Takumi Sato

Three novel mutations of the fibrillin-1 gene and ten single nucleotide polymorphisms of the fibrillin-3 gene in Marfan syndrome patients

R. Kanezaki, T. Toki, Gang Xu, 2004, Journal of Human Genetics.

Biopsy-proven myocardial sequels in Kawasaki disease with giant coronary aneurysms

Tomomi Ueda, Y. Konno, Toru Takahashi, 2010, Cardiology in the Young.

MYH7 mutation identified by next-generation sequencing in three infant siblings with bi-ventricular noncompaction presenting with restrictive hemodynamics: A report of three siblings with a severe phenotype and poor prognosis.

T. Toki, E. Ito, H. Mizukami, 2019, Journal of cardiology cases.

Congenital Long QT Syndrome Associated with Localization-related Epilepsy: Interictal Electroencephalogram Abnormalities Detected after the Second Syncope

Tohru Takahashi, Takumi Sato, Akira Sato, 2016 .

Adams–Oliver syndrome and familial MYH9 mutation

E. Ito, Tohru Takahashi, S. Kunishima, 2012, Pediatrics international : official journal of the Japan Pediatric Society.

Superior mesenteric artery syndrome in a healthy active adolescent

Takumi Sato, Tsuyoshi Okamoto, Yukio Sasaki, 2019, BMJ Case Reports.

Clinical Course and Prognosis of Minor Abnormal Sonographic Findings in Fetal Echocardiography: Five Years of Experience at a Single Institute

Y. Konno, Takumi Sato, Akira Sato, 2014 .

KCNJ2 mutation in intractable ventricular arrhythmia with Andersen's syndrome

T. Toki, E. Ito, Tohru Takahashi, 2005, Pediatrics international : official journal of the Japan Pediatric Society.

The key role of stem cell factor/KIT signaling in the proliferation of blast cells from Down syndrome-related leukemia

G. Xu, R. Kanezaki, T. Toki, 2009, Leukemia.