Disease: Aortic valve stenosis of the child
- A case of dilated cardiomyopathy caused by FHL2 gene variant and a literature review
- A Case of William's Syndrome in a Ugandan Child: A Feasible Diagnosis Even in a Low-Resource Setting
- A case report of Williams syndrome with main clinical manifestation of hypercalcemia and gastrointestinal bleeding as the main clinical manifestations, and with an accompanying literature review
- A comparative study of educational provision for children with neurogenetic syndromes: parent and teacher survey
- A fetal dilated and hypertrophic cardiomyopathy associated with maternal gestational diabetes--a case report
- Alcohol septal ablation after myomectomy failure solutions for unusual cases
- An infant with suspected missed diagnosis of Williams syndrome failed weaning off CPB after surgical correction of pulmonary stenosis: a case report and literature review
- Anatomophysiologic basis of tetralogy of Fallot and its clinical implications
- Aortic valve repair in a low-birth-weight neonate with poor ventricular function: staged tricuspidization of the unicuspid valve
- Aorto-mesenteric and renal allograft transplant: a novel treatment for midaortic syndrome
- Application of single nucleotide polymorphism-array for the diagnosis of Williams-Beuren syndrome in a case
- Approach to the Child with Hypercalcaemia
- Assessment of the influence of background noise on escape-maintained problem behavior and pain behavior in a child with Williams syndrome
- Association between speech-language, general cognitive functioning and behaviour problems in individuals with Williams syndrome
- Behavioral features of Williams Beuren syndrome compared to Fragile X syndrome and subjects with intellectual disability without defined etiology
- Behavioral Profiles of Children With Williams Syndrome From Spain and the United States: Cross-Cultural Similarities and Differences
- Behavioural profile and maternal stress in Greek young children with Williams syndrome
- Bloodless pediatric cardiopulmonary bypass for a 3.2-kg patient whose parents are of Jehovah's Witness faith
- Brief Report: Challenging Behaviors in Toddlers and Preschoolers with Angelman, Prader-Willi, and Williams Syndromes
- Cardiac arrest under anesthesia in a pediatric patient with Williams syndrome: a case report
- Cardiac manifestations of carbohydrate-deficient glycoprotein syndrome
- Characterisation of sleep problems in children with Williams syndrome
- Children with 7q11.23 duplication syndrome: psychological characteristics
- Children with Prader-Willi syndrome vs. Williams syndrome: indirect effects on parents during a jigsaw puzzle task
- Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathy
- Coarctation of the aorta, aortic valvar stenosis, and supravalvar aortic stenosis with left coronary artery ostial stenosis: management using a staged hybrid approach
- Comprehensive Versus Targeted Genetic Testing in Children with Hypertrophic Cardiomyopathy
- Congenital heart disease and acquired valvular lesions in pregnancy
- Congenitally corrected transposition of the great arteries: clues for prenatal diagnosis
- Constructing "best interests": genetic testing of children in families with hypertrophic cardiomyopathy
- Correlations between behavior, memory, sleep-wake and melatonin in Williams-Beuren syndrome
- Cross-sectional and longitudinal assessment of cognitive development in Williams syndrome
- Cyclosporine attenuates cardiomyocyte hypertrophy induced by RAF1 mutants in Noonan and LEOPARD syndromes
- Diagnosis of a case with Williams-Beuren syndrome with nephrocalcinosis using chromosome microarray analysis
- Documented exercise-induced cardiac arrest in a paediatric patient with hypertrophic cardiomyopathy
- Early myoclonic epilepsy, hypertrophic cardiomyopathy and subsequently a nephrotic syndrome in a patient with CoQ10 deficiency caused by mutations in para-hydroxybenzoate-polyprenyl transferase (COQ2)
- Early results of the bovine jugular vein graft used for reconstruction of the right ventricular outflow tract
- Endocrine manifestations in children with Williams-Beuren syndrome
- Executive function as measured by the Behavior Rating Inventory of Executive Function-2: children and adolescents with Williams syndrome
- Fetal Diagnosis of Supravalvular Aortic Stenosis and Pulmonary Stenosis in a Family with Non-Syndromic Elastin Mutation
- Genetic analysis of a child with atypical Williams-Beuren syndrome presenting as supravalvular aortic stenosis
- Genetic diagnosis of a child with aortic stenosis and thumb aplasia
- Health-Related Quality of Life and Functional Status Are Associated with Cardiac Status and Clinical Outcome in Children with Cardiomyopathy
- Huge, invasive, and destructive Abiotrophia defectiva endocarditis of the aortic valve and the aortic wall: a case report of an emergency but successful Ross-Konno operation in a child
- Implantation of a decellularized aortic homograft in a child
- Infantile Hypertrophic Cardiomyopathy and Bronchopneumonia as Causes of an Unexpected Death in an 11-Month-Old Child
- Infantile ictal apneas in a child with williams-beuren syndrome
- Infantile sialic acid storage disease and protein-losing gastroenteropathy
