527 related articles for article (PubMed ID: 17420317)
1. Multiplex families with multiple system atrophy.
Hara K; Momose Y; Tokiguchi S; Shimohata M; Terajima K; Onodera O; Kakita A; Yamada M; Takahashi H; Hirasawa M; Mizuno Y; Ogata K; Goto J; Kanazawa I; Nishizawa M; Tsuji S
Arch Neurol; 2007 Apr; 64(4):545-51. PubMed ID: 17420317
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Heredity in multiple system atrophy.
Soma H; Yabe I; Takei A; Fujiki N; Yanagihara T; Sasaki H
J Neurol Sci; 2006 Jan; 240(1-2):107-10. PubMed ID: 16307759
[TBL] [Abstract][Full Text] [Related]
4. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
Tang B; Xia J; Wang D; Tang X; Shen L; Liu C; Dai H; Yan X; Pan Q; Xiao J; Zhang B; Ou Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):281-4. PubMed ID: 10514531
[TBL] [Abstract][Full Text] [Related]
5. Frequency analysis and clinical characterization of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Korean patients.
Lee WY; Jin DK; Oh MR; Lee JE; Song SM; Lee EA; Kim GM; Chung JS; Lee KH
Arch Neurol; 2003 Jun; 60(6):858-63. PubMed ID: 12810491
[TBL] [Abstract][Full Text] [Related]
6. Analyses of copy number and mRNA expression level of the alpha-synuclein gene in multiple system atrophy.
Jin H; Ishikawa K; Tsunemi T; Ishiguro T; Amino T; Mizusawa H
J Med Dent Sci; 2008 Mar; 55(1):145-53. PubMed ID: 19845160
[TBL] [Abstract][Full Text] [Related]
7. [Molecular genetics and its clinical application in the diagnosis of spinocerebellar ataxias].
Xie QY; Liang XL; Li XH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):71-3. PubMed ID: 15696485
[TBL] [Abstract][Full Text] [Related]
8. Longitudinal MRI study of multiple system atrophy - when do the findings appear, and what is the course?
Horimoto Y; Aiba I; Yasuda T; Ohkawa Y; Katayama T; Yokokawa Y; Goto A; Ito Y
J Neurol; 2002 Jul; 249(7):847-54. PubMed ID: 12140668
[TBL] [Abstract][Full Text] [Related]
9. Multiple system atrophy and CAG repeat length: A genetic screening of polyglutamine disease genes in Italian patients.
Mongelli A; Sarro L; Rizzo E; Nanetti L; Meucci N; Pezzoli G; Goldwurm S; Taroni F; Mariotti C; Gellera C
Neurosci Lett; 2018 Jun; 678():37-42. PubMed ID: 29715545
[TBL] [Abstract][Full Text] [Related]
10. Grading of neuropathology in multiple system atrophy: proposal for a novel scale.
Jellinger KA; Seppi K; Wenning GK
Mov Disord; 2005 Aug; 20 Suppl 12():S29-36. PubMed ID: 16092088
[TBL] [Abstract][Full Text] [Related]
11. Patterns of fractional anisotropy changes in white matter of cerebellar peduncles distinguish spinocerebellar ataxia-1 from multiple system atrophy and other ataxia syndromes.
Prakash N; Hageman N; Hua X; Toga AW; Perlman SL; Salamon N
Neuroimage; 2009 Aug; 47 Suppl 2():T72-81. PubMed ID: 19446636
[TBL] [Abstract][Full Text] [Related]
12. MSA-C is the predominant clinical phenotype of MSA in Japan: analysis of 142 patients with probable MSA.
Yabe I; Soma H; Takei A; Fujiki N; Yanagihara T; Sasaki H
J Neurol Sci; 2006 Nov; 249(2):115-21. PubMed ID: 16828805
[TBL] [Abstract][Full Text] [Related]
13. Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17).
Rolfs A; Koeppen AH; Bauer I; Bauer P; Buhlmann S; Topka H; Schöls L; Riess O
Ann Neurol; 2003 Sep; 54(3):367-75. PubMed ID: 12953269
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. [Multiple system atrophy].
Damon-Perrière N; Tison F; Meissner WG
Psychol Neuropsychiatr Vieil; 2010 Sep; 8(3):179-91. PubMed ID: 20739256
[TBL] [Abstract][Full Text] [Related]
17. Evaluating posterolateral linearization of the putaminal margin with magnetic resonance imaging to diagnose the Parkinson variant of multiple system atrophy.
Ito S; Shirai W; Hattori T
Mov Disord; 2007 Mar; 22(4):578-81. PubMed ID: 17260343
[TBL] [Abstract][Full Text] [Related]
18. Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia.
Le Ber I; Clot F; Vercueil L; Camuzat A; Viémont M; Benamar N; De Liège P; Ouvrard-Hernandez AM; Pollak P; Stevanin G; Brice A; Dürr A
Neurology; 2006 Nov; 67(10):1769-73. PubMed ID: 17130408
[TBL] [Abstract][Full Text] [Related]
19. Screening for premutation in the FMR1 gene in male patients suspected of spinocerebellar ataxia.
Rajkiewicz M; Sułek-Piatkowska A; Krysa W; Zdzienicka E; Szirkowiec W; Zaremba J
Neurol Neurochir Pol; 2008; 42(6):497-504. PubMed ID: 19235102
[TBL] [Abstract][Full Text] [Related]
20. [Towards more efficient clinical trials for multiple system atrophy in Japan].
Ichikawa Y
Brain Nerve; 2012 Oct; 64(10):1141-9. PubMed ID: 23037604
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
