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Frequent association of 22q11.2 deletion with tetralogy of Fallot.
Maeda J, Yamagishi H, Matsuoka R, Ishihara J, Tokumura M, Fukushima H, Ueda H, Takahashi E, Yoshiba S, Kojima Y. Maeda J, et al. Among authors: ishihara j. Am J Med Genet. 2000 Jun 5;92(4):269-72. doi: 10.1002/(sici)1096-8628(20000605)92:4<269::aid-ajmg9>3.0.co;2-l. Am J Med Genet. 2000. PMID: 10842294
Pediatric mumps with laryngeal edema.
Hattori Y, Oi Y, Matsuoka R, Daimon Y, Ito A, Kubota W, Konishi K, Onguchi T, Sato A, Yamashita Y, Ishihara J. Hattori Y, et al. Among authors: ishihara j. Pediatr Emerg Care. 2013 Oct;29(10):1104-6. doi: 10.1097/PEC.0b013e3182a60049. Pediatr Emerg Care. 2013. PMID: 24084609
Prognostic predictive value of gene mutations in Japanese patients with hypertrophic cardiomyopathy.
Chida A, Inai K, Sato H, Shimada E, Nishizawa T, Shimada M, Furutani M, Furutani Y, Kawamura Y, Sugimoto M, Ishihara J, Fujiwara M, Soga T, Kawana M, Fuji S, Tateno S, Kuraishi K, Kogaki S, Nishimura M, Ayusawa M, Ichida F, Yamazawa H, Matsuoka R, Nonoyama S, Nakanishi T. Chida A, et al. Among authors: ishihara j. Heart Vessels. 2017 Jun;32(6):700-707. doi: 10.1007/s00380-016-0920-0. Epub 2016 Nov 24. Heart Vessels. 2017. PMID: 27885498
A neonatal case of HDR syndrome and a vascular ring with a novel GATA3 mutation.
Kusakawa M, Sato T, Hosoda A, Araki E, Matsuzaki Y, Yamashita Y, Ishihara J, Inagaki Y, Uchida N, Ishii T, Hasegawa T. Kusakawa M, et al. Among authors: ishihara j. Hum Genome Var. 2019 Dec 23;6:55. doi: 10.1038/s41439-019-0087-1. eCollection 2019. Hum Genome Var. 2019. PMID: 31885872 Free PMC article.
336 results