Pages that link to "Q39482144"

The following pages link to Three decades of follow-up of aortic and pulmonary vascular lesions in the Williams-Beuren syndrome (Q39482144):

Displaying 43 items.

• Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls (Q24300678) (← links)
• CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes (Q30829917) (← links)
• Peripheral pulmonary artery stenosis as a cause of pulmonary hypertension in adults (Q33165753) (← links)
• Congenital heart disease and genetic syndromes: specific correlation between cardiac phenotype and genotype. (Q34123316) (← links)
• Congenital supravalvar aortic stenosis: a simple lesion? (Q34135033) (← links)
• Familial Williams-Beuren syndrome showing varying clinical expression (Q34136369) (← links)
• Williams syndrome: from genotype through to the cognitive phenotype (Q34141678) (← links)
• Genetic counseling for congenital heart disease: new approaches for a new decade (Q34463389) (← links)
• Echocardiographic findings in patients with Williams-Beuren syndrome. (Q34569940) (← links)
• Further delineation of cardiac abnormalities in Costello syndrome (Q34811131) (← links)
• Cardiovascular manifestations in 75 patients with Williams syndrome (Q35440223) (← links)
• Growth of the aorta in children with Williams syndrome: does surgery make a difference? (Q35646888) (← links)
• Cardiovascular spectrum in Williams-Beuren syndrome: the Mexican experience in 40 patients. (Q36932186) (← links)
• Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome. (Q37152735) (← links)
• Stenosis of the thoracic aorta in Williams syndrome (Q37735734) (← links)
• Abnormalities of Cardiac Repolarization in Williams Syndrome (Q37790477) (← links)
• Extended Single-Patch Repair of Supravalvar Aortic Stenosis: A Simple and Effective Technique (Q37989681) (← links)
• Severe left main coronary artery stenosis with abnormal branching pattern in a patient with mild supravalvar aortic stenosis and Williams-Beuren syndrome (Q38108898) (← links)
• Supravalvar aortic stenosis: current surgical approaches and outcomes (Q38124875) (← links)
• Risk assessment and anesthetic management of patients with Williams syndrome: a comprehensive review (Q38604329) (← links)
• Elastin gene deletions in Williams syndrome patients result in altered deposition of elastic fibers in skin and a subclinical dermal phenotype (Q39531643) (← links)
• Cytogenomic Evaluation of Subjects with Syndromic and Nonsyndromic Conotruncal Heart Defects. (Q40773683) (← links)
• Sudden death in Williams syndrome: report of ten cases (Q41273020) (← links)
• Williams syndrome and Ebstein′s anomaly: A rare association (Q42095870) (← links)
• Pulmonary artery diverticulum: an angiographic marker for Williams syndrome (Q43166539) (← links)
• Occult progressive pulmonary arterial occlusion associated with right ventricular hypertension in patients with systemic arteriopathy (Q43544605) (← links)
• Cardiac outcomes in adults with supravalvar aortic stenosis (Q44977350) (← links)
• Incidence and spectrum of renal abnormalities in Williams-Beuren syndrome (Q44980072) (← links)
• Cardiac catheterization and operative outcomes from a multicenter consortium for children with williams syndrome (Q45351842) (← links)
• Clinical manifestations and molecular investigation of 50 patients with Williams syndrome in the Greek population (Q51932100) (← links)
• Spontaneous development and rupture of pulmonary artery aneurysm: a rare complication in an infant with peripheral pulmonary artery stenoses due to mutation of the elastin gene. (Q53460869) (← links)
• Surgical Correction of Supravalvar Aortic Stenosis: 52 Years' Experience. (Q54960596) (← links)
• Elastin, arterial mechanics, and cardiovascular disease (Q57171390) (← links)
• ELN gene triplication responsible for familial supravalvular aortic aneurysm (Q62870665) (← links)
• Tailored stent treatment for severe supravalvular aortic stenosis (Q71774975) (← links)
• De novo 46,XX,t(6;7)(q27;q11;23) associated with severe cardiovascular manifestations characteristic of supravalvular aortic stenosis and Williams syndrome (Q73531993) (← links)
• Williams-Beuren syndrome 35 years after the diagnosis in one of the first Beuren patients (Q73680947) (← links)
• Composite aortoplasty for recurrent coarctation after neonatal repair in Williams syndrome (Q75271668) (← links)
• Echocardiographic follow-up of children with supravalvular aortic stenosis (Q79338164) (← links)
• Isolated obstruction of the right ventricular infundibulum in a patient with Williams' syndrome (Q79447106) (← links)
• [Williams-Beuren syndrome: presentation of 82 cases] (Q80221072) (← links)
• Pulmonary stenosis is a predictor of unfavorable outcome after surgery for supravalvular aortic stenosis (Q83719245) (← links)
• Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association (Q90669133) (← links)