Warning: simplexml_load_file(): SSL operation failed with code 1. OpenSSL Error messages: error:14095126:SSL routines:ssl3_read_n:unexpected eof while reading in /home/manuscriptpro/public_html/pdf/index.php on line 429



Full Text Journal Articles about
Pulmonic Stenosis

Advertisement

Find full text journal articles






Pulmonary endarteritis and endocarditis complicated with septic embolism: a case report and review of the literature.

Arezoo Khosravi, Zohreh Rostami, Mohammad Javanbakht, Nematollah Jonaidi Jafari, Mohsen Sadeghi Ghahroudi, Mohammad Hassan Kalantar-Motamed, Ramezan Jafari, Behzad Einollahi,

BACKGROUND:Pulmonary endarteritis is a rare clinical phenomenon with congenital heart that can potentially lead to major complications. CASE PRESENTATION:We report a 47-year-old man with pulmonary endarteritis. This patient presented with hypertension, chest pain and a previous history of pulmonary valve disease during childhood. Also, eight-months prior, he was hospitalized with ... Read more >>

BMC Infect. Dis. (BMC infectious diseases)
[2020, 20(1):212]

Cited: 0 times

View full text PDF listing >>



Late Presentation of a Congenitally Corrected Transposition of Great Arteries and Hemodynamically Balanced Ventricles Associated with a Large Ventricular Septal Defect and Severe Pulmonary Stenosis: A Case Report and a Multi-Imaging Approach.

Khaled Elenizi, Rasha Alharthi, Anthony Matta, Abdulrahman Aljuayli, Michel Galinier,

BACKGROUND Congenitally corrected transposition of great arteries (ccTGA) represents a distinct rare group of congenital heart diseases. Survival of unoperated ccTGA in the presence of large ventricular septal defect (VSD) is exceptional. Furthermore, late presentation of such patients in the absence of severe pulmonary hypertension or severe systemic right ventricle ... Read more >>

Am J Case Rep (The American journal of case reports)
[2020, 21:e920822]

Cited: 0 times

View full text PDF listing >>



Advertisement

Main Patterns of Fetal Cardiac Remodeling.

Fàtima Crispi, Álvaro Sepúlveda-Martínez, Francesca Crovetto, Olga Gómez, Bart Bijnens, Eduard Gratacós,

The heart is a central organ in the fetal adaptation to an adverse environment. Fetal cardiac changes may persist postnatally and increase the risk of cardiovascular disease in adulthood. Knowledge about fetal cardiac structural as well as functional remodeling has radically improved over the last few years. As it occurs ... Read more >>

Fetal. Diagn. Ther. (Fetal diagnosis and therapy)
[2020, :1-8]

Cited: 0 times

View full text PDF listing >>



Peters plus syndrome and Chorioretinal findings associated with B3GLCT gene mutation - a case report.

Ye Elaine Wang, Dhariana Acon Ramirez, Ta Chen Chang, Audina Berrocal,

BACKGROUND:Peters plus syndrome (PPS) is a combination of congenital Peters anomaly and systemic abnormalities. It is inherited most commonly in an autosomal recessive pattern with homozygous B3GLCT mutations. Ocular findings consist predominantly anterior segment abnormalities without posterior segment involvement. CASE PRESENTATION:In this presentation, we report a case of PPS with ... Read more >>

BMC Ophthalmol (BMC ophthalmology)
[2020, 20(1):118]

Cited: 0 times

View full text PDF listing >>



Experience with balloon pulmonary valvuloplasty and predictors of outcome: a ten-year study.

Sonia A El-Saeidi, Hala S Hamza, Hala M Agha, Mohammed M Soliman, Wael A Attia, Rania El-Kaffas, Faten Abdel-Aziz, Osama Abdel-Aziz, Sahar Shaker, Amira Esmat, Rasha Ammar, Aya Fattouh, Khalid Mohi-Eldin, Amal M El-Sisi,

BACKGROUND:Balloon pulmonary valvuloplasty is the treatment of choice for patients with moderate to severe pulmonary valve stenosis. METHODS:An observational retrospective cross-sectional study including neonates, small infants, and children who underwent balloon pulmonary valvuloplasty in the period from 2007 to 2016 in the cardiac catheterisation unit of the paediatric cardiology department ... Read more >>

Cardiol Young (Cardiology in the young)
[2020, :1-7]

Cited: 0 times

View full text PDF listing >>



Copy number variations associated with fetal congenital kidney malformations.

