Nishino I - Search Results

1

[A Japanese family with POMT2-related limb girdle muscular dystrophy].

Tomita Y, Matusya N, Narita T, Saito Y, Nishino I, Fukudome T. Tomita Y, et al. Among authors: nishino i. Rinsho Shinkeigaku. 2021 Jun 29;61(6):378-384. doi: 10.5692/clinicalneurol.cn-001547. Epub 2021 May 20. Rinsho Shinkeigaku. 2021. PMID: 34011809 Japanese.

2

Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patients.

Tagawa K, Ogawa M, Kawabe K, Yamanaka G, Matsumura T, Goto K, Nonaka I, Nishino I, Hayashi YK. Tagawa K, et al. Among authors: nishino i. J Neurol Sci. 2003 Jul 15;211(1-2):23-8. doi: 10.1016/s0022-510x(03)00041-8. J Neurol Sci. 2003. PMID: 12767493

3

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.

4

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

5

[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.

6

Congenital muscular dystrophy with glycosylation defects of alpha-dystroglycan in Japan.

Matsumoto H, Hayashi YK, Kim DS, Ogawa M, Murakami T, Noguchi S, Nonaka I, Nakazawa T, Matsuo T, Futagami S, Campbell KP, Nishino I. Matsumoto H, et al. Among authors: nishino i. Neuromuscul Disord. 2005 May;15(5):342-8. doi: 10.1016/j.nmd.2005.01.009. Neuromuscul Disord. 2005. PMID: 15833426

7

[Molecular pathomechanism of distal myopathy with rimmed vacuoles].

Nishino I, Noguchi S, Murayama K, Ohkuma A, Kasahata N, Malicdan MC, Hayashi YK, Nonaka I. Nishino I, et al. Rinsho Shinkeigaku. 2005 Nov;45(11):943-5. Rinsho Shinkeigaku. 2005. PMID: 16447769 Review. Japanese.

8

Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in alpha-dystroglycanopathies.

Taniguchi M, Kurahashi H, Noguchi S, Fukudome T, Okinaga T, Tsukahara T, Tajima Y, Ozono K, Nishino I, Nonaka I, Toda T. Taniguchi M, et al. Among authors: nishino i. Hum Mol Genet. 2006 Apr 15;15(8):1279-89. doi: 10.1093/hmg/ddl045. Epub 2006 Mar 10. Hum Mol Genet. 2006. PMID: 16531417

9

Characterization of lobulated fibers in limb girdle muscular dystrophy type 2A by gene expression profiling.

Keira Y, Noguchi S, Kurokawa R, Fujita M, Minami N, Hayashi YK, Kato T, Nishino I. Keira Y, et al. Among authors: nishino i. Neurosci Res. 2007 Apr;57(4):513-21. doi: 10.1016/j.neures.2006.12.010. Epub 2007 Jan 5. Neurosci Res. 2007. PMID: 17258832

10

Limb-girdle muscular dystrophy due to emerin gene mutations.

Ura S, Hayashi YK, Goto K, Astejada MN, Murakami T, Nagato M, Ohta S, Daimon Y, Takekawa H, Hirata K, Nonaka I, Noguchi S, Nishino I. Ura S, et al. Among authors: nishino i. Arch Neurol. 2007 Jul;64(7):1038-41. doi: 10.1001/archneur.64.7.1038. Arch Neurol. 2007. PMID: 17620497

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