Results 61 to 70 of about 9,224 (129)

Delivery in a 33-year-old woman with fontan palliation

open access: yesJournal of Obstetric Anaesthesia and Critical Care, 2017
Fontan procedure is a surgical treatment used for patients with various forms of congenital heart disease who cannot support biventricular circulation. It is very important in pregnant patients that the right atrium and the single ventricle can tolerate ...
A Viappiani   +4 more
doaj   +1 more source

Himalayan P waves in COPD - A Rare Feature

open access: yesOnline Journal of Health & Allied Sciences, 2014
Himalayan or giant P-waves (amplitude =5 mm) are often known to be classically associated with congenital heart diseases with right to left shunt like tricuspid atresia, Ebstein anomaly, combined tricuspid and pulmonic stenosis, etc, where they indicate ...
Satish Kumar   +5 more
doaj  

Operação de Fontan-Kreutzer em anomalias cardíacas complexas outras que não atresia tricúspide lb, ventrículo único e atresia pulmonar com septo ventricular íntegro The operation of Fontan-Kreutzer in complex congenital anomalies other than lb isolated tricuspid atresia, single ventricle and pulmonary atresia with intact septum

open access: yesBrazilian Journal of Cardiovascular Surgery, 1988
Oitenta e quatro pacientes foram submetidos a operação tipo Fontan, no Instituto do Coração do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, entre 1979 e 1989; as idades variaram entre 5 meses e 31 anos.
Miguel Barbero-Marcial   +7 more
doaj  

Endocardial pacing in a single-ventricle patient with tricuspid atresia-a case report. [PDF]

open access: yesClin Case Rep, 2023
Yamini-Sharif A   +3 more
europepmc   +1 more source

Late Diagnosis of Uncorrected Tricuspid Atresia with Transposition of the Great Arteries in an Adult Patient. [PDF]

open access: yesRadiol Cardiothorac Imaging, 2023
Katekaru-Tokeshi DI   +3 more
europepmc   +1 more source

Raghib Syndrome Presenting as a Cryptogenic Stroke: Role of Cardiac MRI in Accurate Diagnosis

open access: yesCase Reports in Cardiology, 2015
Raghib Syndrome is a rare developmental complex, which consists of persistence of the left superior vena cava (PLSVC) along with coronary sinus ostial atresia and atrial septal defect.
Vistasp J. Daruwalla   +4 more
doaj   +1 more source

Tricuspid atresia in adulthood. [PDF]

open access: yesEur Heart J Case Rep, 2022
Ricci F, Khanji MY, Gallina S.
europepmc   +1 more source

Polycythemia and its determinants among children with unoperated cyanotic congenital heart disease at Tikur Anbessa specialized hospital, Ethiopia: observational cross-sectional study

open access: yesBMC Pediatrics
Background Polycythemia is a physiologic adaptive response to hypoxia seen in children with cyanotic congenital heart disease (Cyanotic CHD). Globally, due to timely cyanotic CHD interventions, polycythemia is underreported or understudied.
Lelise Kaba, Henok Tadele
doaj   +1 more source

Transcatheter Mitral Valve Repair in a Tricuspid Atresia Patient With Potts and Glenn Shunts. [PDF]

open access: yesJACC Case Rep, 2022
Gaignard S   +5 more
europepmc   +1 more source

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