A solution of EDA in DCM (5 ml) and a solution of CHDA in DCM (5 ml) were added (amounts listed in Supplementary Table S1).
Conclusions: In DCM, papillary muscle native T1 time is significantly elevated and related to mitral regurgitant fraction.
We sought to evaluate the potential relationship between papillary muscle T1 time and mitral regurgitation in DCM patients.
Dilute-solution characterization was also made by light scattering and viscometry in DCM at 20 °C.
The complexes bearing tetra acetoxyethylthio) substituents represents aggregation tendency in DCM solution.
A more pronounced response of immobilized Tc is observed in DCM for films polymerized in AN.
Accurate myocardial tissue characterisation is pivotal in DCM patients.
Open image in new window Fig. 10 Key waveforms in DCM Open image in new window Fig. 11 Operating modes in DCM.
More than 100 transcripts were consistently differentially expressed in DCM >1.5-fold (versus pooled nonfailing heart, P < 0.05).
FDG-PET served for longitudinal monitoring of effects of EPO treatment in DCM mice.
The stability analysis of DC/DC converter in DCM is presented in [31, 32].
