435 related articles for article (PubMed ID: 10442462)
1. An autopsy case of spinocerebellar ataxia type 6 with mental symptoms of schizophrenia and dementia.
Tashiro H; Suzuki SO; Hitotsumatsu T; Iwaki T
Clin Neuropathol; 1999; 18(4):198-204. PubMed ID: 10442462
[TBL] [Abstract][Full Text] [Related]
2. Distribution of cerebello-olivary degeneration in idiopathic late cortical cerebellar atrophy: clinicopathological study of four autopsy cases.
Ota S; Tsuchiya K; Anno M; Niizato K; Akiyama H
Neuropathology; 2008 Feb; 28(1):43-50. PubMed ID: 18181834
[TBL] [Abstract][Full Text] [Related]
3. [Autosomal recessive hereditary cortical cerebellar atrophy with striatal degeneration--two siblings showing choreoathetoid movement, ataxia, dementia, and amenorrhea].
Iwabuchi K; Nakazawa Y; Akai J; Yagishita S; Amano N
No To Shinkei; 1994 Jun; 46(6):563-71. PubMed ID: 8068439
[TBL] [Abstract][Full Text] [Related]
4. Hereditary paroxysmal ataxia with mental retardation: a clinicopathological study in relation to episodic ataxia type 2.
Mochizuki Y; Kawata A; Mizutani T; Takamoto K; Hayashi H; Taki K; Morimatsu Y
Acta Neuropathol; 2004 Oct; 108(4):345-9. PubMed ID: 15300451
[TBL] [Abstract][Full Text] [Related]
5. Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.
Gomez CM; Thompson RM; Gammack JT; Perlman SL; Dobyns WB; Truwit CL; Zee DS; Clark HB; Anderson JH
Ann Neurol; 1997 Dec; 42(6):933-50. PubMed ID: 9403487
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Clinical, neuropathological and genetic characteristics of spinocerebellar ataxia type 6 (SCA6)].
Ishikawa K; Mizusawa H
Nihon Rinsho; 1999 Apr; 57(4):880-5. PubMed ID: 10222783
[TBL] [Abstract][Full Text] [Related]
8. [A sporadic case of spinocerebellar ataxia 6 (SCA 6) with large CAG expansion of the CACNL1A4 gene].
Izumi Y; Sawada H; Matsuyama Z; Kawakami H; Udaka F; Nakamura S; Kameyama M
No To Shinkei; 1999 Feb; 51(2):167-70. PubMed ID: 10198907
[TBL] [Abstract][Full Text] [Related]
9. [Autopsy cases of hereditary ataxia pathologically diagnosed as the Japanese type of Joseph disease--cliniconeuropathological findings].
Kogure T; Oda T; Katoh Y
Seishin Shinkeigaku Zasshi; 1990; 92(3):161-83. PubMed ID: 2353076
[TBL] [Abstract][Full Text] [Related]
10. [Some problems on the clinical phenotype of Machado-Joseph disease in relation between their ages at onset].
Iwabuchi K; Kogure T; Oda T; Kato Y; Ohtani K; Endo K; Kosaka K; Amano N; Yagishita S
No To Shinkei; 1993 Mar; 45(3):246-54. PubMed ID: 8323819
[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. 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]
13. [Initial symptoms and mode of neurological progression in spinocerebellar ataxia type 6 (SCA6)].
Yabe I; Sasaki H; Yamashita I; Takei A; Fukazawa T; Hamada T; Tashiro K
Rinsho Shinkeigaku; 1998 Jun; 38(6):489-94. PubMed ID: 9847664
[TBL] [Abstract][Full Text] [Related]
14. An autopsy case of an aged patient with spinocerebellar ataxia type 2.
Ishida C; Komai K; Yonezawa K; Sakajiri K; Nitta E; Kawashima A; Yamada M
Neuropathology; 2011 Oct; 31(5):510-8. PubMed ID: 21134000
[TBL] [Abstract][Full Text] [Related]
15. [An autopsy case of hereditary cerebellar atrophy (Holmes-type) with mental symptoms and rhythmic skeletal myoclonus].
Ohta S; Mizutani Y; Anno M
No To Shinkei; 1994 Jul; 46(7):663-70. PubMed ID: 7946622
[TBL] [Abstract][Full Text] [Related]
16. [An apparently sporadic case with spinocerebellar ataxia type 1 (SCA1)].
Futamura N; Matsumura R; Murata K; Suzumura A; Takayanagi T
Rinsho Shinkeigaku; 1997 Aug; 37(8):708-10. PubMed ID: 9404150
[TBL] [Abstract][Full Text] [Related]
17. Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion.
Babovic-Vuksanovic D; Snow K; Patterson MC; Michels VV
Am J Med Genet; 1998 Oct; 79(5):383-7. PubMed ID: 9779806
[TBL] [Abstract][Full Text] [Related]
18. [An MRI study of hereditary spinocerebellar degenerations].
Konagaya M; Konagaya Y; Morishita S; Nakamuro T
Rinsho Shinkeigaku; 1990 Jun; 30(6):610-6. PubMed ID: 2225653
[TBL] [Abstract][Full Text] [Related]
19. [Clinico-genetic study of type I spinocerebelllar ataxia].
Svetel M; Culjković B; Sternić N; Dragasević B; Stojković I; Romac S; Kostić VS
Srp Arh Celok Lek; 1999; 127(5-6):157-62. PubMed ID: 10500422
[TBL] [Abstract][Full Text] [Related]
20. Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA6).
Sasaki H; Kojima H; Yabe I; Tashiro K; Hamada T; Sawa H; Hiraga H; Nagashima K
Acta Neuropathol; 1998 Feb; 95(2):199-204. PubMed ID: 9498057
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
