Hirano M - Search Results

1

Abnormal cystatin C levels in two patients with bardet-biedl syndrome.

Hirano M, Ohishi M, Yamashita T, Ikuno Y, Iwahashi H, Mano T, Ishihara R, Tanaka I, Yanagihara K, Isono C, Sakamoto H, Nakamura Y, Kusunoki S. Hirano M, et al. Clin Med Insights Case Rep. 2011;4:17-20. doi: 10.4137/CCRep.S6622. Epub 2011 Mar 10. Clin Med Insights Case Rep. 2011. PMID: 21769262 Free PMC article.

2

Treatable fluctuating mental impairment in a patient with Bardet-Biedl syndrome.

Tonomura Y, Hirano M, Shimada K, Asai H, Ikeda M, Kataoka H, Tanaka I, Konishi N, Ueno S. Tonomura Y, et al. Among authors: hirano m. Clin Neurol Neurosurg. 2009 Jan;111(1):102-4. doi: 10.1016/j.clineuro.2008.08.008. Epub 2008 Oct 19. Clin Neurol Neurosurg. 2009. PMID: 18938027

3

Complete recovery of an aged patient with Guillain-Barré syndrome associated with multiple IgM anti-ganglioside antibodies.

Furiya Y, Hirano M, Kusunoki S, Ueda M, Sugie K, Nishiwaki T, Ueno S. Furiya Y, et al. Among authors: hirano m. Muscle Nerve. 2008 Dec;38(6):1630-3. doi: 10.1002/mus.21131. Muscle Nerve. 2008. PMID: 19016534

4

A novel mutation in the calcium channel gene in a family with hypokalemic periodic paralysis.

Hirano M, Kokunai Y, Nagai A, Nakamura Y, Saigoh K, Kusunoki S, Takahashi MP. Hirano M, et al. J Neurol Sci. 2011 Oct 15;309(1-2):9-11. doi: 10.1016/j.jns.2011.07.046. Epub 2011 Aug 19. J Neurol Sci. 2011. PMID: 21855088

5

Risks of inappropriate secretion of antidiuretic hormone in multiple system atrophy.

Samukawa M, Hirano M, Sakamoto H, Kitada M, Kusunoki S, Nakamura Y. Samukawa M, et al. Among authors: hirano m. Mov Disord. 2011 Dec;26(14):2572-3. doi: 10.1002/mds.23904. Epub 2011 Oct 10. Mov Disord. 2011. PMID: 21987432 No abstract available.

6

Refractory acute disseminated encephalomyelitis with anti-galactocerebroside antibody.

Samukawa M, Hirano M, Tsugawa J, Sakamoto H, Tabata E, Takada K, Kuwahara M, Suzuki S, Kitada M, Yamada T, Hara H, Tsuboi Y, Nakamura Y, Kusunoki S. Samukawa M, et al. Among authors: hirano m. Neurosci Res. 2012 Dec;74(3-4):284-9. doi: 10.1016/j.neures.2012.09.006. Epub 2012 Oct 17. Neurosci Res. 2012. PMID: 23085407

7

Details of treatment-related difficulties in men with anti-N-methyl-D-aspartate receptor encephalitis.

Sakamoto H, Hirano M, Samukawa M, Ueno S, Maekura S, Fujimura H, Kuwahara M, Hamada Y, Isono C, Tanaka K, Kusunoki S, Nakamura Y. Sakamoto H, et al. Among authors: hirano m. Eur Neurol. 2013;69(1):21-6. doi: 10.1159/000342023. Epub 2012 Nov 1. Eur Neurol. 2013. PMID: 23128856

8

Mutations in the gene encoding p62 in Japanese patients with amyotrophic lateral sclerosis.

Hirano M, Nakamura Y, Saigoh K, Sakamoto H, Ueno S, Isono C, Miyamoto K, Akamatsu M, Mitsui Y, Kusunoki S. Hirano M, et al. Neurology. 2013 Jan 29;80(5):458-63. doi: 10.1212/WNL.0b013e31827f0fe5. Epub 2013 Jan 9. Neurology. 2013. PMID: 23303844

9

Differences in dysphagia between spinocerebellar ataxia type 3 and type 6.

Isono C, Hirano M, Sakamoto H, Ueno S, Kusunoki S, Nakamura Y. Isono C, et al. Among authors: hirano m. Dysphagia. 2013 Sep;28(3):413-8. doi: 10.1007/s00455-013-9450-4. Epub 2013 Mar 21. Dysphagia. 2013. PMID: 23515636

10

Triple A syndrome in Japan.

Ikeda M, Hirano M, Shinoda K, Katsumata N, Furutama D, Nakamura K, Ikeda S, Tanaka T, Hanafusa T, Kitajima H, Kohno H, Nakagawa M, Nakamura Y, Ueno S. Ikeda M, et al. Among authors: hirano m. Muscle Nerve. 2013 Sep;48(3):381-6. doi: 10.1002/mus.23770. Epub 2013 Jul 17. Muscle Nerve. 2013. PMID: 23861206

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