Aortopathies in mouse models of Pompe, Fabry and Mucopolysaccharidosis IIIB lysosomal storage diseas...
Aortopathies in mouse models of Pompe, Fabry and Mucopolysaccharidosis IIIB lysosomal storage diseases
About this item
Full title
Author / Creator
Belfiore, Maria Paola , Iacobellis, Francesca , Acampora, Emma , Caiazza, Martina , Rubino, Marta , Monda, Emanuele , Magaldi, Maria Rosaria , Tarallo, Antonietta , Sasso, Marcella , De Pasquale, Valeria , Grassi, Roberto , Cappabianca, Salvatore , Calabrò, Paolo , Fecarotta, Simona , Esposito, Salvatore , Esposito, Giovanni , Pisani, Antonio , Pavone, Luigi Michele , Parenti, Giancarlo and Limongelli, Giuseppe
Publisher
United States: Public Library of Science
Journal title
Language
English
Formats
Publication information
Publisher
United States: Public Library of Science
Subjects
More information
Scope and Contents
Contents
Lysosomal storage diseases (LSDs) are rare inherited metabolic diseases characterized by an abnormal accumulation of various toxic materials in the cells as a result of enzyme deficiencies leading to tissue and organ damage. Among clinical manifestations, cardiac diseases are particularly important in Pompe glycogen storage diseases (PD), in glycos...
Alternative Titles
Full title
Aortopathies in mouse models of Pompe, Fabry and Mucopolysaccharidosis IIIB lysosomal storage diseases
Authors, Artists and Contributors
Author / Creator
Iacobellis, Francesca
Acampora, Emma
Caiazza, Martina
Rubino, Marta
Monda, Emanuele
Magaldi, Maria Rosaria
Tarallo, Antonietta
Sasso, Marcella
De Pasquale, Valeria
Grassi, Roberto
Cappabianca, Salvatore
Calabrò, Paolo
Fecarotta, Simona
Esposito, Salvatore
Esposito, Giovanni
Pisani, Antonio
Pavone, Luigi Michele
Parenti, Giancarlo
Limongelli, Giuseppe
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_plos_journals_2404630459
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2404630459
Other Identifiers
ISSN
1932-6203
E-ISSN
1932-6203
DOI
10.1371/journal.pone.0233050
