After qualifying from medical school in Germany, Dr Martina Muggenthaler completed her House Officer and Senior House Officer training in and around London.
In 2005 she became a Cardiology Specialist Registrar.
She finished her CRY Research Fellowship in October 2012. She is currently working at St. George’s University of London.
Martina’s research focuses on the genetic causes for inherited heart conditions, mainly Long QT syndrome and hypertrophic cardiomyopathy.
https://issuu.com/cardiacriskintheyoung/docs/research_newsletter_2016 Cardiac Risk in the Young's research highlights from 2016.
M. Muggenthaler, E. Petropoulou, S. Omer, M.A. Simpson, H. Sahak, A. Rice, H. Raju, F.J. Conti, L.R. Bridges, L.J. Anderson, S. Sharma, E.R. Behr, Y. Jamshidi Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease International Journal of Cardiology, May 2016 {Abstract}
The Terrace Marquee, Westminster - 26th November. Guest of Honour: Lee Mears, former England rugby union international. CRY’s 2014 Parliamentary Reception on Wednesday November 26 was an event packed not only with CRY Representatives, supporters, bereaved families, members of the myheart group and doctors, but also several CRY Patrons and
Read Update 56 online here The CRY Update is the charity’s newsletter, published three times a year, reporting on CRY news and events, cardiac screenings, breaking developments in medical research and CRY supporters’ fundraising over the preceding months.
Read Update 58 online here The CRY Update is the charity’s newsletter, published three times a year, reporting on CRY news and events, cardiac screenings, breaking developments in medical research and CRY supporters’ fundraising over the preceding months.
Preventing young sudden cardiac deaths through awareness, screening and research, and supporting affected families.
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