Results 21 to 30 of about 2,884 (194)
Cirugía Cardiovascular, 2021 Resumen: Presentamos el caso de un neonato de 7 días de vida con diagnóstico prenatal de estenosis aórtica crítica y doble lesión valvular mitral grave, a quien realizamos una reparación biventricular neonatal completa, que consistió en procedimiento de ...
Enrique García +5 more
doaj +1 more source
Morphological and genetic causes of fetal cardiomyopathies
Clinical Genetics, Volume 104, Issue 1, Page 63-72, July 2023., 2023 Fetal cardiomyopathies are rare and could led to in utero fetal death or termination of pregnancy. Morphological analysis of 16 cases allowed to described their characteristics. Genetic analysis on a panel of cardiomyopathy genes has attested of a genetic origin of these cases and also highlighted a particular pattern (high rate of de novo mutation ...
Eva Kohaut +11 more
wiley +1 more source
Echocardiography, Volume 40, Issue 6, Page 483-493, June 2023., 2023 Abstract Objectives We sought to explore a novel left atrial appendage (LAA) strain parameter which could represent the cumulative adverse impact of chronic Atrial fibrillation (AF) on the LAA function, and the relationship between the LAA strain parameter and thrombosis risk in patients with non‐valvular AF.
Bo Su +4 more
wiley +1 more source
Ultrasound in Obstetrics &Gynecology, Volume 61, Issue 5, Page 577-586, May 2023., 2023 ABSTRACT Objectives To report on the early detection of congenital heart disease (CHD) in low‐ and high‐risk populations managed at our hospital; and perform a detailed analysis of false‐negative diagnoses, in order to derive possible recommendations on how to reduce their incidence.
L. Bottelli +4 more
wiley +1 more source
Fetal Arrhythmia Diagnosis and Pharmacologic Management
The Journal of Clinical Pharmacology, Volume 62, Issue S1, Page S53-S66, September 2022., 2022 Abstract One of the most successful achievements of fetal intervention is the pharmacologic management of fetal arrhythmias. This management usually takes place during the second or third trimester. While most arrhythmias in the fetus are benign, both tachy‐ and bradyarrhythmias can lead to fetal hydrops or cardiac dysfunction and require treatment ...
Janette F. Strasburger +4 more
wiley +1 more source
Clinical Case Reports, Volume 10, Issue 8, August 2022., 2022 Frequent premature ventricular complexes as unique electrocardiographic finding in left ventricular non‐compaction cardiomyopathy are rare. Thus, physicians must always pay attention to this “benign” arrythmia in order to allow a proper diagnosis. Abstract Left ventricular non‐compaction (LVNC) cardiomyopathy is an uncommon unclassified or genetic ...
Alejandro Sánchez Velásquez +2 more
wiley +1 more source
Indian Journal of Radiology and Imaging, 2013 Fetal endocardial fibroelastosis (EFE) has been diagnosed by antenatal ultrasonography in the past few years. A typical case of isolated endocardial fibroelastosis is illustrated here, in a fetus of 22 weeks of gestational age exposed to maternal ...
Karippaliyil Balakumar +2 more
doaj +1 more source
Nebulette knockout mice have normal cardiac function, but show Z-line widening and up-regulation of cardiac stress markers [PDF]
, 2015 Aims: Nebulette is a 109 kDa modular protein localized in the sarcomeric Z-line of the heart. In vitro studies have suggested a role of nebulette in stabilizing the thin filament, and missense mutations in the nebulette gene were recently shown to be ...
Bang, Marie-Louise +12 more
core +2 more sources
Ultrasound in Obstetrics &Gynecology, Volume 59, Issue 5, Page 633-641, May 2022., 2022 ABSTRACT ObjectivesTo review our experience with fetal aortic valvuloplasty (FAV) in fetuses with critical aortic stenosis (CAS) and evolving hypoplastic left heart syndrome (eHLHS), including short‐ and medium‐term postnatal outcome, and to refine selection criteria for FAV by identifying preprocedural predictors of biventricular (BV) outcome ...
A. Tulzer +6 more
wiley +1 more source
Results of Late Gadolinium Enhancement in Children Affected by Dilated Cardiomyopathy [PDF]
, 2017 BACKGROUND: Little is known about the clinical value of late gadolinium enhancement (LGE), in children affected by dilated cardiomyopathy (DCM). MATERIALS AND METHODS: We retrospectively evaluated 15 patients (8 ± 6 years, 6 males) with diagnosis of DCM ...
Aurelio Secinaro +8 more
core +1 more source