Kuzuhara S - Search Results

1

Novel chloride channel gene mutations in two unrelated Japanese families with Becker's autosomal recessive generalized myotonia.

Sasaki R, Ichiyasu H, Ito N, Ikeda T, Takano H, Ikeuchi T, Kuzuhara S, Uchino M, Tsuji S, Uyama E. Sasaki R, et al. Among authors: kuzuhara s. Neuromuscul Disord. 1999 Dec;9(8):587-92. doi: 10.1016/s0960-8966(99)00050-4. Neuromuscul Disord. 1999. PMID: 10619717

2

A novel mutation in the gene for the adult skeletal muscle sodium channel alpha-subunit (SCN4A) that causes paramyotonia congenita of von Eulenburg.

Sasaki R, Takano H, Kamakura K, Kaida K, Hirata A, Saito M, Tanaka H, Kuzuhara S, Tsuji S. Sasaki R, et al. Among authors: kuzuhara s. Arch Neurol. 1999 Jun;56(6):692-6. doi: 10.1001/archneur.56.6.692. Arch Neurol. 1999. PMID: 10369308

3

A novel CLCN1 mutation: P480T in a Japanese family with Thomsen's myotonia congenita.

Sasaki R, Ito N, Shimamura M, Murakami T, Kuzuhara S, Uchino M, Uyama E. Sasaki R, et al. Among authors: kuzuhara s. Muscle Nerve. 2001 Mar;24(3):357-63. doi: 10.1002/1097-4598(200103)24:3<357::aid-mus1006>3.0.co;2-e. Muscle Nerve. 2001. PMID: 11353420

4

[Diagnostic criteria for vascular dementia].

Ito N, Kuzuhara S. Ito N, et al. Among authors: kuzuhara s. Nihon Rinsho. 2006 Nov 28;64 Suppl 8:777-82. Nihon Rinsho. 2006. PMID: 17469639 Review. Japanese. No abstract available.

5

[Definition and classification of vascular dementia].

Ito N, Kuzuhara S. Ito N, et al. Among authors: kuzuhara s. Nihon Rinsho. 2006 Nov 28;64 Suppl 8:764-8. Nihon Rinsho. 2006. PMID: 17471662 Review. Japanese. No abstract available.

6

Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27.

Matsumine H, Saito M, Shimoda-Matsubayashi S, Tanaka H, Ishikawa A, Nakagawa-Hattori Y, Yokochi M, Kobayashi T, Igarashi S, Takano H, Sanpei K, Koike R, Mori H, Kondo T, Mizutani Y, Schäffer AA, Yamamura Y, Nakamura S, Kuzuhara S, Tsuji S, Mizuno Y. Matsumine H, et al. Among authors: kuzuhara s. Am J Hum Genet. 1997 Mar;60(3):588-96. Am J Hum Genet. 1997. PMID: 9042918 Free PMC article.

7

[Neurology of vitamin B12 deficiency].

Sasaki R, Kuzuhara S. Sasaki R, et al. Among authors: kuzuhara s. Ryoikibetsu Shokogun Shirizu. 2000;(29 Pt 4):95-7. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11031903 Review. Japanese. No abstract available.

8

A missense mutation in the SOD1 gene in patients with amyotrophic lateral sclerosis from the Kii Peninsula and its vicinity, Japan.

Kikugawa K, Nakano R, Inuzuka T, Kokubo Y, Narita Y, Kuzuhara S, Yoshida S, Tsuji S. Kikugawa K, et al. Among authors: kuzuhara s. Neurogenetics. 1997 Sep;1(2):113-5. doi: 10.1007/s100480050016. Neurogenetics. 1997. PMID: 10732812

9

EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population.

Nishioka K, Funayama M, Vilariño-Güell C, Ogaki K, Li Y, Sasaki R, Kokubo Y, Kuzuhara S, Kachergus JM, Cobb SA, Takahashi H, Mizuno Y, Farrer MJ, Ross OA, Hattori N. Nishioka K, et al. Among authors: kuzuhara s. Parkinsonism Relat Disord. 2014 Jun;20(6):659-61. doi: 10.1016/j.parkreldis.2014.03.004. Epub 2014 Mar 18. Parkinsonism Relat Disord. 2014. PMID: 24704100 Free PMC article.

10

[A family of parkinsonism in which the clinical feature of constituents varied with the age of onset].

Sasaki R, Kuzuhara S, Taniguchi A, Narita Y, Naito Y. Sasaki R, et al. Among authors: kuzuhara s. Rinsho Shinkeigaku. 1994 Jul;34(7):736-8. Rinsho Shinkeigaku. 1994. PMID: 7955737 Japanese.

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