Results 11 to 20 of about 3,853 (183)

Swiss Adult Congenital HEart disease Registry (SACHER) - rationale, design and first results. [PDF]

open access: yes, 2017
In 2013, a prospective registry for adults with congenital heart disease (CHD) was established in Switzerland, providing detailed data on disease characteristics and outcomes: Swiss Adult Congenital HEart disease Registry (SACHER).
Attenhofer Jost, C.   +16 more
core   +1 more source

Management and outcome of Ebstein's anomaly in children [PDF]

open access: yes, 2017
Objectives To assess clinical presentation, treatment, and outcome of children with Ebstein's anomaly. Background Data on long-term outcome of children with Ebstein's anomaly are scarce.
Attenhofer Jost, Christine H.   +8 more
core  

Magnetic resonance imaging of abnormal ventricular septal motion in heart diseases: a pictorial review [PDF]

open access: yes, 2011
The purpose of this article is to illustrate the usefulness of MR imaging in the clinical evaluation of congenital and acquired cardiac diseases characterised by ventricular septal wall motion abnormality.
Cristina Méndez   +6 more
core   +1 more source

NONO‐Related Syndromic X‐Linked Developmental Disability 34: Further Clinical and Molecular Delineation in a Prenatal Cohort

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective To characterize the prenatal sonographic features across different trimesters and genomic spectrum of NONO‐related X‐linked intellectual developmental disorder. Method We analyzed two fetuses presenting with corpus callosum agenesis and rare cardiac anomalies using genome sequencing and exome sequencing.
Yilin Zhao   +13 more
wiley   +1 more source

Cone reconstruction in Ebstein's anomaly repair: early and long-term results [PDF]

open access: yes, 2011
FUNDAMENTO: As principais correções da anomalia de Ebstein (AE) baseiam-se na reconstrução monocúspide da valva tricúspide e são limitadas pela frequente necessidade de substituição ou pela alta reincidência de insuficiência valvar.
BAUMGRATZ, José Francisco   +7 more
core   +4 more sources

Prenatal detection and outcome of major heart defects in a country with universal screening

open access: yesUltrasound in Obstetrics &Gynecology, EarlyView.
ABSTRACT Objective To evaluate the Danish prenatal screening program for major fetal congenital heart defects (mCHD), focusing on incidence, detection rates (DRs), pregnancy outcomes and postnatal mortality. Methods This was a 5‐year nationwide cohort study conducted from January 2018 to December 2022 in Denmark.
C. Vedel   +15 more
wiley   +1 more source

Diagnóstico ecográfico de la malformación de la válvula tricúspide en un perro [PDF]

open access: yes, 1998
Se describe un caso de diplasia de la válvula tricúspide en un perro macho mestizo de nueve meses de ...
Carretero i Romay, Ana   +4 more
core  

Cardiovascular Health in Women—Across the Lifespan

open access: yesClinical Endocrinology, EarlyView.
ABSTRACT Cardiovascular disease (CVD) remains the leading cause of mortality and morbidity among women worldwide. However, CVD continues to be perceived as a predominantly male issue. CVD in women therefore remains understudied, underrecognized and undertreated.
Jaya Chandrasekhar   +5 more
wiley   +1 more source

Anomalía de Ebstein de la válvula tricúspide: comunicación de un caso clínico y revisión de la bibliografía [PDF]

open access: yes, 2009
La anomalía de Ebstein de la válvula tricúspide representa 1% de todas las malformaciones congénitas del corazón. Se asocia con alteraciones de la conducción, como pre-excitación (hasta en 30%). Existen diversos factores de riesgo identificados para este
Cavazos, Manuel de la O.   +4 more
core  

Genetic Diagnoses Among Congenital Anomaly Cases in Europe: Data From the EUROCAT Network

open access: yesPaediatric and Perinatal Epidemiology, EarlyView.
ABSTRACT Background Surveillance of congenital anomaly prevalence over time can identify new teratogens. Anomalies with a genetic cause are excluded from the monitoring. Objectives We examined temporal changes in the proportion of genetic diagnoses among cases with a congenital anomaly.
Jorieke E. H. Bergman   +23 more
wiley   +1 more source

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