Hjermind LE - Search Results

1

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. Petersen MH, et al. Among authors: hjermind le. Mitochondrion. 2014 Jul;17:14-21. doi: 10.1016/j.mito.2014.05.001. Epub 2014 May 15. Mitochondrion. 2014. PMID: 24836434

2

[Hereditary dystonias].

Hjermind LE, Sørensen SA, Werdelin LM. Hjermind LE, et al. Ugeskr Laeger. 2000 Sep 18;162(38):5066-70. Ugeskr Laeger. 2000. PMID: 11014135 Review. Danish.

3

Inherited and de novo mutations in sporadic cases of DYT1-dystonia.

Hjermind LE, Werdelin LM, Sørensen SA. Hjermind LE, et al. Eur J Hum Genet. 2002 Mar;10(3):213-6. doi: 10.1038/sj.ejhg.5200782. Eur J Hum Genet. 2002. PMID: 11973627

4

A novel mutation in the epsilon-sarcoglycan gene causing myoclonus-dystonia syndrome.

Hjermind LE, Werdelin LM, Eiberg H, Krag-Olsen B, Dupont E, Sørensen SA. Hjermind LE, et al. Neurology. 2003 May 13;60(9):1536-9. doi: 10.1212/01.wnl.0000061480.86610.bf. Neurology. 2003. PMID: 12743249

5

Dopa-responsive dystonia and early-onset Parkinson's disease in a patient with GTP cyclohydrolase I deficiency?

Hjermind LE, Johannsen LG, Blau N, Wevers RA, Lucking CB, Hertz JM, Friberg L, Regeur L, Nielsen JE, Sørensen SA. Hjermind LE, et al. Mov Disord. 2006 May;21(5):679-82. doi: 10.1002/mds.20773. Mov Disord. 2006. PMID: 16267845

6

Meiotic CAG repeat instability in spinocerebellar ataxia type 6: maternally transmitted elongation in a presumed sporadic case.

Lindquist SG, Nørremølle A, Hjermind LE, Hasholt L, Nielsen JE. Lindquist SG, et al. Among authors: hjermind le. J Neurol Sci. 2006 Feb 15;241(1-2):95-8. doi: 10.1016/j.jns.2005.10.004. Epub 2005 Nov 28. J Neurol Sci. 2006. PMID: 16310805

7

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. 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

8

[Hereditary Parkinson disease. The Danish Society of Movement Disorders].

Hjermind LE, Nielsen JE; Dansk Selskab for Bevaegeforstyrrelser. Hjermind LE, et al. Ugeskr Laeger. 2008 Mar 17;170(12):1016. Ugeskr Laeger. 2008. PMID: 18397634 Danish. No abstract available.

9

Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegia.

Svenstrup K, Bross P, Koefoed P, Hjermind LE, Eiberg H, Born AP, Vissing J, Gyllenborg J, Nørremølle A, Hasholt L, Nielsen JE. Svenstrup K, et al. Among authors: hjermind le. J Neurol Sci. 2009 Sep 15;284(1-2):90-5. doi: 10.1016/j.jns.2009.04.024. Epub 2009 May 6. J Neurol Sci. 2009. PMID: 19423133

10

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

Bech S, Petersen T, Nørremølle A, Gjedde A, Ehlers L, Eiberg H, Hjermind LE, Hasholt L, Lundorf E, Nielsen JE. Bech S, et al. Among authors: hjermind le. Parkinsonism Relat Disord. 2010 Jan;16(1):12-5. doi: 10.1016/j.parkreldis.2009.06.006. Parkinsonism Relat Disord. 2010. PMID: 19595623

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