Meiying Cai, Na Lin, Linjuan Su, Xiaoqing Wu, Xiaorui Xie, Ying Li, Xuemei Chen, Yuan Lin, Hailong Huang, Liangpu Xu,

Background:Congenital anomalies of the kidney and urinary tract (CAKUT) constitute 20-30% of all congenital malformations. Within the CAKUT phenotypic spectrum, renal hypodysplasia (RHD) is particularly severe. This study aimed to evaluate the applicability of single-nucleotide polymorphism (SNP) array test in prenatal diagnosis of RHD for improving prenatal genetic counseling and ... Read more >>

Mol Cytogenet (Molecular cytogenetics)
[2020, 13:11]

Cited: 0 times

View full text PDF listing >>



Haploinsufficiency of the basic helix-loop-helix transcription factor HAND2 causes congenital heart defects.

Ana S A Cohen, Christopher Simotas, Bryn D Webb, Huanzhi Shi, Wahab A Khan, Lisa Edelmann, Stuart A Scott, Ram Singh,

Congenital heart defects (CHDs) are caused by a disruption in heart morphogenesis, which is dependent, in part, on a network of transcription factors (TFs) that regulate myocardial development. Heterozygous sequence variants in the basic helix-loop-helix TF gene heart and neural crest derivatives expressed 2 (HAND2) have been reported among some ... Read more >>

Am. J. Med. Genet. A (American journal of medical genetics. Part A)
[2020, :]

Cited: 0 times

View full text PDF listing >>



Right Ventricular Growth and Function After Balloon Valvuloplasty for Critical Pulmonary Valve Stenosis in Infants and Neonates.

Hala Agha, Sonia El-Saeidi, Hassan Abou Seif, Mohamed Abd El-Salam, Doaa El Amrousy,

Little data are published about right ventricular (RV) growth and function in infants and neonates after balloon pulmonary valvuloplasty (BPV) for critical valvular pulmonary stenosis (PS). We aimed to assess the RV growth and function during 1 year after BPV for critical valvular PS in neonates and infants. A total of ... Read more >>

Pediatr Cardiol (Pediatric cardiology)
[2020, :]

Cited: 0 times

View full text PDF listing >>



Early postnatal cardiac follow-up of survivors of twin-twin transfusion syndrome treated with fetoscopic laser coagulation.

Manon Gijtenbeek, Monique C Haak, Sanne J Eschbach, Zoë A Buijnsters, Johanna M Middeldorp, Frans J C M Klumper, Dick Oepkes, Arend D J Ten Harkel,

OBJECTIVE:To assess the cardiac function and prevalence of congenital heart defects (CHD) in twin-twin transfusion syndrome (TTTS) survivors. STUDY DESIGN:Prospective follow-up of TTTS pregnancies treated with laser surgery (2015-2018). Echocardiography was performed 1 day and 1 month after birth (corrected for prematurity). Results were compared with a control group of ... Read more >>

J Perinatol (Journal of perinatology : official journal of the California Perinatal Association)
[2020, :]

Cited: 0 times

View full text PDF listing >>



Evaluation of the NuCLEUS-X™ balloon valvuloplasty catheter for severe pulmonic stenosis in dogs.

N L LeBlanc, C C Smith, D D Sisson, K F Scollan,

INTRODUCTION/OBJECTIVES:Balloon instability is commonly encountered during balloon pulmonary valvuloplasty (BPV) and may result in an unsuccessful procedure. The NuCLEUS-X™ catheter is a recently developed BPV catheter with a unique barbell shape and an ordered pattern of inflation that stabilizes the balloon to span the valve annulus before expansion of the ... Read more >>

J Vet Cardiol (Journal of veterinary cardiology : the official journal of the European Society of Veterinary Cardiology)
[2020, 28:11-22]

