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Results: 1 to 20 of 141

Similar articles for PubMed (Select 8557266)

1.

Molecular re-investigation of patients with Huntington's disease in Wessex reveals a family with dentatorubral and pallidoluysian atrophy.

Connarty M, Dennis NR, Patch C, Macpherson JN, Harvey JF.

Hum Genet. 1996 Jan;97(1):76-8.

PMID:
8557266
2.

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p.

Nagafuchi S, Yanagisawa H, Sato K, Shirayama T, Ohsaki E, Bundo M, Takeda T, Tadokoro K, Kondo I, Murayama N, et al.

Nat Genet. 1994 Jan;6(1):14-8.

PMID:
8136826
3.

Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation Danish family.

Nielsen JE, Sørensen SA, Hasholt L, Nørremølle A.

Mov Disord. 1996 Sep;11(5):533-41.

PMID:
8866494
4.

A study on Huntington's disease associated trinucleotide repeat within the Chinese population.

Soong BW, Wang JT.

Proc Natl Sci Counc Repub China B. 1995 Jul;19(3):137-42.

PMID:
7480359
5.

Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigrees.

Becher MW, Rubinsztein DC, Leggo J, Wagster MV, Stine OC, Ranen NG, Franz ML, Abbott MH, Sherr M, MacMillan JC, Barron L, Porteous M, Harper PS, Ross CA.

Mov Disord. 1997 Jul;12(4):519-30. Review.

PMID:
9251070
6.

Huntington's disease: diagnosis by amplification of the CAG repeat.

Upton JD, Avery S, Parkin P, George PM.

N Z Med J. 1995 Mar 8;108(995):78-80.

PMID:
7891947
7.

Study of the Huntington's disease (HD) gene CAG repeats in schizophrenic patients shows overlap of the normal and HD affected ranges but absence of correlation with schizophrenia.

Rubinsztein DC, Leggo J, Goodburn S, Crow TJ, Lofthouse R, DeLisi LE, Barton DE, Ferguson-Smith MA.

J Med Genet. 1994 Sep;31(9):690-3.

8.

Distribution of CAG repeat size in the dentatorubral and pallidoluysian atrophy (DRPLA) gene in a normal population in Taiwan.

Hsieh M, Chiu MH, Lin YH, Lin CH, Lu TM, Li SY, Li C.

Proc Natl Sci Counc Repub China B. 2000 Apr;24(2):76-80.

PMID:
10809084
9.

Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene.

Hummerich H, Baxendale S, Mott R, Kirby SF, MacDonald ME, Gusella J, Lehrach H, Bates GP.

Hum Mol Genet. 1994 Jan;3(1):73-8.

PMID:
8162055
10.

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).

Koide R, Ikeuchi T, Onodera O, Tanaka H, Igarashi S, Endo K, Takahashi H, Kondo R, Ishikawa A, Hayashi T, et al.

Nat Genet. 1994 Jan;6(1):9-13.

PMID:
8136840
11.

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease.

Snell RG, MacMillan JC, Cheadle JP, Fenton I, Lazarou LP, Davies P, MacDonald ME, Gusella JF, Harper PS, Shaw DJ.

Nat Genet. 1993 Aug;4(4):393-7.

PMID:
8401588
13.

Southern analysis for detection of CAG repeat expansions associated with dentatorubral pallidoluysian atrophy.

Alford RL, Margolis RL, Ross CA, Richards CS.

Hum Genet. 1997 Mar;99(3):354-6.

PMID:
9050922
14.

Somatic mosaicism of CAG repeat in dentatorubral-pallidoluysian atrophy (DRPLA).

Ueno S, Kondoh K, Kotani Y, Komure O, Kuno S, Kawai J, Hazama F, Sano A.

Hum Mol Genet. 1995 Apr;4(4):663-6.

PMID:
7633415
15.

Sequence analysis of the CCG polymorphic region adjacent to the CAG triplet repeat of the HD gene in normal and HD chromosomes.

Pêcheux C, Mouret JF, Dürr A, Agid Y, Feingold J, Brice A, Dodé C, Kaplan JC.

J Med Genet. 1995 May;32(5):399-400.

16.

Diagnosis of "sporadic" Huntington's disease.

Dürr A, Dodé C, Hahn V, Pêcheux C, Pillon B, Feingold J, Kaplan JC, Agid Y, Brice A.

J Neurol Sci. 1995 Mar;129(1):51-5.

PMID:
7751845
17.

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.

Stevanin G, Fujigasaki H, Lebre AS, Camuzat A, Jeannequin C, Dode C, Takahashi J, San C, Bellance R, Brice A, Durr A.

Brain. 2003 Jul;126(Pt 7):1599-603. Epub 2003 May 6.

18.

A reproducible assay of polymerase chain reaction to detect trinucleotide repeat expansion of Huntington's disease and senile chorea.

Watanabe M, Abe K, Aoki M, Kameya T, Itoyama Y, Shoji M, Ikeda M, Iizuka T, Hirai S.

Neurol Res. 1996 Feb;18(1):16-8.

PMID:
8714530
19.

Molecular analysis of the IT15 gene in patients with apparently 'sporadic' Huntington's disease.

Mandich P, Di Maria E, Bellone E, Ajmar F, Abbruzzese G.

Eur Neurol. 1996;36(6):348-52.

PMID:
8954302
20.

Somatic mosaicism of expanded CAG repeats in brains of patients with dentatorubral-pallidoluysian atrophy: cellular population-dependent dynamics of mitotic instability.

Takano H, Onodera O, Takahashi H, Igarashi S, Yamada M, Oyake M, Ikeuchi T, Koide R, Tanaka H, Iwabuchi K, Tsuji S.

Am J Hum Genet. 1996 Jun;58(6):1212-22.

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