218 related articles for article (PubMed ID: 21128038)
21. Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7.
Rüb U; Brunt ER; Petrasch-Parwez E; Schöls L; Theegarten D; Auburger G; Seidel K; Schultz C; Gierga K; Paulson H; van Broeckhoven C; Deller T; de Vos RA
Neuropathol Appl Neurobiol; 2006 Dec; 32(6):635-49. PubMed ID: 17083478
[TBL] [Abstract][Full Text] [Related]
22. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia.
Geschwind DH; Perlman S; Figueroa CP; Treiman LJ; Pulst SM
Am J Hum Genet; 1997 Apr; 60(4):842-50. PubMed ID: 9106530
[TBL] [Abstract][Full Text] [Related]
23. Hypergonadotropic hypogonadism in spinocerebellar ataxia type 2: a case report.
Kwon DY; Park MH
J Sex Med; 2009 Jun; 6(6):1779-1782. PubMed ID: 19473475
[TBL] [Abstract][Full Text] [Related]
24. Germ-line CAG repeat instability causes extreme CAG repeat expansion with infantile-onset spinocerebellar ataxia type 2.
Vinther-Jensen T; Ek J; Duno M; Skovby F; Hjermind LE; Nielsen JE; Nielsen TT
Eur J Hum Genet; 2013 Jun; 21(6):626-9. PubMed ID: 23047744
[TBL] [Abstract][Full Text] [Related]
25. Neuropathological staging of spinocerebellar ataxia type 2 by semiquantitative 1C2-positive neuron typing. Nuclear translocation of cytoplasmic 1C2 underlies disease progression of spinocerebellar ataxia type 2.
Koyano S; Yagishita S; Kuroiwa Y; Tanaka F; Uchihara T
Brain Pathol; 2014 Nov; 24(6):599-606. PubMed ID: 24674145
[TBL] [Abstract][Full Text] [Related]
26. The parkinsonian phenotype of spinocerebellar ataxia type 2.
Lu CS; Wu Chou YH; Kuo PC; Chang HC; Weng YH
Arch Neurol; 2004 Jan; 61(1):35-8. PubMed ID: 14732617
[TBL] [Abstract][Full Text] [Related]
27. Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2.
Wang C; Xu Y; Feng X; Ma J; Xie S; Zhang Y; Tang BS; Chan P
Neurobiol Aging; 2015 Jan; 36(1):545.e1-7. PubMed ID: 25189117
[TBL] [Abstract][Full Text] [Related]
28. [Spinocerebellar ataxias type 1 and 2: comparison of clinical, electrophysiological and magnetic resonance evaluation].
Rakowicz M; Zdzienicka E; Poniatowska R; Waliniowska E; Sułek A; Jakubowska T; Niedzielska K; Rola R; Wierzbicka A; Hoffman-Zacharska D; Głazowski C; Jakubczyk T; Niewiadomska M; Zaremba J
Neurol Neurochir Pol; 2005; 39(4):263-275. PubMed ID: 16096942
[TBL] [Abstract][Full Text] [Related]
29. Spinocerebellar ataxia type 7 (SCA7): first report of a systematic neuropathological study of the brain of a patient with a very short expanded CAG-repeat.
Rüb U; Brunt ER; Gierga K; Seidel K; Schultz C; Schöls L; Auburger G; Heinsen H; Ippel PF; Glimmerveen WF; Wittebol-Post D; Arai K; Deller T; de Vos RA
Brain Pathol; 2005 Oct; 15(4):287-95. PubMed ID: 16389941
[TBL] [Abstract][Full Text] [Related]
30. Spinocerebellar ataxia type 2 (SCA2) with white matter involvement.
Armstrong J; Bonaventura I; Rojo A; González G; Corral J; Nadal N; Volpini V; Ferrer I
Neurosci Lett; 2005 Jun; 381(3):247-51. PubMed ID: 15896478
[TBL] [Abstract][Full Text] [Related]
31. CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2).
Hayes S; Turecki G; Brisebois K; Lopes-Cendes I; Gaspar C; Riess O; Ranum LP; Pulst SM; Rouleau GA
Hum Mol Genet; 2000 Jul; 9(12):1753-8. PubMed ID: 10915763
[TBL] [Abstract][Full Text] [Related]
32. Spinocerebellar Ataxia Type 2.
Scoles DR; Pulst SM
Adv Exp Med Biol; 2018; 1049():175-195. PubMed ID: 29427103
[TBL] [Abstract][Full Text] [Related]
33. Genetic profile and clinical characteristics of Chinese patients with spinocerebellar ataxia type 2: A multicenter experience over 10 years.
Yang L; Dong Y; Ma Y; Ni W; Wu ZY
Eur J Neurol; 2021 Mar; 28(3):955-964. PubMed ID: 33070405
[TBL] [Abstract][Full Text] [Related]
34. Thalamic involvement in a spinocerebellar ataxia type 2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevance.
Rüb U; Del Turco D; Del Tredici K; de Vos RA; Brunt ER; Reifenberger G; Seifried C; Schultz C; Auburger G; Braak H
Brain; 2003 Oct; 126(Pt 10):2257-72. PubMed ID: 12847080
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Deranged calcium signaling and neurodegeneration in spinocerebellar ataxia type 2.
Liu J; Tang TS; Tu H; Nelson O; Herndon E; Huynh DP; Pulst SM; Bezprozvanny I
J Neurosci; 2009 Jul; 29(29):9148-62. PubMed ID: 19625506
[TBL] [Abstract][Full Text] [Related]
37. Three spinocerebellar ataxia type 2 siblings with ataxia, parkinsonism, and motor neuronopathy.
Nishikawa N; Nagai M; Tsujii T; Tanabe N; Takashima H; Nomoto M
Intern Med; 2011; 50(13):1429-32. PubMed ID: 21720065
[TBL] [Abstract][Full Text] [Related]
38. Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2.
Van Damme P; Veldink JH; van Blitterswijk M; Corveleyn A; van Vught PW; Thijs V; Dubois B; Matthijs G; van den Berg LH; Robberecht W
Neurology; 2011 Jun; 76(24):2066-72. PubMed ID: 21562247
[TBL] [Abstract][Full Text] [Related]
39. Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA2).
Gierga K; Bürk K; Bauer M; Orozco Diaz G; Auburger G; Schultz C; Vuksic M; Schöls L; de Vos RA; Braak H; Deller T; Rüb U
Acta Neuropathol; 2005 Jun; 109(6):617-31. PubMed ID: 15906049
[TBL] [Abstract][Full Text] [Related]
40. Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset.
Pulst SM; Santos N; Wang D; Yang H; Huynh D; Velazquez L; Figueroa KP
Brain; 2005 Oct; 128(Pt 10):2297-303. PubMed ID: 16000334
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]