Implications of Mutations of Activin Receptor-Like Kinase 1 Gene (ALK1) in Addition to Bone Morphogenetic Protein Receptor II Gene (BMPR2) in Children With Pulmonary Arterial Hyper... von Fujiwara, Maya, Yagi, Hisato, Matsuoka, Rumiko, Akimoto, Kaoru, Furutani, Michiko, Imamura, Shin-ichiro, Uehara, Ritei, Nakayama, Tomotaka, Takao, Atsuyoshi, Nakazawa, Makoto, Saji, Tsutomu

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Role of TBX1 in human del22q11.2 syndrome von Yagi, Hisato, Furutani, Yoshiyuki, Hamada, Hiromichi, Sasaki, Takashi, Asakawa, Shuichi, Minoshima, Shinsei, Ichida, Fukiko, Joo, Kunitaka, Kimura, Misa, Imamura, Shin-ichiro, Kamatani, Naoyuki, Momma, Kazuo, Takao, Atsuyoshi, Nakazawa, Makoto, Shimizu, Nobuyoshi, Matsuoka, Rumiko

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Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect von Hirayama-Yamada, Kayoko, Kamisago, Mitsuhiro, Akimoto, Kaoru, Aotsuka, Hiroyuki, Nakamura, Yoshihide, Tomita, Hideshi, Furutani, Michiko, Imamura, Shin-ichiro, Takao, Atsuyoshi, Nakazawa, Makoto, Matsuoka, Rumiko

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Kieran C. Murphy, Peter J. Scambler (eds): Velo-cardio-facial syndrome: a model for understanding microdeletion disorders: Cambridge University Press, Cambridge, 2005, ISBN 0-521-8... von Takao, Atsuyoshi

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In vivo constriction of the ductus arteriosus by nonsteroidal antiinflammatory drugs in near-term and preterm fetal rats von MOMMA, K, TAKAO, A

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A de novo missense mutation (R1623Q) of the SCN5A gene in a Japanese girl with sporadic long QT syndrome von Yamagishi, Hiroyuki, Furutani, Michiko, Kamisago, Mitsuhiro, Morikawa, Yoshiyuki, Kojima, Yoshifumi, Hino, Yoshiaki, Furutani, Yoshiyuki, Kimura, Misa, Imamura, Shin-ichiro, Takao, Atsuyoshi, Momma, Kazuo, Matsuoka, Rumiko

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Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome von Momma, Kazuo, Kondo, Chisato, Matsuoka, Rumiko, Takao, Atsuyoshi

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Development of myocardial contractile system in the fetal rabbit von NAKANISHI, T, OKUDA, H, KAMATA, K, ABE, K, SEKIGUCHI, M, TAKAO, A

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Novel missense mutation (G601S) of HERG in a Japanese long QT syndrome family von Akimoto, Kaoru, Furutani, Michiko, Imamura, Shin-Ichiro, Furutani, Yoshiyuki, Kasanuki, Hiroshi, Takao, Atsuyoshi, Momma, Kazuo, Matsuoka, Rumiko

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Tetralogy of Fallot associated with chromosome 22q11 deletion von Momma, Kazuo, Kondo, Chisato, Ando, Masahiko, Matsuoka, Rumiko, Takao, Atsuyoshi

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Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome von MATSUOKA, R, KIMURA, M, OYAMA, K, SAJI, T, ANDO, M, TAKAO, A, MOMMA, K, SCAMBLER, P. J, MORROW, B. E, IMAMURA, S.-I, MINOSHIMA, S, SHIMIZU, N, YAMAGISHI, H, JOH-O, K, WATANABE, S

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Natural history of subarterial infundibular ventricular septal defect von Momma, Kazuo, Toyama, Kan, Takao, Atsuyoshi, Ando, Masahiko, Nakazawa, Makoto, Hirosawa, Koshichiro, Imai, Yasuharu

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Systematic visualization of coronary arteries by two-dimensional echocardiography in children and infants: Evaluation in Kawasaki's disease and coronary arteriovenous fistulas von Satomi, Gengi, Nakamura, Kenji, Narai, Sakae, Takao, Atsuyoshi

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ECG findings after myocardial infarction in children after Kawasaki disease von Nakanishi, Toshio, Takao, Atsuyoshi, Kondoh, Chisato, Nakazawa, Makoto, Hiroe, Michiaki, Matsumoto, Yasutoshi

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Announcement from the Editors von Takao, Atsuyoshi

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Announcement from the Editors von Takao, Atsuyoshi

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Announcement from the Editors von Takao, Atsuyoshi

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Expression of slow skeletal myosin heavy chain 2 gene in Purkinje fiber cells in chick heart von Machida, Shuichi, Noda, Setsuko, Takao, Atsuyoshi, Nakazawa, Makoto, Matsuoka, Rumiko

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Systematic diagnostic method of two-dimensional echocardiography in congenital heart disease von Satomi, G, Takao, A

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Thrombocytopenia in patients with 22q11.2 deletion syndrome and its association with glycoprotein lb-[beta] von Kato, Taichi, Kosaka, Kazuki, Kimura, Misa, Imamura, Shin-ichiro, Yamada, Osamu, Iwai, Kazumasa, Ando, Masahiko, Joh-o, Kunitaka, Kuroe, Kenji, Ohtake, Akira, Takao, Atsuyoshi, Momma, Kazuo, Matsuoka, Rumiko

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