Hemolytic anemia secondary to modified blalock-taussig shunt.

abstract：:Identification of heart transplant recipients at highest risk for a poor outcome could lead to improved posttransplantation survival. A chart review of primary heart transplantations from 1993 to 2006 was performed. Analysis was performed to evaluate the risk of graft loss for those with a transplantation age less tha...

journal_title：Pediatric cardiology

authors： Auerbach SR,Richmond ME,Chen JM,Mosca RS,Quaegebeur JM,Addonizio LJ,Hsu DT,Lamour JM

更新日期：2012-01-01 00:00:00

abstract：:Cor triatriatum sinistrum (division of the left atrium) is a recognized clinical and surgical entity. Division of the right atrium, also known as cor triatriatum dexter, is an extremely rare congenital abnormality in which persistence of the right valve of the embryonic systemic sinus venosus divides the right atrium ...

journal_title：Pediatric cardiology

authors： Choudhary D,Sivasankaran S,Venkateshwaran S,Sasidharan B

更新日期：2013-01-01 00:00:00

abstract：:This study identified tracheobronchial cartilage calcification in children with congenital heart disease. Calcification of the tracheobronchial airways has been found previously in adults receiving warfarin and in children receiving warfarin after mitral valve replacement. A 9-year-old girl who had received a Fontan r...

journal_title：Pediatric cardiology

authors： Eckersley L,Stirling J,Occleshaw C,Wilson N

更新日期：2014-08-01 00:00:00

abstract：:Since its first description in Japan 30 years ago, Kawasaki disease has been reported worldwide. Although an infectious etiology is suspected based on the epidemiology and clinical features, a causative agent has not been identified. The majority of the morbidity and mortality associated with this condition is attribu...

journal_title：Pediatric cardiology

authors： Laupland KB,Dele Davies H

更新日期：1999-05-01 00:00:00

abstract：:Left atrial tumor, diagnosed as myxoma at first investigation, was later demonstrated to be a malignant fibrosarcoma with myxoid change. Myxoma should be diagnosed and managed carefully because of its wide range of histopathologic features. ...

journal_title：Pediatric cardiology

authors： Hishitani T,Ogawa K,Hoshino K,Kido S,Nakamura Y,Ogawa Y

更新日期：2001-05-01 00:00:00

abstract：:Angiography remains the gold standard in the preoperative evaluation of complex pulmonary blood supply in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries. In neonates, balloon occlusion aortography using a Berman balloon catheter is a very effective technique. H...

journal_title：Pediatric cardiology

authors： Lim JS,Desai T,Stumper O

更新日期：2004-09-01 00:00:00

abstract：:The case of a transient third degree atrioventricular block in a 4-year-old patient with familial dysautonomia is reported. A review of the literature follows with analysis of the significance of arrhythmias in the natural history of the patient with familial dysautonomia. ...

journal_title：Pediatric cardiology

authors： Rutkowski M,Axelrod FB,Danilowicz D

更新日期：1992-07-01 00:00:00

abstract：:There has been substantial controversy regarding treatment of congenital heart defects in infants with trisomies 13 and 18. Most reports have focused on surgical outcomes versus expectant treatment, and rarely there has been an effort to consolidate existing evidence into a more coherent way to help clinicians with de...

journal_title：Pediatric cardiology

authors： Carvajal HG,Callahan CP,Miller JR,Rensink BL,Eghtesady P

更新日期：2020-10-01 00:00:00

abstract：:Previous studies showed the reliability of cardiac magnetic resonance imaging (cMRI) in the quantification of aortic valve stenosis in adults. The aim of this retrospective study was to assess the ability of cMRI in the quantification of congenital aortic valve stenosis (CAS) in children. Nineteen patients (mean age 1...

journal_title：Pediatric cardiology

authors： Sirin S,Nassenstein K,Neudorf U,Jensen CJ,Mikat C,Schlosser T

更新日期：2014-06-01 00:00:00

abstract：:We report a rare case of tetralogy of Fallot with total anomalous pulmonary venous return, left heart hypoplasia, right lung hypoplasia, and left ocular-mandibular synchinesia (Marcus-Gunn phenomenon), correctly diagnosed by cardiovascular magnetic resonance imaging and successfully operated by modified Glenn anastomo...

