Review: Danon disease: Review of natural history and recent advances-Reference-Cited by-同舟云学术

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Review: Danon disease: Review of natural history and recent advances

Published:2019-11-25 Issue:4 Volume:46 Page:303-322
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathol Appl Neurobiol

Author:

Cenacchi G.¹^ORCID,Papa V.¹,Pegoraro V.²,Marozzo R.²,Fanin M.³,Angelini C.⁴^ORCID

Affiliation:

1. Department of Biomedical and Neuromotor Sciences “Alma Mater” University of Bologna Bologna Italy

2. Neurobiology Laboratory IRCCS San Camillo Hospital VeniceItaly

3. Department of Neurosciences University of Padova Padova Italy

4. Neuromuscular Department IRCCS San Camillo Hospital Venice Italy

Publisher

Wiley

Subject

Physiology (medical),Clinical Neurology,Neurology,Histology,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/nan.12587

Reference150 articles.

1. Lysosomal glycogen storage disease with normal acid maltase

2. Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)

3. Characterization of Danon disease in a male patient and his affected mother

4. Danon Disease as an Underrecognized Cause of Hypertrophic Cardiomyopathy in Children

5. Identification of LAMP2 Mutations in Early-Onset Danon Disease With Hypertrophic Cardiomyopathy by Targeted Next-Generation Sequencing

Cited by 70 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. Altered fatty acid distribution in lysosome-associated membrane protein-2 deficient mice;Biochemistry and Biophysics Reports;2024-12

2. Protein isoform-centric therapeutics: expanding targets and increasing specificity;Nature Reviews Drug Discovery;2024-09-04

3. An International Longitudinal Natural History Study of Danon Disease Patients: Unique Cardiac Trajectories Identified Based on Sex and Heart Failure Outcomes;2024-05-22

4. Endovascular treatment in Danon disease: a case report;Journal of Medical Case Reports;2024-05-12

5. Frameshift mutation of LAMP2:c.667delT in a 17-year-old male with hypertrophic cardiomyopathy and dyslexia: a novel pathogenic variant for Danon disease;Singapore Medical Journal;2024-05-09

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