Results 51 to 60 of about 80,449 (358)

Outcome of Surgical Closure of Atrial Septal Defect in Sulaimani City

Acta Medica Iranica, 2020
An atrial septal defect (ASD), sometimes called a hole in the heart is a type of congenital heart defect in which there is an abnormal opening in the dividing wall between the upper filling chambers of the heart (the atria).
Aso Faeq Salih, Hakam Marwan Mhadi, Shkar Raeof   +2 more
doaj   +1 more source

Halide‐Exchange Arrest Enables Reabsorption‐Free CsPbCl3/CsPbI3 Perovskite Core/Shell Nanocrystals

Advanced Science, EarlyView.
Achieving large Stokes shifts in perovskite nanocrystals is challenging due to halide mobility that disrupts stable core–shell structures. Using CdCl2 passivation, this work stabilizes CsPbCl3/CsPbI3 heterostructures, yielding a ≈1.2 eV Stokes shift, high quantum yield, and fast exciton transfer, enabling reabsorption‐free emitters for advanced ...
Hiba H. Karakkal, Saptarshi Chakraborty, Matteo L. Zaffalon, Jordi Llusar, Shehla Gul, Andrea Fratelli, Leonardo Poletti, Laura Lazzarini, Daniela Erminia Manno, Francesco Meinardi, Francesco Carulli, Francesca Rossi, Ivan Infante, Sergio Brovelli   +13 more
wiley   +1 more source

Building an Intelligent Cardiovascular System Platform: Embedding Artificial Intelligence across All Facets of Cardiovascular Medicine

Advanced Intelligent Systems, EarlyView.
This paper presents an integrated AI‐driven cardiovascular platform unifying multimodal data, predictive analytics, and real‐time monitoring. It demonstrates how artificial intelligence—from deep learning to federated learning—enables early diagnosis, precision treatment, and personalized rehabilitation across the full disease lifecycle, promoting a ...
Mowei Kong, Xingwei Zhao, Qiuting Li, Yang Yu, Chunxiang Zhang   +4 more
wiley   +1 more source

Down syndrome: Prevalence and distribution of congenital heart disease in Brazil

São Paulo Medical Journal
CONTEXT AND OBJECTIVE: Down syndrome is the most common genetic disorder, affecting 1/700 live births. Among the clinical findings, one constant concern is the high prevalence of congenital heart disease. The objective of this study was to determine the
Beatriz Elizabeth Bagatin Veleda Bermudez, Sandra Lira Medeiros, Mariane Bagatin Bermudez, Iolanda Maria Novadzki, Neiva Isabel Rodrigues Magdalena   +4 more
doaj   +1 more source

A surgical approach of an unusual variant of complete atrioventricular defect; A case report

The Cardiothoracic Surgeon, 2021
Background Complete atrioventricular canal is a congenital heart defect that is characterized by an atrial septal defect, ventricular septal defect, and a common atrioventricular valve. Standard surgical techniques for repairing complete atrioventricular
Hamad Qabha, Tariq Alanazi, Mohamad Khouqeer, Mohannad Dawary, Fareed Khouqeer   +4 more
doaj   +1 more source

Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää, Chad R. Haldeman‐Englert, Marja Hietala, Melisa S. Tanverdi, Patrick P. Koty, Diana Brightman, Eniolami Dosunmu, Shailja Tibrewal, Savleen Kaur, Anupriya Kaur, Raj Kumar Verma, Alejandra G. de Alba Campomanes, Virginia Utz, Anne M. Slavotinek, Cynthia Curry   +14 more
wiley   +1 more source

MEF2C regulates outflow tract alignment and transcriptional control of Tdgf1 [PDF]

, 2016
Congenital heart defects are the most common birth defects in humans, and those that affect the proper alignment of the outflow tracts and septation of the ventricles are a highly significant cause of morbidity and mortality in infants.
Barnes, Ralston M., Black, Brian L., Harris, Ian S., Jaehnig, E., McCulley, David J., Norris, Russell A., Rojas González, Anabel, Sauls, Kimberly, Schachterle, William, Sinha, Tanvi   +9 more
core   +1 more source

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

The views of parents concerning the planning of services for rehabilitation of families of children with congenital cardiac disease [PDF]

, 2003
Background and purpose: Although much previous research has focused on the medical aspects of congenital cardiac disease, there is a growing body of research which suggests that families may need help and support with the wider issues associated with the
Kendall, L, Lewin, R. J. P, Parsons, J. M, Sloper, P   +3 more
core   +1 more source

Delayed presentation of ventricular septal defect secondary to penetrating cardiac trauma following stab wound to the chest

Journal of Research in Medical Sciences, 2008
<ul><li>Ventricular septal defect represents an uncommon sequel of penetrating cardiac trauma. A high index of suspicion, follow- up, and a complete evaluation of the patient who survives a penetrating heart injury is required.
Omid Aghadavoudi, Mohsen Mirmohamadsadeghi, Mahmoud Saeidi   +2 more
doaj