen Erik, Ostergaard, L., Scahill, R., Warren, J. D., Rossor, M. N., Fox, N. C., Johannsen, P. & FReJA Consortium, F. C., 2009, In: Dementia and Geriatric Cognitive Disorders. 27, 2, p. 182-6 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Reduced CSF CART in dementia with Lewy bodies
Schultz, K., Wiehager, S., Nilsson, K., Nielsen, Jørgen Erik, Lindquist, Suzanne Granhøj, Hjermind, L. E., Andersen, B. B., Wallin, A., Nilsson, C. & Petersén, A., 2009, In: Neuroscience Letters. 453, 2, p. 104-6 2 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegia
Svenstrup, K., Bross, P., Koefoed, P., Hjermind, L. E., Eiberg, H., Born, A. P., Vissing, J., Gyllenborg, J., Nørremølle, A., Hasholt, L., Nielsen, J. E., Svenstrup, K., Bross, P., Koefoed, P., Hjermind, L. E., Eiberg, H., Born, A. P., Vissing, J., Gyllenborg, J., Nørremølle, A. & 2 others, , 2009, In: Journal of the Neurological Sciences. 284, 1-2, p. 90-5 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2010
- 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
- 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
- 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, , 2010, In: Acta Neuropathologica. 120, 1, p. 33-41 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 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
- 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
- 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, , 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
- 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
- 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, , 1 Sep 2010, In: Epilepsia. 51, 9, p. 1691-8 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 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
- 2011
- Published
Huntington's disease: effect of memantine on FDG-PET brain metabolism?
Hjermind, L. E., Law, Ian, Jønch, A., Stokholm, J. & Nielsen, Jørgen Erik, 2011, In: The Journal of Neuropsychiatry and Clinical Neurosciences. 23, 2, p. 206-10 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY
Orth, M., Handley, O. J., Schwenke, C., Dunnett, S., Wild, E. J., Tabrizi, S. J., Landwehrmeyer, G. B., Hasholt, Lis Frydenreich, Hjermind, L. E., Nørremølle, Anne, Nielsen, Jørgen Erik & European Huntington's Disease Network, E. H. D. N., 2011, In: The Egyptian Journal of Neurology, Psychiatry, and Neurosurgery. 82, 12, p. 1409-12 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 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 proceeding › Book chapter › Communication
- Published
Frontotemporal dementia caused by CHMP2B mutations
Isaacs, A. M., Johannsen, P., Holm, I., Nielsen, Jørgen Erik & FReJA Consortium, F. C., May 2011, In: Current Alzheimer Research. 8, 3, p. 246-51 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders
Bech, S., Nørremølle, Anne, Winge, K., Hasholt, Lis Frydenreich, Tommerup, Niels, Svenstrup, K., Nielsen, Jørgen Erik & Hjermind, L. E., 1 Jun 2011, In: Parkinsonism & Related Disorders. 17, 5, p. 398-9 2 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 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., Hjermind, L. E., Hasholt, Lis Frydenreich, Nørremølle, Anne, Nielsen, Jørgen Erik & European Huntington’s Disease Network, E. H. D. N., Aug 2011, In: European Journal of Human Genetics. 20, 1, p. 20-6 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- Published
No difference between alfacalcidol and paricalcitol in the treatment of secondary hyperparathyroidism in hemodialysis patients: a randomized crossover trial
Hansen, D., Rasmussen, K., Danielsen, H., Meyer-Hofmann, H., Bacevicius, E., Lauridsen, T. G., Madsen, J. K., Tougaard, B. G., Marckmann, P., Thye-Roenn, P., Nielsen, Jørgen Erik, Kreiner, Svend & Brandi, Lisbet, Oct 2011, In: Kidney International. 80, 8, p. 841-850 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutations
Gavassini, B. F., Carboni, N., Nielsen, Jørgen Erik, Danielsen, E. R., Thomsen, C., Svenstrup, K., Bello, L., Maioli, M. A., Marrosu, G., Ticca, A. F., Mura, M., Marrosu, M. G., Soraru, G., Angelini, C., Vissing, John & Pegoraro, E., Nov 2011, In: Muscle & Nerve. 44, 5, p. 703-9 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2012
- 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 journal › Journal article › Research › peer-review
