SCOPUS 정보 검색 플랫폼

Tohoku Journal of Experimental Medicine

Volumn 195, Issue 2, 2001, Pages 85-91

Incidence of genetic subgroups of hereditary spinocerebellar ataxia in fukushima prefecture

(6) Kumagai, Yukie a Sugiura, Yoshihiro a Shimoji, Shinya a Kumagai, T Tomohiro a Tochikubo, Sanae a Yamamoto, Teiji a

a FUKUSHIMA MEDICAL UNIVERSITY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DEMENTIA; DENTATORUBROPALLIDOLUYSIAN ATROPHY; DIAGNOSTIC ERROR; DISEASE CLASSIFICATION; FAMILY HISTORY; GENETIC ANALYSIS; GENETIC DISORDER; GEOGRAPHY; HISTORY; HUMAN; INCIDENCE; JAPAN; MACHADO JOSEPH DISEASE; POPULATION SIZE; PREVALENCE; SPINOCEREBELLAR DEGENERATION;

GENETIC DISEASES, INBORN; HUMANS; INCIDENCE; JAPAN; PREVALENCE; SPINOCEREBELLAR ATAXIAS;

EID: 0035572162 PISSN: 00408727 EISSN: None Source Type: Journal
DOI: 10.1620/tjem.195.85 Document Type: Article

Times cited : (5)

References (34)

1
- 0033108943
- Clinical and genetic characteristics of SCA1
- (in Japanese with English summary)
- (1999) Nippon Rinsho , vol.57 , pp. 796-800
- Abe, K.¹

2
- 0033778477
- Macular degeneration associated with aberrant expansion of trinucleotide repeat of the SCA7 gene in 2 Japanese families
- (2000) Arch. Ophtalmol. , vol.118 , pp. 1415-1421
- Abe, T.¹ Tsuda, T.² Yoshida, M.³ Wada, Y.⁴ Kano, T.⁵ Itoyama, Y.⁶ Tamai, M.⁷

3
- 0006379804
- A Japanese family of spinocerebellar ataxia type 7 (SCA7)
- (in Japanese)
- (1998) Shinkei Naika , vol.49 , pp. 303-304
- Adachi, Y.¹ Ohta, M.² Mori, M.³ Nakajima, K.⁴

4
- 16944364511
- Cloning of the SCA7 gene reveals highly unstable CAG repeat expansion
- (1997) Nature Genet. , vol.17 , pp. 65-70
- David, G.¹ Abbas, N.² Stevanin, G.³ Durr, A.⁴ Yvert, G.⁵ Cancel, G.⁶ Weber, C.⁷ Imbert, G.⁸ Saudou, F.⁹ Antoniou, E.¹⁰ Drabkin, H.¹¹ Gemmill, R.¹² Giunti, P.¹³ Benomar, A.¹⁴ Wood, N.¹⁵ Ruberg, M.¹⁶ Agid, Y.¹⁷ Mandel, J.L.¹⁸ Brice, A.¹⁹

5
- 0029792130
- Autosomal Dominant Spinocerebellar Ataxia with Sensory Axonal Neuropathy (SCA4): Clinical Description and Genetic Localization to Chromosome 16q22.1
- (1996) Am. J. Hum. Genet. , vol.59 , pp. 392-399
- Flanigan, K.¹ Gardner, K.² Alderson, K.³ Galster, B.⁴ Otterud, B.⁵ Leppert, M.F.⁶ Kaplan, C.⁷ Ptacek, L.J.⁸

6
- 0033093291
- Genetic analysis of a dendatorubral-pallidoluysian atrophy family: Relevance to apparent sporadic cases
- (1999) Intern. Med. , vol.38 , pp. 287-289
- Hattori, M.¹ Yuasa, H.² Takada, K.³ Yamada, T.⁴ Yamada, K.⁵ Kamimoto, K.⁶ Uchida, M.⁷

7
- 0006343775
- Epidemiological investigation of motor ataxia syndrome (spinocerebellar ataxia and Shy-Drager syndrome) in all country; the third report
- Specified Disease Motor Ataxia Syndrome Investigation Study Group of Ministry of Health and Welfare, Study Reports of the 1991th, edited by K. Hirayama, Kagaku Toshyo Insatsu Co., Tokyo
- (1991) , pp. 29-44
- Hirayama, K.¹ Takayanagi, T.² Yanagisawa, N.³ Nakamura, R.⁴ Hattori, T.⁵ Kita, K.⁶ Satomura, Y.⁷

