211 related articles for article (PubMed ID: 10090679)
1. Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies.
Estrada R; Galarraga J; Orozco G; Nodarse A; Auburger G
Acta Neuropathol; 1999 Mar; 97(3):306-10. PubMed ID: 10090679
[TBL] [Abstract][Full Text] [Related]
2. Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.
Bürk K; Abele M; Fetter M; Dichgans J; Skalej M; Laccone F; Didierjean O; Brice A; Klockgether T
Brain; 1996 Oct; 119 ( Pt 5)():1497-505. PubMed ID: 8931575
[TBL] [Abstract][Full Text] [Related]
3. Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions.
Gilman S; Sima AA; Junck L; Kluin KJ; Koeppe RA; Lohman ME; Little R
Ann Neurol; 1996 Feb; 39(2):241-55. PubMed ID: 8967756
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Autosomal dominant cerebellar ataxia type I. MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3.
Klockgether T; Skalej M; Wedekind D; Luft AR; Welte D; Schulz JB; Abele M; Bürk K; Laccone F; Brice A; Dichgans J
Brain; 1998 Sep; 121 ( Pt 9)():1687-93. PubMed ID: 9762957
[TBL] [Abstract][Full Text] [Related]
6. Supratentorial atrophy in spinocerebellar ataxia type 2: MRI study of 20 patients.
Giuffrida S; Saponara R; Restivo DA; Trovato Salinaro A; Tomarchio L; Pugliares P; Fabbri G; Maccagnano C
J Neurol; 1999 May; 246(5):383-8. PubMed ID: 10399871
[TBL] [Abstract][Full Text] [Related]
7. [Correlation of clinichopathological features and CAG repeats in SCA2].
Koyano S; Iwabuchi K
Nihon Rinsho; 1999 Apr; 57(4):805-10. PubMed ID: 10222770
[TBL] [Abstract][Full Text] [Related]
8. Infantile-onset spinocerebellar ataxia: MR and CT findings.
Koskinen T; Valanne L; Ketonen LM; Pihko H
AJNR Am J Neuroradiol; 1995 Aug; 16(7):1427-33. PubMed ID: 7484627
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family.
Martin JJ; Van Regemorter N; Krols L; Brucher JM; de Barsy T; Szliwowski H; Evrard P; Ceuterick C; Tassignon MJ; Smet-Dieleman H
Acta Neuropathol; 1994; 88(4):277-86. PubMed ID: 7839819
[TBL] [Abstract][Full Text] [Related]
11. Clinicopathology of spinocerebellar degeneration: its correlation to the unstable CAG repeat of the affected gene.
Yagishita S; Inoue M
Pathol Int; 1997 Jan; 47(1):1-15. PubMed ID: 9051687
[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. ADC mapping of neurodegeneration in the brainstem and cerebellum of patients with progressive ataxias.
Della Nave R; Foresti S; Tessa C; Moretti M; Ginestroni A; Gavazzi C; Guerrini L; Salvi F; Piacentini S; Mascalchi M
Neuroimage; 2004 Jun; 22(2):698-705. PubMed ID: 15193598
[TBL] [Abstract][Full Text] [Related]
14. [Autopsy case of SCA2 with Parkinsonian phenotype].
Yomono HS; Kurisaki H; Hebisawa A; Sakiyama Y; Saito Y; Murayama S
Rinsho Shinkeigaku; 2010 Mar; 50(3):156-62. PubMed ID: 20235484
[TBL] [Abstract][Full Text] [Related]
15. Brain acetylcholinesterase activity is markedly reduced in dominantly-inherited olivopontocerebellar atrophy.
Kish SJ; Schut L; Simmons J; Gilbert J; Chang LJ; Rebbetoy M
J Neurol Neurosurg Psychiatry; 1988 Apr; 51(4):544-8. PubMed ID: 3164041
[TBL] [Abstract][Full Text] [Related]
16. Neuropathological background of oculomotor disturbances in olivopontocerebellar atrophy with special reference to slow saccade.
Mizutani T; Satoh J; Morimatsu Y
Clin Neuropathol; 1988; 7(2):53-61. PubMed ID: 3164663
[TBL] [Abstract][Full Text] [Related]
17. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.
Pujana MA; Corral J; Gratacòs M; Combarros O; Berciano J; Genís D; Banchs I; Estivill X; Volpini V
Hum Genet; 1999 Jun; 104(6):516-22. PubMed ID: 10453742
[TBL] [Abstract][Full Text] [Related]
18. Brain phospholipids and fatty acids in Friedreich's ataxia and spinocerebellar atrophy type-1.
Eder K; Kish SJ; Kirchgessner M; Ross BM
Mov Disord; 1998 Sep; 13(5):813-9. PubMed ID: 9756151
[TBL] [Abstract][Full Text] [Related]
19. Brainstem neurodegeneration correlates with clinical dysfunction in SCA1 but not in SCA2. A quantitative volumetric, diffusion and proton spectroscopy MR study.
Guerrini L; Lolli F; Ginestroni A; Belli G; Della Nave R; Tessa C; Foresti S; Cosottini M; Piacentini S; Salvi F; Plasmati R; De Grandis D; Siciliano G; Filla A; Mascalchi M
Brain; 2004 Aug; 127(Pt 8):1785-95. PubMed ID: 15240431
[TBL] [Abstract][Full Text] [Related]
20. Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings.
Orozco G; Estrada R; Perry TL; Araña J; Fernandez R; Gonzalez-Quevedo A; Galarraga J; Hansen S
J Neurol Sci; 1989 Oct; 93(1):37-50. PubMed ID: 2809629
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
