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Items: 10

1.

New type of encephalomyelitis responsive to trimethoprim/sulfamethoxazole treatment in Japan.

Sakiyama Y, Kanda N, Higuchi Y, Yoshimura M, Wakaguri H, Takata Y, Watanabe O, Yuan J, Tashiro Y, Saigo R, Nozuma S, Yoshimura A, Arishima S, Ikeda K, Shinohara K, Arata H, Michizono K, Higashi K, Hashiguchi A, Okamoto Y, Hirano R, Shiraishi T, Matsuura E, Okubo R, Higuchi I, Goto M, Hirano H, Sano A, Iwasaki T, Matsuda F, Izumo S, Takashima H.

Neurol Neuroimmunol Neuroinflamm. 2015 Aug 13;2(5):e143. doi: 10.1212/NXI.0000000000000143. eCollection 2015 Oct.

2.

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.

Intern Med. 2014;53(14):1563-8. Epub 2014 Jul 15.

3.

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.

Acta Neuropathol. 2011 Jun;121(6):775-83. doi: 10.1007/s00401-011-0818-y. Epub 2011 Mar 22.

4.

[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.

Rinsho Shinkeigaku. 2011 Jan;51(1):38-42. Japanese.

PMID:
21387699
5.

SET binding factor 2 (SBF2) mutation causes CMT4B with juvenile onset glaucoma.

Hirano R, Takashima H, Umehara F, Arimura H, Michizono K, Okamoto Y, Nakagawa M, Boerkoel CF, Lupski JR, Osame M, Arimura K.

Neurology. 2004 Aug 10;63(3):577-80.

PMID:
15304601
6.

Involvement of Fas/Fas ligand system in the spinal cords of HTLV-I-associated myelopathy.

Umehara F, Itoh K, Michizono K, Abe M, Izumo S, Osame M.

Acta Neuropathol. 2002 Apr;103(4):384-90. Epub 2001 Dec 15.

PMID:
11904759
7.

Usefulness of transcutaneous Doppler jugular venous echo to predict pulmonary hypertension in COPD patients.

Matsuyama W, Ohkubo R, Michizono K, Abe M, Nakamura Y, Kawabata M, Osame M.

Eur Respir J. 2001 Jun;17(6):1128-31.

8.

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.

Neurology. 2001 Mar 27;56(6):807-10.

PMID:
11274326
9.

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.

Neurology. 2000 Aug 8;55(3):392-7.

PMID:
10932274
10.

Autosomal dominant early onset dementia and leukoencephalopathy in a Japanese family: clinical, neuroimaging and genetic studies.

Utatsu Y, Takashima H, Michizono K, Kanda N, Endou K, Mitsuyama Y, Fujimoto T, Nagai M, Umehara F, Higuchi I, Arimura K, Nakagawa M, Osame M.

J Neurol Sci. 1997 Mar 20;147(1):55-62.

PMID:
9094061

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