Nonaka I - Search Results

1

Central core disease and congenital neuromuscular disease with uniform type 1 fibers in one family.

Tojo M, Ozawa M, Nonaka I. Tojo M, et al. Among authors: nonaka i. Brain Dev. 2000 Jun;22(4):262-4. doi: 10.1016/s0387-7604(00)00108-x. Brain Dev. 2000. PMID: 10838116

2

Peripheral nerve involvement in Werdnig-Hoffmann disease.

Chien YY, Nonaka I. Chien YY, et al. Among authors: nonaka i. Brain Dev. 1989;11(4):221-9. doi: 10.1016/s0387-7604(89)80040-3. Brain Dev. 1989. PMID: 2774090

3

[Strongly succinate dehydrogenase-reactive blood vessels (SSV) in various neuromuscular diseases].

Matsuoka T, Hasegawa H, Nonaka I. Matsuoka T, et al. Among authors: nonaka i. Rinsho Shinkeigaku. 1992 Jun;32(6):645-7. Rinsho Shinkeigaku. 1992. PMID: 1424348 Japanese.

4

[Significance of rimmed vacuoles in neuromuscular disorders--a comparative immunohistochemical study of inclusion body myositis and distal myopathy with rimmed vacuole formation].

Murakami N, Takemitsu M, Kurashige T, Nonaka I. Murakami N, et al. Among authors: nonaka i. Rinsho Shinkeigaku. 1994 Aug;34(8):782-7. Rinsho Shinkeigaku. 1994. PMID: 7994984 Japanese.

5

[A patient with lysosomal glycogen storage disease with normal acid maltase].

Itoh M, Asano Y, Shimohira M, Iwakawa Y, Goto Y, Nonaka I. Itoh M, et al. Among authors: nonaka i. No To Hattatsu. 1993 Sep;25(5):459-64. No To Hattatsu. 1993. PMID: 8398237 Japanese.

6

14-3-3 proteins, particularly of the epsilon isoform, are detectable in cerebrospinal fluids of cerebellar diseases in children.

Fujii K, Uchikawa H, Tanabe Y, Omata T, Nonaka I, Kohno Y. Fujii K, et al. Among authors: nonaka i. Brain Dev. 2013 Jun;35(6):555-60. doi: 10.1016/j.braindev.2012.09.007. Epub 2012 Oct 15. Brain Dev. 2013. PMID: 23078967

7

Bilateral occipital cortical dysplasia and white matter T2 hyperintensity with mild non-specific myopathy: two sibling cases.

Okanishi T, Ishikawa T, Kobayashi S, Ando N, Nishino I, Togari H, Nonaka I. Okanishi T, et al. Among authors: nonaka i. Brain Dev. 2010 Apr;32(4):342-6. doi: 10.1016/j.braindev.2009.11.006. Epub 2009 Dec 22. Brain Dev. 2010. PMID: 20022722

8

A novel FKRP gene mutation in a Taiwanese patient with limb-girdle muscular dystrophy 2I.

Lin YC, Murakami T, Hayashi YK, Nishino I, Nonaka I, Yuo CY, Jong YJ. Lin YC, et al. Among authors: nonaka i. Brain Dev. 2007 May;29(4):234-8. doi: 10.1016/j.braindev.2006.09.006. Epub 2006 Oct 20. Brain Dev. 2007. PMID: 17055682

9

A case of congenital neuromuscular disease with uniform type 1 fibers.

Sakamoto HM, Yoshioka M, Tsuji M, Kuroki S, Higuchi Y, Nonaka I, Nishino I. Sakamoto HM, et al. Among authors: nonaka i. Brain Dev. 2006 Apr;28(3):202-5. doi: 10.1016/j.braindev.2005.06.008. Epub 2006 Jan 18. Brain Dev. 2006. PMID: 16413720

10

Intranuclear rods myopathy with autonomic dysfunction.

Chou PC, Liang WC, Nonaka I, Mitsuhashi S, Nishino I, Jong YJ. Chou PC, et al. Among authors: nonaka i. Brain Dev. 2013 Aug;35(7):686-9. doi: 10.1016/j.braindev.2012.09.011. Epub 2012 Oct 25. Brain Dev. 2013. PMID: 23102861

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