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1 in and I(f) in the sinus node and blunts the sinus bradycardia.
2 3-day postnatal Postn-Cre H2CKO pups exhibit sinus bradycardia.
3 n part may account for autoimmune-associated sinus bradycardia.
4 ), and not S1P(1), is directly implicated in sinus bradycardia.
5 ost common TRAEs were visual effects (56%), (sinus) bradycardia (44%), fatigue (26%), and nausea (15%
6 ith a higher risk of potentially symptomatic sinus bradycardia ( 50 bpm) than lumefantrine (risk diff
8 1D Ca channel in mice results in significant sinus bradycardia and atrioventricular block, a phenotyp
9 pproximately 50% of TG(N488I) mice displayed sinus bradycardia and features suggestive of pre-excitat
10 reover, Slc26a6(-/)(-) mice show evidence of sinus bradycardia and fragmented QRS complex, supporting
12 monstrated that Possum mice exhibited marked sinus bradycardia and R-R variability upon scruffing, ab
13 ation, general supraventricular tachycardia, sinus bradycardia and sinus rhythm including sinus irreg
14 or Calm2(N98S/+) (Calm2(S/+)) mice exhibited sinus bradycardia and were more susceptible to arrhythmi
15 Later changes, such as intra-atrial block, sinus bradycardia, and atrial flutter, may be attributed
18 atrial rhythm, A-V rhythm, A-V dissociation, sinus bradycardia, atrial flutter, escape-capture bigemi
19 able, progressive conduction-system disease (sinus bradycardia, atrioventricular conduction block, or
21 we investigated the functional basis of this sinus bradycardia by characterizing the effects of antib
22 and/or 2 degrees atrioventricular block, but sinus bradycardia, defined as fetal heart rate<3% for ge
25 k of CHB is complete atrioventricular block, sinus bradycardia has been reported recently in animal m
29 literature describe patients presenting with sinus bradycardia in association with left ventricular n
34 rtant clinical significance and suggest that sinus bradycardia may be a potential marker in the detec
35 Before ablation, Cav3.1(-/-) mice showed sinus bradycardia (mean+/-SEM; RR intervals, 148+/-3 ver
36 fetus with persistent bradycardia, including sinus bradycardia or functional 2:1 atrioventricular blo
40 s could provide, in part, the ionic basis of sinus bradycardia reported in animal models of CHB and c
42 e characterized by sinus dysrhythmia, severe sinus bradycardia, sinus pauses and chronotropic incompe
43 ion induces electrical changes, resulting in sinus bradycardia, sinus pauses, and a susceptibility to
46 use model of heart failure in which there is sinus bradycardia, there is upregulation of a microRNA (
49 ng sofosbuvir and daclatasvir for 3 days and sinus bradycardia was recorded each day, 2 hrs after int
50 common in the family with D1595H, but rather sinus bradycardia was the predominant clinical finding.
51 mily and a cohort of unrelated probands with sinus bradycardia were examined by electrocardiography,
54 g, kcnma1b, in zebrafish embryos resulted in sinus bradycardia with dilatation and reduced contractio