8
- 0032727249
- Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12
- (1999) Nature Genet. , vol.23 , pp. 391-392
- Holmes, S.E.¹ O'Hearn, E.E.² McInnis, M.G.³ Gorelick-Feldman, D.A.⁴ Kleiderlein, J.J.⁵ Callahan, C.⁶ Kwak, N.G.⁷ Ingersoll-Ashworth, R.G.⁸ Sherr, M.⁹ Sumner, A.J.¹⁰ Sharp, A.H.¹¹ Anath, U.¹² Seltzer, W.K.¹³ Boss, M.A.¹⁴ Vieria-Saecker Riess, O.¹⁵ Ross, C.A.¹⁶ Margolis, R.L.¹⁷

9
- 0006379267
- Regional feature of hereditary spinocerebellar degeneration in Kanto district of Japan
- (in Japanese)
- (2000) Shinkei Naika , vol.53 , pp. 104-110
- Ichikawa, Y.¹ Goto, J.²

10
- 0034700999
- Molecular and clinical analyses of spinocerebellar ataxia type 8 in Japan
- (2000) Neurology , vol.54 , pp. 950-955
- Ikeda, Y.¹ Shizuka, M.² Watanabe, M.³ Okamoto, K.⁴ Shoji, M.⁵

11
- 0030294345
- Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
- (Group 1), (Group 2)
- (1996) Nature Genet. , vol.14 , pp. 285-291
- Imbert, G.¹ Saudou, F.² Yvert, G.³ Devys, D.⁴ Trottier, Y.⁵ Garnier, J.M.⁶ Weber, C.⁷ Mandel, J.L.⁸ Cancel, G.⁹ Abbas, N.¹⁰ Durr, A.¹¹ Didierjean, O.¹² Stevanin, G.¹³ Agid, Y.¹⁴ Brice, A.¹⁵

12
- 0006379268
- Dementia and psychological symptoms of DRPLA
- edited by S. Tsuji, H. Naito & Oyanagi, S. Igaku Shoin Co., Tokyo
- (1997) DRPLA , pp. 61-67
- Inazuki, G.¹

13
- 0029049256
- Analysis of spinocerebellar ataxia type 1 (SCA1)-related CAG trinucleotide expansion in Japan
- (1995) Neurology , vol.45 , pp. 1587-1694
- Kameya, T.¹ Abe, K.² Aoki, M.³ Sahara, M.⁴ Tobita, M.⁵ Konno, H.⁶ Itoyama, Y.⁷

14
- 0006343776
- Spinocerebellar ataxia type 1
- edited by Y. Itoyama & K. Abe, Shinkoh Igaku Shuppan Co., Tokyo
- (1996) Spinocerebellar Degeneration , pp. 9-14
- Kameya, T.¹

15
- 0028143527
- CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1
- (1994) Nature Genet. , vol.8 , pp. 221-228
- Kawaguchi, Y.¹ Okamoto, T.² Taniwaki, M.³ Aizawa, M.⁴ Inoue, M.⁵ Katayama, S.⁶ Kawakami, H.⁷ Nakmura, S.⁸ Nishimura, M.⁹ Akiguchi, I.¹⁰ Kimura, J.¹¹ Narumiya, S.¹² Kakizuka, A.¹³

16
- 0028216760
- Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)
- (1994) Nature Genet. , vol.6 , pp. 9-13
- Koide, R.¹ Ikeuchi, T.² Onodera, O.³ Tanaka, H.⁴ Igarashi, S.⁵ Endo, K.⁶ Takahashi, H.⁷ Kondo, R.⁸ Ishikawa, A.⁹ Hayashi, T.¹⁰ Saito, M.¹¹ Tomoda, A.¹² Miike, T.¹³ Naito, H.¹⁴ Ikuta, F.¹⁵ Tsuji, S.¹⁶

