Neonatal heart failure and noncompaction/dilated cardiomyopathy from mucopolysaccharidosis. First description in literature-Reference-Cited by-同舟云学术

Neonatal heart failure and noncompaction/dilated cardiomyopathy from mucopolysaccharidosis. First description in literature

Published:2021-03 Issue: Volume:26 Page:100714
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Miselli Francesca,Brambilla Alice,Calabri Giovanni Battista,Favilli Silvia,Sanvito Maria Chiara,Ragni Luca,Torcetta Francesco,Rossi Katia,Donati Maria Alice,Procopio Elena

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference14 articles.

1. Residual α-L-iduronidase activity in fibroblasts of mild to severe Mucopolysaccharidosis type I patients;Oussoren;Mol. Genet. Metab.,2013

2. Guidelines for the management of mucopolysaccharidosis type I;Martins;J. Pediatr.,2009

3. Genetic infiltrative Cardiomyopathies;Sweet;Heart Fail. Clin.,2018

4. Left ventricular noncompaction: A distinct genetic cardiomyopathy?;Arbustini;J. Am. Coll. Cardiol.,2016

5. Mitochondrial Cardiomyopathies;El-Hattab;Front Cardiovasc Med.,2016

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1. Hematopoietic cell transplantation for Mucopolysaccharidosis I in the presence of decreased cardiac function;Molecular Genetics and Metabolism;2023-11

2. Early Neonatal Cardiac Phenotype in Hurler Syndrome: Case Report and Literature Review;Genes;2022-07-22

3. Pre-operative Considerations in Adult Mucopolysaccharidosis Patients Planned for Cardiac Intervention;Frontiers in Cardiovascular Medicine;2022-04-04