Nishino I - Search Results

1

Sarcoplasmic MxA expression: A valuable marker of dermatomyositis.

Uruha A, Nishikawa A, Tsuburaya RS, Hamanaka K, Kuwana M, Watanabe Y, Suzuki S, Suzuki N, Nishino I. Uruha A, et al. Among authors: nishino i. Neurology. 2017 Jan 31;88(5):493-500. doi: 10.1212/WNL.0000000000003568. Epub 2016 Dec 30. Neurology. 2017. PMID: 28039312

2

[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.

3

Diagnostic significance of membrane attack complex and vitronectin in childhood dermatomyositis.

Sakuta R, Murakami N, Jin Y, Nagai T, Nonaka I, Nishino I. Sakuta R, et al. Among authors: nishino i. J Child Neurol. 2005 Jul;20(7):597-602. doi: 10.1177/08830738050200071201. J Child Neurol. 2005. PMID: 16159528

4

Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness.

Murakami T, Hayashi YK, Noguchi S, Ogawa M, Nonaka I, Tanabe Y, Ogino M, Takada F, Eriguchi M, Kotooka N, Campbell KP, Osawa M, Nishino I. Murakami T, et al. Among authors: nishino i. Ann Neurol. 2006 Nov;60(5):597-602. doi: 10.1002/ana.20973. Ann Neurol. 2006. PMID: 17036286

5

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

6

Myotubular/centronuclear myopathy and central core disease.

Fujimura-Kiyono C, Racz GZ, Nishino I. Fujimura-Kiyono C, et al. Among authors: nishino i. Neurol India. 2008 Jul-Sep;56(3):325-32. doi: 10.4103/0028-3886.43451. Neurol India. 2008. PMID: 18974559 Free article. Review.

7

TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathy.

Liang WC, Mitsuhashi H, Keduka E, Nonaka I, Noguchi S, Nishino I, Hayashi YK. Liang WC, et al. Among authors: nishino i. Ann Neurol. 2011 Jun;69(6):1005-13. doi: 10.1002/ana.22338. Epub 2011 Mar 9. Ann Neurol. 2011. PMID: 21391237

8

Lobulated fibers in a patient with 46-year history of limb-girdle muscle weakness.

Tsuburaya R, Suzuki T, Saiki K, Nonaka I, Sugita H, Hayashi YK, Nishino I. Tsuburaya R, et al. Among authors: nishino i. Neuropathology. 2011 Aug;31(4):455-7. doi: 10.1111/j.1440-1789.2011.01221.x. Epub 2011 Apr 26. Neuropathology. 2011. PMID: 21518015 No abstract available.

9

Inflammatory changes in infantile-onset LMNA-associated myopathy.

Komaki H, Hayashi YK, Tsuburaya R, Sugie K, Kato M, Nagai T, Imataka G, Suzuki S, Saitoh S, Asahina N, Honke K, Higuchi Y, Sakuma H, Saito Y, Nakagawa E, Sugai K, Sasaki M, Nonaka I, Nishino I. Komaki H, et al. Among authors: nishino i. Neuromuscul Disord. 2011 Aug;21(8):563-8. doi: 10.1016/j.nmd.2011.04.010. Epub 2011 May 31. Neuromuscul Disord. 2011. PMID: 21632249

10

Anti-signal recognition particle myopathy in the first decade of life.

Suzuki S, Ohta M, Shimizu Y, Hayashi YK, Nishino I. Suzuki S, et al. Among authors: nishino i. Pediatr Neurol. 2011 Aug;45(2):114-6. doi: 10.1016/j.pediatrneurol.2011.04.009. Pediatr Neurol. 2011. PMID: 21763952

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