journal_title：Pediatric cardiology

authors： Festa P,Lamia AA,Murzi B,Bini MR

更新日期：2005-07-01 00:00:00

abstract：:The aim of this study is to evaluate the relationship between maternal single nucleotide polymorphisms (SNPs) of methylenetetrahydrofolate reductase (MTHFR) gene with plasma homocysteine (HCY) level and offspring congenital heart diseases (CHDs). 338 mothers with offspring CHDs as case group and 306 mothers of normal ...

journal_title：Pediatric cardiology

authors： Shi H,Yang S,Lin N,Huang P,Yu R,Chen M,Wang L,Jiang Z,Sun X

更新日期：2020-11-21 00:00:00

abstract：:A 6-year-old girl presented with respiratory distress. Chest radiographs exhibited calcifications in the mediastinum. Further imaging revealed extensive cardiac calcifications on computed tomography of the chest. The laboratory parameters were consistent with findings of secondary hyperparathyroidism. Detailed review ...

journal_title：Pediatric cardiology

authors： Zaidi AN,Ceneviva GD,Phipps LM,Dettorre MD,Mart CR,Thomas NJ

更新日期：2005-07-01 00:00:00

abstract：:Adult studies suggest a better functional outcome after aortic valve replacement with a pulmonary autograft compared with mechanical or homograft valves. Little is known about functional results after Ross surgery in growing children. This study reports formal exercise stress echocardiographic data from 26 pediatric R...

journal_title：Pediatric cardiology

authors： Pauliks LB,Brian Clark J,Rogerson A,DiPietro A,Myers JL,Cyran SE

更新日期：2012-06-01 00:00:00

abstract：BACKGROUND:The purpose of this study was to investigate the associations between clinical factors and cardiac function as measured by pressure-volume loops (PVLs) in a pediatric heart transplant cohort. METHODS:Patients (age < 20 years) who underwent heart transplantation presenting for a clinically indicated catheter...

journal_title：Pediatric cardiology

authors： Schroeder LW,Chowdhury SM,Burnette AL,Kavarana MN,Hamilton Baker G,Savage AJ,Atz AM,Butts RJ

更新日期：2018-02-01 00:00:00

abstract：:Over the past decade, revolutionary advances in ultrasound imaging technology have allowed the study of the evolution of congenital heart disease during fetal life. The frustration arising from watching the prenatal progression of severe semilunar valve obstructions and therapy-refractory fetal arrhythmias has prompte...

journal_title：Pediatric cardiology

authors： Kohl T

更新日期：2002-05-01 00:00:00

abstract：:Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a heritable cardiomyopathy characterized by fibro-fatty replacement of right ventricular myocardium. Diagnostic criteria, established in 1994 and modified in 2010, are based on predominately adult manifestations of ARVC/D. The goal of this paper is ...

journal_title：Pediatric cardiology

authors： Deshpande SR,Herman HK,Quigley PC,Shinnick JK,Cundiff CA,Caltharp S,Shehata BM

更新日期：2016-04-01 00:00:00

abstract：:Fifty infants with interrupted aortic arch (IAA), admitted between 1979 and 1988, were reviewed. They usually presented early in severe cardiac failure or shock. In the initial 5-year period, 17 of the 21 infants underwent diagnostic or confirmatory cardiac catheterization, in contrast with the latter 5 years when onl...

journal_title：Pediatric cardiology

authors： Menahem S,Rahayoe AU,Brawn WJ,Mee RB

更新日期：1992-10-01 00:00:00

abstract：:Very young mammals have an impressive cardiac regeneration capacity. In contrast, cardiac regeneration is very limited in adult humans. The hearts of young children have a higher regenerative capacity compared with adults, as, for example, seen after surgical correction of an anomalous left coronary artery arising fro...

journal_title：Pediatric cardiology

authors： Rupp S,Schranz D

更新日期：2015-04-01 00:00:00

abstract：:Cardiovascular disease is a leading cause of mortality among patients with diabetes, and heart failure exists even in the absence of coronary disease. Myocardial metabolism is altered in the diabetic heart as a result of changes in substrate availability secondary to insulin resistance. The nuclear receptor peroxisome...

journal_title：Pediatric cardiology

authors： Duncan JG

更新日期：2011-03-01 00:00:00

abstract：:All 91,823 children born in 1980 in Bohemia (population 6.314 million; area 52,478 square kilometers) were examined at least four times during infancy and at the age of three and four years. All children who died were autopsied and those with heart disease were selected. A total of 779 children (8.223/1000 live births...

