Shinichiro Sakaki

ORCID: 0000-0003-0221-6860
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About
Contact & Profiles
Research Areas
  • Congenital Heart Disease Studies
  • Congenital Diaphragmatic Hernia Studies
  • Cardiac Valve Diseases and Treatments
  • Cardiovascular Issues in Pregnancy
  • Parvovirus B19 Infection Studies
  • Mechanical Circulatory Support Devices
  • Cerebrovascular and Carotid Artery Diseases
  • Viral-associated cancers and disorders
  • COVID-19 Impact on Reproduction
  • Herpesvirus Infections and Treatments
  • Infectious Encephalopathies and Encephalitis
  • T-cell and Retrovirus Studies
  • Kawasaki Disease and Coronary Complications
  • Tracheal and airway disorders
  • Toxin Mechanisms and Immunotoxins
  • Cytomegalovirus and herpesvirus research
  • Coronary Artery Anomalies
  • Vector-Borne Animal Diseases

Kanagawa Children's Medical Center
2024

National Center For Child Health and Development
2019

Chiba Hospital
2018

10.1016/j.jpeds.2017.10.013 article EN The Journal of Pediatrics 2017-12-07

Isolated left-sided innominate artery, a rare congenital anomaly in which the artery arises from main pulmonary trunk, is usually diagnosed incidentally children and adults. Limited reports exist on its prenatal diagnosis, with none comprehensively describing associated perinatal haemodynamic changes. We report case of prenatally isolated postnatal clinical course.

10.1017/s1047951124025307 article EN Cardiology in the Young 2024-05-27

10.1292/jvms1932.48.361 article EN Journal of the Central Society for Veterinary Medicine 1935-01-01

A 5-month-old girl with single ventricle, interrupted inferior vena cava and polysplenia syndrome palliated bilateral Blalock-Taussig shunts developed severe cyanosis despite apparently increased pulmonary blood flow. Angiography revealed diffuse arteriolar capillary dilatation early venous filling, suggesting the presence of arteriovenous malformations. Abdominal angiography at 6 months demonstrated a large extrahepatic portosystemic shunt, which was percutaneously closed vascular plug....

10.1136/bcr-2019-229491 article EN BMJ Case Reports 2019-07-01
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