Saito M - Search Results

1

Refinement of the gene locus for autosomal recessive juvenile parkinsonism (AR-JP) on chromosome 6q25.2-27 and identification of markers exhibiting linkage disequilibrium.

Saito M, Matsumine H, Tanaka H, Ishikawa A, Shimoda-Matsubayashi S, Schäffer AA, Mizuno Y, Tsuji S. Saito M, et al. J Hum Genet. 1998;43(1):22-31. doi: 10.1007/s100380050032. J Hum Genet. 1998. PMID: 9609994

2

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: saito m. Am J Hum Genet. 1997 Mar;60(3):588-96. Am J Hum Genet. 1997. PMID: 9042918 Free PMC article.

3

Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9.

Ikeuchi T, Asaka T, Saito M, Tanaka H, Higuchi S, Tanaka K, Saida K, Uyama E, Mizusawa H, Fukuhara N, Nonaka I, Takamori M, Tsuji S. Ikeuchi T, et al. Among authors: saito m. Ann Neurol. 1997 Apr;41(4):432-7. doi: 10.1002/ana.410410405. Ann Neurol. 1997. PMID: 9124799

4

Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.

Ishikawa K, Tanaka H, Saito M, Ohkoshi N, Fujita T, Yoshizawa K, Ikeuchi T, Watanabe M, Hayashi A, Takiyama Y, Nishizawa M, Nakano I, Matsubayashi K, Miwa M, Shoji S, Kanazawa I, Tsuji S, Mizusawa H. Ishikawa K, et al. Among authors: saito m. Am J Hum Genet. 1997 Aug;61(2):336-46. doi: 10.1086/514867. Am J Hum Genet. 1997. PMID: 9311738 Free PMC article.

5

Linkage mapping of the gene for Charcot-Marie-Tooth disease type 2 to chromosome 1p (CMT2A) and the clinical features of CMT2A.

Saito M, Hayashi Y, Suzuki T, Tanaka H, Hozumi I, Tsuji S. Saito M, et al. Neurology. 1997 Dec;49(6):1630-5. doi: 10.1212/wnl.49.6.1630. Neurology. 1997. PMID: 9409358

6

Dopamine cell death by a single genetic mechanism: phenotypic analysis and linkage study of autosomal recessive juvenile parkinsonism.

Matsumine H, Saito M, Ishikawa A, Yokochi M, Yamamura Y, Tsuji S, Mizuno Y. Matsumine H, et al. Among authors: saito m. Adv Neurol. 1999;80:187-94. Adv Neurol. 1999. PMID: 10410720 Review. No abstract available.

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: saito m. 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

Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism.

Maruyama M, Ikeuchi T, Saito M, Ishikawa A, Yuasa T, Tanaka H, Hayashi S, Wakabayashi K, Takahashi H, Tsuji S. Maruyama M, et al. Among authors: saito m. Ann Neurol. 2000 Aug;48(2):245-50. Ann Neurol. 2000. PMID: 10939576

9

An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene.

Hayashi S, Wakabayashi K, Ishikawa A, Nagai H, Saito M, Maruyama M, Takahashi T, Ozawa T, Tsuji S, Takahashi H. Hayashi S, et al. Among authors: saito m. Mov Disord. 2000 Sep;15(5):884-8. doi: 10.1002/1531-8257(200009)15:5<884::aid-mds1019>3.0.co;2-8. Mov Disord. 2000. PMID: 11009195

10

Strong linkage disequilibrium and haplotype analysis in Japanese pedigrees with Machado-Joseph disease.

Endo K, Sasaki H, Wakisaka A, Tanaka H, Saito M, Igarashi S, Takiyama Y, Sanpei K, Iwabuchi K, Suzuki Y, Onari K, Suzuki T, Weissenbach J, Weber JL, Nomura Y, Segawa M, Nishizawa M, Tsuji S. Endo K, et al. Among authors: saito m. Am J Med Genet. 1996 Sep 20;67(5):437-44. doi: 10.1002/(SICI)1096-8628(19960920)67:5<437::AID-AJMG1>3.0.CO;2-H. Am J Med Genet. 1996. PMID: 8886159

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

8,385 results

Search Page

Filters