180 related articles for article (PubMed ID: 12235319)
1. Paradoxical absence of nuclear inclusion in cerebellar Purkinje cells of hereditary ataxias linked to CAG expansion.
Koyano S; Iwabuchi K; Yagishita S; Kuroiwa Y; Uchihara T
J Neurol Neurosurg Psychiatry; 2002 Oct; 73(4):450-2. PubMed ID: 12235319
[TBL] [Abstract][Full Text] [Related]
2. Progress in pathogenesis studies of spinocerebellar ataxia type 1.
Cummings CJ; Orr HT; Zoghbi HY
Philos Trans R Soc Lond B Biol Sci; 1999 Jun; 354(1386):1079-81. PubMed ID: 10434309
[TBL] [Abstract][Full Text] [Related]
3. Non-expanded polyglutamine proteins in intranuclear inclusions of hereditary ataxias--triple-labeling immunofluorescence study.
Uchihara T; Fujigasaki H; Koyano S; Nakamura A; Yagishita S; Iwabuchi K
Acta Neuropathol; 2001 Aug; 102(2):149-52. PubMed ID: 11563629
[TBL] [Abstract][Full Text] [Related]
4. Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases.
Pang JT; Giunti P; Chamberlain S; An SF; Vitaliani R; Scaravilli T; Martinian L; Wood NW; Scaravilli F; Ansorge O
Brain; 2002 Mar; 125(Pt 3):656-63. PubMed ID: 11872620
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions.
Holmberg M; Duyckaerts C; Dürr A; Cancel G; Gourfinkel-An I; Damier P; Faucheux B; Trottier Y; Hirsch EC; Agid Y; Brice A
Hum Mol Genet; 1998 May; 7(5):913-8. PubMed ID: 9536097
[TBL] [Abstract][Full Text] [Related]
7. Nuclear inclusions in spinocerebellar ataxia type 1.
Duyckaerts C; Dürr A; Cancel G; Brice A
Acta Neuropathol; 1999 Feb; 97(2):201-7. PubMed ID: 9928833
[TBL] [Abstract][Full Text] [Related]
8. Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: triple-labeling immunofluorescent study.
Koyano S; Uchihara T; Fujigasaki H; Nakamura A; Yagishita S; Iwabuchi K
Neurosci Lett; 1999 Oct; 273(2):117-20. PubMed ID: 10505630
[TBL] [Abstract][Full Text] [Related]
9. Abundant expression and cytoplasmic aggregations of [alpha]1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6.
Ishikawa K; Fujigasaki H; Saegusa H; Ohwada K; Fujita T; Iwamoto H; Komatsuzaki Y; Toru S; Toriyama H; Watanabe M; Ohkoshi N; Shoji S; Kanazawa I; Tanabe T; Mizusawa H
Hum Mol Genet; 1999 Jul; 8(7):1185-93. PubMed ID: 10369863
[TBL] [Abstract][Full Text] [Related]
10. Mapping of Purkinje neuron loss and polyglucosan body accumulation in hereditary cerebellar degeneration in Scottish terriers.
Urkasemsin G; Linder KE; Bell JS; de Lahunta A; Olby NJ
Vet Pathol; 2012 Sep; 49(5):852-9. PubMed ID: 21753036
[TBL] [Abstract][Full Text] [Related]
11. Increased protein kinase C gamma activity induces Purkinje cell pathology in a mouse model of spinocerebellar ataxia 14.
Ji J; Hassler ML; Shimobayashi E; Paka N; Streit R; Kapfhammer JP
Neurobiol Dis; 2014 Oct; 70():1-11. PubMed ID: 24937631
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. Spinocerebellar ataxia type 4 (SCA4): Initial pathoanatomical study reveals widespread cerebellar and brainstem degeneration.
Hellenbroich Y; Gierga K; Reusche E; Schwinger E; Deller T; de Vos RA; Zühlke C; Rüb U
J Neural Transm (Vienna); 2006 Jul; 113(7):829-43. PubMed ID: 16362839
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Clinicopathologic investigation of a family with expanded SCA8 CTA/CTG repeats.
Ito H; Kawakami H; Wate R; Matsumoto S; Imai T; Hirano A; Kusaka H
Neurology; 2006 Oct; 67(8):1479-81. PubMed ID: 17060579
[TBL] [Abstract][Full Text] [Related]
16. Presenile onset of spinocerebellar ataxia type 1 presenting with conspicuous psychiatric symptoms and widespread anti-expanded polyglutamine antibody- and fused in sarcoma antibody-immunopositive pathology.
Iwasaki Y; Mori K; Ito M; Mimuro M; Yoshida M
Psychogeriatrics; 2015 Sep; 15(3):212-7. PubMed ID: 25920043
[TBL] [Abstract][Full Text] [Related]
17. Autosomal dominant spinocerebellar degenerations. Clinical, pathological, and genetic correlations.
Iwabuchi K; Tsuchiya K; Uchihara T; Yagishita S
Rev Neurol (Paris); 1999 Apr; 155(4):255-70. PubMed ID: 10367323
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. Familial frontotemporal dementia with neuronal intranuclear inclusions is not a polyglutamine expansion disease.
Mackenzie IR; Butland SL; Devon RS; Dwosh E; Feldman H; Lindholm C; Neal SJ; Ouellette BF; Leavitt BR
BMC Neurol; 2006 Aug; 6():32. PubMed ID: 16945149
[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]