- 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, , Mar 2012, In: Neurology. 78, 10, p. 690-5 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 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, 2Research output: Contribution to journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 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. 73Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The DJ-1 concentration in cerebrospinal fluid does not differentiate among parkinsonian syndromes
Salvesen, Lisette, Bech, S., Løkkegaard, Annemette, Hjermind, L. E., Nielsen, Jørgen Erik, Pakkenberg, B., Tanassi, J. T., Heegaard, N. H. H. & Winge, K., Aug 2012, In: Parkinsonism & Related Disorders. 18, 7, p. 899-901 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 2013
- 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, Jørgen Erik & Nielsen, T. T., 2013, In: European Journal of Human Genetics. 21, 6, p. 626-9 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Cognitive impairment in the preclinical stage of dementia in FTD-3 CHMP2B mutation carriers: A longitudinal prospective study
Stokholm, J., Teasdale, T. W., Johannsen, P., Nielsen, Jørgen Erik, Nielsen, T. T., Isaacs, A., Brown, J. M., Gade, A. & and the Frontotemporal dementia Research in Jutland Association (FReJA) consortium, A. T. F. D. R. I. J. A. (. C., Feb 2013, In: Journal of Neurology, Neurosurgery and Psychiatry. 84, 2, p. 170-176 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease
Lindquist, S., Duno, M., Batbayli, M., Puschmann, A., Braendgaard, H., Mardosiene, S., Svenstrup, K., Pinborg, L., Vestergaard, K., Hjermind, L., Stokholm, J., Andersen, B., Johannsen, P. & Nielsen, Jørgen Erik, Mar 2013, In: Clinical Genetics. 83, 3, p. 279-283 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients
Metzger, S., Walter, C., Riess, O., Roos, R. A. C., Nielsen, Jørgen Erik, Craufurd, D., Nguyen, H. P. & REGISTRY Investigators of the European Huntington’s Disease Network, R. I. O. T. E. H. D. N., Jul 2013, In: PLOS ONE. 8, 7, p. e68951Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Antisense gene silencing: therapy for neurodegenerative disorders?
Nielsen, T. T. & Nielsen, Jørgen Erik, 10 Sep 2013, In: Genes. 4, 3, p. 457-84 28 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2014
- Published
Reduction in mitochondrial DNA copy number in peripheral leukocytes after onset of Huntington's disease
Petersen, M. H., Budtz-Joergensen, Esben, Sørensen, S. A., Nielsen, Jørgen Erik, Hjermind, L. E., Vinther-Jensen, T., Nielsen, S. M. B. & Nørremølle, Anne, 2014, In: Mitochondrion. 17, p. 14-21 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Hereditary spastic paraplegia is not associated with C9ORF72 repeat expansions in a Danish cohort
Nielsen, T. T., Svenstrup, K., Duno, M. & Nielsen, Jørgen Erik, Jan 2014, In: Spinal Cord. 52, 1, p. 77-79 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Reduced ceramide synthase 2 activity causes progressive myoclonic epilepsy
Mosbech, M., Olsen, A. S. B., Neess, D., Ben-David, O., Klitten, L. L., Larsen, J., Sabers, A., Vissing, John, Nielsen, Jørgen Erik, Hasholt, Lis Frydenreich, Klein, A. D., Tsoory, M. M., Hjalgrim, H., Tommerup, Niels, Futerman, A. H., Møller, R. S. & Færgeman, N. J., 28 Feb 2014, In: Annals of Clinical and Translational Neurology. 1, 2, p. 88-98 11 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
CYP7B1: novel mutations and magnetic resonance spectroscopy abnormalities in hereditary spastic paraplegia type 5A
Roos, P., Svenstrup, K., Danielsen, E. R., Thomsen, C. & Nielsen, Jørgen Erik, May 2014, In: Acta Neurologica Scandinavica. 129, 5, p. 330-4 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 9689629
Most downloads
-
461
downloads
Patient iPSC-derived neurons for disease modeling of frontotemporal dementia with mutation in CHMP2B
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
330
downloads
Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.A11
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
299
downloads
Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.B11
Research output: Contribution to journal › Journal article › Research › peer-review
Published