Cited: 0 times

View full text PDF listing >>



Clinical epidemiology of congenital heart diseases in dogs: prevalence, popularity and volatility throughout twenty years of clinical practice

PG Brambilla, Polli, Pradelli, Papa, Rizzi, Bagardi, Bussadori,

Abstract The epidemiology of Congenital Heart Diseases (CHDs) has changed over the past twenty years. We evaluated the prevalence of CHDs in the population of dogs recruited in a single referral center (RC); compared the epidemiological features of CHDs in screened breeds (Boxers) versus nonscreened (French and English Bulldogs and ... Read more >>

()
[, :]

Cited: 0 times

View full text PDF listing >>



Multisystem burden of neurofibromatosis 1 in Denmark: registry- and population-based rates of hospitalizations over the life span.

Line Kenborg, Anne Katrine Duun-Henriksen, Susanne O Dalton, Pernille E Bidstrup, Karoline Doser, Kathrine Rugbjerg, Camilla Pedersen, Anja Krøyer, Christoffer Johansen, Klaus Kaae Andersen, John R Østergaard, Hanne Hove, Sven Asger Sørensen, Vincent M Riccardi, John J Mulvihill, Jeanette F Winther,

PURPOSE:The aim was to assess lifetime risk for hospitalization in individuals with neurofibromatosis 1 (NF1). METHODS:The 2467 individuals discharged with a diagnosis indicating NF1 or followed in a clinical center for NF1 were matched to 20,132 general population comparisons. Based on diagnoses in 12 main diagnostic groups and 146 subcategories, ... Read more >>

Genet. Med. (Genetics in medicine : official journal of the American College of Medical Genetics)
[2020, :]

Cited: 0 times

View full text PDF listing >>



Venoarterial extracorporeal membrane oxygenation in heart surgery post-operative pediatric patients: A retrospective study at Christus Muguerza Hospital, Monterrey, Mexico.

Gerardo Vargas-Camacho, Verónica Contreras-Cepeda, Rene Gómez-Gutierrez, Guillermo Quezada-Valenzuela, Adriana Nieto-Sanjuanero, Jesús Santos-Guzmán, Francisco González-Salazar,

Objectives:Extracorporeal membrane oxygenation is a life support procedure developed to offer cardiorespiratory support when conventional therapies have failed. The purpose of this study is to describe the findings during the first years using venoarterial extracorporeal membrane oxygenation in pediatric patients after cardiovascular surgery at Christus Muguerza High Specialty Hospital in ... Read more >>

SAGE Open Med (SAGE Open Medicine)
[2020, 8:2050312120910353]

Cited: 0 times

View full text PDF listing >>



Tricuspid Intervention Following Pulmonary Valve Replacement in Adults With Congenital Heart Disease.

Catherine Deshaies, Helen Trottier, Paul Khairy, Mohammed Al-Aklabi, Luc Beauchesne, Pierre-Luc Bernier, Santokh Dhillon, Sanjiv K Gandhi, Christoph Haller, Camille L Hancock Friesen, Edward J Hickey, David Horne, Frédéric Jacques, Marla C Kiess, Jean Perron, Maria Rodriguez, Nancy C Poirier, ,

BACKGROUND:Tricuspid regurgitation (TR) is common among adults with corrected tetralogy of Fallot (TOF) or pulmonary stenosis (PS) referred for pulmonary valve replacement (PVR). Yet, combined valve surgery remains controversial. OBJECTIVES:This study sought to evaluate the impact of concomitant tricuspid valve intervention (TVI) on post-operative TR, length of hospital stay, and on ... Read more >>

J. Am. Coll. Cardiol. (Journal of the American College of Cardiology)
[2020, 75(9):1033-1043]

Cited: 0 times

View full text PDF listing >>



Outcomes after combined percutaneous balloon valvuloplasty and external beam radiation therapy for the treatment of congenital pulmonic stenosis in four dogs.

K Nagata, A E Coleman,

Valve restenosis after percutaneous balloon pulmonary valvuloplasty (BPV) for the treatment of congenital pulmonic stenosis (PS) may occur in up to 17% of canine cases. Outcomes in dogs with PS that are treated with repeat BPV after restenosis have not been described. The present report details the clinical courses of ... Read more >>

J Vet Cardiol (Journal of veterinary cardiology : the official journal of the European Society of Veterinary Cardiology)
[2020, 28:1-10]

Cited: 0 times

View full text PDF listing >>



Long-term follow-up after transatrial-transpulmonary repair of tetralogy of Fallot: influence of timing on outcome.

