NS041547/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2004	3
2005	1
2006	4
2007	6
2008	1
2009	1
2010	3
2011	2
2012	5
2013	5
2014	1
2015	2
2024	0

1

How much expansion to be diseased?: toward repeat size and myotonic dystrophy type 2.

Schoser B, Ashizawa T. Schoser B, et al. Neurology. 2009 Feb 10;72(6):484-5. doi: 10.1212/01.wnl.0000341937.70150.64. Neurology. 2009. PMID: 19204257 No abstract available.

2

Spinocerebellar ataxia type 10.

Ashizawa T. Ashizawa T. Handb Clin Neurol. 2012;103:507-19. doi: 10.1016/B978-0-444-51892-7.00032-2. Handb Clin Neurol. 2012. PMID: 21827910 Free PMC article. Review. No abstract available.

3

Bolivian kindred with combined spinocerebellar ataxia types 2 and 10.

Baizabal-Carvallo JF, Xia G, Botros P, Laguna J, Ashizawa T, Jankovic J. Baizabal-Carvallo JF, et al. Acta Neurol Scand. 2015 Aug;132(2):139-42. doi: 10.1111/ane.12371. Epub 2015 Jan 28. Acta Neurol Scand. 2015. PMID: 25630585 Free PMC article.

4

Olfactory impairment in familial ataxias.

Moscovich M, Munhoz RP, Teive HA, Raskin S, Carvalho Mde J, Barbosa ER, Ranvaud R, Liu J, McFarland K, Ashizawa T, Lees AJ, Silveira-Moriyama L. Moscovich M, et al. J Neurol Neurosurg Psychiatry. 2012 Oct;83(10):970-4. doi: 10.1136/jnnp-2012-302770. Epub 2012 Jul 11. J Neurol Neurosurg Psychiatry. 2012. PMID: 22791905 Free PMC article.

5

Transgenic models of spinocerebellar ataxia type 10: modeling a repeat expansion disorder.

McFarland KN, Ashizawa T. McFarland KN, et al. Genes (Basel). 2012 Jul 30;3(3):481-491. doi: 10.3390/genes3030481. eCollection 2012 Sep. Genes (Basel). 2012. PMID: 24533179 Free PMC article. Review.

6

Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families.

Teive HA, Munhoz RP, Arruda WO, Lopes-Cendes I, Raskin S, Werneck LC, Ashizawa T. Teive HA, et al. Clinics (Sao Paulo). 2012;67(5):443-9. doi: 10.6061/clinics/2012(05)07. Clinics (Sao Paulo). 2012. PMID: 22666787 Free PMC article.

7

Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population.

Alonso E, Martínez-Ruano L, De Biase I, Mader C, Ochoa A, Yescas P, Gutiérrez R, White M, Ruano L, Fragoso-Benítez M, Ashizawa T, Bidichandani SI, Rasmussen A. Alonso E, et al. Mov Disord. 2007 May 15;22(7):1050-3. doi: 10.1002/mds.21470. Mov Disord. 2007. PMID: 17427938

8

Spinocerebellar ataxia type 10: Frequency of epilepsy in a large sample of Brazilian patients.

Teive HA, Munhoz RP, Raskin S, Arruda WO, de Paola L, Werneck LC, Ashizawa T. Teive HA, et al. Mov Disord. 2010 Dec 15;25(16):2875-8. doi: 10.1002/mds.23324. Mov Disord. 2010. PMID: 20818609 Free PMC article.

9

Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17.

Rasmussen A, De Biase I, Fragoso-Benítez M, Macías-Flores MA, Yescas P, Ochoa A, Ashizawa T, Alonso ME, Bidichandani SI. Rasmussen A, et al. Ann Neurol. 2007 Jun;61(6):607-10. doi: 10.1002/ana.21139. Ann Neurol. 2007. PMID: 17474109

10

Detection of large pathogenic expansions in FRDA1, SCA10, and SCA12 genes using a simple fluorescent repeat-primed PCR assay.

Cagnoli C, Michielotto C, Matsuura T, Ashizawa T, Margolis RL, Holmes SE, Gellera C, Migone N, Brusco A. Cagnoli C, et al. J Mol Diagn. 2004 May;6(2):96-100. doi: 10.1016/S1525-1578(10)60496-5. J Mol Diagn. 2004. PMID: 15096564 Free PMC article.

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