Hara K - Search Results

1

Gardner RJ, Knight MA, Hara K, Tsuji S, Forrest SM, Storey E. Gardner RJ, et al. Among authors: hara k. Cerebellum. 2005;4(1):47-50. doi: 10.1080/14734220410019029. Cerebellum. 2005. PMID: 15895559 Review.

2

Novel locus for benign hereditary chorea with adult onset maps to chromosome 8q21.3 q23.3.

Shimohata T, Hara K, Sanpei K, Nunomura J, Maeda T, Kawachi I, Kanazawa M, Kasuga K, Miyashita A, Kuwano R, Hirota K, Tsuji S, Onodera O, Nishizawa M, Honma Y. Shimohata T, et al. Among authors: hara k. Brain. 2007 Sep;130(Pt 9):2302-9. doi: 10.1093/brain/awm036. Epub 2007 Apr 2. Brain. 2007. PMID: 17405764

3

Multiplex families with multiple system atrophy.

Hara K, Momose Y, Tokiguchi S, Shimohata M, Terajima K, Onodera O, Kakita A, Yamada M, Takahashi H, Hirasawa M, Mizuno Y, Ogata K, Goto J, Kanazawa I, Nishizawa M, Tsuji S. Hara K, et al. Arch Neurol. 2007 Apr;64(4):545-51. doi: 10.1001/archneur.64.4.545. Arch Neurol. 2007. PMID: 17420317

4

Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families.

Hara K, Shiga A, Nozaki H, Mitsui J, Takahashi Y, Ishiguro H, Yomono H, Kurisaki H, Goto J, Ikeuchi T, Tsuji S, Nishizawa M, Onodera O. Hara K, et al. Neurology. 2008 Aug 19;71(8):547-51. doi: 10.1212/01.wnl.0000311277.71046.a0. Epub 2008 Jun 25. Neurology. 2008. PMID: 18579805

5

TRPM7 is not associated with amyotrophic lateral sclerosis-parkinsonism dementia complex in the Kii peninsula of Japan.

Hara K, Kokubo Y, Ishiura H, Fukuda Y, Miyashita A, Kuwano R, Sasaki R, Goto J, Nishizawa M, Kuzuhara S, Tsuji S. Hara K, et al. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):310-3. doi: 10.1002/ajmg.b.30966. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19405049

6

Mutations in COQ2 in familial and sporadic multiple-system atrophy.

Multiple-System Atrophy Research Collaboration. Multiple-System Atrophy Research Collaboration. N Engl J Med. 2013 Jul 18;369(3):233-44. doi: 10.1056/NEJMoa1212115. Epub 2013 Jun 12. N Engl J Med. 2013. PMID: 23758206 Free article.

7

A wide spectrum of clinical and brain MRI findings in patients with SLC19A3 mutations.

Yamada K, Miura K, Hara K, Suzuki M, Nakanishi K, Kumagai T, Ishihara N, Yamada Y, Kuwano R, Tsuji S, Wakamatsu N. Yamada K, et al. Among authors: hara k. BMC Med Genet. 2010 Dec 22;11:171. doi: 10.1186/1471-2350-11-171. BMC Med Genet. 2010. PMID: 21176162 Free PMC article.

8

[Oral cyclophosphamide therapy for multifocal fibrosclerosis with hypertrophic intracranial pachymeningitis].

Tada M, Onodera O, Hara K, Tanaka K, Takahashi H, Tsuji S, Nishizawa M. Tada M, et al. Among authors: hara k. Rinsho Shinkeigaku. 2006 Feb;46(2):128-33. Rinsho Shinkeigaku. 2006. PMID: 16619837 Japanese.

9

[Molecular genetic analysis of amyotrophic lateral sclerosis/parkinsonism-dementia complex (ALS/PDC) in the Kii peninsula].

Hara K, Kuwano R, Miyashita A, Kokubo Y, Sasaki R, Nakahara Y, Goto J, Nishizawa M, Kuzuhara S, Tsuji S. Hara K, et al. Rinsho Shinkeigaku. 2007 Nov;47(11):974-6. Rinsho Shinkeigaku. 2007. PMID: 18210852 Japanese.

10

Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease.

Hara K, Shiga A, Fukutake T, Nozaki H, Miyashita A, Yokoseki A, Kawata H, Koyama A, Arima K, Takahashi T, Ikeda M, Shiota H, Tamura M, Shimoe Y, Hirayama M, Arisato T, Yanagawa S, Tanaka A, Nakano I, Ikeda S, Yoshida Y, Yamamoto T, Ikeuchi T, Kuwano R, Nishizawa M, Tsuji S, Onodera O. Hara K, et al. N Engl J Med. 2009 Apr 23;360(17):1729-39. doi: 10.1056/NEJMoa0801560. N Engl J Med. 2009. PMID: 19387015 Free article.

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