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Spectrum of mutations and genotype-phenotype analysis in Noonan syndrome patients with RIT1 mutations.
Yaoita M, Niihori T, Mizuno S, Okamoto N, Hayashi S, Watanabe A, Yokozawa M, Suzumura H, Nakahara A, Nakano Y, Hokosaki T, Ohmori A, Sawada H, Migita O, Mima A, Lapunzina P, Santos-Simarro F, García-Miñaúr S, Ogata T, Kawame H, Kurosawa K, Ohashi H, Inoue S, Matsubara Y, Kure S, Aoki Y. Yaoita M, et al. Among authors: yokozawa m. Hum Genet. 2016 Feb;135(2):209-22. doi: 10.1007/s00439-015-1627-5. Epub 2015 Dec 29. Hum Genet. 2016. PMID: 26714497
Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.
Sato N, Katsumata N, Kagami M, Hasegawa T, Hori N, Kawakita S, Minowada S, Shimotsuka A, Shishiba Y, Yokozawa M, Yasuda T, Nagasaki K, Hasegawa D, Hasegawa Y, Tachibana K, Naiki Y, Horikawa R, Tanaka T, Ogata T. Sato N, et al. Among authors: yokozawa m. J Clin Endocrinol Metab. 2004 Mar;89(3):1079-88. doi: 10.1210/jc.2003-030476. J Clin Endocrinol Metab. 2004. PMID: 15001591
Double outlet right ventricle with intact ventricular septum.
Sakurai N, Fuse S, Takamuro M, Yokozawa M, Kikuchi S, Horita N, Tsutsumi H. Sakurai N, et al. Among authors: yokozawa m. Pediatr Int. 2007 Apr;49(2):248-50. doi: 10.1111/j.1442-200X.2007.02347.x. Pediatr Int. 2007. PMID: 17445049 No abstract available.
Genesis stent implantation without using a long sheath in two children.
Kobayashi T, Tomita H, Yokozawa M, Takamuro M, Hatakeyama K, Kim SH, Ono Y, Sakamoto K. Kobayashi T, et al. Among authors: yokozawa m. J Cardiol. 2008 Dec;52(3):296-9. doi: 10.1016/j.jjcc.2008.06.002. Epub 2008 Jul 23. J Cardiol. 2008. PMID: 19027610 Free article.
52 results