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1 ardia and atrioventricular (AV) dysfunction (heart block).
2 s; and 6) the introduction of the concept of heart block.
3 chronically instrumented dogs with complete heart block.
4 from inherited cardiac arrhythmias, notably heart block.
5 insight into the pathogenesis of congenital heart block.
6 rial fibrillation without producing complete heart block.
7 led him to discover the mechanism of partial heart block.
8 mportant risk factor for having a child with heart block.
9 RS complex, 4 resulted in transient complete heart block.
10 ite their strong association with congenital heart block.
11 larly 52Ro, in the development of congenital heart block.
12 rothers of another family had arrhythmia and heart block.
13 intractable ventricular arrhythmias, and/or heart block.
14 s 69%; P=0.034), but with a 23% incidence of heart block.
15 diogenic shock, cardiac arrest, and complete heart block.
16 4 years) received a PPM due to postoperative heart block.
17 reat profound bradycardia caused by complete heart block.
18 support in both rats and pigs with complete heart block.
19 prior asystole from sinus arrest or complete heart block.
20 a bilateral ocular involvement and complete heart block.
21 a bilateral ocular involvement and complete heart block.
22 similar time course to that of postsurgical heart block.
23 adverse events on all cases was queried for heart block.
24 icular conduction in a rat model of complete heart block.
25 PM4 have been linked to progressive familial heart block.
26 lar nodal cells, accounting for the observed heart block.
27 r contractions, tachycardia, and high-degree heart block.
28 sistent with bradyarrhythmia and progressive heart block.
29 lower success rate and a higher incidence of heart block.
30 a may be characteristic of an acute stage of heart block.
31 ns to ventricular arrhythmias and congenital heart block.
32 5%) who required permanent pacing because of heart block.
33 was frequently followed by atrioventricular heart block.
34 ne of the most common pathologies underlying heart blocks.
35 int occurred in 14.3% consisting of 1 (2.9%) heart block, 1 (2.9%) femoral artery dissection, and 3 (
36 n fraction <60% (1.72; 1.22-2.40; P = .002), heart block (2.22; 1.41-3.47; P = .001), tachyarrhythmia
37 r arrhythmia (9 patients, or 14 percent), or heart block (3 patients, or 5 percent), although in some
38 s 13.1%; P<0.001), as were rates of complete heart block (3.5% versus 11.2%; P<0.001) and new-onset l
39 z type II atrioventricular block or complete heart block; (3) ventricular fibrillation; (4) ventricul
40 mortality; reduced first- and second-degree heart block 4.6- and 4-fold, respectively; and prevented
43 portantly, DMPK+/- mice develop first-degree heart block, a conduction defect strikingly similar to t
45 One procedure was complicated by complete heart block after ablation of a high-risk midseptal AP.
46 used to identify patients with postoperative heart block after CHS between January 1, 1960, and Decem
48 help identify patients at risk for complete heart block after septal reduction procedures for HCM.
50 bradyarrhythmia characterized by progressive heart block and impaired ventricular depolarization.
51 others with a previous child with congenital heart block and in 3 of 74 pregnancies (4%) in mothers w
52 the near universal association of congenital heart block and maternal Abs to SSA/Ro and SSB/La, the i
55 egment depression, complete atrioventricular heart block and right precordial ST segment elevation.
56 nt mice develop progressive atrioventricular heart block and significant ultrastructural changes in b
57 nother patient with syncope had intermittent heart block and survived as the result of pacing feature
58 s anticipated, 3 patients developed complete heart block and underwent pacemaker implantation, wherea
59 cts with progressive development of complete heart block and various arrhythmias, all of whom died su
62 e >=3 s, anytime sinus pause >=6 s, complete heart block, and a composite end point demonstrated an a
66 irth, developed significant bradycardia with heart block, and died within the first weeks after birth
67 ctural defects but have progressive complete heart block, and massive trabecular muscle overgrowth fo
72 diomyopathy are at risk for acute high-grade heart block, and, in this cohort, bradycardic events rep
73 ailure, cardiac arrest, arrhythmia, complete heart block, and/or stroke requiring hospitalization <1
74 o deaths were caused by development of acute heart block; another patient with syncope had intermitte
76 sociated cardiac defects, operative history, heart block, arrhythmias and tricuspid (i.e., systemic a
77 s conduction system abnormalities that cause heart block, arrhythmias, and sudden death are more comm
80 with neonatal lupus erythematosus (NLE) and heart block, as well as patients with Sjogren's syndrome
81 aily to prevent the recurrence of congenital heart block associated with anti-SSA/Ro (anti-Sjogren's
82 t groups more likely to develop third-degree heart block associated with Lyme carditis is essential t
83 risk for atrial and ventricular arrhythmias, heart block, asystole, development of pulmonary congesti
84 ing the DN allele displayed slow conduction, heart block, atrial fibrillation, ventricular tachycardi
85 ate cardiac erosions, thrombus formation and heart block; (b) the transcatheter closure of muscular v
86 evelop ventricular arrhythmias or high-grade heart block because the treatment is different and drama
87 e elinogrel arms, but there were no cases of heart block, bradycardia, hypotension, or liver failure.
