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Heart (British Cardiac Society), 2014-05, Vol.100 (10), p.806-813
2014

Details

Autor(en) / Beteiligte
Titel
Coronary microvascular dysfunction in primary cardiomyopathies
Ist Teil von
  • Heart (British Cardiac Society), 2014-05, Vol.100 (10), p.806-813
Ort / Verlag
England: BMJ Publishing Group LTD
Erscheinungsjahr
2014
Link zum Volltext
Quelle
BMJ Journals Archiv - DFG Nationallizenzen
Beschreibungen/Notizen
  • [...]a low CFR does not necessarily reflect a reduction of maximum flow, but it can be caused by an abnormally elevated resting flow in the face of a normal hyperaemic flow.w3 CMD is found both in primary and secondary cardiomyopathies with very important prognostic implications. Cardiomyopathies are grouped into specific morphological and functional phenotypes; each phenotype is then sub-classified into familial and non-familial forms. 3 Prompted by recent work by Camici et al on CMD in left ventricular (LV) hypertrophy, both of primary and secondary aetiology, we decided to perform a more focused review on myocardial ischaemia in primary cardiomyopathies.w4 Hypertrophic cardiomyopathy HCM is the most common genetic heart disease, with prevalence in the general population of 1:500, and characterised by extreme heterogeneity with regard to phenotypic expression, pathophysiology, and clinical course. 4 w5-w8 HCM is the most common cause of sudden cardiac death in the young, but also a major cause of heart failure and disability at any age.w9-w12 Myocardial ischaemia due to severe CMD is an established pathophysiologic feature in HCM ( table 1 ) and may be associated with important disease related complications that have an impact on the clinical outcome, including adverse LV remodelling and systolic dysfunction ( figure 1 ).
Sprache
Englisch
Identifikatoren
ISSN: 1355-6037
eISSN: 1468-201X
DOI: 10.1136/heartjnl-2013-304291
Titel-ID: cdi_proquest_miscellaneous_1517881045

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