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771 results

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Different clinicopathological features between Japanese siblings with facioscapulohumeral muscular dystrophy 2 with a novel nonsense SMCHD1 mutation (Arg552∗).
Ohta Y, Tadokoro K, Sasaki R, Takahashi Y, Sato K, Takemoto M, Hishikawa N, Shang J, Yamashita T, Takehisa Y, Nishino I, Abe K. Ohta Y, et al. Among authors: nishino i. J Clin Neurosci. 2018 Dec;58:215-217. doi: 10.1016/j.jocn.2018.10.021. Epub 2018 Oct 13. J Clin Neurosci. 2018. PMID: 30327220
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
Oculopharyngeal muscular dystrophy associated with dementia.
Mizoi Y, Yamamoto T, Minami N, Ohkuma A, Nonaka I, Nishino I, Tamura N, Amano T, Araki N. Mizoi Y, et al. Among authors: nishino i. Intern Med. 2011;50(20):2409-12. doi: 10.2169/internalmedicine.50.5577. Epub 2011 Oct 15. Intern Med. 2011. PMID: 22001477 Free article.
Myotonic dystrophy type 2 is rare in the Japanese population.
Matsuura T, Minami N, Arahata H, Ohno K, Abe K, Hayashi YK, Nishino I. Matsuura T, et al. Among authors: nishino i. J Hum Genet. 2012 Mar;57(3):219-20. doi: 10.1038/jhg.2011.152. Epub 2012 Jan 19. J Hum Genet. 2012. PMID: 22258159 No abstract available.
771 results