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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
17 n additional reoperation: 4 received CABG, 2 MVR, and 2 MV repair.
18              There were 33 AVR (5.4%) and 38 MVR (7.9%) hospital deaths.
19 alve replacement) (35, 0.9%), AVR (231, 6%), MVR (41, 1.06%), CABG + others (95, 2.46%), and others (
20 re were 46 patients identified (37 MVP and 9 MVR).
21 y in 370 patients undergoing VR (249 AVR, 93 MVR, 28 DVR).
22 19 patients with an EF < or = 30% received a MVR using an undersized nonflexible complete ring.
23 l valve deterioration of bioprosthesis after MVR is higher than after AVR; after AVR, homografts and
24 th chronic MR before and 10 to 14 days after MVR.
25                      The decline in EF after MVR for chronic MR is traditionally thought to be a cons
26 r AVR, and postoperative renal failure after MVR.
27     Significant limitation of function after MVR is uncommon.
28                        Early mortality after MVR can be predicted on the basis of diagnosis and the s
29 survival was 95 +/- 1%; when mortality after MVR is included, 7-year survival was 83 +/- 6%.
30 thesis (66% vs. 79%, p = 0.02) but not after MVR.
31  after repair was better than survival after MVR for both PL-MVP (at 15 years, 41+/-5% versus 31+/-6%
32                                          All MVR and control patients underwent ablation under therap
33                                P = .022) and MVR/SVP (66.2 +/- 12.4%, P = .017) groups than the MVR/N
34 was lower in the repair (1.8%, P = .046) and MVR/SVP (1.5%.
35 ion was BMVP in 64 patients, SMVP in 33, and MVR in 11.
36                      Mortality after AVR and MVR is high at 10 to 15 years because of the associated
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
41                                           As MVR increases the likelihood of postsynaptic receptor sa
42           Operative mortality rates for AVR, MVR, combined CABG/AVR and combined CABG/ MVR were 4.00%
43  a mechanism by which a combination of basal MVR and low receptor saturation allow the presynaptic ac
44    These data can assist in choosing between MVR and alternative palliative strategies.
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.
47 ad CABG/mitral repair versus 56 who had CABG/MVR with preservation of the subvalvular apparatus.
48 ter CABG with mitral valve replacement (CABG/MVR).
49 t no valve replacement (n = 6), conventional MVR with chordal excision (n = 7), or chordal-sparing MV
50                           After conventional MVR, baseline theta max fell by 66% to 81% in the antero
51 ular-ventricular integrity with conventional MVR reduced regional LV systolic torsion in the anterior
52  within an active zone is coordinated during MVR.
53 arious methods of chorda preservation during MVR to assess their impact on left ventricular systolic
54                                  We examined MVR at a ribbon synapse in a retinal slice preparation u
55  patients having smaller prostheses at first MVR (18.7+/-0.8 mm versus 22.4+/-3.6 mm, P=0.017).
56 (age <2 years and prosthesis <20 mm at first MVR) had an OR=46.3 compared with low-risk patients (age
57 or=2 years and prosthesis >or=20 mm at first MVR) over similar follow-up intervals.
58 sthesis survival was predicted only by first MVR age: odds ratio (OR) 7.7 (95% confidence interval [C
59 sis survival can be predicted based on first MVR age and prosthesis size.
60 had second MVR, prosthesis sizes were: first MVR 19+/-2 mm and second MVR 22+/-3 mm, and their body w
61 he 73 who did not have a second MVR on first-MVR demographic and perioperative variables.
62                                  Using first-MVR weight-matched controls, body weight increased simil
63 l LV torsional deformation acutely following MVR with and without chordal preservation.
64                   Predictors of TE following MVR/DVR were raised mean platelet volume (4.0), raised f
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
67 rial survival rates, 84% for AVR and 80% for MVR at 5 years, were not affected by VAI.
68 patients > or =60 to 65 years of age and for MVR in patients > or =65 to 70 years of age; in younger
69           Unadjusted operative mortality for MVR only was 5.60% for blacks versus 6.18% for whites (O
70 nd June 2001, 1,195 consecutive patients had MVR with ring annuloplasty.
71                                     However, MVR should be considered for high-risk patients and thos
72                                      Initial MVR and younger age were associated with worse survival.
73                  Complications after initial MVR included heart block requiring pacemaker (16%), endo
74 , which included 102 survivors after initial MVR, was analyzed.
75 ority of deaths occurred early after initial MVR, with little late attrition despite repeat MVR and c
76 an interval of 4.8+/-3.8 years after initial MVR.
77                               Age at initial MVR was 1.9+/-1.4 years.
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
80 l dual-blade device; (2) microvitreoretinal (MVR) blade; and (3) Trabectome.
81 icant morphological predictors necessitating MVR were found.
82 y (a) morphological predictors necessitating MVR, and (b) predictors of future reoperation within the
83                  At last follow-up, 82.7% of MVR patients had their arrhythmia controlled (69.1% not
84 over an extended period, but the dynamics of MVR at ribbon synapses is unknown.
85 n the synaptic cleft, a result indicative of MVR, and suggests that MVR can be modified by long-term
86 h current solutions and clinical outcomes of MVR with mitral valve allograft.
87                 We find that the presence of MVR and receptor saturation at this synapse alters the c
88 These findings indicate that late results of MVR after minimally invasive surgery and after anterior
89 xible" patients required a repeat operation, MVR (1), and 2 patients required a transplant.
