Ozawa T - Search Results

1

No mutation in the entire coding region of the alpha-synuclein gene in pathologically confirmed cases of multiple system atrophy.

Ozawa T, Takano H, Onodera O, Kobayashi H, Ikeuchi T, Koide R, Okuizumi K, Shimohata T, Wakabayashi K, Takahashi H, Tsuji S. Ozawa T, et al. Neurosci Lett. 1999 Jul 30;270(2):110-2. doi: 10.1016/s0304-3940(99)00475-9. Neurosci Lett. 1999. PMID: 10462110

2

Analysis of the expression level of alpha-synuclein mRNA using postmortem brain samples from pathologically confirmed cases of multiple system atrophy.

Ozawa T, Okuizumi K, Ikeuchi T, Wakabayashi K, Takahashi H, Tsuji S. Ozawa T, et al. Acta Neuropathol. 2001 Aug;102(2):188-90. doi: 10.1007/s004010100367. Acta Neuropathol. 2001. PMID: 11563635

3

The phenotype spectrum of Japanese multiple system atrophy.

Ozawa T, Tada M, Kakita A, Onodera O, Tada M, Ishihara T, Morita T, Shimohata T, Wakabayashi K, Takahashi H, Nishizawa M. Ozawa T, et al. J Neurol Neurosurg Psychiatry. 2010 Nov;81(11):1253-5. doi: 10.1136/jnnp.2009.182576. Epub 2010 Jun 22. J Neurol Neurosurg Psychiatry. 2010. PMID: 20571046

4

Suprachiasmatic nucleus in a patient with multiple system atrophy with abnormal circadian rhythm of arginine-vasopressin secretion into plasma.

Ozawa T, Oyanagi K, Tanaka H, Horikawa Y, Takahashi H, Morita T, Tsuji S. Ozawa T, et al. J Neurol Sci. 1998 Jan 21;154(1):116-21. doi: 10.1016/s0022-510x(97)00210-4. J Neurol Sci. 1998. PMID: 9543334

5

Nocturnal decrease in vasopressin secretion into plasma in patients with multiple system atrophy.

Ozawa T, Tanaka H, Nakano R, Sato M, Inuzuka T, Soma Y, Yoshimura N, Fukuhara N, Tsuji S. Ozawa T, et al. J Neurol Neurosurg Psychiatry. 1999 Oct;67(4):542-5. doi: 10.1136/jnnp.67.4.542. J Neurol Neurosurg Psychiatry. 1999. PMID: 10486410 Free PMC article.

6

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: ozawa t. 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

7

Frequency of nocturnal sudden death in patients with multiple system atrophy.

Shimohata T, Ozawa T, Nakayama H, Tomita M, Shinoda H, Nishizawa M. Shimohata T, et al. Among authors: ozawa t. J Neurol. 2008 Oct;255(10):1483-5. doi: 10.1007/s00415-008-0941-4. Epub 2008 Jul 28. J Neurol. 2008. PMID: 18670800

8

[Prevertebral abscesses with a protracted insidious clinical course and subsequent lethal, acute pyogenic meningitis and septic shock].

Ozawa T, Onodera O, Kakita A, Aoki K, Tanaka K, Soma Y, Takahashi H, Tsuji S. Ozawa T, et al. No To Shinkei. 1998 Jan;50(1):75-9. No To Shinkei. 1998. PMID: 9493203 Japanese.

9

A de novo splice donor site mutation causes in-frame deletion of 14 amino acids in the proteolipid protein in Pelizaeus-Merzbacher disease.

Aoyagi Y, Kobayashi H, Tanaka K, Ozawa T, Nitta H, Tsuji S. Aoyagi Y, et al. Among authors: ozawa t. Ann Neurol. 1999 Jul;46(1):112-5. doi: 10.1002/1531-8249(199907)46:1<112::aid-ana16>3.0.co;2-u. Ann Neurol. 1999. PMID: 10401787

10

Floppy epiglottis as a contraindication of CPAP in patients with multiple system atrophy.

Shimohata T, Tomita M, Nakayama H, Aizawa N, Ozawa T, Nishizawa M. Shimohata T, et al. Among authors: ozawa t. Neurology. 2011 May 24;76(21):1841-2. doi: 10.1212/WNL.0b013e31821ccd07. Neurology. 2011. PMID: 21606457 No abstract available.

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