Hidenori Yamamoto

发表

Prediction of postnatal clinical course in primary congenital dilated cardiomyopathy

Yoshiyuki Takahashi, K. Omoya, K. Yasuda, 2019, Pediatrics international : official journal of the Japan Pediatric Society.

Severe fetal cardiomegaly caused by multiple non-giant placental chorioangiomas

Taichi Kato, Hidenori Yamamoto, Yoshie Fukasawa, 2019, Cardiology in the Young.

Mesenchymal stem/stromal cells stably transduced with an inhibitor of CC chemokine ligand 2 ameliorate bronchopulmonary dysplasia and pulmonary hypertension.

M. Hayakawa, Yoshiyuki Takahashi, Atsuto Onoda, 2020, Cytotherapy.

Familial cardiac septal defect due to a novel nine-base deletion in TBX20.

H. Kurahashi, H. Inagaki, Satoshi Hayano, 2022, Pediatrics international : official journal of the Japan Pediatric Society.

Influence of Percutaneous Occlusion of Atrial Septal Defect on Left Atrial Function Evaluated Using 2D Speckle Tracking Echocardiography.

S. Saitoh, S. Takeda, H. Nishikawa, 2020, International heart journal.

Mid-term Results of an Ascending Aortic Extension Technique Using Autologous Tissue for Patients with Narrowing of the Retroaortic Space: Five Cases

M. Noda, M. Nakayama, H. Nishikawa, 2018 .

A Case of Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery Developed Acute Heart Failure by Transcatheter Ductus Arteriosus Closure

M. Noda, S. Takeda, H. Nishikawa, 2016 .

Ventricular tachycardia and chest pain due to foreign body in the pericardium caused by self-injurious behaviour

Taichi Kato, Hidenori Yamamoto, Yoshie Fukasawa, 2019, Cardiology in the Young.

Case report: High-dose epoprostenol therapy in pediatric patients with pulmonary hypertension and developmental lung disease

M. Hayakawa, Yoshiaki Sato, Miharu Ito, 2023, Frontiers in Pediatrics.

Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor.

T. Taketani, I. Nishino, Y. Okuno, 2021, The Journal of allergy and clinical immunology.

Phosphorylated proteome analysis of a novel germline ABL1 mutation causing an autosomal dominant syndrome with ventricular septal defect.

S. Saitoh, Y. Okuno, Yoshiyuki Takahashi, 2020, International journal of cardiology.