Tsujino S - Search Results

1

Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosis.

Yoshida T, Sasaki M, Yoshida M, Namekawa M, Okamoto Y, Tsujino S, Sasayama H, Mizuta I, Nakagawa M; Alexander Disease Study Group in Japan. Yoshida T, et al. Among authors: tsujino s. J Neurol. 2011 Nov;258(11):1998-2008. doi: 10.1007/s00415-011-6056-3. Epub 2011 May 1. J Neurol. 2011. PMID: 21533827

2

Novel deletion mutation in GFAP gene in an infantile form of Alexander disease.

Murakami N, Tsuchiya T, Kanazawa N, Tsujino S, Nagai T. Murakami N, et al. Among authors: tsujino s. Pediatr Neurol. 2008 Jan;38(1):50-2. doi: 10.1016/j.pediatrneurol.2007.08.017. Pediatr Neurol. 2008. PMID: 18054694

3

An infantile-juvenile form of Alexander disease caused by a R79H mutation in GFAP.

Asahina N, Okamoto T, Sudo A, Kanazawa N, Tsujino S, Saitoh S. Asahina N, et al. Among authors: tsujino s. Brain Dev. 2006 Mar;28(2):131-3. doi: 10.1016/j.braindev.2005.05.004. Epub 2005 Sep 15. Brain Dev. 2006. PMID: 16168593 Free article.

4

Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L.

Shiroma N, Kanazawa N, Kato Z, Shimozawa N, Imamura A, Ito M, Ohtani K, Oka A, Wakabayashi K, Iai M, Sugai K, Sasaki M, Kaga M, Ohta T, Tsujino S. Shiroma N, et al. Among authors: tsujino s. Brain Dev. 2003 Mar;25(2):116-21. doi: 10.1016/s0387-7604(02)00167-5. Brain Dev. 2003. PMID: 12581808

5

Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis.

Shiroma N, Kanazawa N, Izumi M, Sugai K, Fukumizu M, Sasaki M, Hanaoka S, Kaga M, Tsujino S. Shiroma N, et al. Among authors: tsujino s. J Hum Genet. 2001;46(10):579-82. doi: 10.1007/s100380170024. J Hum Genet. 2001. PMID: 11587071

6

A case of infantile Alexander disease with a milder phenotype and a novel GFAP mutation, L90P.

Suzuki Y, Kanazawa N, Takenaka J, Okumura A, Negoro T, Tsujino S. Suzuki Y, et al. Among authors: tsujino s. Brain Dev. 2004 Apr;26(3):206-8. doi: 10.1016/S0387-7604(03)00132-3. Brain Dev. 2004. PMID: 15030911

7

A case of infantile Alexander disease diagnosed by magnetic resonance imaging and genetic analysis.

Sakakibara T, Takahashi Y, Fukuda K, Inoue T, Kurosawa T, Nishikubo T, Shima M, Taoka T, Aida N, Tsujino S, Kanazawa N, Yoshioka A. Sakakibara T, et al. Among authors: tsujino s. Brain Dev. 2007 Sep;29(8):525-8. doi: 10.1016/j.braindev.2007.02.002. Epub 2007 Mar 23. Brain Dev. 2007. PMID: 17383133

8

[A case of long-term survival of a patient with infantile Alexander disease diagnosed by DNA analysis].

Wakabayashi K, Lai M, Masuko K, Yamashita S, Yamada M, Iwamoto H, Aida N, Shiroma N, Kanazawa N, Tsujino S. Wakabayashi K, et al. Among authors: tsujino s. No To Hattatsu. 2005 Jan;37(1):55-9. No To Hattatsu. 2005. PMID: 15675360 Review. Japanese.

9

Diagnosis of McArdle's disease by molecular genetic analysis of blood.

el-Schahawi M, Tsujino S, Shanske S, DiMauro S. el-Schahawi M, et al. Among authors: tsujino s. Neurology. 1996 Aug;47(2):579-80. doi: 10.1212/wnl.47.2.579. Neurology. 1996. PMID: 8757044

10

New GAA mutations in Japanese patients with GSDII (Pompe disease).

Pipo JR, Feng JH, Yamamoto T, Ohsaki Y, Nanba E, Tsujino S, Sakuragawa N, Martiniuk F, Ninomiya H, Oka A, Ohno K. Pipo JR, et al. Among authors: tsujino s. Pediatr Neurol. 2003 Oct;29(4):284-7. doi: 10.1016/s0887-8994(03)00267-4. Pediatr Neurol. 2003. PMID: 14643388

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

162 results

Search Page

Filters