266 related articles for article (PubMed ID: 22353852)
1. Spinocerebellar ataxia type 31 exists in northeast China.
Ouyang Y; He Z; Li L; Qin X; Zhao Y; Yuan L
J Neurol Sci; 2012 May; 316(1-2):164-7. PubMed ID: 22353852
[TBL] [Abstract][Full Text] [Related]
2. Comparisons of acoustic function in SCA31 and other forms of ataxias.
Ikeda Y; Nagai M; Kurata T; Yamashita T; Ohta Y; Nagotani S; Deguchi K; Takehisa Y; Shiro Y; Matsuura T; Abe K
Neurol Res; 2011 May; 33(4):427-32. PubMed ID: 21535943
[TBL] [Abstract][Full Text] [Related]
3. Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration.
Wolf NI; Koenig M
Handb Clin Neurol; 2013; 113():1869-78. PubMed ID: 23622410
[TBL] [Abstract][Full Text] [Related]
4. Spinocerebellar ataxia 13 and 25.
Stevanin G; Dürr A
Handb Clin Neurol; 2012; 103():549-53. PubMed ID: 21827913
[TBL] [Abstract][Full Text] [Related]
5. Rare frequency of downbeat positioning nystagmus in spinocerebellar ataxia type 31.
Yabe I; Matsushima M; Yoshida K; Ishikawa K; Shirai S; Takahashi I; Sasaki H
J Neurol Sci; 2015 Mar; 350(1-2):90-2. PubMed ID: 25684342
[TBL] [Abstract][Full Text] [Related]
6. Spinocerebellar ataxia type 31: A clinical and radiological literature review.
Saucier J; Al-Qadi M; Amor MB; Ishikawa K; Chamard-Witkowski L
J Neurol Sci; 2023 Jan; 444():120527. PubMed ID: 36563608
[TBL] [Abstract][Full Text] [Related]
7. Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan.
Sakai H; Yoshida K; Shimizu Y; Morita H; Ikeda S; Matsumoto N
Neurogenetics; 2010 Oct; 11(4):409-15. PubMed ID: 20424877
[TBL] [Abstract][Full Text] [Related]
8. [Clinical features and MRI findings in spinocerebellar ataxia type 31 (SCA31) comparing with spinocerebellar ataxia type 6 (SCA6)].
Sakakibara S; Aiba I; Saito Y; Inukai A; Ishikawa K; Mizusawa H
Rinsho Shinkeigaku; 2014; 54(6):473-9. PubMed ID: 24990830
[TBL] [Abstract][Full Text] [Related]
9. Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4.
Hiramoto K; Kawakami H; Inoue K; Seki T; Maruyama H; Morino H; Matsumoto M; Kurisu K; Sakai N
Mov Disord; 2006 Sep; 21(9):1355-60. PubMed ID: 16763984
[TBL] [Abstract][Full Text] [Related]
10. Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31.
Ohmori H; Hara A; Ishikawa K; Mizusawa H; Ando Y
J Neurogenet; 2015; 29(2-3):80-4. PubMed ID: 26004545
[TBL] [Abstract][Full Text] [Related]
11. Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese.
Onodera Y; Aoki M; Mizuno H; Warita H; Shiga Y; Itoyama Y
Neurology; 2006 Oct; 67(7):1300-2. PubMed ID: 17030774
[TBL] [Abstract][Full Text] [Related]
12. Clinical and genetic characterization of 16q-linked autosomal dominant spinocerebellar ataxia in South Kyushu, Japan.
Hirano R; Takashima H; Okubo R; Okamoto Y; Maki Y; Ishida S; Suehara M; Hokezu Y; Arimura K
J Hum Genet; 2009 Jul; 54(7):377-81. PubMed ID: 19444286
[TBL] [Abstract][Full Text] [Related]
13. Abnormal RNA structures (RNA foci) containing a penta-nucleotide repeat (UGGAA)n in the Purkinje cell nucleus is associated with spinocerebellar ataxia type 31 pathogenesis.
Niimi Y; Takahashi M; Sugawara E; Umeda S; Obayashi M; Sato N; Ishiguro T; Higashi M; Eishi Y; Mizusawa H; Ishikawa K
Neuropathology; 2013 Dec; 33(6):600-11. PubMed ID: 23607545
[TBL] [Abstract][Full Text] [Related]
14. Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics.
Fujioka S; Sundal C; Wszolek ZK
Orphanet J Rare Dis; 2013 Jan; 8():14. PubMed ID: 23331413
[TBL] [Abstract][Full Text] [Related]
15. A large family with spinocerebellar ataxia type 6 in Iran: a clinical and genetic study.
Shimazaki H; Vazifehmand R; Heidari MH; Khorram-Khorshid HR; Saber S; Hejazi S; Aghakhani-Moghadam F; Ouyang Y; Honda J; Nakano I; Takiyama Y
Arch Iran Med; 2008 Jul; 11(4):459-62. PubMed ID: 18588381
[TBL] [Abstract][Full Text] [Related]
16. [Overview of Hereditary Spinocerebellar Ataxias in Japan].
Tada M; Yokoseki A; Onodera O
Brain Nerve; 2017 Aug; 69(8):879-890. PubMed ID: 28819072
[TBL] [Abstract][Full Text] [Related]
17. Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients.
Dragasević NT; Culjković B; Klein C; Ristić A; Keckarević M; Topisirović I; Vukosavić S; Svetel M; Kock N; Stefanova E; Romac S; Kostić VS
Mov Disord; 2006 Feb; 21(2):187-91. PubMed ID: 16149098
[TBL] [Abstract][Full Text] [Related]
18. Case of infantile onset spinocerebellar ataxia type 5.
Jacob FD; Ho ES; Martinez-Ojeda M; Darras BT; Khwaja OS
J Child Neurol; 2013 Oct; 28(10):1292-5. PubMed ID: 22914369
[TBL] [Abstract][Full Text] [Related]
19. Clinical and genetic epidemiological study of 16q22.1-linked autosomal dominant cerebellar ataxia in western Japan.
Hayashi M; Adachi Y; Mori M; Nakano T; Nakashima K
Acta Neurol Scand; 2007 Aug; 116(2):123-7. PubMed ID: 17661799
[TBL] [Abstract][Full Text] [Related]
20. Natural History of Spinocerebellar Ataxia Type 31: a 4-Year Prospective Study.
Nakamura K; Yoshida K; Matsushima A; Shimizu Y; Sato S; Yahikozawa H; Ohara S; Yazawa M; Ushiyama M; Sato M; Morita H; Inoue A; Ikeda SI
Cerebellum; 2017 Apr; 16(2):518-524. PubMed ID: 27830516
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
