Nishino I - Search Results

1

Characteristics of the muscle involvement along the disease progression in a large cohort of oculopharyngodistal myopathy compared to oculopharyngeal muscular dystrophy.

Eura N, Noguchi S, Ogasawara M, Kumutpongpanich T, Hayashi S, Nishino I; OPDM/OPMD Image Study Group. Eura N, et al. Among authors: nishino i. J Neurol. 2023 Dec;270(12):5988-5998. doi: 10.1007/s00415-023-11906-9. Epub 2023 Aug 27. J Neurol. 2023. PMID: 37634163

2

Muscular dystrophies.

Nishino I, Ozawa E. Nishino I, et al. Curr Opin Neurol. 2002 Oct;15(5):539-44. doi: 10.1097/00019052-200210000-00004. Curr Opin Neurol. 2002. PMID: 12351997 Review.

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

Reduction of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distal myopathy with rimmed vacuoles.

Noguchi S, Keira Y, Murayama K, Ogawa M, Fujita M, Kawahara G, Oya Y, Imazawa M, Goto Y, Hayashi YK, Nonaka I, Nishino I. Noguchi S, et al. Among authors: nishino i. J Biol Chem. 2004 Mar 19;279(12):11402-7. doi: 10.1074/jbc.M313171200. Epub 2004 Jan 5. J Biol Chem. 2004. PMID: 14707127 Free article.

6

Subcellular localization of fukutin and fukutin-related protein in muscle cells.

Matsumoto H, Noguchi S, Sugie K, Ogawa M, Murayama K, Hayashi YK, Nishino I. Matsumoto H, et al. Among authors: nishino i. J Biochem. 2004 Jun;135(6):709-12. doi: 10.1093/jb/mvh086. J Biochem. 2004. PMID: 15213246 Free article.

7

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

8

[The pathomechanism and the direction of therapy development in view of cDNA microarray].

Nishino I, Hayashi YK, Noguchi S. Nishino I, et al. Rinsho Shinkeigaku. 2004 Nov;44(11):905-7. Rinsho Shinkeigaku. 2004. PMID: 15651327 Review. Japanese.

9

Distal myopathy with rimmed vacuoles and hereditary inclusion body myopathy.

Nonaka I, Noguchi S, Nishino I. Nonaka I, et al. Among authors: nishino i. Curr Neurol Neurosci Rep. 2005 Feb;5(1):61-5. doi: 10.1007/s11910-005-0025-0. Curr Neurol Neurosci Rep. 2005. PMID: 15676110 Review.

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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