Hayashi M - Search Results

1

A mutation of COX6A1 causes a recessive axonal or mixed form of Charcot-Marie-Tooth disease.

Tamiya G, Makino S, Hayashi M, Abe A, Numakura C, Ueki M, Tanaka A, Ito C, Toshimori K, Ogawa N, Terashima T, Maegawa H, Yanagisawa D, Tooyama I, Tada M, Onodera O, Hayasaka K. Tamiya G, et al. Among authors: hayashi m. Am J Hum Genet. 2014 Sep 4;95(3):294-300. doi: 10.1016/j.ajhg.2014.07.013. Epub 2014 Aug 21. Am J Hum Genet. 2014. PMID: 25152455 Free PMC article.

2

Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan.

Abe A, Numakura C, Kijima K, Hayashi M, Hashimoto T, Hayasaka K. Abe A, et al. Among authors: hayashi m. J Hum Genet. 2011 May;56(5):364-8. doi: 10.1038/jhg.2011.20. Epub 2011 Feb 17. J Hum Genet. 2011. PMID: 21326314

3

Molecular analysis of the genes causing recessive demyelinating Charcot-Marie-Tooth disease in Japan.

Hayashi M, Abe A, Murakami T, Yamao S, Arai H, Hattori H, Iai M, Watanabe K, Oka N, Chida K, Kishikawa Y, Hayasaka K. Hayashi M, et al. J Hum Genet. 2013 May;58(5):273-8. doi: 10.1038/jhg.2013.15. Epub 2013 Mar 7. J Hum Genet. 2013. PMID: 23466821

4

The first Japanese case of Charcot-Marie-Tooth disease type 4H with a novel FGD4 c.837-1G>A mutation.

Arai H, Hayashi M, Hayasaka K, Kanda T, Tanabe Y. Arai H, et al. Among authors: hayashi m. Neuromuscul Disord. 2013 Aug;23(8):652-5. doi: 10.1016/j.nmd.2013.04.010. Epub 2013 Jun 14. Neuromuscul Disord. 2013. PMID: 23770104

5

Mild phenotype of Charcot-Marie-Tooth disease type 4B1.

Murakami T, Kutoku Y, Nishimura H, Hayashi M, Abe A, Hayasaka K, Sunada Y. Murakami T, et al. Among authors: hayashi m. J Neurol Sci. 2013 Nov 15;334(1-2):176-9. doi: 10.1016/j.jns.2013.08.001. Epub 2013 Aug 9. J Neurol Sci. 2013. PMID: 23962696

6

Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome.

Meguro T, Yoshida Y, Hayashi M, Toyota K, Otagiri T, Mochizuki N, Kishikawa Y, Sasaki A, Hayasaka K. Meguro T, et al. Among authors: hayashi m. J Hum Genet. 2012 May;57(5):335-7. doi: 10.1038/jhg.2012.27. Epub 2012 Mar 22. J Hum Genet. 2012. PMID: 22437207

7

INF2 mutations in Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis.

Toyota K, Ogino D, Hayashi M, Taki M, Saito K, Abe A, Hashimoto T, Umetsu K, Tsukaguchi H, Hayasaka K. Toyota K, et al. Among authors: hayashi m. J Peripher Nerv Syst. 2013 Mar;18(1):97-8. doi: 10.1111/jns5.12014. J Peripher Nerv Syst. 2013. PMID: 23521651 No abstract available.

8

Prognostic Impact of CDKN2A Mutations Associated With Smoking and Drinking History in Japanese Digestive Cancers.

Fujita K, Hayashi M, Nakagawa N, Kurimoto K, Inokawa Y, Takami H, Nakanishi K, Umeda S, Shimizu D, Hattori N, Kanda M, Tanaka C, Nakayama G, Kodera Y. Fujita K, et al. Among authors: hayashi m. Anticancer Res. 2024 Jun;44(6):2699-2707. doi: 10.21873/anticanres.17077. Anticancer Res. 2024. PMID: 38821577

9

A low baseline serum myostatin concentration is associated with poor clinical outcome in patients with primary biliary cholangitis.

Hayashi M, Abe K, Sugaya T, Takahata Y, Fujita M, Takahashi A, Ohira H. Hayashi M, et al. J Gastroenterol Hepatol. 2024 May 30. doi: 10.1111/jgh.16639. Online ahead of print. J Gastroenterol Hepatol. 2024. PMID: 38816894

10

Serum miR‑29 is increased in mice with early liver fibrosis.

Matsumoto K, Ohsugi Y, Tayama C, Hayashi M, Kato Y, Ohashi M, Chiba M. Matsumoto K, et al. Among authors: hayashi m. Exp Ther Med. 2024 May 15;28(1):285. doi: 10.3892/etm.2024.12573. eCollection 2024 Jul. Exp Ther Med. 2024. PMID: 38800048 Free PMC article.

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