790 related articles for article (PubMed ID: 9124808)
1. Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and spinocerebellar ataxia type 1.
Hashida H; Goto J; Kurisaki H; Mizusawa H; Kanazawa I
Ann Neurol; 1997 Apr; 41(4):505-11. PubMed ID: 9124808
[TBL] [Abstract][Full Text] [Related]
2. Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and Machado-Joseph disease.
Lopes-Cendes I; Maciel P; Kish S; Gaspar C; Robitaille Y; Clark HB; Koeppen AH; Nance M; Schut L; Silveira I; Coutinho P; Sequeiros J; Rouleau GA
Ann Neurol; 1996 Aug; 40(2):199-206. PubMed ID: 8773601
[TBL] [Abstract][Full Text] [Related]
3. Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population.
Ikeuchi T; Takano H; Koide R; Horikawa Y; Honma Y; Onishi Y; Igarashi S; Tanaka H; Nakao N; Sahashi K; Tsukagoshi H; Inoue K; Takahashi H; Tsuji S
Ann Neurol; 1997 Dec; 42(6):879-84. PubMed ID: 9403480
[TBL] [Abstract][Full Text] [Related]
4. Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado-Joseph disease.
Cancel G; Gourfinkel-An I; Stevanin G; Didierjean O; Abbas N; Hirsch E; Agid Y; Brice A
Hum Mutat; 1998; 11(1):23-7. PubMed ID: 9450899
[TBL] [Abstract][Full Text] [Related]
5. [Molecular basis of heterogeneities of clinical presentation of dentatorubral pallidoluysian atrophy (DRPLA)].
Tsuji S
Rinsho Shinkeigaku; 1994 Dec; 34(12):1227-9. PubMed ID: 7774119
[TBL] [Abstract][Full Text] [Related]
6. Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease.
Matilla T; McCall A; Subramony SH; Zoghbi HY
Ann Neurol; 1995 Jul; 38(1):68-72. PubMed ID: 7611728
[TBL] [Abstract][Full Text] [Related]
7. Mendelian segregation of normal CAG trinucleotide repeat alleles at three autosomal loci.
MacMillan JC; Voisey J; Healey SC; Martin NG
J Med Genet; 1999 Mar; 36(3):258-9. PubMed ID: 10204858
[TBL] [Abstract][Full Text] [Related]
8. Molecular pathology of dentatorubral-pallidoluysian atrophy.
Kanazawa I
Philos Trans R Soc Lond B Biol Sci; 1999 Jun; 354(1386):1069-74. PubMed ID: 10434307
[TBL] [Abstract][Full Text] [Related]
9. Dentatorubral-pallidoluysian atrophy (DRPLA). Molecular basis for wide clinical features of DRPLA.
Ikeuchi T; Koide R; Onodera O; Tanaka H; Oyake M; Takano H; Tsuji S
Clin Neurosci; 1995; 3(1):23-7. PubMed ID: 7614090
[TBL] [Abstract][Full Text] [Related]
10. Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.
Dürr A; Stevanin G; Cancel G; Duyckaerts C; Abbas N; Didierjean O; Chneiweiss H; Benomar A; Lyon-Caen O; Julien J; Serdaru M; Penet C; Agid Y; Brice A
Ann Neurol; 1996 Apr; 39(4):490-9. PubMed ID: 8619527
[TBL] [Abstract][Full Text] [Related]
11. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
Oda M; Maruyama H; Komure O; Morino H; Terasawa H; Izumi Y; Imamura T; Yasuda M; Ichikawa K; Ogawa M; Matsumoto M; Kawakami H
Arch Neurol; 2004 Feb; 61(2):209-12. PubMed ID: 14967767
[TBL] [Abstract][Full Text] [Related]
12. Differential pattern in tissue-specific somatic mosaicism of expanded CAG trinucleotide repeats in dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and X-linked recessive spinal and bulbar muscular atrophy.
Tanaka F; Sobue G; Doyu M; Ito Y; Yamamoto M; Shimada N; Yamamoto K; Riku S; Hshizume Y; Mitsuma T
J Neurol Sci; 1996 Jan; 135(1):43-50. PubMed ID: 8926495
[TBL] [Abstract][Full Text] [Related]
13. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
Tang B; Xia J; Wang D; Tang X; Shen L; Liu C; Dai H; Yan X; Pan Q; Xiao J; Zhang B; Ou Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):281-4. PubMed ID: 10514531
[TBL] [Abstract][Full Text] [Related]
14. [Molecular and clinical features in spinocerebellar ataxia type 6 (SCA6) in Japanese].
Ikeuchi T
Nihon Rinsho; 1999 Apr; 57(4):891-5. PubMed ID: 10222785
[TBL] [Abstract][Full Text] [Related]
15. Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat.
Ikeuchi T; Koide R; Tanaka H; Onodera O; Igarashi S; Takahashi H; Kondo R; Ishikawa A; Tomoda A; Miike T
Ann Neurol; 1995 Jun; 37(6):769-75. PubMed ID: 7778850
[TBL] [Abstract][Full Text] [Related]
16. [A sporadic case of dentatorubral-pallidoluysian atrophy (DRPLA) having an elderly age of onset].
Horikawa H; Futamura N; Uetakagaito M
Rinsho Shinkeigaku; 1996 Apr; 36(4):584-6. PubMed ID: 8810854
[TBL] [Abstract][Full Text] [Related]
17. Long-term disability and prognosis in dentatorubral-pallidoluysian atrophy: a correlation with CAG repeat length.
Hasegawa A; Ikeuchi T; Koike R; Matsubara N; Tsuchiya M; Nozaki H; Homma A; Idezuka J; Nishizawa M; Onodera O
Mov Disord; 2010 Aug; 25(11):1694-700. PubMed ID: 20589872
[TBL] [Abstract][Full Text] [Related]
18. [Autosomal dominant spinocerebellar ataxia].
Legros B; Manto MU
Rev Med Brux; 1999 Dec; 20(6):495-503. PubMed ID: 10672773
[TBL] [Abstract][Full Text] [Related]
19. Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain.
Yazawa I; Nukina N; Hashida H; Goto J; Yamada M; Kanazawa I
Nat Genet; 1995 May; 10(1):99-103. PubMed ID: 7647802
[TBL] [Abstract][Full Text] [Related]
20. 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
Nat Genet; 1994 Jan; 6(1):9-13. PubMed ID: 8136840
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
