Nielsen JE - Search Results

1

No muscle involvement in myoclonus-dystonia caused by epsilon-sarcoglycan gene mutations.

Hjermind LE, Vissing J, Asmus F, Krag T, Lochmüller H, Walter MC, Erdal J, Blake DJ, Nielsen JE. Hjermind LE, et al. Among authors: nielsen je. Eur J Neurol. 2008 May;15(5):525-9. doi: 10.1111/j.1468-1331.2008.02116.x. Epub 2008 Mar 18. Eur J Neurol. 2008. PMID: 18355305

2

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

Vinther-Jensen T, Simonsen AH, Budtz-Jørgensen E, Hjermind LE, Nielsen JE. Vinther-Jensen T, et al. Among authors: nielsen je. Eur J Neurol. 2015 Oct;22(10):1378-84. doi: 10.1111/ene.12750. Epub 2015 Jun 13. Eur J Neurol. 2015. PMID: 26073975

3

Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9).

Eiberg H, Hansen L, Korbo L, Nielsen IM, Svenstrup K, Bech S, Pinborg LH, Friberg L, Hjermind LE, Olsen OR, Nielsen JE. Eiberg H, et al. Among authors: nielsen je, nielsen im. Clin Genet. 2012 Sep;82(3):256-63. doi: 10.1111/j.1399-0004.2011.01745.x. Epub 2011 Jul 18. Clin Genet. 2012. PMID: 21696388

4

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 JE, Lindquist SG, Hjermind LE, Andersen BB, Wallin A, Nilsson C, Petersén A. Schultz K, et al. Among authors: nielsen je. Eur J Neurol. 2010 Mar;17(3):456-60. doi: 10.1111/j.1468-1331.2009.02841.x. Epub 2009 Nov 17. Eur J Neurol. 2010. PMID: 19922456

5

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

Lindquist SG, Duno M, Batbayli M, Puschmann A, Braendgaard H, Mardosiene S, Svenstrup K, Pinborg LH, Vestergaard K, Hjermind LE, Stokholm J, Andersen BB, Johannsen P, Nielsen JE. Lindquist SG, et al. Among authors: nielsen je. Clin Genet. 2013 Mar;83(3):279-83. doi: 10.1111/j.1399-0004.2012.01903.x. Epub 2012 Jul 4. Clin Genet. 2013. PMID: 22650353

6

An Exploratory Study Investigating Autonomy in Huntington's Disease Gene Expansion Carriers.

Hendel RK, Hellem MNN, Hjermind LE, Nielsen JE, Vogel A. Hendel RK, et al. Among authors: nielsen je. J Huntingtons Dis. 2022;11(4):373-381. doi: 10.3233/JHD-220540. J Huntingtons Dis. 2022. PMID: 35964199

7

Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.

Nielsen JE, Johnsen B, Koefoed P, Scheuer KH, Grønbech-Jensen M, Law I, Krabbe K, Nørremølle A, Eiberg H, Søndergård H, Dam M, Rehfeld JF, Krarup C, Paulson OB, Hasholt L, Sørensen SA. Nielsen JE, et al. Eur J Neurol. 2004 Dec;11(12):817-24. doi: 10.1111/j.1468-1331.2004.00888.x. Eur J Neurol. 2004. PMID: 15667412

8

NIPA1 mutation in complex hereditary spastic paraplegia with epilepsy.

Svenstrup K, Møller RS, Christensen J, Budtz-Jørgensen E, Gilling M, Nielsen JE. Svenstrup K, et al. Among authors: nielsen je. Eur J Neurol. 2011 Sep;18(9):1197-9. doi: 10.1111/j.1468-1331.2011.03359.x. Epub 2011 Feb 22. Eur J Neurol. 2011. PMID: 21599812

9

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

Vinther-Jensen T, Nielsen TT, Budtz-Jørgensen E, Larsen IU, Hansen MM, Hasholt L, Hjermind LE, Nielsen JE, Nørremølle A. Vinther-Jensen T, et al. Among authors: nielsen tt, nielsen je. Clin Genet. 2016 Mar;89(3):320-7. doi: 10.1111/cge.12628. Epub 2015 Jul 17. Clin Genet. 2016. PMID: 26081309

10

Increased intracortical facilitation in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p.

Nielsen JE, Jennum P, Fenger K, Sørensen SA, Fuglsang-Frederiksen A. Nielsen JE, et al. Eur J Neurol. 2001 Jul;8(4):335-9. doi: 10.1046/j.1468-1331.2001.00249.x. Eur J Neurol. 2001. PMID: 11422430

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