Sato K - Search Results

1

Meta-iodobenzylguanidine myocardial scintigraphy in Perry disease.

Mishima T, Fujioka S, Nishioka K, Li Y, Sato K, Houzen H, Yabe I, Shiomi K, Eriguchi M, Hara H, Hattori N, Tsuboi Y. Mishima T, et al. Among authors: sato k. Parkinsonism Relat Disord. 2021 Feb;83:49-53. doi: 10.1016/j.parkreldis.2020.12.017. Epub 2021 Jan 12. Parkinsonism Relat Disord. 2021. PMID: 33476877

2

[A case of deep cerebral venous thrombosis with sudden convulsion after delivery].

Hata D, Sato K, Chiba M, Ohtaki M, Tsumura N, Houzen H. Hata D, et al. Among authors: sato k. No To Shinkei. 2003 Jul;55(7):629-32. No To Shinkei. 2003. PMID: 12910999 Japanese.

3

Herpes simplex encephalitis.

Hata D, Sato K, Houzen H. Hata D, et al. Among authors: sato k. Intern Med. 2003 Oct;42(10):1057-8. doi: 10.2169/internalmedicine.42.1057. Intern Med. 2003. PMID: 14606730 Free article. No abstract available.

4

Transient subacute cerebellar ataxia in a patient with Lambert-Eaton myasthenic syndrome after intracranial aneurysm surgery.

Nakamura M, Yabe I, Sato K, Nakano F, Yaguchi H, Tsuji S, Shiraishi H, Yoneda M, Tanaka K, Motomura M, Sasaki H. Nakamura M, et al. Among authors: sato k. Clin Neurol Neurosurg. 2008 May;110(5):480-3. doi: 10.1016/j.clineuro.2008.01.002. Epub 2008 Mar 4. Clin Neurol Neurosurg. 2008. PMID: 18295972 Free article.

5

[Progressive cerebellar ataxia with euthyroid Hashimoto's disease--implication of autoantibodies associated with Hashimoto's disease in progressive cerebellar ataxia].

Yabe I, Sato K, Soma H, Sasaki H. Yabe I, et al. Among authors: sato k. Rinsho Shinkeigaku. 2008 Sep;48(9):640-5. doi: 10.5692/clinicalneurol.48.640. Rinsho Shinkeigaku. 2008. PMID: 19048946 Japanese.

6

[Reliability of the Japanese version of the Scale for the Assessment and Rating of Ataxia (SARA)].

Sato K, Yabe I, Soma H, Yasui K, Ito M, Shimohata T, Onodera O, Nakashima K, Sobue G, Nishizawa M, Sasaki H. Sato K, et al. Brain Nerve. 2009 May;61(5):591-5. Brain Nerve. 2009. PMID: 19514520 Japanese.

7

Estimation of skeletal muscle energy metabolism in Machado-Joseph disease using (31)P-MR spectroscopy.

Yabe I, Tha KK, Yokota T, Sato K, Soma H, Takei A, Terae S, Okita K, Sasaki H. Yabe I, et al. Among authors: sato k. Mov Disord. 2011 Jan;26(1):165-8. doi: 10.1002/mds.23335. Epub 2010 Sep 3. Mov Disord. 2011. PMID: 20818604

8

Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.

Sato K, Yabe I, Fukuda Y, Soma H, Nakahara Y, Tsuji S, Sasaki H. Sato K, et al. Arch Neurol. 2010 Oct;67(10):1257-62. doi: 10.1001/archneurol.2010.231. Arch Neurol. 2010. PMID: 20937954

9

Genetic analysis of two Japanese families with progressive external ophthalmoplegia and parkinsonism.

Sato K, Yabe I, Yaguchi H, Nakano F, Kunieda Y, Saitoh S, Sasaki H. Sato K, et al. J Neurol. 2011 Jul;258(7):1327-32. doi: 10.1007/s00415-011-5936-x. Epub 2011 Feb 8. J Neurol. 2011. PMID: 21301859 Free article.

10

Clinical, pathological, and genetic mutation analysis of sporadic inclusion body myositis in Japanese people.

Cai H, Yabe I, Sato K, Kano T, Nakamura M, Hozen H, Sasaki H. Cai H, et al. Among authors: sato k. J Neurol. 2012 Sep;259(9):1913-22. doi: 10.1007/s00415-012-6439-0. Epub 2012 Feb 17. J Neurol. 2012. PMID: 22349865 Free article.

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