SHAINE MORRIS to Adolescent
This is a "connection" page, showing publications SHAINE MORRIS has written about Adolescent.
Connection Strength
0.884
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Mitral annular disjunction and its progression during childhood in Marfan syndrome. Eur Heart J Cardiovasc Imaging. 2024 Aug 26; 25(9):1306-1314.
Score: 0.066
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Cardiovascular Management of Aortopathy in Children: A Scientific Statement From the American Heart Association. Circulation. 2024 Sep 10; 150(11):e228-e254.
Score: 0.066
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Evidence of cardiomyopathy associated with Marfan syndrome in children. Heart. 2024 Jun 17; 110(13):887-891.
Score: 0.065
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An Analysis of Hospital Mortality After Cardiac Operations in Children With Down Syndrome. Semin Thorac Cardiovasc Surg. 2020 Winter; 32(4):947-957.
Score: 0.050
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Thoracic Aortic, Aortic Valve, and Mitral Valve Surgery in Pediatric and Young Adult Patients With Marfan Syndrome: Characteristics and Outcomes. Semin Thorac Cardiovasc Surg. 2019; 31(4):818-825.
Score: 0.046
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Obstetric Management of Loeys-Dietz Syndrome. Obstet Gynecol. 2018 06; 131(6):1080-1084.
Score: 0.043
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A population-based analysis of mortality in patients with Turner syndrome and hypoplastic left heart syndrome using the Texas Birth Defects Registry. Congenit Heart Dis. 2017 Jan; 12(1):105-112.
Score: 0.038
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Thoracic aortic dissection and rupture in conotruncal cardiac defects: A population-based study. Int J Cardiol. 2015 Apr 01; 184:521-527.
Score: 0.034
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Aortic dissection in hospitalized children and young adults: a multiinstitutional study. Congenit Heart Dis. 2014 Jan-Feb; 9(1):54-62.
Score: 0.030
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Impact of obesity on ventricular size and function in children, adolescents and adults with Tetralogy of Fallot after initial repair. Am J Cardiol. 2013 Aug 15; 112(4):594-8.
Score: 0.030
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Increased vertebral artery tortuosity index is associated with adverse outcomes in children and young adults with connective tissue disorders. Circulation. 2011 Jul 26; 124(4):388-96.
Score: 0.027
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Aortic and arterial manifestations and clinical features in TGFB3-related heritable thoracic aortic disease: results from the Montalcino Aortic Consortium. J Med Genet. 2025 Jan 27; 62(2):82-88.
Score: 0.017
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Caught in the Act: A Detailed Analysis of Cardiac Event Monitoring in a Cohort of Pediatric and ACHD Patients. Pacing Clin Electrophysiol. 2024 Dec; 47(12):1593-1603.
Score: 0.017
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Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016-2023). Am J Med Genet A. 2024 Oct; 194(10):e63638.
Score: 0.016
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Design and implementation of multicenter pediatric and congenital studies with cardiovascular magnetic resonance: Big data in smaller bodies. J Cardiovasc Magn Reson. 2024; 26(1):101041.
Score: 0.016
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Abnormal Left Ventricular Strain Correlates with Left Ventricular Dysfunction but not Aortic Pathology in Marfan Syndrome in Children. Pediatr Cardiol. 2023 Oct; 44(7):1536-1545.
Score: 0.015
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Natural history of TANGO2 deficiency disorder: Baseline assessment of 73 patients. Genet Med. 2023 04; 25(4):100352.
Score: 0.015
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Lesion-Specific Congenital Heart Disease Mortality Trends in Children: 1999 to 2017. Pediatrics. 2022 10 01; 150(4).
Score: 0.014
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Hospital outcomes for pediatric heart transplant recipients undergoing tracheostomy: A multi-institutional analysis. Pediatr Transplant. 2021 May; 25(3):e13904.
Score: 0.013
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The first reported case of Loeys-Dietz syndrome in a patient with biallelic SMAD3 variants. Am J Med Genet A. 2020 11; 182(11):2755-2760.
Score: 0.013
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Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome. J Pediatr. 2020 07; 222:213-220.e5.
Score: 0.012
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Neurovascular findings in children and young adults with Loeys-Dietz syndromes: Informing recommendations for screening. J Neurol Sci. 2020 Feb 15; 409:116633.
Score: 0.012
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Association of Wolff-Parkinson-White With Left Ventricular Noncompaction Cardiomyopathy in Children. J Card Fail. 2019 Dec; 25(12):1004-1008.
Score: 0.012
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Improved 6 Minute Walk Distance and Brain-Type Natriuretic Peptide After Continuous-Flow Ventricular Assist Device Placement in Children. ASAIO J. 2019 Sep/Oct; 65(7):725-730.
