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1 MVR and receptor saturation both occur at some high p sy
2 MVR blade treatment across 170.0 +/- 14.1 degrees of TM
3 MVR consequently represents a widespread mechanism that
4 MVR data suggest that mouse minisatellites mutate mainly
5 MVR determines the temporal and spatial dispersion of tr
6 MVR may be an appropriate strategy for children <5 years
7 MVR or MV repair after previous CABG is associated with
8 MVR permits small presynaptic voltage changes to elicit
9 MVR typing could, therefore, improve the ascertainment o
10 MVR typing of rare-length alleles indicates that they ar
11 MVR typing of the common alleles a1, a2, a3, and a4 show
12 MVR via conventional sternotomy has been an established
13 MVR was initially identified at specialized synapses but
14 MVR was performed 176 times on 139 patients.
15 MVR, however, is preferred for select patients.
16 MVR-calibrated measurements of allele length yield rare
19 alve replacement) (35, 0.9%), AVR (231, 6%), MVR (41, 1.06%), CABG + others (95, 2.46%), and others (
23 l valve deterioration of bioprosthesis after MVR is higher than after AVR; after AVR, homografts and
31 after repair was better than survival after MVR for both PL-MVP (at 15 years, 41+/-5% versus 31+/-6%
37 greater with bioprosthesis, both for AVR and MVR, and occurred at a much higher rate in those aged <6
38 pect to age (P = .002) and in the repair and MVR/SVP groups with respect to NYHA functional class and
39 odds ratio, 0.27, P < .05) and of repair and MVR/SVP on overall mortality (hazard ratios, 0.43, P < .
40 after either the sham procedure or anterior MVR; however, after posterior chordal-sparing MVR, theta
43 a mechanism by which a combination of basal MVR and low receptor saturation allow the presynaptic ac
45 ortic valve replacement) (228, 5.9%), CABG + MVR (mitral valve replacement) (35, 0.9%), AVR (231, 6%)
46 R, MVR, combined CABG/AVR and combined CABG/ MVR were 4.00%, 6.04%, 6.80% and 13.29%, respectively.
49 t no valve replacement (n = 6), conventional MVR with chordal excision (n = 7), or chordal-sparing MV
51 ular-ventricular integrity with conventional MVR reduced regional LV systolic torsion in the anterior
53 arious methods of chorda preservation during MVR to assess their impact on left ventricular systolic
56 (age <2 years and prosthesis <20 mm at first MVR) had an OR=46.3 compared with low-risk patients (age
58 sthesis survival was predicted only by first MVR age: odds ratio (OR) 7.7 (95% confidence interval [C
60 had second MVR, prosthesis sizes were: first MVR 19+/-2 mm and second MVR 22+/-3 mm, and their body w
65 0.001 for AVR and 44% vs. 4%, p = 0.0001 for MVR), and in patients > or =65 years after AVR, primary
66 years, 20+/-5% for repair versus 23+/-5% for MVR; P=0.4) or separately in PL-MVP (P=0.3) or AL-MVP (P
68 patients > or =60 to 65 years of age and for MVR in patients > or =65 to 70 years of age; in younger
75 ority of deaths occurred early after initial MVR, with little late attrition despite repeat MVR and c
78 ality was 4.7% overall and 1.4% for isolated MVR (1.1% for minimally invasive surgery vs. 1.6% for co
79 using minisatellite variant repeat mapping (MVR) by PCR to gain insight into allelic diversity and t
82 y (a) morphological predictors necessitating MVR, and (b) predictors of future reoperation within the
85 n the synaptic cleft, a result indicative of MVR, and suggests that MVR can be modified by long-term
88 These findings indicate that late results of MVR after minimally invasive surgery and after anterior
91 ications: prolonged ventilation after AVR or MVR, postoperative stay >14 days after AVR or MVR, reope
92 VR, postoperative stay >14 days after AVR or MVR, reoperation for bleeding after AVR, and postoperati
96 redictor of operative mortality after AVR or MVR; however, black race was associated with an increase
97 of operative mortality after isolated AVR or MVR; however, there is evidence of an association betwee
98 f those patients who underwent either MVP or MVR between January 1, 1988, and December 31, 1998, for
99 ation rate was not different after repair or MVR overall (at 19 years, 20+/-5% for repair versus 23+/
100 free from failure of biventricular repair or MVR was 79% at 1 month and 55% at 5 years, with worse ou
102 minisatellite variant repeat mapping by PCR (MVR-PCR), which determines the distribution of variant r
105 of peak oxygen consumption in the CABG plus MVR group compared with the CABG group (3.3 mL/kg/min ve
106 in the secondary end points in the CABG plus MVR group compared with the CABG group: left ventricular
107 ps: 3% and 9%, respectively in the CABG plus MVR group, versus 3% (P=1.00) and 5% (P=0.66), respectiv
111 eformation (theta max) did not fall from pre-MVR values in the baseline state after the sham procedur
112 fluoroscopic marker images were obtained pre-MVR in the baseline state and with inotropic stimulation
114 d replacement with subvalvular preservation (MVR/SVP), and 318 had replacement without subvalvular pr
115 ents undergoing mitral valve reconstruction (MVR) with either a flexible or nonflexible complete ring
116 ave a high degree of multivesicular release (MVR) in the absence of postsynaptic receptor saturation.
