Watanabe O - Search Results

1

Hereditary motor and sensory neuropathy with myelin folding and juvenile onset glaucoma.

Kiwaki T, Umehara F, Takashima H, Nakagawa M, Kamimura K, Kashio N, Sakamoto Y, Unoki K, Nobuhara Y, Michizono K, Watanabe O, Arimura H, Osame M. Kiwaki T, et al. Among authors: watanabe o. Neurology. 2000 Aug 8;55(3):392-7. doi: 10.1212/wnl.55.3.392. Neurology. 2000. PMID: 10932274

2

Circulating levels of MMP-1, -2, -3, -9, and TIMP-1 are increased in POEMS syndrome.

Michizono K, Umehara F, Hashiguchi T, Arimura K, Matsuura E, Watanabe O, Fujimoto N, Okada Y, Osame M. Michizono K, et al. Among authors: watanabe o. Neurology. 2001 Mar 27;56(6):807-10. doi: 10.1212/wnl.56.6.807. Neurology. 2001. PMID: 11274326

3

[A case of a syndrome resembling PSP after aortic arch replacement under deep hypothermic circulatory arrest].

Sakiyama Y, Michizono K, Tomari S, Watanabe O, Nakahara K, Takashima H. Sakiyama Y, et al. Among authors: watanabe o. Rinsho Shinkeigaku. 2011 Jan;51(1):38-42. doi: 10.5692/clinicalneurol.51.38. Rinsho Shinkeigaku. 2011. PMID: 21387699 Japanese.

4

A new mitochondria-related disease showing myopathy with episodic hyper-creatine kinase-emia.

Okamoto Y, Higuchi I, Sakiyama Y, Tokunaga S, Watanabe O, Arimura K, Nakagawa M, Takashima H. Okamoto Y, et al. Among authors: watanabe o. Ann Neurol. 2011 Sep;70(3):486-92. doi: 10.1002/ana.22498. Ann Neurol. 2011. PMID: 21905081

5

A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy.

Sakiyama Y, Okamoto Y, Higuchi I, Inamori Y, Sangatsuda Y, Michizono K, Watanabe O, Hatakeyama H, Goto Y, Arimura K, Takashima H. Sakiyama Y, et al. Among authors: watanabe o. Acta Neuropathol. 2011 Jun;121(6):775-83. doi: 10.1007/s00401-011-0818-y. Epub 2011 Mar 22. Acta Neuropathol. 2011. PMID: 21424749 Free PMC article.

6

Mechanism of action of voltage-gated K+ channel antibodies in acquired neuromyotonia.

Tomimitsu H, Arimura K, Nagado T, Watanabe O, Otsuka R, Kurono A, Sonoda Y, Osame M, Kameyama M. Tomimitsu H, et al. Among authors: watanabe o. Ann Neurol. 2004 Sep;56(3):440-4. doi: 10.1002/ana.20221. Ann Neurol. 2004. PMID: 15349875

7

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. 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

8

[A case of reversible cerebral vasoconstriction syndrome (RCVS) triggered by a Chinese herbal medicine].

Ichiki M, Watanabe O, Okamoto Y, Ikeda K, Takashima H, Arimura K. Ichiki M, et al. Among authors: watanabe o. Rinsho Shinkeigaku. 2008 Apr;48(4):267-70. doi: 10.5692/clinicalneurol.48.267. Rinsho Shinkeigaku. 2008. PMID: 18453160 Japanese.

9

[A case of Lyme neuroborreliosis coexistent with T-cell lymphoma].

Nagata R, Inamori Y, Takata Y, Ikeda K, Watanabe O, Takashima H. Nagata R, et al. Among authors: watanabe o. Rinsho Shinkeigaku. 2014;54(2):146-50. doi: 10.5692/clinicalneurol.54.146. Rinsho Shinkeigaku. 2014. PMID: 24583590 Japanese.

10

Partial deficiency of emerin caused by a splice site mutation in EMD.

Yuan J, Ando M, Higuchi I, Sakiyama Y, Matsuura E, Michizono K, Watanabe O, Nagano S, Inamori Y, Hashiguchi A, Higuchi Y, Yoshimura A, Takashima H. Yuan J, et al. Among authors: watanabe o. Intern Med. 2014;53(14):1563-8. doi: 10.2169/internalmedicine.53.8922. Epub 2014 Jul 15. Intern Med. 2014. PMID: 25030574 Free article.

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