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Results: 1 to 20 of 35

1.

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.

Clin Genet. 2015 Jun 17. doi: 10.1111/cge.12628. [Epub ahead of print]

PMID:
26081309
2.

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

Vinther-Jensen T, Simonsen AH, Budtz-Jørgensen E, Hjermind LE, Nielsen JE.

Eur J Neurol. 2015 Jun 13. doi: 10.1111/ene.12750. [Epub ahead of print]

PMID:
26073975
3.

Familial hemiplegic migraine type 1 associated with parkinsonism: a case report.

Bruun M, Hjermind LE, Thomsen C, Danielsen E, Thomsen LL, Pinborg LH, Khabbazbavani N, Nielsen JE.

Case Rep Neurol. 2015 Apr 14;7(1):84-9. doi: 10.1159/000381827. eCollection 2015 Jan-Apr.

4.

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 AH, Nielsen JE, Hjermind LE.

Parkinsonism Relat Disord. 2014 Nov;20(11):1301-3. doi: 10.1016/j.parkreldis.2014.08.011. Epub 2014 Aug 28. No abstract available.

PMID:
25219973
5.

Diagnostic genetic testing for Huntington's disease.

Craufurd D, MacLeod R, Frontali M, Quarrell O, Bijlsma EK, Davis M, Hjermind LE, Lahiri N, Mandich P, Martinez A, Tibben A, Roos RA; Working Group on Genetic Counselling and Testing of the European Huntington's Disease Network (EHDN).

Pract Neurol. 2015 Feb;15(1):80-4. doi: 10.1136/practneurol-2013-000790. Epub 2014 Aug 28. No abstract available.

PMID:
25169240
6.

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

Vinther-Jensen T, Larsen IU, Hjermind LE, Budtz-Jørgensen E, Nielsen TT, Nørremølle A, Nielsen JE, Vogel A.

Orphanet J Rare Dis. 2014 Jul 17;9:114. doi: 10.1186/s13023-014-0114-8.

7.

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

Ferrari R, Hernandez DG, Nalls MA, Rohrer JD, Ramasamy A, Kwok JB, Dobson-Stone C, Brooks WS, Schofield PR, Halliday GM, Hodges JR, Piguet O, Bartley L, Thompson E, Haan E, Hernández I, Ruiz A, Boada M, Borroni B, Padovani A, Cruchaga C, Cairns NJ, Benussi L, Binetti G, Ghidoni R, Forloni G, Galimberti D, Fenoglio C, Serpente M, Scarpini E, Clarimón J, Lleó A, Blesa R, Waldö ML, Nilsson K, Nilsson C, Mackenzie IR, Hsiung GY, Mann DM, Grafman J, Morris CM, Attems J, Griffiths TD, McKeith IG, Thomas AJ, Pietrini P, Huey ED, Wassermann EM, Baborie A, Jaros E, Tierney MC, 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 JB, Schlachetzki JC, Uphill J, Collinge J, Mead S, Danek A, Van Deerlin VM, Grossman M, Trojanowski JQ, van der Zee J, Deschamps W, Van Langenhove T, Cruts M, Van Broeckhoven C, Cappa SF, Le Ber I, Hannequin D, Golfier V, Vercelletto M, Brice A, Nacmias B, Sorbi S, Bagnoli S, Piaceri I, Nielsen JE, Hjermind LE, Riemenschneider M, Mayhaus M, Ibach B, Gasparoni G, Pichler S, Gu W, Rossor MN, Fox NC, Warren JD, Spillantini MG, Morris HR, Rizzu P, Heutink P, Snowden JS, Rollinson S, Richardson A, Gerhard A, Bruni AC, Maletta R, Frangipane F, Cupidi C, Bernardi L, Anfossi M, Gallo M, Conidi ME, Smirne N, Rademakers R, Baker M, Dickson DW, Graff-Radford NR, Petersen RC, Knopman D, Josephs KA, Boeve BF, Parisi JE, Seeley WW, Miller BL, Karydas AM, Rosen H, van Swieten JC, Dopper EG, Seelaar H, Pijnenburg YA, Scheltens P, Logroscino G, Capozzo R, Novelli V, Puca AA, Franceschi M, Postiglione A, Milan G, Sorrentino P, Kristiansen M, Chiang HH, Graff C, Pasquier F, Rollin A, Deramecourt V, Lebert F, Kapogiannis D, Ferrucci L, Pickering-Brown S, Singleton AB, Hardy J, Momeni P.

Lancet Neurol. 2014 Jul;13(7):686-99. doi: 10.1016/S1474-4422(14)70065-1.

8.

Missense dopamine transporter mutations associate with adult parkinsonism and ADHD.

