Soma H - Search Results

1

X-linked Charcot-Marie-Tooth disease (CMTX) in a severely affected female patient with scattered lesions in cerebral white matter.

Basri R, Yabe I, Soma H, Matsushima M, Tsuji S, Sasaki H. Basri R, et al. Among authors: soma h. Intern Med. 2007;46(13):1023-7. doi: 10.2169/internalmedicine.46.0047. Epub 2007 Jul 2. Intern Med. 2007. PMID: 17603245 Free article.

2

Unusual retinal phenotypes in an SCA7 family.

Inaba H, Yabe I, Yashima M, Soma H, Nakamura Y, Houzen H, Sasaki H. Inaba H, et al. Among authors: soma h. Intern Med. 2009;48(16):1461-4. doi: 10.2169/internalmedicine.48.2072. Epub 2009 Aug 17. Intern Med. 2009. PMID: 19687599 Free article.

3

[Spastic paraplegia caused by a novel mutation in the spastin gene (1207C-->G, P361R)--clinical features of a patient without family history].

Machino Y, Kokubo Y, Soma H, Yabe I, Sasaki H, Kuzuhara S. Machino Y, et al. Among authors: soma h. Brain Nerve. 2008 Feb;60(2):187-9. Brain Nerve. 2008. PMID: 18306668 Japanese.

4

Downbeat positioning nystagmus is a common clinical feature despite variable phenotypes in an FHM1 family.

Yabe I, Kitagawa M, Suzuki Y, Fujiwara K, Wada T, Tsubuku T, Takeichi N, Sakushima K, Soma H, Tsuji S, Niino M, Saitoh S, Sasaki H. Yabe I, et al. Among authors: soma h. J Neurol. 2008 Oct;255(10):1541-4. doi: 10.1007/s00415-008-0970-z. Epub 2008 Jul 28. J Neurol. 2008. PMID: 18670797 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: soma h. Rinsho Shinkeigaku. 2008 Sep;48(9):640-5. doi: 10.5692/clinicalneurol.48.640. Rinsho Shinkeigaku. 2008. PMID: 19048946 Japanese.

6

Microstructural white matter abnormalities of multiple system atrophy: in vivo topographic illustration by using diffusion-tensor MR imaging.

Tha KK, Terae S, Yabe I, Miyamoto T, Soma H, Zaitsu Y, Fujima N, Kudo K, Sasaki H, Shirato H. Tha KK, et al. Among authors: soma h. Radiology. 2010 May;255(2):563-9. doi: 10.1148/radiol.10090988. Radiology. 2010. PMID: 20413765

7

Cat Scratch Disease-associated Encephalitis Followed by Parkinsonism.

Nakamura M, Ura S, Yabe I, Otsuki M, Soma H, Ogata A. Nakamura M, et al. Among authors: soma h. Intern Med. 2022 Oct 15;61(20):3115-3120. doi: 10.2169/internalmedicine.9047-21. Epub 2022 Mar 19. Intern Med. 2022. PMID: 35314550 Free PMC article.

8

Heredity in multiple system atrophy.

Soma H, Yabe I, Takei A, Fujiki N, Yanagihara T, Sasaki H. Soma H, et al. J Neurol Sci. 2006 Jan 15;240(1-2):107-10. doi: 10.1016/j.jns.2005.09.003. Epub 2005 Nov 22. J Neurol Sci. 2006. PMID: 16307759 Free article.

9

Four mutations of the spastin gene in Japanese families with spastic paraplegia.

Basri R, Yabe I, Soma H, Takei A, Nishimura H, Machino Y, Kokubo Y, Kosugi M, Okada R, Yukitake M, Tachibana H, Kuroda Y, Kuzuhara S, Sasaki H. Basri R, et al. Among authors: soma h. J Hum Genet. 2006;51(8):711-715. doi: 10.1007/s10038-006-0412-7. Epub 2006 Jun 21. J Hum Genet. 2006. PMID: 16788734 Free article.

10

Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families.

Basri R, Yabe I, Soma H, Sasaki H. Basri R, et al. Among authors: soma h. J Hum Genet. 2007;52(10):848-855. doi: 10.1007/s10038-007-0182-x. Epub 2007 Sep 5. J Hum Genet. 2007. PMID: 17805477 Free article.

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