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Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation Danish family.
Nielsen JE, Sørensen SA, Hasholt L, Nørremølle A. Nielsen JE, et al. Among authors: norremolle a. Mov Disord. 1996 Sep;11(5):533-41. doi: 10.1002/mds.870110508. Mov Disord. 1996. PMID: 8866494
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
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. Clin Genet. 1995 Mar;47(3):113-7. doi: 10.1111/j.1399-0004.1995.tb03941.x. Clin Genet. 1995. PMID: 7634532
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
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
DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington disease.
Andrew S, Theilmann J, Almqvist E, Norremolle A, Lucotte G, Anvret M, Sorensen SA, Turpin JC, Hayden MR. Andrew S, et al. Among authors: norremolle a. Clin Genet. 1993 Jun;43(6):286-94. doi: 10.1111/j.1399-0004.1993.tb03820.x. Clin Genet. 1993. PMID: 8370147
Mapping of the human NMDA receptor subunit (NMDAR1) and the proposed NMDA receptor glutamate-binding subunit (NMDARA1) to chromosomes 9q34.3 and chromosome 8, respectively.
Collins C, Duff C, Duncan AM, Planells-Cases R, Sun W, Norremolle A, Michaelis E, Montal M, Worton R, Hayden MR. Collins C, et al. Among authors: norremolle a. Genomics. 1993 Jul;17(1):237-9. doi: 10.1006/geno.1993.1311. Genomics. 1993. PMID: 8406459
Antisense downregulation of mutant huntingtin in a cell model.
Hasholt L, Abell K, Nørremølle A, Nellemann C, Fenger K, Sørensen SA. Hasholt L, et al. Among authors: norremolle a. J Gene Med. 2003 Jun;5(6):528-38. doi: 10.1002/jgm.378. J Gene Med. 2003. PMID: 12797118
Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG4) using direct mutation detection.
Nielsen JE, Koefoed P, Kjaergaard S, Jensen LN, Nørremølle A, Hasholt L. Nielsen JE, et al. Among authors: norremolle a. Prenat Diagn. 2004 May;24(5):363-6. doi: 10.1002/pd.875. Prenat Diagn. 2004. PMID: 15164410
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. 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
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