Hansen FH, Skjørringe T, Yasmeen S, Arends NV, Sahai MA, Erreger K, Andreassen TF, Holy M, Hamilton PJ, Neergheen V, Karlsborg M, Newman AH, Pope S, Heales SJ, Friberg L, Law I, Pinborg LH, Sitte HH, Loland C, Shi L, Weinstein H, Galli A, Hjermind LE, Møller LB, Gether U.

J Clin Invest. 2014 Jul;124(7):3107-20. doi: 10.1172/JCI73778. Epub 2014 Jun 9.

9.

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

Petersen MH, Budtz-Jørgensen E, Sørensen SA, Nielsen JE, Hjermind LE, Vinther-Jensen T, Nielsen SM, Nørremølle A.

Mitochondrion. 2014 Jul;17:14-21. doi: 10.1016/j.mito.2014.05.001. Epub 2014 May 15.

PMID:
24836434
10.

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

Schjerling L, Hjermind LE, Jespersen B, Madsen FF, Brennum J, Jensen SR, Løkkegaard A, Karlsborg M.

J Neurosurg. 2013 Dec;119(6):1537-45. doi: 10.3171/2013.8.JNS13844. Epub 2013 Oct 11. Erratum in: J Neurosurg. 2014 Jan;120(1):295.

PMID:
24116723
11.

Chromosomal rearrangements in Tourette syndrome: implications for identification of candidate susceptibility genes and review of the literature.

Bertelsen B, Debes NM, Hjermind LE, Skov L, Brøndum-Nielsen K, Tümer Z.

Neurogenetics. 2013 Nov;14(3-4):197-203. doi: 10.1007/s10048-013-0372-y. Epub 2013 Aug 29.

PMID:
23989977
12.

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 LE, Nielsen JE, Nielsen TT.

Eur J Hum Genet. 2013 Jun;21(6):626-9. doi: 10.1038/ejhg.2012.231. Epub 2012 Oct 10.

13.

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.

Clin Genet. 2013 Mar;83(3):279-83. doi: 10.1111/j.1399-0004.2012.01903.x. Epub 2012 Jul 4.

PMID:
22650353
14.

The DJ-1 concentration in cerebrospinal fluid does not differentiate among Parkinsonian syndromes.

Salvesen L, Bech S, Lokkegaard A, Hjermind LE, Nielsen JE, Pakkenberg B, Tanassi JT, Heegaard NH, Winge K.

Parkinsonism Relat Disord. 2012 Aug;18(7):899-901. doi: 10.1016/j.parkreldis.2012.03.013. Epub 2012 Apr 11. No abstract available.

PMID:
22503539
15.

Amyloid-related biomarkers and axonal damage proteins in parkinsonian syndromes.

Bech S, Hjermind LE, Salvesen L, Nielsen JE, Heegaard NH, Jørgensen HL, Rosengren L, Blennow K, Zetterberg H, Winge K.

Parkinsonism Relat Disord. 2012 Jan;18(1):69-72. doi: 10.1016/j.parkreldis.2011.08.012. Epub 2011 Aug 27.

PMID:
21873100
16.

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.

Clin Genet. 2012 Sep;82(3):256-63. doi: 10.1111/j.1399-0004.2011.01745.x. Epub 2011 Jul 18.

PMID:
21696388
17.

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

Hjermind LE, Law I, Jønch A, Stokholm J, Nielsen JE.

J Neuropsychiatry Clin Neurosci. 2011 Spring;23(2):206-10. doi: 10.1176/appi.neuropsych.23.2.206.

PMID:
21677252
18.

The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders.

Bech S, Nørremølle A, Winge K, Hasholt L, Tommerup N, Svenstrup K, Nielsen JE, Hjermind LE.

Parkinsonism Relat Disord. 2011 Jun;17(5):398-9. doi: 10.1016/j.parkreldis.2011.01.016. Epub 2011 Feb 25. No abstract available.

PMID:
21353620
19.

Proteomic investigations of the ventriculo-lumbar gradient in human CSF.

Simonsen AH, Bech S, Laursen I, Salvesen L, Winge K, Waldemar G, Werdelin L, Nielsen JE, McGuire JN, Hjermind LE.

J Neurosci Methods. 2010 Aug 30;191(2):244-8. doi: 10.1016/j.jneumeth.2010.06.017. Epub 2010 Jun 25.

PMID:
20599557
20.

Behavioral variant of frontotemporal dementia mimicking Huntington's disease.

Nielsen TR, Bruhn P, Nielsen JE, Hjermind LE.

Int Psychogeriatr. 2010 Jun;22(4):674-7. doi: 10.1017/S1041610210000098. Epub 2010 Feb 22.

PMID:
20170589
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