Kaida KI - Search Results

1

Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy.

Ishiura H, Doi K, Mitsui J, Yoshimura J, Matsukawa MK, Fujiyama A, Toyoshima Y, Kakita A, Takahashi H, Suzuki Y, Sugano S, Qu W, Ichikawa K, Yurino H, Higasa K, Shibata S, Mitsue A, Tanaka M, Ichikawa Y, Takahashi Y, Date H, Matsukawa T, Kanda J, Nakamoto FK, Higashihara M, Abe K, Koike R, Sasagawa M, Kuroha Y, Hasegawa N, Kanesawa N, Kondo T, Hitomi T, Tada M, Takano H, Saito Y, Sanpei K, Onodera O, Nishizawa M, Nakamura M, Yasuda T, Sakiyama Y, Otsuka M, Ueki A, Kaida KI, Shimizu J, Hanajima R, Hayashi T, Terao Y, Inomata-Terada S, Hamada M, Shirota Y, Kubota A, Ugawa Y, Koh K, Takiyama Y, Ohsawa-Yoshida N, Ishiura S, Yamasaki R, Tamaoka A, Akiyama H, Otsuki T, Sano A, Ikeda A, Goto J, Morishita S, Tsuji S. Ishiura H, et al. Among authors: kaida ki. Nat Genet. 2018 Apr;50(4):581-590. doi: 10.1038/s41588-018-0067-2. Epub 2018 Mar 5. Nat Genet. 2018. PMID: 29507423

2

A novel mutation in the gene for the adult skeletal muscle sodium channel alpha-subunit (SCN4A) that causes paramyotonia congenita of von Eulenburg.

Sasaki R, Takano H, Kamakura K, Kaida K, Hirata A, Saito M, Tanaka H, Kuzuhara S, Tsuji S. Sasaki R, et al. Arch Neurol. 1999 Jun;56(6):692-6. doi: 10.1001/archneur.56.6.692. Arch Neurol. 1999. PMID: 10369308

3

Far-field potentials in hypothenar motor unit number estimation.

Higashihara M, Sonoo M, Yamamoto T, Kawamura Y, Nagashima Y, Terao Y, Kaida K, Kimura F, Ugawa Y, Tsuji S. Higashihara M, et al. Muscle Nerve. 2013 Aug;48(2):191-7. doi: 10.1002/mus.23734. Epub 2013 Feb 4. Muscle Nerve. 2013. PMID: 23381934

4

[Case report: a case of chronic inflammatory demyelinating polyneuropathy (CIDP) exacerbated by influenza vaccination].

Morooka M, Maekawa R, Hida A, Shimizu J, Kaida K, Naruse H, Nagashima Y, Shiio Y. Morooka M, et al. Nihon Naika Gakkai Zasshi. 2013 Apr 10;102(4):963-5. doi: 10.2169/naika.102.963. Nihon Naika Gakkai Zasshi. 2013. PMID: 23772511 Japanese. No abstract available.

5

Recurrent K3E mutation in Cu/Zn superoxide dismutase gene associated with amyotrophic lateral sclerosis.

Kuźma-Kozakiewicz M, Berdyński M, Morita M, Takahashi Y, Kawata A, Kaida K, Kaźmierczak B, Lusakowska A, Goto J, Tsuji S, Zekanowski C, Kwieciński H. Kuźma-Kozakiewicz M, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2013 Dec;14(7-8):608-14. doi: 10.3109/21678421.2013.812119. Epub 2013 Jul 30. Amyotroph Lateral Scler Frontotemporal Degener. 2013. PMID: 23898858

6

[Case of wall-eyed bilateral internuclear ophthalmoplegia (WEBINO) syndrome with cerebellar ataxia and facial dysesthesia].

Kadoya M, Onoue H, Kadoya A, Higashihara M, Ikewaki K, Kaida K. Kadoya M, et al. Rinsho Shinkeigaku. 2014;54(4):317-20. doi: 10.5692/clinicalneurol.54.317. Rinsho Shinkeigaku. 2014. PMID: 24807275 Japanese.

7

Repeated treatments with rituximab in a patient with amyloid-like IgM deposition neuropathy.

Kadoya M, Kadoya A, Onoue H, Ikewaki K, Shimizu J, Kaida K. Kadoya M, et al. Neurol Neuroimmunol Neuroinflamm. 2016 Mar 31;3(3):e220. doi: 10.1212/NXI.0000000000000220. eCollection 2016 Jun. Neurol Neuroimmunol Neuroinflamm. 2016. PMID: 27088116 Free PMC article. No abstract available.

8

IgG4 anti-neurofascin155 antibodies in chronic inflammatory demyelinating polyradiculoneuropathy: Clinical significance and diagnostic utility of a conventional assay.

Kadoya M, Kaida K, Koike H, Takazaki H, Ogata H, Moriguchi K, Shimizu J, Nagata E, Takizawa S, Chiba A, Yamasaki R, Kira JI, Sobue G, Ikewaki K. Kadoya M, et al. J Neuroimmunol. 2016 Dec 15;301:16-22. doi: 10.1016/j.jneuroim.2016.10.013. Epub 2016 Nov 9. J Neuroimmunol. 2016. PMID: 27852440

9

Clinicopathologic features of myositis patients with CD8-MHC-1 complex pathology.

Ikenaga C, Kubota A, Kadoya M, Taira K, Uchio N, Hida A, Maeda MH, Nagashima Y, Ishiura H, Kaida K, Goto J, Tsuji S, Shimizu J. Ikenaga C, et al. Neurology. 2017 Sep 5;89(10):1060-1068. doi: 10.1212/WNL.0000000000004333. Epub 2017 Aug 9. Neurology. 2017. PMID: 28794251

10

Familial paroxysmal dystonic choreoathetosis: clinical findings in a large Japanese family and genetic linkage to 2q.

Matsuo H, Kamakura K, Saito M, Okano M, Nagase T, Tadano Y, Kaida K, Hirata A, Miyamoto N, Masaki T, Nakamura R, Motoyoshi K, Tanaka H, Tsuji S. Matsuo H, et al. Arch Neurol. 1999 Jun;56(6):721-6. doi: 10.1001/archneur.56.6.721. Arch Neurol. 1999. PMID: 10369313

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