17
- 0032900772
- An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
- (1999) Nature Genet. , vol.21 , pp. 379-384
- Koob, M.D.¹ Moseley, M.L.² Schut, L.J.³ Benzow, K.A.⁴ Bird, T.D.⁵ Day, J.W.⁶ Ranum, L.P.W.⁷

18
- 0027297703
- Novel triplet repeat containing genes in human brain: Cloning, expression, and length polymorphisms
- (1993) Genomics , vol.16 , pp. 572-579
- Li, S.H.¹ Mcinnis, M.G.² Margolis, R.L.³ Antonarakis, S.E.⁴ Ross, C.A.⁵

19
- 0033771685
- Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10
- (2000) Nature Genet. , vol.26 , pp. 191-194
- Matsuura, T.¹ Yamagata, T.² Burgess, D.L.³ Rasmussen, A.⁴ Grewal, R.P.⁵ Watase, K.⁶ Khajavani, M.⁷ McCall, A.E.⁸ Davis, C.F.⁹ Zu, L.¹⁰ Achari, M.¹¹ Pulst, S.M.¹² Alonso, E.¹³ Noebels, J.L.¹⁴ Nelson, D.L.¹⁵ Zoghbi, H.Y.¹⁶ Ashizawa, T.¹⁷

20
- 0028335386
- Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p
- (1994) Nature Genet. , vol.6 , pp. 14-18
- Nagafuchi, S.¹ Yanagisawa, H.² Sato, K.³ Shirayama, T.⁴ Ohsaki, E.⁵ Bundo, M.⁶ Takeda, T.⁷ Tadokoro, K.⁸ Kondo, I.⁹ Murayama, N.¹⁰ Tanaka, Y.¹¹ Kikushima, H.¹² Umino, K.¹³ Kurosawa, H.¹⁴ Furukawa, T.¹⁵ Nihei, K.¹⁶ Inoue, T.¹⁷ Sano, A.¹⁸ Komure, O.¹⁹ Takahashi Yoshizawa, T.²⁰ Kanazawa, I.²¹ Yamada, M.²² more..

21
- 0033120421
- Regional differences in genetic subgroup frequency in hereditary cerebellar ataxia and morphometrical study of brain MR images in SCA1, MJD and SCA6
- (1999) J. Nerol. Sci. , vol.164 , pp. 187-194
- Nagaoka, U.¹ Suzuki, Y.² Kawanami, T.³ Kurita, K.⁴ Shikama, Y.⁵ Honda, K.⁶ Abe, K.⁷ Nakajima, T.⁸ Kato, T.⁹

22
- 0006358477
- Psychiatric symptoms of dentatorubral-pallidoluysian atrophy (DRPLA)
- (in Japanese)
- (1991) Rinsho Seishin Igaku , vol.20 , pp. 1195-1204
- Naito, H.¹ Inazuki, G.²

23
- 0000876223
- Regional feature of hereditary spinocerebellar degeneration in Tohoku district of Japan
- (in Japanese)
- (2000) Shinkei Naika , vol.53 , pp. 99-103
- Onodera, Y.¹ Tsuda, T.² Itoyama, Y.³

24
- 0027164698
- Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
- (1993) Nature Genet. , vol.4 , pp. 221-226
- Orr, H.T.¹ Chung, M.Y.² Banfi, S.³ Kwiatkowski T.J., Jr.⁴ Servadio, A.⁵ Beaudet, A.L.⁶ McCall, A.E.⁷ Duvick, L.A.⁸ Ranum, L.P.⁹ Zoghbi, H.Y.¹⁰

25
- 0030292488
- Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
- (1996) Nature Genet. , vol.14 , pp. 269-276
- Pulst, S.M.¹ Nechiporuk, A.² Nichiporuk, T.³ Gispert, S.⁴ Chen, X.N.⁵ Lopes-Cendes, I.⁶ Perlman, S.⁷ Starkman, S.⁸ Orozco-Diaz, G.⁹ Lunkes, A.¹⁰ Dejong, P.¹¹ Rouleau, G.A.¹² Auburger, G.¹³ Korenberg, J.R.¹⁴ Figueroa, C.¹⁵ Sahba, S.¹⁶

26
- 0028020605
- Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11
- (1994) Nature Genet. , vol.8 , pp. 280-284
- Ranum, L.P.¹ Schut, L.J.² Lundgren, J.K.³ Orr, H.T.⁴ Livingston, D.M.⁵

