Ashizawa T - Search Results

1

Rosa AL, Ashizawa T. Rosa AL, et al. Among authors: ashizawa t. Neurol Clin. 2002 Aug;20(3):727-57, vii. doi: 10.1016/s0733-8619(02)00008-7. Neurol Clin. 2002. PMID: 12432828 Review.

2

Screening for mutations in the MECP2 (Rett syndrome) gene in Gilles de la Tourette syndrome.

Rosa AL, Jankovic J, Ashizawa T. Rosa AL, et al. Among authors: ashizawa t. Arch Neurol. 2003 Apr;60(4):502-3. doi: 10.1001/archneur.60.4.502. Arch Neurol. 2003. PMID: 12707062 No abstract available.

3

MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a Drosophila model of myotonic dystrophy type 1.

de Haro M, Al-Ramahi I, De Gouyon B, Ukani L, Rosa A, Faustino NA, Ashizawa T, Cooper TA, Botas J. de Haro M, et al. Among authors: ashizawa t. Hum Mol Genet. 2006 Jul 1;15(13):2138-45. doi: 10.1093/hmg/ddl137. Epub 2006 May 24. Hum Mol Genet. 2006. PMID: 16723374

4

Ataxia.

Akbar U, Ashizawa T. Akbar U, et al. Among authors: ashizawa t. Neurol Clin. 2015 Feb;33(1):225-48. doi: 10.1016/j.ncl.2014.09.004. Neurol Clin. 2015. PMID: 25432731 Free PMC article. Review.

5

Molecular basis of neuromuscular diseases.

Chance PF, Ashizawa T, Hoffman EP, Crawford TO. Chance PF, et al. Among authors: ashizawa t. Phys Med Rehabil Clin N Am. 1998 Feb;9(1):49-81, vi. Phys Med Rehabil Clin N Am. 1998. PMID: 9894134 Review.

6

Genetic testing in spinocerebellar ataxias: defining a clinical role.

Tan EK, Ashizawa T. Tan EK, et al. Among authors: ashizawa t. Arch Neurol. 2001 Feb;58(2):191-5. doi: 10.1001/archneur.58.2.191. Arch Neurol. 2001. PMID: 11176956 Review.

7

Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10.

Rasmussen A, Matsuura T, Ruano L, Yescas P, Ochoa A, Ashizawa T, Alonso E. Rasmussen A, et al. Among authors: ashizawa t. Ann Neurol. 2001 Aug;50(2):234-9. doi: 10.1002/ana.1081. Ann Neurol. 2001. PMID: 11506407

8

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. Among authors: ashizawa t. Ann Neurol. 2007 Jun;61(6):607-10. doi: 10.1002/ana.21139. Ann Neurol. 2007. PMID: 17474109

9

Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy.

Matsuura T, Achari M, Khajavi M, Bachinski LL, Zoghbi HY, Ashizawa T. Matsuura T, et al. Among authors: ashizawa t. Ann Neurol. 1999 Mar;45(3):407-11. doi: 10.1002/1531-8249(199903)45:3<407::aid-ana21>3.0.co;2-d. Ann Neurol. 1999. PMID: 10072060

10

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. Among authors: ashizawa t. Mov Disord. 2007 May 15;22(7):1050-3. doi: 10.1002/mds.21470. Mov Disord. 2007. PMID: 17427938

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