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1 e, proven with positive bone scintigraphy or endomyocardial biopsy).
2 oronary computed tomography angiography, and endomyocardial biopsies).
3 cally, the diagnosis of myocarditis required endomyocardial biopsy.
4 en shown to correlate with the results of an endomyocardial biopsy.
5 the standard method of tissue histology from endomyocardial biopsy.
6 Nine patients underwent endomyocardial biopsy.
7 and serial echocardiography; five underwent endomyocardial biopsy.
8 gs in the diagnosis of amyloidosis proven by endomyocardial biopsy.
9 assessed by the rejection grade on the first endomyocardial biopsy.
10 osis on the basis of clinical evaluation and endomyocardial biopsy.
11 of MMF trough level at the time of scheduled endomyocardial biopsy.
12 c transplants revolves around the use of the endomyocardial biopsy.
13 DSE at the time of their regularly scheduled endomyocardial biopsy.
14 lantation at the time of serial surveillance endomyocardial biopsy.
15 uded, of whom 142 underwent TTE before first endomyocardial biopsy.
16 asive coronary angiography, cardiac MRI, and endomyocardial biopsy.
17 nical signs and symptoms and low accuracy of endomyocardial biopsy.
18 highly selected cases undergoing autopsy or endomyocardial biopsy.
19 owed positive dd-cfDNA results with negative endomyocardial biopsy.
20 ts without evidence of rejection observed on endomyocardial biopsy.
21 ntify clinically relevant non-HLA from donor endomyocardial biopsy.
22 ransplantation (ISHLT) grade 2R or higher at endomyocardial biopsy.
23 ic work-up, including genetic evaluation and endomyocardial biopsy.
24 ditis was defined by ongoing inflammation on endomyocardial biopsy.
25 Twenty-eight (88%) patients underwent endomyocardial biopsy.
26 ars) had undergone diagnostic cardiac MR and endomyocardial biopsy.
27 mic myocardial (18)F-NOS PET/CT, followed by endomyocardial biopsy.
28 nd immunoglobulins) and microvasculopathy in endomyocardial biopsy.
29 onresponse to CRT in patients with DCM using endomyocardial biopsies.
30 in human atrial tissue and right ventricular endomyocardial biopsies.
31 Egr-1 mRNA expression and rejection grade in endomyocardial biopsies.
32 men was used, and rejection was monitored by endomyocardial biopsies.
33 nd arteriolar endothelial ICAM-1 in matching endomyocardial biopsies.
34 were measured in 186 patients undergoing 365 endomyocardial biopsies.
35 187 adult HTx patients with contemporaneous endomyocardial biopsies.
36 not predominantly lymphocytic myocarditis in endomyocardial biopsies.
37 expression by sequencing RNA extracted from endomyocardial biopsies.
38 ilure and rejection and may undergo repeated endomyocardial biopsies.
39 ents could obviate the need for surveillance endomyocardial biopsies.
42 9%) had history of myocarditis diagnosed by endomyocardial biopsy (59%) and/or cardiac magnetic reso
43 hs, 64% occurred within 3 months of the last endomyocardial biopsy, 96% had normal biopsies, and the
44 ation relies on histopathological grading of endomyocardial biopsies according to International Socie
45 ter nucleic acids had been extracted from an endomyocardial biopsy, an explant, or autopsy samples, P
49 We evaluated PIMI in the first four weekly endomyocardial biopsies and/or autopsy myocardium from 1
51 retrospectively identified who had undergone endomyocardial biopsy and cardiac MR at one institution
53 Acute allograft rejection was diagnosed by endomyocardial biopsy and graded according to the Intern
55 transplant recipients underwent simultaneous endomyocardial biopsy and intravascular ultrasound (IVUS
56 nts require more invasive procedures such as endomyocardial biopsy and may aid in reducing the number
57 ave myocarditis according to the findings on endomyocardial biopsy and the Dallas histopathological c
59 ant recipients who were referred for routine endomyocardial biopsy and/or surveillance coronary angio
60 with histologically proven amyloid (374 with endomyocardial biopsies) and 360 patients subsequently c
61 ranscriptional profiling was performed on 26 endomyocardial biopsies, and expression patterns were co
66 the major limitations, and currently, serial endomyocardial biopsies are required to diagnose rejecti
69 jection in humans might obviate the need for endomyocardial biopsy as well as improve the accuracy of
71 including TD imaging, along with transmural endomyocardial biopsy at the time of coronary bypass sur
72 sis of 196 consecutive patients referred for endomyocardial biopsy because of clinical suspicion of c
73 of patients with DCM, 99 patients underwent endomyocardial biopsies before CRT implantation, with hi
78 that transcriptomic biomarkers from a single endomyocardial biopsy can improve the clinical detection
79 nological factors at the time of a low-grade endomyocardial biopsy can predict progression to high-gr
80 were also found to be clonally explanted in endomyocardial biopsies collected 17 and 21 mo earlier f
81 cular atheroma excised at endarterectomy and endomyocardial biopsies contained purely variant fibrino
82 schemic changes in early posttransplantation endomyocardial biopsies correlate with the later develop
83 criptomic signature, generated from a single endomyocardial biopsy, could serve as a novel prognostic
85 transplant recipients following inadvertent endomyocardial biopsy disruption of the tricuspid appara
86 GF) mRNA expression was determined in serial endomyocardial biopsies during the first year after tran
90 pathology were addressed: (a) Improvement of endomyocardial biopsy (EMB) accuracy for the diagnosis o
93 diac magnetic resonance (CMR) mapping versus endomyocardial biopsy (EMB) has not been determined.
