Arisato T - Search Results

1

Recombinant thrombomodulin inhibits thrombin-induced vascular endothelial growth factor production in neuronal cells.

Sarker KP, Yamahata H, Nakata M, Arisato T, Nakajima T, Kitajima I, Maruyama I. Sarker KP, et al. Among authors: arisato t. Haemostasis. 1999 Nov-Dec;29(6):343-52. doi: 10.1159/000022522. Haemostasis. 1999. PMID: 10844408

2

The agonist of the protease-activated receptor-1 (PAR) but not PAR3 mimics thrombin-induced vascular endothelial growth factor release in human smooth muscle cells.

Arisato T, Sarker KP, Kawahara K, Nakata M, Hashiguchi T, Osame M, Kitajima I, Maruyama I. Arisato T, et al. Cell Mol Life Sci. 2003 Aug;60(8):1716-24. doi: 10.1007/s00018-003-3140-6. Cell Mol Life Sci. 2003. PMID: 14513837 Free PMC article.

3

Highly accumulated platelet vascular endothelial growth factor in coagulant thrombotic region.

Arisato T, Hashiguchi T, Sarker KP, Arimura K, Asano M, Matsuo K, Osame M, Maruyama I. Arisato T, et al. J Thromb Haemost. 2003 Dec;1(12):2589-93. doi: 10.1046/j.1538-7836.2003.00475.x. J Thromb Haemost. 2003. PMID: 14675094 Free article.

4

Overproduction of vascular endothelial growth factor/vascular permeability factor is causative in Crow-Fukase (POEMS) syndrome.

Watanabe O, Maruyama I, Arimura K, Kitajima I, Arimura H, Hanatani M, Matsuo K, Arisato T, Osame M. Watanabe O, et al. Among authors: arisato t. Muscle Nerve. 1998 Nov;21(11):1390-7. doi: 10.1002/(sici)1097-4598(199811)21:11<1390::aid-mus5>3.0.co;2-4. Muscle Nerve. 1998. PMID: 9771661

5

Paraneoplastic vasculitic neuropathy: immunohistochemical studies on a biopsied nerve and post-mortem examination.

Matsumuro K, Izumo S, Umehara F, Arisato T, Maruyama I, Yonezawa S, Shirahama H, Sato E, Osame M. Matsumuro K, et al. Among authors: arisato t. J Intern Med. 1994 Aug;236(2):225-30. doi: 10.1111/j.1365-2796.1994.tb01287.x. J Intern Med. 1994. PMID: 8046323 Review.

6

[n-Hexane polyneuropathy presenting with CIDP-like features].

Takata Y, Shiraishi T, Matsuura E, Arisato T, Okubo R, Higuchi I, Umehara F, Osame M, Arimura K, Hashiguchi K. Takata Y, et al. Among authors: arisato t. Nihon Naika Gakkai Zasshi. 2006 May 10;95(5):933-5. doi: 10.2169/naika.95.933. Nihon Naika Gakkai Zasshi. 2006. PMID: 16774070 Japanese. No abstract available.

7

[Juvenile Binswanger-type encephalopathy with alopecia and spondylosis deformans--a case report].

Arisato T, Hokezu Y, Suehara M, Kiwaki S, Kuriyama M, Osame M. Arisato T, et al. Rinsho Shinkeigaku. 1993 Apr;33(4):400-4. Rinsho Shinkeigaku. 1993. PMID: 8370202 Review. Japanese.

8

Clinical and pathological studies of familial amyotrophic lateral sclerosis (FALS) with SOD1 H46R mutation in large Japanese families.

Arisato T, Okubo R, Arata H, Abe K, Fukada K, Sakoda S, Shimizu A, Qin XH, Izumo S, Osame M, Nakagawa M. Arisato T, et al. Acta Neuropathol. 2003 Dec;106(6):561-8. doi: 10.1007/s00401-003-0763-5. Epub 2003 Sep 27. Acta Neuropathol. 2003. PMID: 14517684

9

Early clinical signs and imaging findings in Gerstmann-Sträussler-Scheinker syndrome (Pro102Leu).

Arata H, Takashima H, Hirano R, Tomimitsu H, Machigashira K, Izumi K, Kikuno M, Ng AR, Umehara F, Arisato T, Ohkubo R, Nakabeppu Y, Nakajo M, Osame M, Arimura K. Arata H, et al. Among authors: arisato t. Neurology. 2006 Jun 13;66(11):1672-8. doi: 10.1212/01.wnl.0000218211.85675.18. Neurology. 2006. PMID: 16769939 Clinical Trial.

10

Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.

Hirano R, Takashima H, Okubo R, Tajima K, Okamoto Y, Ishida S, Tsuruta K, Arisato T, Arata H, Nakagawa M, Osame M, Arimura K. Hirano R, et al. Among authors: arisato t. Neurogenetics. 2004 Dec;5(4):215-21. doi: 10.1007/s10048-004-0194-z. Epub 2004 Sep 29. Neurogenetics. 2004. PMID: 15455264

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