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Multiple stenotic arteriopathy in a 72-year-old female with Williams syndrome.
Unuma K, Harada K, Furutani M, Furutani Y, Nakajima M, Nakanishi T, Matsuoka R, Yoshida K. Unuma K, et al. Among authors: furutani m, furutani y. J Clin Pathol. 2011 Apr;64(4):368-70. doi: 10.1136/jcp.2010.085803. Epub 2011 Jan 5. J Clin Pathol. 2011. PMID: 21212057 No abstract available.
Outcomes of childhood pulmonary arterial hypertension in BMPR2 and ALK1 mutation carriers.
Chida A, Shintani M, Yagi H, Fujiwara M, Kojima Y, Sato H, Imamura S, Yokozawa M, Onodera N, Horigome H, Kobayashi T, Hatai Y, Nakayama T, Fukushima H, Nishiyama M, Doi S, Ono Y, Yasukouchi S, Ichida F, Fujimoto K, Ohtsuki S, Teshima H, Kawano T, Nomura Y, Gu H, Ishiwata T, Furutani Y, Inai K, Saji T, Matsuoka R, Nonoyama S, Nakanishi T. Chida A, et al. Among authors: furutani y. Am J Cardiol. 2012 Aug 15;110(4):586-93. doi: 10.1016/j.amjcard.2012.04.035. Epub 2012 May 25. Am J Cardiol. 2012. PMID: 22632830
Mutations of NOTCH3 in childhood pulmonary arterial hypertension.
Chida A, Shintani M, Matsushita Y, Sato H, Eitoku T, Nakayama T, Furutani Y, Hayama E, Kawamura Y, Inai K, Ohtsuki S, Saji T, Nonoyama S, Nakanishi T. Chida A, et al. Among authors: furutani y. Mol Genet Genomic Med. 2014 May;2(3):229-39. doi: 10.1002/mgg3.58. Epub 2014 Apr 1. Mol Genet Genomic Med. 2014. PMID: 24936512 Free PMC article.
Compound Mutations Cause Increased Cardiac Events in Children with Long QT Syndrome: Can the Sequence Homology-Based Tools be Applied for Prediction of Phenotypic Severity?
Izumi G, Hayama E, Yamazawa H, Inai K, Shimada M, Furutani M, Nishizawa T, Furutani Y, Matsuoka R, Nakanishi T. Izumi G, et al. Among authors: furutani m, furutani y. Pediatr Cardiol. 2016 Jun;37(5):962-70. doi: 10.1007/s00246-016-1378-7. Epub 2016 Apr 4. Pediatr Cardiol. 2016. PMID: 27041096
316 results