Survival Implications: Hypertrophic Cardiomyopathy in Noonan Syndrome-Reference-Cited by-同舟云学术

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Survival Implications: Hypertrophic Cardiomyopathy in Noonan Syndrome

Published:2011-01 Issue:1 Volume:6 Page:41-47
ISSN:1747-079X
Container-title:Congenital Heart Disease
language:en
Short-container-title:

Author:

Hickey Edward J.,Mehta Rohit,Elmi Maryam,Asoh Kentaro,McCrindle Brian W.,Williams William G.,Manlhiot Cedric,Benson Lee

Publisher

Computers, Materials and Continua (Tech Science Press)

Subject

Cardiology and Cardiovascular Medicine,Radiology Nuclear Medicine and imaging,General Medicine,Surgery,Pediatrics, Perinatology, and Child Health

Reference29 articles.

1. Cardiologic abnormalities in Noonan syndrome: phenotypic diagnosis and echocardiographic assessment of 118 patients;Burch;J Am Coll Cardiol.,1993

2. Cardiovascular abnormalities in Noonan syndrome: the clinical findings and treatments;Ishizawa;Acta Paediatr Jpn.,1996

3. Hypertrophic cardiomyopathy in Noonan syndrome;Nishikawa;Acta Paediatr Jpn.,1996

4. Echocardiographic and electrocardiographic identification of those children with hypertrophic cardiomyopathy who should be considered at high-risk of dying suddenly;Ostman-Smith;Cardiol Young.,2005

5. Myocardial disarray in Noonan syndrome;Burch;Br Heart J.,1992

Cited by 59 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mutation-induced LZTR1 polymerization provokes cardiac pathology in recessive Noonan syndrome;Cell Reports;2024-07

2. Unique Aspects of Hypertrophic Cardiomyopathy in Children;Canadian Journal of Cardiology;2024-05

3. MEK Inhibition for RASopathy-Associated Hypertrophic Cardiomyopathy: Clinical Application of a Basic Concept;Canadian Journal of Cardiology;2024-05

4. General anesthesia with remimazolam for tooth extraction in a patient with Noonan syndrome and hypertrophic obstructive cardiomyopathy: A case report;Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology;2024-05

5. Preclinical evaluation of CRISPR-based therapies for Noonan syndrome caused by deep-intronic LZTR1 variants;Molecular Therapy - Nucleic Acids;2024-03

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