Acute infantile cardiomyopathy as a presenting feature of mucopolysaccharidosis VI-Reference-Cited by-同舟云学术

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Acute infantile cardiomyopathy as a presenting feature of mucopolysaccharidosis VI

Published:1992-02 Issue:2 Volume:120 Page:269-272
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Hayflick S.,Rowe S.,Kavanaugh-McHugh A.,Olson J.L.,Valle D.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference7 articles.

1. Mucopolysaccharidosis VI (Maroteaux-Lamy's disease);Spranger;Helv Paediatr Acta,1970

2. Cardiovascular manifestations of the genetic mucopolysaccharidoses;Krovetz;Birth Defects,1972

3. Hurler syndrome with cardiomyopathy in infancy;Donaldson;J Pediatr,1989

4. Mucopolysaccharidosis type VI presenting in infancy with endocardial fibroelastosis and heart failure;Miller;Pediatr Cardiol,1983

5. Endocardial fibroelastosis in mucopolysaccharidosis type VI;Fong;Clin Cardiol,1987

Cited by 51 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. The articular and the craniocervical abnormalities are of confusing age of onset in patients with Maroteaux-Lamy disease (MPS VI);Minerva Pediatrics;2023-04

2. Cardiovascular System;Keeling's Fetal and Neonatal Pathology;2022

3. Mucopolysaccharidoses;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2021

4. Mucopolysaccharidosis type VI: case report with first neonatal presentation with ascites fetalis and rapidly progressive cardiac manifestation;BMC Medical Genetics;2020-02-19

5. Identification of eleven different mutations including six novel, in the arylsulfatase B gene in Iranian patients with mucopolysaccharidosis type VI;Molecular Biology Reports;2019-04-13

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