Evmorfia Petropoulou

Evmorfia Petropoulou

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Evmorfia Petropoulou

Evmorfia Petropoulou

Publications by authors named "Evmorfia Petropoulou"

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Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy.

Eur J Med Genet 2017 Sep 19;60(9):485-488. Epub 2017 Jun 19.

Cardiovascular and Cell Sciences Institute, St George's University of London, Cranmer Terrace, London, UK. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S17697212173004
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http://dx.doi.org/10.1016/j.ejmg.2017.06.008DOI Listing
September 2017

Coagulation Gene Expression Profiling in Infants With Necrotizing Enterocolitis.

J Pediatr Gastroenterol Nutr 2016 12;63(6):e169-e175

*Department of Paediatric and Neonatal Surgery, St George's University Hospitals NHS Foundation Trust †Human Genetics Research Centre, Institute of Cardiovascular and Cell Sciences, St George's University of London ‡Department of Neonatal Intensive Care Unit, St George's University Hospitals NHS Foundation Trust, London, UK.

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http://dx.doi.org/10.1097/MPG.0000000000001215DOI Listing
December 2016

The genetics of pro-arrhythmic adverse drug reactions.

Br J Clin Pharmacol 2014 Apr;77(4):618-25

Human Genetics Research Centre, Division of Biomedical Sciences, St George's Hospital Medical School, London, SW17 0RE, UK.

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http://dx.doi.org/10.1111/bcp.12208DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3971979PMC
April 2014