Score: 0.012
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Impact of Treatment Modality on Vascular Function in Coarctation of the Aorta: The LOVE - COARCT Study. J Am Heart Assoc. 2019 04 02; 8(7):e011536.
Score: 0.011
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Cervical lymphatic malformations: Prenatal characteristics and ex utero intrapartum treatment. Prenat Diagn. 2019 03; 39(4):287-292.
Score: 0.011
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Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations. Genet Med. 2018 10; 20(10):1206-1215.
Score: 0.010
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Allometric considerations when assessing aortic aneurysms in Turner syndrome: Implications for activity recommendations and medical decision-making. Am J Med Genet A. 2018 Feb; 176(2):277-282.
Score: 0.010
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Fatal cardiac arrest in pediatric heart transplant recipients: Query of the UNOS database. Pediatr Transplant. 2018 02; 22(1).
Score: 0.010
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Heterotaxy syndrome and associated arrhythmias in pediatric patients. Heart Rhythm. 2018 04; 15(4):548-554.
Score: 0.010
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Bicuspid and unicuspid aortic valves: Different phenotypes of the same disease? Insight from the GenTAC Registry. Congenit Heart Dis. 2017 Dec; 12(6):740-745.
Score: 0.010
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Aortic Dilatation Associated With Bicuspid Aortic Valve: Relation to Sex, Hemodynamics, and Valve Morphology (the National Heart Lung and Blood Institute-Sponsored National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions). Am J Cardiol. 2017 Oct 01; 120(7):1171-1175.
Score: 0.010
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Assessment of large copy number variants in patients with apparently isolated congenital left-sided cardiac lesions reveals clinically relevant genomic events. Am J Med Genet A. 2017 Aug; 173(8):2176-2188.
Score: 0.010
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Associations of Age and Sex With Marfan Phenotype: The National Heart, Lung, and Blood Institute GenTAC (Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions) Registry. Circ Cardiovasc Genet. 2017 Jun; 10(3).
Score: 0.010
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Diminished Global Longitudinal Strain Predicts?Late Allograft Failure in Pediatric?Heart Transplant Recipients. JACC Cardiovasc Imaging. 2017 12; 10(12):1529-1531.
Score: 0.010
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Aortic Complications Associated With Pregnancy in Marfan Syndrome: The NHLBI National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC). J Am Heart Assoc. 2016 08 11; 5(8).
Score: 0.009
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Echocardiographic Parameters and Outcomes in Primary Fetal Cardiomyopathy. J Ultrasound Med. 2016 Sep; 35(9):1949-55.
Score: 0.009
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Disrupted nitric oxide signaling due to GUCY1A3 mutations increases risk for moyamoya disease, achalasia and hypertension. Clin Genet. 2016 10; 90(4):351-60.
Score: 0.009
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The Need for Standardized Methods for Measuring the Aorta: Multimodality Core Lab Experience From the GenTAC Registry. JACC Cardiovasc Imaging. 2016 Mar; 9(3):219-26.
Score: 0.009
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Reassessing Risk Factors in Pediatric Patients With Pacemakers Implanted for Atrioventricular Block: The Impact of Nonsustained Ventricular Tachycardia. J Cardiovasc Electrophysiol. 2016 Apr; 27(4):471-9.
Score: 0.009
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Segmental Aortic Stiffness in Children and Young Adults With Connective Tissue Disorders: Relationships With Age, Aortic Size, Rate of Dilation, and Surgical Root Replacement. Circulation. 2015 Aug 18; 132(7):595-602.
Score: 0.009
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Echocardiographic Parameters of Right Ventricular Diastolic Function in Repaired Tetralogy of Fallot Are Associated with Important Findings on Magnetic Resonance Imaging. Congenit Heart Dis. 2015 May-Jun; 10(3):E113-22.
Score: 0.009
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Pediatric ventricular assist device use as a bridge to transplantation does not affect long-term quality of life. J Thorac Cardiovasc Surg. 2014 Apr; 147(4):1334-43.
Score: 0.008
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Low incidence of arrhythmias in the right ventricular infundibulum sparing approach to tetralogy of Fallot repair. Pediatr Cardiol. 2014 Feb; 35(2):261-9.
Score: 0.008
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Economic and safety implications of introducing fast tracking in congenital heart surgery. Circ Cardiovasc Qual Outcomes. 2013 Mar 01; 6(2):201-7.
Score: 0.007
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Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q. Am J Med Genet. 1999 Aug 27; 85(5):455-62.
Score: 0.003