Kitada T - Search Results

1

Molecular cloning, gene expression, and identification of a splicing variant of the mouse parkin gene.

Kitada T, Asakawa S, Minoshima S, Mizuno Y, Shimizu N. Kitada T, et al. Mamm Genome. 2000 Jun;11(6):417-21. doi: 10.1007/s003350010080. Mamm Genome. 2000. PMID: 10818204

2

[A 50-year-old man with metamorphopsia and optic nerve swelling].

Nakajima Y, Kitada T, Mizutani Y, Yamamoto Y, Kuwabara N, Sato T, Kondo T, Mizuno Y. Nakajima Y, et al. Among authors: kitada t. No To Shinkei. 1993 May;45(5):485-92. No To Shinkei. 1993. PMID: 8192734 Japanese.

3

[A 62-year-old man with multiple cranial nerve palsies on the right side and a pelvic mass].

Tanaka S, Kitada T, Kanazawa A, Ueda G, Noguchi K, Mori H, Kondo T, Shirai T, Mizuno Y. Tanaka S, et al. Among authors: kitada t. No To Shinkei. 1993 Aug;45(8):777-87. No To Shinkei. 1993. PMID: 8217405 Japanese.

4

[A 81-year-old man with dementia, gait disturbance, hemiparesis, and sympathetic apraxia].

Nishi K, Kitada T, Mori H, Wada T, Kuwabara N, Imai H, Sato T, Mizuno Y. Nishi K, et al. Among authors: kitada t. No To Shinkei. 1993 Apr;45(4):389-95. No To Shinkei. 1993. PMID: 8334025 Japanese.

5

[A 34-year-old woman with delayed motor milestones, high arched palate, and proximal muscle weakness].

Yamamoto T, Kitada T, Hirasawa E, Mori H, Mizuno Y. Yamamoto T, et al. Among authors: kitada t. No To Shinkei. 1996 Jul;48(7):677-84. No To Shinkei. 1996. PMID: 8753005 Japanese.

6

[A 56-year-old man with fever, backache and tetraparesis].

Hattori T, Kitada T, Suzuki H, Imai H, Mizuno Y. Hattori T, et al. Among authors: kitada t. No To Shinkei. 1996 Feb;48(2):183-93. No To Shinkei. 1996. PMID: 8962786 Japanese.

7

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.

Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N. Kitada T, et al. Nature. 1998 Apr 9;392(6676):605-8. doi: 10.1038/33416. Nature. 1998. PMID: 9560156

8

A microdeletion of D6S305 in a family of autosomal recessive juvenile parkinsonism (PARK2).

Matsumine H, Yamamura Y, Hattori N, Kobayashi T, Kitada T, Yoritaka A, Mizuno Y. Matsumine H, et al. Among authors: kitada t. Genomics. 1998 Apr 1;49(1):143-6. doi: 10.1006/geno.1997.5196. Genomics. 1998. PMID: 9570960

9

Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene.

Hattori N, Matsumine H, Asakawa S, Kitada T, Yoshino H, Elibol B, Brookes AJ, Yamamura Y, Kobayashi T, Wang M, Yoritaka A, Minoshima S, Shimizu N, Mizuno Y. Hattori N, et al. Among authors: kitada t. Biochem Biophys Res Commun. 1998 Aug 28;249(3):754-8. doi: 10.1006/bbrc.1998.9134. Biochem Biophys Res Commun. 1998. PMID: 9731209

10

Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals.

Hattori N, Kitada T, Matsumine H, Asakawa S, Yamamura Y, Yoshino H, Kobayashi T, Yokochi M, Wang M, Yoritaka A, Kondo T, Kuzuhara S, Nakamura S, Shimizu N, Mizuno Y. Hattori N, et al. Among authors: kitada t. Ann Neurol. 1998 Dec;44(6):935-41. doi: 10.1002/ana.410440612. Ann Neurol. 1998. PMID: 9851438

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