journal_title：Pediatric cardiology

authors： Samánek M,Slavík Z,Zborilová B,Hrobonová V,Vorísková M,Skovránek J

更新日期：1989-10-01 00:00:00

abstract：:Mammalian cardiomyocytes withdraw from the cell cycle soon after birth. This process is called terminal differentiation. The c-kit, a receptor tyrosine kinase, is expressed on cardiomyocytes immediately after birth but for only a few days. In mice with genetic c-kit dysfunction, adult cardiomyocytes are phenotypically...

journal_title：Pediatric cardiology

authors： Naqvi N,Li M,Yahiro E,Graham RM,Husain A

更新日期：2009-07-01 00:00:00

abstract：:Use of extracorporeal membrane oxygenation (ECMO) in infants with congenital heart disease is becoming more frequent. We present the first reported use of balloon atrial septostomy during ECMO support and describe possible complications of such procedures unique to ECMO therapy. ...

journal_title：Pediatric cardiology

authors： O'Connor TA,Downing GJ,Ewing LL,Gowdamarajan R

更新日期：1993-07-01 00:00:00

abstract：:A ventriculoseptal defect (VSD) usually is present in patients with a double-outlet right ventricle. This report describes a case of double-outlet right ventricle with a completely shrouded inlet VSD and no interventricular shunting. This was associated with a severely regurgitant dysplastic mitral valve. The anatomy ...

journal_title：Pediatric cardiology

authors： Singla M,Al-Radi O,Mertens L

更新日期：2013-01-01 00:00:00

abstract：:Hyperplastic left heart syndrome (HLHS) patients are palliated by creating a Fontan-type circulation passing from different surgical stages. The aim of this work is to describe the evolution of ventricular energetics parameters in HLHS patients during the different stages of palliation including the hybrid, the Norwoo...

journal_title：Pediatric cardiology

authors： Di Molfetta A,Iacobelli R,Guccione P,Di Chiara L,Rocchi M,Cobianchi Belisari F,Campanale M,Gagliardi MG,Filippelli S,Ferrari G,Amodeo A

更新日期：2017-12-01 00:00:00

abstract：:Twenty-three children with diabetes mellitus, their ages ranging from 0.2-9.8 years, but with no sign of diabetic microvascular disease were investigated by M-mode and Doppler echocardiography, along with a comparable group of control subjects. In the diabetics, the fractional shortening and the mean velocity of fract...

journal_title：Pediatric cardiology

authors： Gøtzsche O,Sørensen K,McIntyre B,Henningsen P

更新日期：1991-04-01 00:00:00

abstract：:Intramural coronary artery is known to be a risk factor for early death after an arterial switch operation (ASO). We evaluated the early and mid-term results of ASO for patients with intramural coronary artery. From September 2008 to March 2012, seven patients with an intramural coronary artery underwent ASO at our ho...

journal_title：Pediatric cardiology

authors： Chen X,Cui H,Chen W,Yang S,Cui Y,Xia Y,Ma L

更新日期：2015-01-01 00:00:00

abstract：:Kearns-Sayre syndrome (KSS) is a rare mitochondrial disorder characterized by large-scale deletions of mitochondrial DNA. Neuromuscular and cardiac conduction systems are most commonly involved in these patients. Here, we discuss a 10-year-old patient with diabetes mellitus who presented in complete heart block leadin...

journal_title：Pediatric cardiology

authors： Chawla S,Coku J,Forbes T,Kannan S

更新日期：2008-05-01 00:00:00

abstract：:A case of aneurysmal enlargement of the right atrium was found accidentally during a routine examination. The patient was asymptomatic and free of palpitations or proven rhythm disturbances. The results of echocardiography, magnetic resonance imaging, and cardiac catheterization excluded cardiac malformation, which co...

journal_title：Pediatric cardiology

authors： Kozelj M,Angelski R,Pavcnik D,Zorman D

更新日期：1998-09-01 00:00:00

abstract：:Ebstein anomaly of mitral valve (MV) is an extremely rare congenital heart disease. In the current report, we present a case of Ebstein of MV that was diagnosed prenatally. Fetal echocardiogram showed that the posterior leaflet of MV was tethered to the lateral wall of left ventricle (LV) with downward displacement in...

journal_title：Pediatric cardiology

authors： Aly S,Bokowski J,Diab K,Muller BA

更新日期：2018-08-01 00:00:00

abstract：:The original version of the article unfortunately contained an alignment error in Table 1. The correct version of Table 1 is given below. ...

journal_title：Pediatric cardiology

authors： Şişli E,Tuncer ON,Şenkaya S,Doğan E,Şahin H,Ayık MF,Atay Y

更新日期：2019-01-01 00:00:00