90 dels were developed: one for isolated AVR or MVR and one for CABG plus AVR or CABG plus MVR.
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
93 atients undergoing CABG combined with AVR or MVR.
94 ep sternal wound infection for either AVR or MVR.
95 en race and operative mortality after AVR or MVR.
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
101 scularization alone, mitral valve repair, or MVR.
102 minisatellite variant repeat mapping by PCR (MVR-PCR), which determines the distribution of variant r
103          A minisatellite variant repeat PCR (MVR-PCR) system gives Y-specific DNA codes, with a virtu
104 on >30% were randomized to receive CABG plus MVR (34 patients) or CABG only (39 patients).
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
108  stay duration were greater in the CABG plus MVR group.
109 r MVR and one for CABG plus AVR or CABG plus MVR.
110 t closure and recovery from anesthesia, post-MVR data were acquired.
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
113 eplacement without subvalvular preservation (MVR/NoSVP).
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
118           Pronounced multivesicular release (MVR) occurs at the ribbon synapses of sensory neurones t
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
122 ther it can increase multivesicular release (MVR).
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
125             The role of mitral valve repair (MVR) during coronary artery bypass grafting (CABG) in pa
126 R, with little late attrition despite repeat MVR and chronic anticoagulation.
127 nvestigated by Minisatellite Variant Repeat (MVR) analysis in a sample of >100 autochthonous individu
128 region using a minisatellite variant repeat (MVR)-PCR approach.
129         Using minisatellite variant repeat ("MVR") mapping, and compound haplotypes composed of the m
130 med in 46 patients (58%) and MV replacement (MVR) in 34.
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
133 atients undergoing mitral valve replacement (MVR) for chronic MR.
134                    Mitral valve replacement (MVR) has a high mortality and morbidity.
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
138 nd to discuss when mitral valve replacement (MVR) may be favored over mitral valve repair.
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
145 ts with mechanical mitral valve replacement (MVR).
146 red after elective mitral valve replacement (MVR).
147 placement (AVR) or mitral valve replacement (MVR).
148 terioration (SVD) (mitral valve replacement [MVR] > AVR) and, therefore, for replacement of the PHV.
149 ue to MVP (679 repairs and 238 replacements [MVRs]) was performed between 1980 and 1995.
150              Myocardial vascular resistance (MVR) increased with increasing triglyceride levels (r=0.
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
155 y for patients <2 years old who had a second MVR versus those who did not.
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+
158 is an increment in prosthesis size at second MVR, suggesting continued annular growth.
159                           Reasons for second MVR were prosthetic valve stenosis 24 (83%), thrombosis
160 comparable regardless of the need for second MVR.
161                     For those who had second MVR, prosthesis sizes were: first MVR 19+/-2 mm and seco
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.
164 ng with repeat 7, characteristic "signature" MVR patterns emerge for each common allele.
165  Sham operation and anterior chordal-sparing MVR did not affect regional LV torsion; however, loss of
166                    Posterior chordal-sparing MVR impaired torsion only after calcium administration.
167 , and the chordae tendineac, chordal-sparing MVR is popular.
168 ure or anterior or posterior chordal-sparing MVR procedure (P > or = .10).
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
174        Based on these data, it is clear that MVR mapping is a very useful tool for the analysis of zo
175                These findings establish that MVR and postsynaptic receptor saturation can influence t
176                    Furthermore, we show that MVR may occur under baseline physiological conditions, a
177                              We suggest that MVR occurs at SC-CA1 synapses when Pr is elevated by fac
178  result indicative of MVR, and suggests that MVR can be modified by long-term plasticity.
179                                          The MVR blade exhibited minimal removal of TM and obvious in
180                      P = NS) groups than the MVR/NoSVP group (5.0%).
181 P (66.2 +/- 12.4%, P = .017) groups than the MVR/NoSVP group (63.5 +/- 3.4%).
182 of complete heart block was noted within the MVR group (37.5%).
183 d complete mitral annuloplasty ring as their MVR procedure.
184              Of patients who did not undergo MVR or repeat CBC, 8% were in New York Heart Association
185               In elderly patients undergoing MVR, actuarial analysis overestimates the 10-year risk o
186  outcomes in infants and patients undergoing MVR, but has improved in our more recent experience.
187 eedom from VD in elderly patients undergoing MVR.
188 nts were subclassified into those undergoing MVR with chordal preservation (group Ia) and those under
189 preservation (group Ia) and those undergoing MVR with chordal transection (group Ib).
190 04 patients > or = 70 years of age underwent MVR at our institution.
191 lack and 46,249 white patients who underwent MVR alone or AVR alone from 1999 through 2002.
192 nsory synapses overcome this problem and use MVR to encode signals of widely varying intensities.
193                                        Using MVR-PCR, 20 to 25 repeats at the 5' end of the VNTR can
194  three different retinal synapses to utilize MVR.
195 eservation of the subvalvular apparatus with MVR has a theoretical advantage in terms of ventricular
196 tion techniques are used in combination with MVR.
197 ue to MVP, mitral valve repair compared with MVR provides improved very long-term survival after surg
198 oved left ventricular function compared with MVR.
199                                Patients with MVR had larger atria (p < 0.0001), lower left ventricula
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
202 ation is feasible and safe for patients with MVR.
203 7-year event-free survival (survival without MVR or repeat CBC) was 80 +/- 4%, 77 +/- 4%, 65 +/- 6%,

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