Nørremølle A - Search Results

1

Haploinsufficiency of ARHGAP42 is associated with hypertension.

Fjorder AS, Rasmussen MB, Mehrjouy MM, Nazaryan-Petersen L, Hansen C, Bak M, Grarup N, Nørremølle A, Larsen LA, Vestergaard H, Hansen T, Tommerup N, Bache I. Fjorder AS, et al. Among authors: norremolle a. Eur J Hum Genet. 2019 Aug;27(8):1296-1303. doi: 10.1038/s41431-019-0382-9. Epub 2019 Mar 21. Eur J Hum Genet. 2019. PMID: 30903111 Free PMC article.

2

Elongated CAG repeats of the B37 gene in a Danish family with dentato-rubro-pallido-luysian atrophy.

Nørremølle A, Nielsen JE, Sørensen SA, Hasholt L. Nørremølle A, et al. Hum Genet. 1995 Mar;95(3):313-8. doi: 10.1007/BF00225200. Hum Genet. 1995. PMID: 7868125

3

4p16.3 haplotype modifying age at onset of Huntington disease.

Nørremølle A, Budtz-Jørgensen E, Fenger K, Nielsen JE, Sørensen SA, Hasholt L. Nørremølle A, et al. Clin Genet. 2009 Mar;75(3):244-50. doi: 10.1111/j.1399-0004.2008.01136.x. Clin Genet. 2009. PMID: 19250382

4

Huntington's disease does not appear to increase the risk of diabetes mellitus.

Boesgaard TW, Nielsen TT, Josefsen K, Hansen T, Jørgensen T, Pedersen O, Nørremølle A, Nielsen JE, Hasholt L. Boesgaard TW, et al. Among authors: norremolle a. J Neuroendocrinol. 2009 Sep;21(9):770-6. doi: 10.1111/j.1365-2826.2009.01898.x. Epub 2009 Jul 7. J Neuroendocrinol. 2009. PMID: 19602103

5

Simulation based virtual learning environment in medical genetics counseling: an example of bridging the gap between theory and practice in medical education.

Makransky G, Bonde MT, Wulff JS, Wandall J, Hood M, Creed PA, Bache I, Silahtaroglu A, Nørremølle A. Makransky G, et al. Among authors: norremolle a. BMC Med Educ. 2016 Mar 25;16:98. doi: 10.1186/s12909-016-0620-6. BMC Med Educ. 2016. PMID: 27012245 Free PMC article.

6

Paroxysmal Cranial Dyskinesia and Nail-Patella Syndrome Caused by a Novel Variant in the LMX1B Gene.

Bech S, Løkkegaard A, Nielsen TT, Nørremølle A, Grønborg S, Hasholt L, Steffensen GK, Graehn G, Olesen JH, Tommerup N, Mang Y, Bak M, Nielsen JE, Eiberg H, Hjermind LE. Bech S, et al. Among authors: norremolle a. Mov Disord. 2020 Dec;35(12):2343-2347. doi: 10.1002/mds.28244. Epub 2020 Sep 19. Mov Disord. 2020. PMID: 32949189 Free PMC article.

7

Trinucleotide repeat elongation in the Huntingtin gene in Huntington disease patients from 71 Danish families.

Nørremølle A, Riess O, Epplen JT, Fenger K, Hasholt L, Sørensen SA. Nørremølle A, et al. Hum Mol Genet. 1993 Sep;2(9):1475-6. doi: 10.1093/hmg/2.9.1475. Hum Mol Genet. 1993. PMID: 8242074

8

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. Bech S, et al. Among authors: norremolle a. Parkinsonism Relat Disord. 2011 Jun;17(5):398-9. doi: 10.1016/j.parkreldis.2011.01.016. Epub 2011 Feb 25. Parkinsonism Relat Disord. 2011. PMID: 21353620 No abstract available.

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: norremolle a. Clin Genet. 2016 Mar;89(3):320-7. doi: 10.1111/cge.12628. Epub 2015 Jul 17. Clin Genet. 2016. PMID: 26081309

10

Nucleotide sequence and PCR-amplification of a polymorphic MboI site in human DNA marker D4S95 linked to the Huntington disease locus.

Nørremølle A, Sørensen SA, Arctander P. Nørremølle A, et al. Clin Genet. 1992 Oct;42(4):210-1. doi: 10.1111/j.1399-0004.1992.tb03240.x. Clin Genet. 1992. PMID: 1358489

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