27
- 0030292368
- Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT
- (1996) Nature Genet. , vol.14 , pp. 277-284
- Sampei, K.¹ Takano, H.² Igarashi, S.³ Sato, T.⁴ Oyake, M.⁵ Sasaki, H.⁶ Wakisaka, A.⁷ Tashiro, K.⁸ Ishida, Y.⁹ Ikeuchi, T.¹⁰ Koide, R.¹¹ Saito, M.¹² Tanaka, T.¹³ Hnyu, S.¹⁴ Takiyama, Y.¹⁵ Nishizawa, M.¹⁶ Shimizu, N.¹⁷ Nomura, Y.¹⁸ Segawa, M.¹⁹ Iwabuchi Tanaka, H.²⁰ Takahashi, H.²¹ Tsuji, S.²² more..

28
- 0030015722
- A sporadic case of dentatorubral pallidoluysian atrophy (DRPLA) with CAG repeat expansion but no clinical abnormalities in the father
- (1996) J. Neurol. Neurosurg. Psychiatry , vol.61 , pp. 113-114
- Shimizu, N.¹ Yamami, T.² Nakayama, M.³ Ikeuchi, T.⁴ Koide, R.⁵ Tsuji, S.⁶

29
- 0006378967
- Regional feature of hereditary spinocerebellar degeneration in Shinetsu · Hokuriku district of Japan
- (in Japanese)
- (2000) Shinkei Naika , vol.53 , pp. 111-115
- Shimohata, M.¹ Onodera, S.² Tsuji, S.³

30
- 6544229058
- Hereditary ataxias in Akita prefecture
- (in Japanese with English abstract)
- (1999) Rinsho Shinkeigaku , vol.39 , pp. 763-766
- Sugawara, M.¹ Toyoshima, I.² Kato, K.³ Wada, C.⁴ Imota, T.⁵ Hirota, K.⁶ Ishiguro, H.⁷ Kagaya, H.⁸ Hirata, A.⁹ Ogasawara, M.¹⁰ Masamune, O.¹¹

31
- 0032231668
- Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations
- (1998) Am. J. Hum. Genet. , vol.63 , pp. 1060-1066
- Takano, H.¹ Cancel, G.² Ikeudhi, T.³ Lorenzetti, D.⁴ Mawad, R.⁵ Stevanin, G.⁶ Didierjean, O.⁷ Durr, A.⁸ Oyake, M.⁹ Shimohata, T.¹⁰ Sasaki, R.¹¹ Koide, R.¹² Igarashi, S.¹³ Hayashi, S.¹⁴ Takiyama, Y.¹⁵ Nishizawa, M.¹⁶ Tanaka, H.¹⁷ Zohbi, H.¹⁸ Brice, A.¹⁹ Tsuji, S.²⁰ more..

32
- 0029121944
- Spinocerebellar ataxia type 1 (SCA1) in the Japanese in Hokkaido may derive from a single common ancestry
- (1995) J. Med. Genet. , vol.32 , pp. 590-592
- Wakisaka, A.¹ Sasaki, H.² Takada, A.³ Fukazawa, T.⁴ Suzuki, Y.⁵ Hamada, T.⁶ Iwabuchi, K.⁷ Tashiro, K.⁸ Yoshiki, T.⁹

33
- 0033358555
- Autosomal Dominant Cerebellar Ataxia Type III: Linkage in a Large British Family to a 7. 6-cM Region on Chromosome 15q14-21.3
- (1999) Am. J. Hum. Genet. , vol.65 , pp. 420-426
- Worth, P.F.¹ Giunti, P.² Gardner-Thorpe, C.³ Dixon, P.H.⁴ Davis, M.B.⁵ Wood, N.W.⁶

34
- 0031012399
- Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel
- (1997) Nature Genet. , vol.15 , pp. 62-69
- Zhuchenko, O.¹ Bailey, J.² Bonnen, P.³ Ashizawa, T.⁴ Stockton, D.W.⁵ Amos, C.⁶ Dobyns, W.B.⁷ Subramony, S.H.⁸ Zoghbi, H.Y.⁹ Lee, C.C.¹⁰

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.