Eva van den Bosch, Ad J J C Bogers, Jolien W Roos-Hesselink, Arie P J van Dijk, Marie H E J van Wijngaarden, Eric Boersma, Aagje Nijveld, Linda W G Luijten, Ronald Tanke, Laurens P Koopman, Willem A Helbing,

OBJECTIVES:Our goal was to report the long-term serial follow-up after transatrial-transpulmonary repair of tetralogy of Fallot (TOF) and to describe the influence of the timing of the repair on outcome. METHODS:We included all patients with TOF who had undergone transatrial-transpulmonary repair between 1970 and 2012. Records were reviewed for patient ... Read more >>

Eur J Cardiothorac Surg (European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery)
[2020, 57(4):635-643]

Cited: 0 times

View full text PDF listing >>



Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations.

Jeevana Praharsha Athota, Meenakshi Bhat, Sheela Nampoothiri, Kalpana Gowrishankar, Sanjeeva Ghanti Narayanachar, Vinuth Puttamallesh, Mohammed Oomer Farooque, Swathi Shetty,

BACKGROUND:Noonan syndrome (NS), an autosomal dominant developmental genetic disorder, is caused by germline mutations in genes associated with the RAS / mitogen-activated protein kinase (MAPK) pathway. In several studies PTPN11 is one of the genes with a significant number of pathogenic variants in NS-affected patients. Therefore, clinically diagnosed NS individuals ... Read more >>

BMC Med. Genet. (BMC medical genetics)
[2020, 21(1):50]

Cited: 0 times

View full text PDF listing >>



Right and left ventricular interactions, strain, and remodeling in repaired pulmonary stenosis patients with preserved right ventricular ejection fraction: A cardiac magnetic resonance study.

Shi-Yu Wang, Rong-Zhen OuYang, Li-Wei Hu, Wei-Hui Xie, Ya-Feng Peng, Lei Wang, Fa-Bao Gao, Yu-Min Zhong,

BACKGROUND:Right ventricular dilation and dysfunction is a common long-term complication in patients with repaired pulmonary stenosis (rPS). Additionally, abnormal right and left ventricular interactions have been reported in right-sided heart defect after intervention, including in pulmonary stenosis. PURPOSE:To analyze ventricular strain, remodeling, and left and right ventricular interactions in rPS ... Read more >>

J Magn Reson Imaging (Journal of magnetic resonance imaging : JMRI)
[2020, :]

Cited: 0 times

View full text PDF listing >>



Congenital heart defects in Noonan syndrome: Diagnosis, management, and treatment.

Léa Linglart, Bruce D Gelb,

Noonan syndrome is a pleomorphic genetic disorder, in which a high percentage of affected individuals have cardiovascular involvement, most prevalently various forms of congenital heart disease (i.e., pulmonary valve stenosis, septal defects, left-sided lesions, and complex forms with multiple anomalies). Care includes attentiveness to several comorbidities, some directly impacting cardiac ... Read more >>

Am J Med Genet C Semin Med Genet (American journal of medical genetics. Part C, Seminars in medical genetics)
[2020, 184(1):73-80]

Cited: 0 times

View full text PDF listing >>



[Application of arterial duct stent in ductus-dependent hypoplastic right heart syndrome].

G Luo, A Liu, K L Wang, W Yao, Z X Ji, Q S Xing, S L Pan,

Objective: To summarize the experience of arterial duct (AD) stenting in children with ductus-dependent hypoplastic right heart syndrome (HRHS). Methods: Seven children including 4 cases of pulmonary atresia with intact ventricular septum (PA-IVS) with HRHS and 3 cases of critical pulmonary stenosis (CPS)-IVS with HRHS underwent AD stenting in Qingdao ... Read more >>

Zhonghua Er Ke Za Zhi (Zhonghua er ke za zhi = Chinese journal of pediatrics)
[2020, 58(4):319-323]

Cited: 0 times

View full text PDF listing >>



Early and late outcomes of surgical repair of double-chambered right ventricle: a single-centre experience.