- Is the child 'father of the man'? evaluating the stability of genetic influences across development
- Left ventricular rehabilitation in an infant with transposition of the great arteries, intact ventricular septum, pulmonary stenosis and small left ventricle
- Management of aortic coarctation at the adult age
- Management of valvar aortic stenosis in children
- Maternal stress among mothers of children with Williams-Beuren syndrome, Down's syndrome and mental retardation of non-syndromal etiology in comparison to mothers of non-disabled children
- Metopic and Sagittal Craniosynostosis in Williams Syndrome
- Naxos disease in an Arab family is not caused by the Pk2157del2 mutation. Evidence for exclusion of the plakoglobin gene
- Neurocognitive profile in psychotic versus nonpsychotic individuals with 22q11.2 deletion syndrome
- Novel mutation in ELN gene causes cardiac abnormalities and inguinal hernia: case report
- Outcome of surgical commissurotomy for aortic valve stenosis in early infancy
- Outcomes of an 8-Week Treadmill Training Program for a Toddler With Williams Syndrome: A Case Report
- Outcomes of Mitral Valve Replacement after Closed Mitral Valvotomy: A Retrospective Cohort Study
- Parental smoking during early pregnancy and congenital heart defects
- Parents' attributions of their child's jigsaw-puzzle performance: comparing two genetic syndromes
- Parents' experiences of having an asymptomatic child diagnosed with hypertrophic cardiomyopathy through family screening
- Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four-break rearrangement
- Penetrance of hypertrophic cardiomyopathy in children and adolescents: a 12-year follow-up study of clinical screening and predictive genetic testing
- Percutaneous transluminal septal myocardial ablation in a child with hypertrophic obstructive cardiomyopathy and Noonan syndrome
- Physician or seer? Very early diagnosis and prognosis. The example of William's syndrome
- Prenatal therapy of non-immunologic hydrops fetalis caused by severe aortic stenosis
- Progressive intracranial vascular disease with strokes and seizures in a boy with progeria
- Proximal trisomy of 1q mosaicism in a girl with hypertrophic cardiomyopathy associated with Wolff-Parkinson-White syndrome and multiple congenital anomalies
- Psychopathological and behavior impairments in Williams-Beuren syndrome: the influence of gender, chronological age, and cognition
- Psychopathology and behavior problems in children and adolescents with Williams syndrome: Distinctive relationships with cognition
- Quality of life of Brazilian families who have children with Williams syndrome
- Repair, replacement, Ross: how I approach the older child with mixed aortic stenosis/aortic insufficiency
- Reproduction problems in women with cardiovascular diseases
- Resynchronization or dyssynchronization--successful treatment with biventricular stimulation of a child with obstructive hypertrophic cardiomyopathy without dyssynchrony
- Ross mitral procedure for massive congenital mitral insufficiency
- Ross Procedure for Aortic Valve Replacement
- Ross Procedure for Aortic Valve Replacement
- Short-term longitudinal study of a child with Williams syndrome
- Siblings of children with Williams syndrome: Correlates of psychosocial adjustment and sibling relationship quality
- Sleep characteristics and problems of 2-year-olds with Williams syndrome: relations with language and behavior
- Special dental management in patients with Williams syndrome
- Structural validity of the Child Behavior Checklist (CBCL) for preschoolers with neurogenetic syndromes
- Studies of age-correlated features of cognitive-behavioral development in children and adolescents with genetic disorders
- Sudden death of an infant with cardiac, nervous system and genetic involvement--a case report
- Supravalvular aortic stenosis surgical repair using modified Sousa's technique
- Surgical repair of aorto-ventricular tunnel
- Surgical repair of interrupted right-sided cervical aortic arch with hypoplasia of the descending thoracic aorta in a child with PHACE syndrome
- Surgical valvuloplasty versus balloon aortic dilation for congenital aortic stenosis: are evidence-based outcomes relevant?
- Tetralogy of Fallot with aortic valvular stenosis: surgical correction in one case
- The assessment of left ventricular function in cardiac and extracardiac disorders in children
- The child from families with type 1 diabetes
- The impact of physical activity modification on the well-being of a cohort of children with an inherited arrhythmia or cardiomyopathy
- The Impact on the Family of Four Neurogenetic Syndromes: A Comparative Study of Parental Views
- The surgical treatment of critical aortic stenosis in a child by the Ross-Konno technic
- Transcatheter aortic valve replacement (TAVR) as bridge therapy restoring eligibility for liver transplantation in cirrhotic patients
- Treating food refusal in a child with Williams syndrome using the parent as therapist in the home setting
- Trileaflet Semilunar Valve Reconstruction: Acute Porcine in Vivo Evaluation
- Visuo-spatial and linguistic abilities in a twin with Williams syndrome