Found: 6
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Percutaneous embolization of lymphatic fistulae as treatment for protein‐losing enteropathy and plastic bronchitis in patients with failing Fontan circulation.
- Published in:
- Catheterization & Cardiovascular Interventions, 2019, v. 94, n. 7, p. 996, doi. 10.1002/ccd.28501
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- Publication type:
- Article
Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 1, p. 1, doi. 10.1371/journal.pgen.1007138
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- Publication type:
- Article
Persistent Markers of Kidney Injury in Children Who Developed Acute Kidney Injury After Pediatric Cardiac Surgery: A Prospective Cohort Study.
- Published in:
- 2022
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- Publication type:
- journal article
The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 8, p. 1822, doi. 10.1002/ajmg.a.37108
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- Publication type:
- Article
MEIS2 involvement in cardiac development, cleft palate, and intellectual disability.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 5, p. 1142, doi. 10.1002/ajmg.a.36989
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- Publication type:
- Article
Haploinsufficiency of elastin gene may lead to familial cardiopathy and pulmonary emphysema.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 8, p. 2053, doi. 10.1002/ajmg.a.35464
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- Publication type:
- Article