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Ehjcardiovascrec

When we divided our FRDA patients into two groups based on a cut-off value of 1.1 cm of PWd and/or IVSd thickness, we found no difference in cardiac PCr/ATP ratios between patients with wall ...

Cardiovascular Research, Lodi, R., Rajagopalan, B., Crilley, J.G., Cooper, J.Mark, Styles, P., Schapira, A.H.V.

Date : 01/06/2002 Item size : 118083 bytes
Ehjcardiovascrec

Introduction Familial hypertrophic cardiomyopathy (HCM) is a primary disorder of cardiac muscle, and is associated with thickened ventricular wall and ventricular septum, increased myocardial ...

Cardiovascular Research, Han, Lu, Li, Yang, Tchao, Jason, Kaplan, Aaron D., Lin, Bo, Li, You, Mich-Basso, Jocelyn, Lis, Agnieszka, Hassan, Narmeen, London, Barry, Bett, Glenna C.L., Tobita, Kimimasa, ...

Date : 01/11/2014 Item size : 371089 bytes
Ehjcardiovascrec

[...]we propose an alternative interpretation for the discrepancy between iPSC-derived cardiomyocytes and model simulations: the model is not an accurate representation of the cardiomyocytes under ...

Cardiovascular Research, Han, Lu, Li, Yang, Tchao, Jason, Kaplan, Aaron D., Lin, Bo, Li, You, Mich-Basso, Jocelyn, Lis, Agnieszka, Hassan, Narmeen, London, Barry, Bett, Glenna C.L., Tobita, Kimimasa, ...

Date : 01/04/2015 Item size : 136670 bytes
Ehjcardiovascrec

Hypertrophied cells, already manifesting marked potassium channel abnormalities, are highly sensitive to metabolic conditions such as hypokalemia, or QT prolonging drugs that further prolong ...

Cardiovascular Research, Kowey, Peter R., Yan, Gan-Xin, Xu, Xiaoping

Date : 01/08/2000 Item size : 148624 bytes
Ehjcardiovascrec

Abstract Aims Familial hypertrophic cardiomyopathy (HCM), frequently caused by sarcomeric gene mutations, is characterized by cellular dysfunction and asymmetric left-ventricular (LV) ...

Cardiovascular Research, Witjas-Paalberends, E. Rosalie, Piroddi, Nicoletta, Stam, Kelly, van Dijk, Sabine J., Oliviera, Vasco Sequeira, Ferrara, Claudia, Scellini, Beatrice, Hazebroek, Mark, ten ...

Date : 01/08/2013
Ehjcardiovascrec

In clinical terms, 25 years ago patients with unexplained left ventricular hypertrophy suffering from dyspnoea and potentially life-threatening arrhythmias were observed, since then underlying ...

Cardiovascular Research, Hasenfuss, Gerd

Date : 01/04/2015
Ehjcardiovascrec

Study familial hypertrophic cardiomyopathy using patient-specific induced pluripotent stem cells recently published in Cardiovascular Research1 Life-threatening ventricular arrhythmias in ...

Cardiovascular Research, Christ, Torsten, Koivumäki, Jussi T., Eschenhagen, Thomas

Date : 01/04/2015
Ehjcardiovascrec

Introduction Familial hypertrophic cardiomyopathy (FHC) is a relatively common autosomal dominant genetic disease characterized by ventricular hypertrophy, myofibrillar disarray, often clinically ...

Cardiovascular Research, Abraham, Theodore P., Jones, Michelle, Kazmierczak, Katarzyna, Liang, Hsin-Yueh, Pinheiro, Aurelio C., Wagg, Cory S., Lopaschuk, Gary D., Szczesna-Cordary, Danuta

Date : 01/04/2009
Ehjournal

Abstract Aims To study the diagnostic value of a new 2D left ventricle hypertrophy (2D LVH) score in families with hypertrophic cardiomyopathy (HCM) in comparison with the conventional maximal wall ...

European Heart Journal, Forissier, Jean F., Charron, Philippe, du Montcel, Sophie Tezenas, Hagège, Albert, Isnard, Richard, Carrier, Lucie, Richard, Pascale, Desnos, Michel, Bouhour, Jean B., ...

Date : 01/09/2005
Ehjournal

Introduction Hypertrophic cardiomyopathy is defined by the presence of increased ventricular wall thickness or mass in the absence of loading conditions (hypertension, valve disease) sufficient to ...

European Heart Journal, Friedrich, Felix W., Bausero, Pedro, Sun, Yuli, Treszl, Andras, Krämer, Elisabeth, Juhr, Denise, Richard, Pascale, Wegscheider, Karl, Schwartz, Ketty, Brito, Dulce, ...

Date : 01/07/2009