Results 41 to 50 of about 1,177,569 (320)

Pediatric Liver Transplantation: Then and Now [PDF]

open access: yes, 2020
This paper reviews the past 50 years of liver transplantation in children from the perspective of patient demographics, perioperative patient management, surgical techniques, immunosuppression and patient ...
Banh, DPT   +4 more
core   +1 more source

Prenatal diagnosis of tetralogy of Fallot with pulmonary atresia using: Fetal Intelligent Navigation Echocardiography (FINE)

open access: yesJournal of Maternal-Fetal & Neonatal Medicine, 2018
Tetralogy of Fallot with pulmonary atresia, a severe form of tetralogy of Fallot, is characterized by the absence of flow from the right ventricle to the pulmonary arteries.
L. Yeo, Dor Markush, R. Romero
semanticscholar   +1 more source

Bilateral Ductal Stenting for Discontinuity of the Pulmonary Artery via the Femoral and Carotid Arteries in an Infant

open access: yesCase Reports in Cardiology, 2015
Bilateral ductal stenting should be performed in cases of discontinuity of the pulmonary branches and pulmonary atresia. Performing this procedure via the carotid artery in small infants can be very difficult and challenging.
Osman Baspinar, Derya Aydin Sahin
doaj   +1 more source

Physiological and clinical consequences of relief of right ventricular outflow tract obstruction late after repair of congenital heart defects. [PDF]

open access: yes, 2006
BACKGROUND: Right ventricular outflow tract obstruction (RVOTO) is a common problem after repair of congenital heart disease. Percutaneous pulmonary valve implantation (PPVI) can treat this condition without consequent pulmonary regurgitation or ...
Bonhoeffer, P   +10 more
core   +1 more source

Management of pulmonary atresia [PDF]

open access: yesHeart, 1970
Based on experience with 48 patients, a new simple classification of pulmonary atresia, according to pulmonary artery development is suggested. The need for extensive investigation including biplane aortography and right ventricular angiocardiography is emphasized. Adequate display of the anatomy is required to plan the surgical management.
openaire   +2 more sources

Inflammation, Active Fibroplasia, and End-stage Fibrosis in 172 Biliary Atresia Remnants Correlate Poorly With Age at Kasai Portoenterostomy, Visceral Heterotaxy, and Outcome [PDF]

open access: yes, 2018
Published histologic studies of the hilar plate or entire biliary remnant at the time of Kasai portoenterostomy (KHPE) have not provided deep insight into the pathogenesis of biliary atresia, relation to age at surgery, prognosis or the basis for ...
Arva   +32 more
core   +1 more source

Transcatheter pulmonary valve perforation using chronic total occlusion wire in pulmonary atresia with intact ventricular septum

open access: yesAnnals of Pediatric Cardiology, 2017
Background: Perforation of pulmonary valve using radiofrequency ablation in pulmonary atresia with intact ventricular septum (PA IVS) is a treatment of choice.
Shweta Bakhru   +6 more
semanticscholar   +1 more source

Remarkable case of uncorrected type IC tricuspid atresia with adaptive pulmonary trunk dilatation to allow prolonged survival: Case report and CT fly-through

open access: yesTranslational Research in Anatomy, 2017
A remarkable case of a surgically uncorrected Type IC (no great artery transposition, no pulmonary stenosis) tricuspid atresia surviving to adulthood is presented.
Zeke J. McKinney   +2 more
doaj   +1 more source

Pulmonary hypertension and congenital bronchial atresia: A time factor association

open access: yesRespiratory Medicine Case Reports, 2019
Congenital bronchial atresia is rarely symptomatic in adults. Recurrent lung infection and pneumothorax are the feared complications of this otherwise benign condition.
Prince A. Alebna   +3 more
doaj   +1 more source

54. Radiofrequency perforation of pulmonary valve and PDA stenting in a preterm neonate

open access: yesJournal of the Saudi Heart Association, 2016
Transcatheter radiofrequency perforation of the pulmonary valve and PDA stenting is considered as a modality for pulmonary atresia and intact ventricular septum with mildly hypoplastic tripartate right ventricle.
D. Khaymaf, K. Al Dhahri, V. Arulselvam
doaj   +1 more source

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