Tsuji S - Search Results

1

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: tsuji s. BMC Med Genet. 2010 Dec 22;11:171. doi: 10.1186/1471-2350-11-171. BMC Med Genet. 2010. PMID: 21176162 Free PMC article.

2

A novel exon mutation in the human beta-hexosaminidase beta subunit gene affects 3' splice site selection.

Wakamatsu N, Kobayashi H, Miyatake T, Tsuji S. Wakamatsu N, et al. Among authors: tsuji s. J Biol Chem. 1992 Feb 5;267(4):2406-13. J Biol Chem. 1992. PMID: 1531140 Free article.

3

Identification of a mutation in the arylsulfatase A gene of a patient with adult-type metachromatic leukodystrophy.

Kondo R, Wakamatsu N, Yoshino H, Fukuhara N, Miyatake T, Tsuji S. Kondo R, et al. Among authors: tsuji s. Am J Hum Genet. 1991 May;48(5):971-8. Am J Hum Genet. 1991. PMID: 1673291 Free PMC article.

4

Stability of messenger RNA in postmortem human brains and construction of human brain cDNA libraries.

Kobayashi H, Sakimura K, Kuwano R, Sato S, Ikuta F, Takahashi Y, Miyatake T, Tsuji S. Kobayashi H, et al. Among authors: tsuji s. J Mol Neurosci. 1990;2(1):29-34. doi: 10.1007/BF02896923. J Mol Neurosci. 1990. PMID: 1701658

5

[Lysosome disease--Sandhoff disease].

Eguchi I, Wakamatsu N, Nakano R, Tsuji S. Eguchi I, et al. Among authors: tsuji s. Nihon Rinsho. 1993 Sep;51(9):2276-80. Nihon Rinsho. 1993. PMID: 8411702 Review. Japanese.

6

Mutations producing premature termination of translation and an amino acid substitution in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis associated with parkinsonism.

Wakamatsu N, Hayashi M, Kawai H, Kondo H, Gotoda Y, Nishida Y, Kondo R, Tsuji S, Matsumoto T. Wakamatsu N, et al. Among authors: tsuji s. J Neurol Neurosurg Psychiatry. 1999 Aug;67(2):195-8. doi: 10.1136/jnnp.67.2.195. J Neurol Neurosurg Psychiatry. 1999. PMID: 10406988 Free PMC article.

7

Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1.

Tomita Ha, Nagamitsu S, Wakui K, Fukushima Y, Yamada K, Sadamatsu M, Masui A, Konishi T, Matsuishi T, Aihara M, Shimizu K, Hashimoto K, Mineta M, Matsushima M, Tsujita T, Saito M, Tanaka H, Tsuji S, Takagi T, Nakamura Y, Nanko S, Kato N, Nakane Y, Niikawa N. Tomita Ha, et al. Among authors: tsuji s. Am J Hum Genet. 1999 Dec;65(6):1688-97. doi: 10.1086/302682. Am J Hum Genet. 1999. PMID: 10577923 Free PMC article.

8

Japanese SCA families with an unusual phenotype linked to a locus overlapping with SCA15 locus.

Hara K, Fukushima T, Suzuki T, Shimohata T, Oyake M, Ishiguro H, Hirota K, Miyashita A, Kuwano R, Kurisaki H, Yomono H, Goto J, Kanazawa I, Tsuji S. Hara K, et al. Among authors: tsuji s. Neurology. 2004 Feb 24;62(4):648-51. doi: 10.1212/01.wnl.0000110190.08412.25. Neurology. 2004. PMID: 14981189

9

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: tsuji s. Brain. 2007 Sep;130(Pt 9):2302-9. doi: 10.1093/brain/awm036. Epub 2007 Apr 2. Brain. 2007. PMID: 17405764

10

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. Among authors: tsuji s. Arch Neurol. 2007 Apr;64(4):545-51. doi: 10.1001/archneur.64.4.545. Arch Neurol. 2007. PMID: 17420317

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