117 possibility is that multivesicular release (MVR) is determined by the instantaneous release probabil
119 from univesicular to multivesicular release (MVR) when two Ca channels/AZ open at potentials above th
120 equency stimulation, multivesicular release (MVR), or asynchronous release can each activate NMDARs.
121 several vesicles, or multivesicular release (MVR), represents a simple mechanism to overcome the intr
123 vidual release site [multivesicular release (MVR)] and whether fusion of a single vesicle leads to re
124 f multiple vesicles (multivesicular release; MVR) from single active zones occurs at some central syn
127 nvestigated by Minisatellite Variant Repeat (MVR) analysis in a sample of >100 autochthonous individu
131 placement (AVR) or mitral valve replacement (MVR) and from 43,463 patients undergoing CABG combined w
132 placement (AVR) or mitral valve replacement (MVR) at 13 VA medical centers were randomized to receive
135 al excision during mitral valve replacement (MVR) impairs left ventricular (LV) systolic function, bu
136 initial mechanical mitral valve replacement (MVR) in children <5 years of age are poorly defined.
137 s after prosthetic mitral valve replacement (MVR) in children aged <5 years are ill-defined and gener
139 ) and 482 isolated mitral valve replacement (MVR) operations with the St Jude Medical valve were stud
140 Early attempts at mitral valve replacement (MVR) with mitral valve allograft were unsuccessful mainl
141 ave suggested that mitral valve replacement (MVR) with sparing of the subvalvular apparatus had compa
142 plasty (SMVP), and mitral valve replacement (MVR), although the optimal therapeutic strategy is uncle
143 patients requiring mitral valve replacement (MVR), mechanical prostheses (MPs) have been reported to
144 ; the alternative, mitral valve replacement (MVR), necessitates commitment to future valve replacemen
148 terioration (SVD) (mitral valve replacement [MVR] > AVR) and, therefore, for replacement of the PHV.
151 F-MLI synapses but, while some showed robust MVR with increased release probability, most were limite
152 ctors for having a second MVR, the 29 second MVR survivors were compared with the 73 who did not have
153 Twenty-nine survivors had undergone a second MVR at an interval of 4.8+/-3.8 years after initial MVR.
154 mpared with the 73 who did not have a second MVR on first-MVR demographic and perioperative variables
156 To identify risk factors for having a second MVR, the 29 second MVR survivors were compared with the
157 s sizes were: first MVR 19+/-2 mm and second MVR 22+/-3 mm, and their body weight increased from 7.4+
162 dren <5 years old despite the risk of second MVR in the youngest patients in whom the smallest prosth
163 however, differed significantly, with second MVR patients having smaller prostheses at first MVR (18.
165 Sham operation and anterior chordal-sparing MVR did not affect regional LV torsion; however, loss of
169 chordal excision (n = 7), or chordal-sparing MVR with preservation of the posterior leaflet and reatt
170 VR; however, after posterior chordal-sparing MVR, theta max fell in the lateral, posterior, and poste
171 ctive zones occurs at some central synapses, MVR is not thought to require coordination among release
172 ese results suggest that at PF-MLI synapses, MVR occurs under control conditions and is increased whe
173 when Pr is elevated by facilitation and that MVR may be a phenomenon common to many synapses througho
186 outcomes in infants and patients undergoing MVR, but has improved in our more recent experience.
188 nts were subclassified into those undergoing MVR with chordal preservation (group Ia) and those under
192 nsory synapses overcome this problem and use MVR to encode signals of widely varying intensities.
195 eservation of the subvalvular apparatus with MVR has a theoretical advantage in terms of ventricular
197 ue to MVP, mitral valve repair compared with MVR provides improved very long-term survival after surg
200 he role of ablative therapy in patients with MVR is not yet established, with safety concerns and ver
201 cember 2008, we followed up 81 patients with MVR undergoing first-time AF ablation (compared with 162
203 7-year event-free survival (survival without MVR or repeat CBC) was 80 +/- 4%, 77 +/- 4%, 65 +/- 6%,
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