Cardiac profile of the Czech population of Duchenne muscular dystrophy patients: a cardiovascular magnetic resonance study with T1 mapping-Reference-Cited by-同舟云学术

Cardiac profile of the Czech population of Duchenne muscular dystrophy patients: a cardiovascular magnetic resonance study with T1 mapping

Published:2019-01-09 Issue:1 Volume:14 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

Panovský Roman^ORCID,Pešl Martin,Holeček Tomáš,Máchal Jan,Feitová Věra,Mrázová Lenka,Haberlová Jana,Slabá Alžběta,Vít Pavel,Stará Veronika,Kincl Vladimír

Funder

Ministerstvo Školství, Mládeže a Tělovýchovy

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics (clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-018-0986-0.pdf

Reference37 articles.

1. Birnkrant DJ, Bushby K, Bann CM, et al. DMD care considerations working group. Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management. Lancet Neurol. 2018;17(4):347–61.

2. McNally EM. New approaches in the therapy of cardiomyopathy in muscular dystrophy. Ann Rev Med. 2007;58:75–88.

3. Mu X, Tang Y, Lu A, et al. The role of notch signaling in muscle progenitor cell depletion and the rapid onset of histopathology in muscular dystrophy. Hum Mol Genet. 2015;24(10):2923–37.

4. Berry SE, Andruszkiewicz P, Chun JL, Hong J. Nestin expression in end-stage disease in dystrophin-deficient heart: implications for regeneration from endogenous cardiac stem cells. Stem Cells Transl Med. 2013;2(11):848–61.

5. Aartsma-Rus A, Van Deutekom JC, Fokkema IF, Van Ommen GJ, Den Dunnen JT. Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule. Muscle Nerve. 2006;34(2):135–44.

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