88 or until a significant arrhythmia (asystole, heart block, bradycardia, supraventricular or ventricula
89 e molecular basis of atrial fibrillation and heart block but also may suggest targets for the develop
90 eading to sudden cardiac death from complete heart block, but no longer developed DCM or the other ph
91 a significantly higher incidence of complete heart block, but the risk was reduced with contrast echo
93 dence and determinants of permanent complete heart block (CHB) after nonsurgical septal reduction the
95 etermine the temporal occurrence of complete heart block (CHB) and ventricular tachyarrhythmia (VT) a
96 description and understanding of congenital heart block (CHB) came in the 1970s with the observation
102 It is a widely held view that congenital heart block (CHB) is caused by the transplacental transf
103 lesion of autoantibody-associated congenital heart block (CHB) is fibrosis of the conducting tissue.
106 ewed all cases of second degree and complete heart block (CHB) on POD 0 from August 2009 through Dece
108 ce rates of autoimmune-associated congenital heart block (CHB) using information from the Research Re
109 relevant in autoimmune-associated congenital heart block (CHB) where the obligate factor is a materna
110 e report 16 infants with complete congenital heart block (CHB) who developed late-onset dilated cardi
113 necessary for the development of congenital heart block (CHB), the low frequency suggests that fetal
117 3 children (22 with rash, 35 with congenital heart block [CHB], 26 unaffected siblings) and 58 mother
119 imary cardiac arrest, and sustained complete heart block, classified by a reviewer blinded to preoper
121 is associated with cardioskeletal myopathy, heart block, delayed growth and early postnatal death.
124 Destructive counterparts include familial heart block ending in fatal arrhythmias, similar results
125 after in utero identification of congenital heart block, especially in fetuses with associated myoca
126 utoantibodies with the genesis of congenital heart block, female BALB/c mice were immunized with huma
128 plays progressive muscle wasting, cataracts, heart block, gonadal atrophy, insulin resistance and neu
129 ce developing cardiomyopathy associated with heart block, impaired repolarization, and ventricular ar
132 anisms resulting in immune-mediated complete heart block in a small subset of 'at-risk' fetuses is un
134 There was a trend toward more congenital heart block in fetuses of women with previously affected
138 at hydroxychloroquine may prevent congenital heart block in pregnancies exposed to SSA/Ro antibodies.
141 radually progressive development of complete heart block in young people often is associated with car
142 inically relevant porcine models of complete heart block, intramyocardially injected TBX18 mRNA provi
148 ti-SSA/Ro-associated third-degree congenital heart block is irreversible, prompting a search for earl
152 rse effects include infections, bradycardia, heart blocks, macular edema, infusion reactions, injecti
153 ta suggest that patients affected by SSS and heart block may benefit from IKACh suppression achieved
154 able analysis identified older age, complete heart block, MV repair without annuloplasty ring, and th
155 ded tamponade (n = 4), pericarditis (n = 3), heart block (n = 1, prior to radiofrequency application)
157 ses fulminant heart failure, arrhythmias, or heart block, necessitating aggressive immunosuppression,
158 or for the composite of in-hospital death or heart block (noninferiority, P<0.001; superiority, P=0.0
164 patients with pacing indications of complete heart block or atrioventricular nodal ablation (LP: 10.3
166 ailure predicted IGCM, and presentation with heart block or more than nine weeks of symptoms predicte
167 ailure predicted IGCM, and presentation with heart block or more than nine weeks of symptoms predicte
169 =3 s, anytime sinus pause of >=6 s, complete heart block, or a composite of these bradyarrhythmias fr
170 mber of deaths (4 versus 1), final degree of heart block, or requirement for a pacemaker (14 versus 1
171 omposite outcome of in-hospital mortality or heart block, outcomes were compared (sequential noninfer
172 s6795970 is associated with a higher risk of heart block (P < 0.05) and a lower risk of ventricular f
173 sence of arrhythmias (P > 0.2), first-degree heart block (P = 0.12), bundle-branch block (P > 0.2), a
174 8.6%) had serious adverse events of complete heart block, peri-hepatic bleeding, and rupture of tricu
179 Complications after initial MVR included heart block requiring pacemaker (16%), endocarditis (6%)
180 gnificantly increased the risk of a complete heart block requiring pacemaker implantation (8.1% versu
181 by a rise in the incidence of postoperative heart block requiring permanent pacemaker (PPM) implanta
186 -D reconstruction of SN network in clarified heart blocks revealed significant changes in the physiol
187 is of neonatal lupus syndrome and congenital heart block reveals important information about prospect
188 gene transfer of SEK-1(KR) to the adult rat heart blocks SAPK activation by pressure overload, demon
191 heral artery disease, second or third degree heart block, stroke (ischaemic, haemorrhagic, and unspec
192 hol ablation, but with a higher incidence of heart block than in cases where only surgery is performe
193 d arrhythmias, but their combination induced heart block that could be abrogated by nicotinic recepto
194 d by heart failure, ventricular arrhythmias, heart blocks, thromboembolic phenomena, and sudden death
195 nt patients who exhibit evidence of neonatal heart block, treatment with dexamethasone is preferred o
196 bundle-branch disorder progressive familial heart block type I (PFHBI) and isolated cardiac conducti
197 -in a large family with progressive familial heart block type I and showed that these mutations preve
198 mon adverse effects associated with TAVI are heart block, vascular complications, and renal failure.
202 dence of pacemaker implantation for complete heart block was higher (22% vs. 2% in surgery; p = 0.02)