Results 51 to 60 of about 3,161 (171)

Noncompaction cardiomyopathy and heterotaxy syndrome [PDF]

open access: yes, 2017
Left ventricular noncompaction cardiomyopathy (LVNC) is characterized by compact and trabecular layers of the left ventricular myocardium. This cardiomyopathy may occur with congenital heart disease (CHD).
Martinez, Hugo R.   +3 more
core   +1 more source

Undetected cases after implementation of first‐trimester anomaly scan in low‐risk population: insights from the IMITAS study

open access: yesUltrasound in Obstetrics &Gynecology, Volume 67, Issue 1, Page 27-33, January 2026.
ABSTRACT Objective To assess the effectiveness of the first‐trimester anomaly scan (FTAS) performed as part of a centrally steered national screening program in The Netherlands by investigating false‐negative cases with a fetal structural anomaly that was not detected at the FTAS.
K. Bronsgeest   +18 more
wiley   +1 more source

Obstetric outcome in women with congenital heart disease: A nationwide cohort in Sweden

open access: yesActa Obstetricia et Gynecologica Scandinavica, Volume 105, Issue 1, Page 7-17, January 2026.
In this large national case–control study in women with congenital heart disease, we showed an increased likelihood of giving birth prematurely, by cesarean section, and having a small‐for‐gestational‐age neonate compared to matched controls. Abstract Introduction Survival and healthcare for patients with congenital heart disease have improved, and the
Frida Wedlund   +10 more
wiley   +1 more source

Anomalia de Ebstein da válvula tricúspide. Tolerância clínca até aos 38 anos de idade e ao estado de gravidez.

open access: yesActa Médica Portuguesa, 1994
Ebstein's Anomaly of the tricuspid valve has a variable degree of abnormality with a continuous change between mild and severe forms and, consequently, a variable clinical course. Pregnancy can also be well tolerated with a good fetal outcome.
J M Santos   +5 more
doaj   +1 more source

Thoracic Skeletal Muscle and Exercise Capacity in Adults With Congenital Heart Disease: A Cross‐Sectional Imaging Analysis

open access: yesJournal of Cachexia, Sarcopenia and Muscle, Volume 16, Issue 6, December 2025.
ABSTRACT Background The growing population of adults with congenital heart disease (ACHD) faces lifelong morbidities despite advancements in medical and surgical care. Sarcopenia, characterized by loss of muscle mass and strength, is linked to increased disability, poor quality of life and mortality.
Jacob D. Steffen   +7 more
wiley   +1 more source

Zero Fluoroscopy Ablation of Arrhythmias in Patients With Congenital Heart Disease

open access: yesJournal of Arrhythmia, Volume 41, Issue 6, December 2025.
Zero‐fluoroscopy radiofrequency ablation using 3D electroanatomic mapping was performed in 42 patients with mild, moderate, or great complexity congenital heart disease. Acute success was 100%, with no complications and minimal recurrence over 48 months. This approach eliminates radiation exposure while maintaining safety and efficacy across select yet
Shailendra Upadhyay   +4 more
wiley   +1 more source

Abnormal ECG Findings in Athletes: Clinical Evaluation and Considerations. [PDF]

open access: yes, 2019
PURPOSE OF REVIEW: Pre-participation cardiovascular evaluation with electrocardiography is normal practice for most sporting bodies. Awareness about sudden cardiac death in athletes and recognizing how screening can help identify vulnerable athletes have
A Biffi   +83 more
core   +1 more source

Transcatheter Management of Severe Paravalvular Leak in the Inferior Vena Cava Prosthesis of the TricValve Bicaval Valve System

open access: yesCatheterization and Cardiovascular Interventions, Volume 106, Issue 5, Page 2945-2948, November 1, 2025.
ABSTRACT We present a 74‐year‐old female with a history of mechanical aortic and mitral valve implantation and non‐Hodgkin lymphoma. She presented with right sided heart failure due to severe functional tricuspid regurgitation and was treated with transcatheter TricValve bicaval system implantation.
Marcel A. Beijk   +2 more
wiley   +1 more source

Familial 22q11.2 Duplication/Deletion Syndrome: A Testament to the Long‐Standing Clinical Utility of FISH

open access: yesClinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT While the standard diagnostic test for suspected 22q copy number disorders is by chromosomal microarray, this case highlights the importance of utilizing FISH to localize allelic copy number when there is a family history of deletion/duplication syndrome for accurate recurrence risk assessment.
Laura M. Bryant   +5 more
wiley   +1 more source

ECLS in Pediatric Cardiac Patients [PDF]

open access: yes, 2016
Extracorporeal life support (ECLS) is an important device in the management of children with severe refractory cardiac and or pulmonary failure. Actually, two forms of ECLS are available for neonates and children: extracorporeal membrane oxygenation ...
Antonio Amodeo   +5 more
core   +2 more sources

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