Nishino I - Search Results

1

Sarcolemmopathy: muscular dystrophies with cell membrane defects.

Ozawa E, Nishino I, Nonaka I. Ozawa E, et al. Among authors: nishino i. Brain Pathol. 2001 Apr;11(2):218-30. doi: 10.1111/j.1750-3639.2001.tb00394.x. Brain Pathol. 2001. PMID: 11303797 Free PMC article. Review.

2

A new congenital muscular dystrophy with mitochondrial structural abnormalities.

Nishino I, Kobayashi O, Goto Y, Kurihara M, Kumagai K, Fujita T, Hashimoto K, Horai S, Nonaka I. Nishino I, et al. Muscle Nerve. 1998 Jan;21(1):40-7. doi: 10.1002/(sici)1097-4598(199801)21:1<40::aid-mus6>3.0.co;2-g. Muscle Nerve. 1998. PMID: 9427222

3

Newly recognized exons induced by a splicing abnormality from an intronic mutation of the dystrophin gene resulting in Duchenne muscular dystrophy. Mutations in brief no. 213. Online.

Ikezawa M, Nishino I, Goto Y, Miike T, Nonaka I. Ikezawa M, et al. Among authors: nishino i. Hum Mutat. 1999;13(2):170. doi: 10.1002/(SICI)1098-1004(1999)13:2<170::AID-HUMU12>3.0.CO;2-7. Hum Mutat. 1999. PMID: 10094556

4

Mutations of calpain 3 gene in patients with sporadic limb-girdle muscular dystrophy in Japan.

Minami N, Nishino I, Kobayashi O, Ikezoe K, Goto Y, Nonaka I. Minami N, et al. Among authors: nishino i. J Neurol Sci. 1999 Dec 1;171(1):31-7. doi: 10.1016/s0022-510x(99)00245-2. J Neurol Sci. 1999. PMID: 10567047

5

Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease).

Nishino I, Fu J, Tanji K, Yamada T, Shimojo S, Koori T, Mora M, Riggs JE, Oh SJ, Koga Y, Sue CM, Yamamoto A, Murakami N, Shanske S, Byrne E, Bonilla E, Nonaka I, DiMauro S, Hirano M. Nishino I, et al. Nature. 2000 Aug 24;406(6798):906-10. doi: 10.1038/35022604. Nature. 2000. PMID: 10972294

6

The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle.

Matsuda C, Hayashi YK, Ogawa M, Aoki M, Murayama K, Nishino I, Nonaka I, Arahata K, Brown RH Jr. Matsuda C, et al. Among authors: nishino i. Hum Mol Genet. 2001 Aug 15;10(17):1761-6. doi: 10.1093/hmg/10.17.1761. Hum Mol Genet. 2001. PMID: 11532985

7

Infantile autophagic vacuolar myopathy is distinct from Danon disease.

Yamamoto A, Morisawa Y, Verloes A, Murakami N, Hirano M, Nonaka I, Nishino I. Yamamoto A, et al. Among authors: nishino i. Neurology. 2001 Sep 11;57(5):903-5. doi: 10.1212/wnl.57.5.903. Neurology. 2001. PMID: 11552028

8

Ullrich disease: collagen VI deficiency: EM suggests a new basis for muscular weakness.

Ishikawa H, Sugie K, Murayama K, Ito M, Minami N, Nishino I, Nonaka I. Ishikawa H, et al. Among authors: nishino i. Neurology. 2002 Sep 24;59(6):920-3. doi: 10.1212/wnl.59.6.920. Neurology. 2002. PMID: 12297580

9

Ullrich disease due to deficiency of collagen VI in the sarcolemma.

Ishikawa H, Sugie K, Murayama K, Awaya A, Suzuki Y, Noguchi S, Hayashi YK, Nonaka I, Nishino I. Ishikawa H, et al. Among authors: nishino i. Neurology. 2004 Feb 24;62(4):620-3. doi: 10.1212/01.wnl.0000113023.84421.00. Neurology. 2004. PMID: 14981181

10

Molecular pathomechanism of distal myopathy with rimmed vacuoles.

Nishino I, Malicdan MC, Murayama K, Nonaka I, Hayashi YK, Noguchi S. Nishino I, et al. Acta Myol. 2005 Oct;24(2):80-3. Acta Myol. 2005. PMID: 16550921 Review.

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