Goto K - Search Results

1

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: goto k. 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

2

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: goto k. 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

3

Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy.

Goto K, Nishino I, Hayashi YK. Goto K, et al. Neuromuscul Disord. 2006 Apr;16(4):256-61. doi: 10.1016/j.nmd.2006.01.008. Epub 2006 Mar 20. Neuromuscul Disord. 2006. PMID: 16545566

4

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: goto k. Arch Neurol. 2007 Jul;64(7):1038-41. doi: 10.1001/archneur.64.7.1038. Arch Neurol. 2007. PMID: 17620497

5

Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy.

Hayashi YK, Matsuda C, Ogawa M, Goto K, Tominaga K, Mitsuhashi S, Park YE, Nonaka I, Hino-Fukuyo N, Haginoya K, Sugano H, Nishino I. Hayashi YK, et al. Among authors: goto k. J Clin Invest. 2009 Sep;119(9):2623-33. doi: 10.1172/JCI38660. Epub 2009 Aug 10. J Clin Invest. 2009. PMID: 19726876 Free PMC article.

6

Congenital fiber type disproportion myopathy caused by LMNA mutations.

Kajino S, Ishihara K, Goto K, Ishigaki K, Noguchi S, Nonaka I, Osawa M, Nishino I, Hayashi YK. Kajino S, et al. Among authors: goto k. J Neurol Sci. 2014 May 15;340(1-2):94-8. doi: 10.1016/j.jns.2014.02.036. Epub 2014 Mar 5. J Neurol Sci. 2014. PMID: 24642510

7

Dysferlin mutation analysis in a group of Italian patients with limb-girdle muscular dystrophy and Miyoshi myopathy.

Kawabe K, Goto K, Nishino I, Angelini C, Hayashi YK. Kawabe K, et al. Among authors: goto k. Eur J Neurol. 2004 Oct;11(10):657-61. doi: 10.1111/j.1468-1331.2004.00755.x. Eur J Neurol. 2004. PMID: 15469449

8

Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan.

Astejada MN, Goto K, Nagano A, Ura S, Noguchi S, Nonaka I, Nishino I, Hayashi YK. Astejada MN, et al. Among authors: goto k. Acta Myol. 2007 Dec;26(3):159-64. Acta Myol. 2007. PMID: 18646565 Free PMC article. Review.

9

Abnormal localization of laminin subunits in muscular dystrophies.

Hayashi YK, Engvall E, Arikawa-Hirasawa E, Goto K, Koga R, Nonaka I, Sugita H, Arahata K. Hayashi YK, et al. Among authors: goto k. J Neurol Sci. 1993 Oct;119(1):53-64. doi: 10.1016/0022-510x(93)90191-z. J Neurol Sci. 1993. PMID: 8246011

10

[Clinical and genetical features of Japanese early-onset facioscapulohumeral muscular dystrophy].

Yamanaka G, Goto K, Hayashi YK, Miyajima T, Hoshika A, Arahata K. Yamanaka G, et al. Among authors: goto k. No To Hattatsu. 2002 Jul;34(4):318-24. No To Hattatsu. 2002. PMID: 12134683 Japanese.

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