記事一覧

• Tabara Y, Tachibana-Iimori R, Yamamoto M, Abe M, Kondo I, Miki T, Kohara K.
  Hypotension associated with prone body position: a possible overlooked postural hypotension.
  Hypertens Res 2014以前; 28:741-746.

• Tamaki S, Nakamura Y, Tabara Y, Okumura T, Kita Y, Kadowaki T, Tsujita Y, Horie M, Miki T, Ueshima H.
  Combined analysis of polymorphisms in angitotensinogen and adducing genes and their effects on hypertension in a Japanese sample: The Shigaraki Study.
  Hypertens Res 2014以前; 28:645-650.

• Okuda Y, Tabara Y, Kondo I, Suyama K, Miki T, Kohara K.
  Delayed reflection pressure wave: new aspects for postprandial hypotension.
  J Am Geriatr Soc 2014以前; 53:1833-1834.

• Masuyama T, Matsuo M, Jing JJ, Tabara Y, Kitsuki K, Yamagata H, Kan Y, Miki T, Ishii K, Kondo I.
  Classic Rett syndrome in a boy with R133C mutation of MECP2.
  Brain Dev 2014以前; 27:439-442.

• Zhong, W, Yamagata H, Taguchi K, Akatsu H, Kamino K, Yamamoto T, Kosaka K, Takeda M, Kondo K, Miki T.
  Lymphocyte-specific protein tyrosine kinase is a novel risk gene for Alzheimer disease.
  J Neurol Sci 2014以前; 238:53-57.

• Osawa H, Onuma H, Ochi M, Murakami A, Yamauchi J, Takasuka T, Tanabe F, Shimizu I, Kato K, Nishida W, Yamada K, Tabara Y, Yasukawa M, Fujii Y, Ohashi J, Miki T, Makino H.
  Resistin SNP-420 determines its monocyte mRNA and serum levels inducing type 2 diabetes.
  Biochem Biophys Res Commun 2014以前; 335:596-602.

• Abe M, Wu Z, Yamamoto M, Jin JJ, Tabara Y, Mogi M, Kohara K, Miki T, Nakura J.
  Association of dopamine beta-hydroxylase polymorphism with hypertension through interaction with fasting plasma glucose in Japanese.
  Hypertens Res 2014以前; 28:215-221.

• Ogimoto A, Hamada M, Miki T, Higaki J.
  Angiotensin I-converting enzyme insertion/insertion genotype as a genetic risk factor for cardiovascular disease.
  Am Heart J 2014以前; 150:1

• Kohara K, Tabara Y, Oshiumi A, Miyawaki Y, Kobayashi T, Miki T.
  Radial augmentation index: a useful and easily obtainable parameter for vascular aging.
  Am J Hypertens 2014以前; 18:11S-14S.

• Ogimoto A, Shigematsu Y, Nakura J, Hara Y, Ohtsuka T, Kohara K, Hamada M, Miki T, Higaki J.
  Endothelial nitric oxide synthase gene polymorphism (Glu298Asp) in patients with coexistent hypertrophic cardiomyopathy and coronary spastic angina.
  J Mol Med 2014以前; 83:619-625.

• Takemura Y, Sakurai Y, Yokoya S, Otaki J, Matsuoka T, Ban N, Hirata I, Miki T, Tsuda T.
  Open-ended questions: are they really beneficial for gathering medical information from patients?
  Tohoku J Exp Med 2014以前; 206:151-154.

• Fukuda T, Yamashita Y, Nagamitsu S, Miyamoto K, Jin JJ, Ohmori I, Ohtsuka Y, Kuwajima K, Endo S, Iwai T, Yamagata H, Tabara Y, Miki T, Matsuishi T, Kondo I.
  Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms.
  Brain Dev 2014以前; 27:211-217.