S. Yonesaka

发表

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.

Dilated cardiomyopathy: diagnostic accuracy of endomyocardial biopsy.

A. Becker, S. Yonesaka, 1987, British heart journal.

Coronary Arterial Calcification in Kawasaki Disease

T. Matsubara, T. Nakada, H. Furukawa, 1991, Acta paediatrica Japonica : Overseas edition.

Congenital left ventricular aneurysm coexisting with left ventricular non‐compaction in a newborn

E. Ito, Y. Konno, Toru Takahashi, 2014, Pediatrics international : official journal of the Japan Pediatric Society.

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

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

Clinical and histopathological studies in children with supraventricular tachycardia.

T. Nakada, H. Furukawa, T. Takahashi, 1996, Japanese circulation journal.

Histopathological study on Kawasaki disease with special reference to the relation between the myocardial sequelae and regional wall motion abnormalities of the left ventricle.

T. Nakada, H. Furukawa, T. Takahashi, 1992, Japanese circulation journal.

Endomyocardial Biopsy in Children with Kawasaki Disease

T. Nakada, Toru Takahashi, S. Yonesaka, 1989, Acta paediatrica Japonica : Overseas edition.

‘Hypertrophic cardiomyopathy’ in a girl with adult‐type myotonic dystrophy

T. Nakada, S. Yonesaka, 1999, Pediatrics international : official journal of the Japan Pediatric Society.

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.

Interruption of aortic arch type A in two siblings

T. Nakada, S. Yonesaka, 1996, Acta paediatrica Japonica : Overseas edition.

Adams–Oliver syndrome and familial MYH9 mutation

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

Progressive pulmonary vascular disease after pulmonary artery banding and total correction in a case of ventricular septal defect and pulmonary hypertension.

T. Takahashi, S. Suzuki, K. Ouchi, 1999, The Japanese journal of thoracic and cardiovascular surgery : official publication of the Japanese Association for Thoracic Surgery = Nihon Kyobu Geka Gakkai zasshi.

Dual‐chamber pacing in hypertrophic obstructive cardiomyopathy with biventricular outflow tract obstruction and severe drug‐refractory symptoms in a 9‐year‐old girl

Tohru Takahashi, S. Satoh, Shuji Eto, 2003, Pediatrics international : official journal of the Japan Pediatric Society.

Lung biopsy diagnosis of operative indication in secundum atrial septal defect with severe pulmonary vascular disease.

K. Maeda, K. Tabayashi, M. Kumate, 2004, Chest.

[Histopathological studies of endomyocardial biopsy on the children with Kawasaki disease].

T. Nakada, H. Furukawa, T. Takahashi, 1989, Kokyu to junkan. Respiration & circulation.

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.

A case of Familial Tachycardia-electrophysiological and histopathological studies

I. Sakurai, S. Yonesaka, K. Kamimura, 1983 .