A human MYBPC3 mutation appearing about 10 centuries ago results in a hypertrophic cardiomyopathy with delayed onset, moderate evolution but with a risk of sudden death

Autor: Danielle Majoor-Krakauer, François Pernot, Jean Boutarin, Florence Fellmann, Michaël Stumpf, Gilles Millat, Carolien H Teirlinck, Xavier André-Fouët, Rajae El Malti, Patrice Bouvagnet, Faïza Senni

Publikováno v: BMC Medical Genetics
BMC Medical Genetics, vol. 13, no. 105, pp. 1-9
BMC Medical Genetics, Vol 13, Iss 1, p 105 (2012)
BMC Medical Genetics, 13. BioMed Central Ltd.

Background Hypertrophic Cardiomyopathy (HCM) is a genetically heterogeneous disease. One specific mutation in the MYBPC3 gene is highly prevalent in center east of France giving an opportunity to define the clinical profile of this specific mutation.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63a73d91bce55f9210e9f6e7115c21ce
https://doi.org/10.1186/1471-2350-13-105

Coronary-to-bronchial artery anastomosis complicated with myocardial infarction

Autor: Michel Gallet, Aupetit Jf, Jean Boutarin

Publikováno v: International journal of cardiology. 18(1)

A patient with bronchiectasis had an inferolateral myocardial infarction. Coronary arteriography revealed a large anastomosis from the left circumflex artery to the left lower lobe bronchial arteries. The relationship between the patient's myocardial

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d04c62b2a04f7f736dc8928e682e23a
https://pubmed.ncbi.nlm.nih.gov/3343067