A5017531561- Liver Disease Diagnosis and Treatment
- Cardiovascular Function and Risk Factors
- Cardiac Imaging and Diagnostics
- Congenital Heart Disease Studies
- Hepatocellular Carcinoma Treatment and Prognosis
- Kawasaki Disease and Coronary Complications
- Liver Disease and Transplantation
- Cardiac Structural Anomalies and Repair
- Iron Metabolism and Disorders
- Coronary Artery Anomalies
- Cardiovascular Disease and Adiposity
Universidade de São Paulo
2023-2024
Universidade Brasil
2024
Hospital Samaritano de São Paulo
2023
Krankenhaus Salem
2017-2019
Heidelberg University
2017-2019
Resumo Fundamento: As complicações cardiovasculares são a principal causa de morte em pacientes pediátricos com doença renal crônica (DRC). A avaliação ecocardiográfica da função diastólica na DRC tem se limitado à espectral por Doppler e tecidual, técnicas sabidamente menos confiáveis pediatria. O strain do átrio esquerdo (AE) pela técnica speckle tracking bidimensional (2DST) foi recentemente confirmada como uma medida robusta diastólica. Objetivos: Investigar o papel AE crianças...
Abstract Background: Cardiovascular complications are the leading cause of mortality in pediatric patients with chronic kidney disease (CKD). Echocardiographic assessment diastolic function CKD has been limited to spectral and tissue Doppler imaging, known be less reliable techniques pediatrics. Two-dimensional Speckle tracking echocardiography (2DST) derived left atrial (LA) strain recently confirmed as a robust measure function. Objectives: To investigate LA role children at different...
Patients with alcoholic liver disease (ALD) develop prognostically unfavourable hepatic iron overload (HIO) and anemia, however, the underlying molecular mechanisms role of systemic masterswitch hepcidin are poorly understood. Herein, we investigate effect hemolysis in disruption physiological regulation.
Host genetic factors play an important role in the development of alcohol-related cirrhosis. Hepatocellular carcinoma (HCC) complicates course this disorder approximately 20% affected individuals. The variant rs738409 patatin-like phospholipase domain containing-3 (PNPLA3) is established risk for cirrhosis and HCC. Recently, a loss-of-function splice rs72613567:TA gene coding hydroxysteroid 17-beta dehydrogenase 13 (HSD17B13) was reported not only to be associated with reduced developing but...