Tsuji S - Search Results

1

The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15.

Saffari A, Kellner M, Jordan C, Rosengarten H, Mo A, Zhang B, Strelko O, Neuser S, Davis MY, Yoshikura N, Futamura N, Takeuchi T, Nabatame S, Ishiura H, Tsuji S, Aldeen HS, Cali E, Rocca C, Houlden H, Efthymiou S, Assmann B, Yoon G, Trombetta BA, Kivisäkk P, Eichler F, Nan H, Takiyama Y, Tessa A, Santorelli FM, Sahin M, Blackstone C, Yang E, Schüle R, Ebrahimi-Fakhari D. Saffari A, et al. Among authors: tsuji s. Brain. 2023 May 2;146(5):2003-2015. doi: 10.1093/brain/awac391. Brain. 2023. PMID: 36315648 Free PMC article.

2

Direct detection of expanded (CAG/CTG) repeats in the myotonin-protein kinase genes of myotonic dystrophy patients using a high-stringency hybridization method.

Sanpei K, Igarashi S, Eguchi I, Takiyama Y, Tanaka H, Tsuji S. Sanpei K, et al. Among authors: tsuji s. Biochem Biophys Res Commun. 1995 Jul 17;212(2):341-6. doi: 10.1006/bbrc.1995.1975. Biochem Biophys Res Commun. 1995. PMID: 7626046

3

[The characteristics and the gene locus of Machado Joseph disease].

Takiyama Y, Tsuji S. Takiyama Y, et al. Among authors: tsuji s. No To Shinkei. 1995 Feb;47(2):117-29. No To Shinkei. 1995. PMID: 7669410 Review. Japanese. No abstract available.

4

A clinical and pathologic study of a large Japanese family with Machado-Joseph disease tightly linked to the DNA markers on chromosome 14q.

Takiyama Y, Oyanagi S, Kawashima S, Sakamoto H, Saito K, Yoshida M, Tsuji S, Mizuno Y, Nishizawa M. Takiyama Y, et al. Among authors: tsuji s. Neurology. 1994 Jul;44(7):1302-8. doi: 10.1212/wnl.44.7.1302. Neurology. 1994. PMID: 8035935

5

Pure cerebellar ataxia phenotype in Machado-Joseph disease.

Ishikawa K, Mizusawa H, Igarashi S, Takiyama Y, Tanaka H, Ohkoshi N, Shoji S, Tsuji S. Ishikawa K, et al. Among authors: tsuji s. Neurology. 1996 Jun;46(6):1776-7. doi: 10.1212/wnl.46.6.1776. Neurology. 1996. PMID: 8649595 No abstract available.

6

Autosomal dominant pure cerebellar ataxia. A clinical and genetic analysis of eight Japanese families.

Ishikawa K, Mizusawa H, Saito M, Tanaka H, Nakajima N, Kondo N, Kanazawa I, Shoji S, Tsuji S. Ishikawa K, et al. Among authors: tsuji s. Brain. 1996 Aug;119 ( Pt 4):1173-82. doi: 10.1093/brain/119.4.1173. Brain. 1996. PMID: 8813281

7

Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy.

Illarioshkin SN, Ivanova-Smolenskaya IA, Tanaka H, Vereshchagin NV, Markova ED, Poleshchuk VV, Lozhnikova SM, Sukhorukov VS, Limborska SA, Slominsky PA, Bulayeva KB, Tsuji S. Illarioshkin SN, et al. Among authors: tsuji s. Brain. 1996 Dec;119 ( Pt 6):1895-909. doi: 10.1093/brain/119.6.1895. Brain. 1996. PMID: 9009996

8

Progressive atrophy of cerebellum and brainstem as a function of age and the size of the expanded CAG repeats in the MJD1 gene in Machado-Joseph disease.

Onodera O, Idezuka J, Igarashi S, Takiyama Y, Endo K, Takano H, Oyake M, Tanaka H, Inuzuka T, Hayashi T, Yuasa T, Ito J, Miyatake T, Tsuji S. Onodera O, et al. Among authors: tsuji s. Ann Neurol. 1998 Mar;43(3):288-96. doi: 10.1002/ana.410430305. Ann Neurol. 1998. PMID: 9506544

9

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: the aprataxin gene mutations.

Shimazaki H, Takiyama Y, Sakoe K, Ikeguchi K, Niijima K, Kaneko J, Namekawa M, Ogawa T, Date H, Tsuji S, Nakano I, Nishizawa M. Shimazaki H, et al. Among authors: tsuji s. Neurology. 2002 Aug 27;59(4):590-5. doi: 10.1212/wnl.59.4.590. Neurology. 2002. PMID: 12196655

10

Lymphomatoid granulomatosis involving central nervous system successfully treated with rituximab alone.

Ishiura H, Morikawa M, Hamada M, Watanabe T, Kako S, Chiba S, Motokura T, Hangaishi A, Shibahara J, Akahane M, Goto J, Kwak S, Kurokawa M, Tsuji S. Ishiura H, et al. Among authors: tsuji s. Arch Neurol. 2008 May;65(5):662-5. doi: 10.1001/archneur.65.5.662. Arch Neurol. 2008. PMID: 18474745

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