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Page 1
Meta-iodobenzylguanidine myocardial scintigraphy in Perry disease.
Mishima T, Fujioka S, Nishioka K, Li Y, Sato K, Houzen H, Yabe I, Shiomi K, Eriguchi M, Hara H, Hattori N, Tsuboi Y. Mishima T, et al. Among authors: houzen h. Parkinsonism Relat Disord. 2021 Feb;83:49-53. doi: 10.1016/j.parkreldis.2020.12.017. Epub 2021 Jan 12. Parkinsonism Relat Disord. 2021. PMID: 33476877
Herpes simplex encephalitis.
Hata D, Sato K, Houzen H. Hata D, et al. Among authors: houzen h. Intern Med. 2003 Oct;42(10):1057-8. doi: 10.2169/internalmedicine.42.1057. Intern Med. 2003. PMID: 14606730 Free article. No abstract available.
An autopsy case of Sjögren's syndrome with acute encephalomyelopathy.
Yaguchi H, Houzen H, Kikuchi K, Hata D, Ura S, Takeda T, Yabe I, Sasaki H. Yaguchi H, et al. Among authors: houzen h. Intern Med. 2008;47(19):1675-80. doi: 10.2169/internalmedicine.47.0207. Epub 2008 Oct 1. Intern Med. 2008. PMID: 18827415 Free article.
Unusual retinal phenotypes in an SCA7 family.
Inaba H, Yabe I, Yashima M, Soma H, Nakamura Y, Houzen H, Sasaki H. Inaba H, et al. Among authors: houzen h. Intern Med. 2009;48(16):1461-4. doi: 10.2169/internalmedicine.48.2072. Epub 2009 Aug 17. Intern Med. 2009. PMID: 19687599 Free article.
DNAJB6 myopathy in an Asian cohort and cytoplasmic/nuclear inclusions.
Sato T, Hayashi YK, Oya Y, Kondo T, Sugie K, Kaneda D, Houzen H, Yabe I, Sasaki H, Noguchi S, Nonaka I, Osawa M, Nishino I. Sato T, et al. Among authors: houzen h. Neuromuscul Disord. 2013 Mar;23(3):269-76. doi: 10.1016/j.nmd.2012.12.010. Epub 2013 Feb 6. Neuromuscul Disord. 2013. PMID: 23394708
Novel GNE compound heterozygous mutations in a GNE myopathy patient.
Cai H, Yabe I, Shirai S, Nishimura H, Hirotani M, Kano T, Houzen H, Yoshida K, Sasaki H. Cai H, et al. Among authors: houzen h. Muscle Nerve. 2013 Oct;48(4):594-8. doi: 10.1002/mus.23862. Epub 2013 Aug 30. Muscle Nerve. 2013. PMID: 23558691
44 results