Sørensen SA - Search Results

1

The Danish HD Registry-a nationwide family registry of HD families in Denmark.

Gilling M, Budtz-Jørgensen E, Boonen SE, Lildballe D, Bojesen A, Hertz JM, Sørensen SA. Gilling M, et al. Among authors: sorensen sa. Clin Genet. 2017 Sep;92(3):338-341. doi: 10.1111/cge.12984. Epub 2017 Mar 28. Clin Genet. 2017. PMID: 28155235

2

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. Among authors: sorensen sa. Clin Genet. 2009 Mar;75(3):244-50. doi: 10.1111/j.1399-0004.2008.01136.x. Clin Genet. 2009. PMID: 19250382

3

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: sorensen sa. Mitochondrion. 2014 Jul;17:14-21. doi: 10.1016/j.mito.2014.05.001. Epub 2014 May 15. Mitochondrion. 2014. PMID: 24836434

4

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. Among authors: sorensen sa. Hum Mol Genet. 1993 Sep;2(9):1475-6. doi: 10.1093/hmg/2.9.1475. Hum Mol Genet. 1993. PMID: 8242074

5

Correlation between magnitude of CAG repeat length alterations and length of the paternal repeat in paternally inherited Huntington's disease.

Nørremølle A, Sørensen SA, Fenger K, Hasholt L. Nørremølle A, et al. Among authors: sorensen sa. Clin Genet. 1995 Mar;47(3):113-7. doi: 10.1111/j.1399-0004.1995.tb03941.x. Clin Genet. 1995. PMID: 7634532

6

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. Among authors: sorensen sa. Hum Genet. 1995 Mar;95(3):313-8. doi: 10.1007/BF00225200. Hum Genet. 1995. PMID: 7868125

7

Mosaicism of the CAG repeat sequence in the Huntington disease gene in a pair of monozygotic twins.

Nørremølle A, Hasholt L, Petersen CB, Eiberg H, Hasselbalch SG, Gideon P, Nielsen JE, Sørensen SA. Nørremølle A, et al. Among authors: sorensen sa. Am J Med Genet A. 2004 Oct 1;130A(2):154-9. doi: 10.1002/ajmg.a.30128. Am J Med Genet A. 2004. PMID: 15372528

8

Causes of death in patients with Huntington's disease and in unaffected first degree relatives.

Sørensen SA, Fenger K. Sørensen SA, et al. J Med Genet. 1992 Dec;29(12):911-4. doi: 10.1136/jmg.29.12.911. J Med Genet. 1992. PMID: 1479606 Free PMC article.

9

Fabry's disease.

Hasholt L, Wandall A, Sørensen SA. Hasholt L, et al. Among authors: sorensen sa. Clin Genet. 1989 Nov;36(5):335-6. doi: 10.1111/j.1399-0004.1989.tb03208.x. Clin Genet. 1989. PMID: 2513152

10

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. Among authors: sorensen sa. Mov Disord. 2006 May;21(5):679-82. doi: 10.1002/mds.20773. Mov Disord. 2006. PMID: 16267845

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