Murat Surucu, İlkay Erdoğan, Birgül Varan, Murat Özkan, N Kürşad Tokel, Sait Aşlamacı,

OBJECTIVE:Double-chambered right ventricle is characterised by division of the outlet portion of the right ventricle by hypertrophy of the septoparietal trabeculations into two parts. We aim to report our experiences regarding the presenting symptoms of double-chambered right ventricle, long-term prognosis, including the recurrence rate and incidence of arrhythmias after surgery. ... Read more >>

Cardiol Young (Cardiology in the young)
[2020, 30(3):409-412]

Cited: 0 times

View full text PDF listing >>



Fetal cardiovascular alterations in twin-to-twin transfusion syndrome.

Ioana Cristina Rotar, Gabriela Zaharie, Adelina Staicu, Andreia Preda, Daniel Mureşan,

Twin-to-twin transfusion syndrome (TTTS) is the consequence of vascular anastomoses of the shared placenta of monochorionic twin pregnancies. Both circulating inter-twin blood flow and vasoactive mediators imbalance cause hypovolemia in the donor and hypervolemia in the recipient fetus. If left untreated, TTTS has a high perinatal mortality rate and adverse ... Read more >>

Med Pharm Rep (Medicine and pharmacy reports)
[2020, 93(1):5-11]

Cited: 0 times

View full text PDF listing >>



Congenital heart disease in school children in Lagos, Nigeria: Prevalence and the diagnostic gap.

Ekanem N Ekure, Ogochukwu Sokunbi, Nnenna Kalu, Akinsanya Olusegun-Joseph, Oyewole Kushimo, Casmir Amadi, Olayinka Hassan, Desmond Ikebudu, Sophia Onyia, Chinonso Onwudiwe, Victor Nwankwo, Remi Akinwunmi, Fukpode Awusa, Zainab Akere, Olaolu Dele-Salawu, Elizabeth Ajayi, Olagoke Ale, Dorothy Muoneke, Maximillian Muenke, Paul Kruszka, Andrea Beaton, Craig Sable, Adebowale Adeyemo,

Congenital heart disease (CHD) in low-and-middle income countries (LMIC) is often characterized by late presentation resulting from inadequate screening and healthcare access in these regions. Accurate estimates of the burden of CHD among school children are often lacking. The objective of this study was to determine the prevalence and distribution ... Read more >>

Am J Med Genet C Semin Med Genet (American journal of medical genetics. Part C, Seminars in medical genetics)
[2020, 184(1):47-52]

Cited: 0 times

View full text PDF listing >>



Left main coronary artery compression by the right pulmonary artery in a patient with congenital pulmonic stenosis.

Eduardo Bahena-López, Jorge Loya-Centurión,

Congenital pulmonary stenosis (PS) can be associated with pulmonary artery (PA) dilatation. In some cases, this can cause compression of nearby structures including the left main coronary artery (LMCA). This compression causes angina and is considered an indication for surgical treatment. We present the case of a patient with PS ... Read more >>

Arch Cardiol Mex (Archivos de cardiologia de Mexico)
[2020, 90(1):55-57]

Cited: 0 times

View full text PDF listing >>



Pulmonary ductal coarctation and left pulmonary artery interruption; pathology and role of neural crest and second heart field during development

Adriana Gittenberger-de Groot, Joshua Peterson, Lambertus Wisse, Arno A.W. Roest, Robert Poelmann, Regina Bökenkamp, Nynke Elzenga, Mark Hazekamp, Margot Bartelings, Monique R.M. Jongbloed, Marco DeRuiter,

Abstract Objectives In congenital heart malformations with pulmonary stenosis to atresia an abnormal lateral ductus arteriosus to left pulmonary artery connection can lead to a localised narrowing (pulmonary ductal coarctation) or even interruption We investigated embryonic remodelling and pathogenesis of this area. Material and methods. Normal development was studied in ... Read more >>

()
[, :]

Cited: 0 times

View full text PDF listing >>



Advertisement

Disclaimer
2.2323 s