Nishino I - Search Results

1

A symptomatic male carrier of Duchenne muscular dystrophy with Klinefelter's syndrome mimicking Becker muscular dystrophy.

Takizawa H, Mori-Yoshimura M, Minami N, Murakami N, Yatabe K, Taira K, Hashimoto Y, Aoki Y, Nishino I, Takahashi Y. Takizawa H, et al. Among authors: nishino i. Neuromuscul Disord. 2021 Jul;31(7):666-672. doi: 10.1016/j.nmd.2021.04.006. Epub 2021 Apr 27. Neuromuscul Disord. 2021. PMID: 34172357

2

Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene.

Yamasoba T, Goto Yi, Oka Y, Nishino I, Tsukuda K, Nonaka I. Yamasoba T, et al. Among authors: nishino i. Neuromuscul Disord. 2002 Jun;12(5):506-12. doi: 10.1016/s0960-8966(01)00329-7. Neuromuscul Disord. 2002. PMID: 12031626

3

cDNA microarray analysis of individual Duchenne muscular dystrophy patients.

Noguchi S, Tsukahara T, Fujita M, Kurokawa R, Tachikawa M, Toda T, Tsujimoto A, Arahata K, Nishino I. Noguchi S, et al. Among authors: nishino i. Hum Mol Genet. 2003 Mar 15;12(6):595-600. Hum Mol Genet. 2003. PMID: 12620965

4

Localization of calpain 3 in human skeletal muscle and its alteration in limb-girdle muscular dystrophy 2A muscle.

Keira Y, Noguchi S, Minami N, Hayashi YK, Nishino I. Keira Y, et al. Among authors: nishino i. J Biochem. 2003 May;133(5):659-64. doi: 10.1093/jb/mvg084. J Biochem. 2003. PMID: 12801918 Free article.

5

[Appearance of numerous lobulated fibers after a protracted course of 18 years in a case of dermatomyositis].

Onodera N, Miyamoto K, Matsubara S, Hayashi H, Minami N, Nishino I. Onodera N, et al. Among authors: nishino i. Rinsho Shinkeigaku. 2003 May;43(5):270-3. Rinsho Shinkeigaku. 2003. PMID: 12931633 Japanese.

6

Characterization of Danon disease in a male patient and his affected mother.

Sugie K, Koori T, Yamamoto A, Ogawa M, Hirano M, Inoue K, Nonaka I, Nishino I. Sugie K, et al. Among authors: nishino i. Neuromuscul Disord. 2003 Nov;13(9):708-11. doi: 10.1016/s0960-8966(03)00105-6. Neuromuscul Disord. 2003. PMID: 14561493

7

FSHD-like patients without 4q35 deletion.

Yamanaka G, Goto K, Ishihara T, Oya Y, Miyajima T, Hoshika A, Nishino I, Hayashi YK. Yamanaka G, et al. Among authors: nishino i. J Neurol Sci. 2004 Apr 15;219(1-2):89-93. doi: 10.1016/j.jns.2003.12.010. J Neurol Sci. 2004. PMID: 15050443

8

Two novel CAV3 gene mutations in Japanese families.

Sugie K, Murayama K, Noguchi S, Murakami N, Mochizuki M, Hayashi YK, Nonaka I, Nishino I. Sugie K, et al. Among authors: nishino i. Neuromuscul Disord. 2004 Dec;14(12):810-4. doi: 10.1016/j.nmd.2004.08.008. Neuromuscul Disord. 2004. PMID: 15564037

9

Dysferlinopathy associated with rigid spine syndrome.

Nagashima T, Chuma T, Mano Y, Goto Y, Hayashi YK, Minami N, Nishino I, Nonaka I, Takahashi T, Sawa H, Aoki M, Nagashima K. Nagashima T, et al. Among authors: nishino i. Neuropathology. 2004 Dec;24(4):341-6. doi: 10.1111/j.1440-1789.2004.00573.x. Neuropathology. 2004. PMID: 15641596

10

Characterization of MTM1 mutations in 31 Japanese families with myotubular myopathy, including a patient carrying 240 kb deletion in Xq28 without male hypogenitalism.

Tsai TC, Horinouchi H, Noguchi S, Minami N, Murayama K, Hayashi YK, Nonaka I, Nishino I. Tsai TC, et al. Among authors: nishino i. Neuromuscul Disord. 2005 Mar;15(3):245-52. doi: 10.1016/j.nmd.2004.12.005. Epub 2005 Jan 28. Neuromuscul Disord. 2005. PMID: 15725586

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