Association between genetic variants in the HIF1A-VEGF pathway and left ventricular regional myocardial deformation in patients with hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

Association between genetic variants in the HIF1A-VEGF pathway and left ventricular regional myocardial deformation in patients with hypertrophic cardiomyopathy

Published:2020-05-06 Issue:3 Volume:89 Page:628-635
ISSN:0031-3998
Container-title:Pediatric Research
language:en
Short-container-title:Pediatr Res

Author:

Pieles Guido E.,Alkon Jaime,Manlhiot Cedric,Fan Chun-Po Steve,Kinnear Caroline,Benson Leland N.,Mital Seema,Friedberg Mark K.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://www.nature.com/articles/s41390-020-0929-z.pdf

Reference41 articles.

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2. Watkins, H., Ashrafian, H. & Redwood, C. Inherited cardiomyopathies. N. Engl. J. Med. 364, 1643–1656 (2011).

3. Alkon, J. et al. Genetic variations in hypoxia response genes influence hypertrophic cardiomyopathy phenotype. Pediatr. Res. 72, 583–592 (2012).

4. McMahon, C. J. et al. Characterization of left ventricular diastolic function by tissue Doppler imaging and clinical status in children with hypertrophic cardiomyopathy. Circulation 109, 1756–1762 (2004).

5. Ha, J. W. et al. Tissue Doppler-derived indices predict exercise capacity in patients with apical hypertrophic cardiomyopathy. Chest 128, 3428–3433 (2005).

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