Hayashi YK - Search Results

1

Tanboon J, Viravan S, Hayashi YK, Nishino I, Sangruchi T. Tanboon J, et al. Among authors: hayashi yk. Brain Pathol. 2015 Sep;25(5):651-2. doi: 10.1111/bpa.12284. Brain Pathol. 2015. PMID: 26276028 Free PMC article. No abstract available.

2

A 31-Year-Old Man with Slowly Progressive Limb Muscle Weakness and Respiratory Insufficiency.

Uruha A, Hayashi YK, Mori-Yoshimura M, Oya Y, Kanai M, Murata M, Nishino I. Uruha A, et al. Among authors: hayashi yk. Brain Pathol. 2018 Jan;28(1):123-124. doi: 10.1111/bpa.12575. Brain Pathol. 2018. PMID: 29265629 Free PMC article. No abstract available.

3

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: hayashi yk. 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

4

Kyphoscoliosis and easy fatigability in a 14-year-old boy.

Tanboon J, Hayashi YK, Nishino I, Sangruchi T. Tanboon J, et al. Among authors: hayashi yk. Neuropathology. 2015 Feb;35(1):91-3. doi: 10.1111/neup.12147. Epub 2014 Aug 28. Neuropathology. 2015. PMID: 25168271 No abstract available.

5

Muscle from a 20-week-old myotubular myopathy fetus is not myotubular.

Hamanaka K, Inami I, Wada T, Mitsuhashi S, Noguchi S, Hayashi YK, Nishino I. Hamanaka K, et al. Among authors: hayashi yk. Neuromuscul Disord. 2016 Mar;26(3):234-5. doi: 10.1016/j.nmd.2015.11.010. Epub 2015 Dec 3. Neuromuscul Disord. 2016. PMID: 26898940 No abstract available.

6

Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuoles.

Ozawa R, Hayashi YK, Ogawa M, Kurokawa R, Matsumoto H, Noguchi S, Nonaka I, Nishino I. Ozawa R, et al. Among authors: hayashi yk. Am J Pathol. 2006 Mar;168(3):907-17. doi: 10.2353/ajpath.2006.050564. Am J Pathol. 2006. PMID: 16507906 Free PMC article.

7

Central core disease is due to RYR1 mutations in more than 90% of patients.

Wu S, Ibarra MC, Malicdan MC, Murayama K, Ichihara Y, Kikuchi H, Nonaka I, Noguchi S, Hayashi YK, Nishino I. Wu S, et al. Among authors: hayashi yk. Brain. 2006 Jun;129(Pt 6):1470-80. doi: 10.1093/brain/awl077. Epub 2006 Apr 18. Brain. 2006. PMID: 16621918

8

Mutation analysis of the GNE gene in distal myopathy with rimmed vacuoles (DMRV) patients in Thailand.

Liewluck T, Pho-Iam T, Limwongse C, Thongnoppakhun W, Boonyapisit K, Raksadawan N, Murayama K, Hayashi YK, Nishino I, Sangruchi T. Liewluck T, et al. Among authors: hayashi yk. Muscle Nerve. 2006 Dec;34(6):775-8. doi: 10.1002/mus.20583. Muscle Nerve. 2006. PMID: 16810679

9

A Gne knockout mouse expressing human V572L mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy.

Malicdan MC, Noguchi S, Nonaka I, Hayashi YK, Nishino I. Malicdan MC, et al. Among authors: hayashi yk. Hum Mol Genet. 2007 Jan 15;16(2):115-28. doi: 10.1093/hmg/ddl446. Epub 2006 Dec 12. Hum Mol Genet. 2007. Retraction in: Hum Mol Genet. 2007 Nov 1;16(21):2647. doi: 10.1093/hmg/ddm231 PMID: 17164266 Retracted.

10

A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy.

Malicdan MC, Noguchi S, Nonaka I, Hayashi YK, Nishino I. Malicdan MC, et al. Among authors: hayashi yk. Hum Mol Genet. 2007 Nov 15;16(22):2669-82. doi: 10.1093/hmg/ddm220. Epub 2007 Aug 18. Hum Mol Genet. 2007. PMID: 17704511

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