94 ration and frequency of routine surveillance endomyocardial biopsy (EMB) have been questioned in the
95 d many to question the yield of surveillance endomyocardial biopsy (EMB) in heart transplantation (HT
102 tic resonance (CMR), cardiac biomarkers, and endomyocardial biopsy (EMB) results to predict left vent
108 ons between genome-wide molecular changes in endomyocardial biopsies (EMBs) and plasma dd-cfDNA.
109 on after heart transplant (HT), surveillance endomyocardial biopsies (EMBs) are often continued for y
110 To determine the utility of surveillance endomyocardial biopsies (EMBs) during a 14-day OKT3 indu
111 e total Treg population, we examined Treg in endomyocardial biopsies (EMBs) of both patients who deve
112 lyzing digital pathology images from routine endomyocardial biopsies (EMBs) to develop a precision me
113 d for the presence of viral genome in serial endomyocardial biopsies (EMBs) using polymerase chain re
118 nological factors at the time of a low-grade endomyocardial biopsy enables prospective stratification
119 ited utilization and the poor sensitivity of endomyocardial biopsies (especially for patchy diseases
124 ional research that influence the utility of endomyocardial biopsy for the management of inflammatory
126 ir receptors CXCR3 and CCR5 was tested in 60 endomyocardial biopsies from 24 patients using quantitat
128 ern of vascular cardiac allograft rejection, endomyocardial biopsies from 344 heart transplant recipi
129 D We analyzed pretreatment and posttreatment endomyocardial biopsies from 58 Fabry patients enrolled
133 the presence of acute cellular rejection in endomyocardial biopsies from cardiac transplant recipien
134 ve RT-PCR in RNA from right ventricular (RV) endomyocardial biopsies from intact nonfailing hearts, a
135 properties of mCSCs and vCSCs isolated from endomyocardial biopsies from patients with advanced hear
136 d (P=0.012) and 5.1-fold (P=0.038) higher in endomyocardial biopsies from patients with CVB3-positive
137 ntiated adult heart muscle cells, studies in endomyocardial biopsies from patients with dilated and i
138 luorescence, and immunoperoxidase studies of endomyocardial biopsies from such patients often reveal
139 echocardiograms, hemodynamic parameters, and endomyocardial biopsys from 137 patients with heart tran
145 res surrogate cardiac imaging biomarkers, as endomyocardial biopsy has relatively low yield, even wit
149 erum samples were retrospectively matched to endomyocardial biopsies in 98 cardiac transplant recipie
155 nvasive test holds promise for replacing the endomyocardial biopsy in heart transplant recipients and
156 9 (terminal pathway), at the time of routine endomyocardial biopsy in heart transplant recipients.
157 uptake on bone scintigraphy and/or positive endomyocardial biopsy in the absence of monoclonal prote
158 This article reviews the current role of the endomyocardial biopsy in the management of patients foll
159 ression profiling or with the use of routine endomyocardial biopsies, in addition to clinical and ech
160 ve addressed important issues concerning the endomyocardial biopsy, including the reliability of the
162 istic regression, odds of identifying ACR on endomyocardial biopsy increased with doubling of CXCL10
163 e DNA from the donor genome at times when an endomyocardial biopsy independently established the pres
164 n-fixed, paraffin-embedded right ventricular endomyocardial biopsies is diagnostic of immunopathologi
165 +) T cells and the CXCR3 ligand IP-10 within endomyocardial biopsies is strongly associated with acut
172 are often used as initial diagnostic tests, endomyocardial biopsy is required for definitive diagnos
177 n the invasive and low-sensitivity nature of endomyocardial biopsy, its diagnostic focus shifted to a
181 in pathologic processes, Egr-1 expression in endomyocardial biopsies may act as a surrogate marker of
184 ntation has traditionally relied on numerous endomyocardial biopsies, most of which occur during the
185 ig), and their receptor CXCR3 in consecutive endomyocardial biopsies (n = 133) from human cardiac all
187 ion of VEGF by immunohistochemistry in human endomyocardial biopsies (n=101) from 10 cardiac transpla
189 ood mononuclear cells (n=24), plasma (n=27), endomyocardial biopsies (n=2), and cardiac tissue sample
192 rdiac tissues obtained from autopsies (n=3), endomyocardial biopsy (n=1), or cardiac transplants (n=2
194 of ATTR-CM without the need for confirmatory endomyocardial biopsies; observational studies indicate
196 observed an increase in MYOCD levels in the endomyocardial biopsies of DCM patients associated with
197 Egr-1 protein expression was analyzed in endomyocardial biopsies of different rejection grades by
200 ling of protein-coding genes and 754 miRs in endomyocardial biopsies of test cohorts was performed at
202 ology and sarcomere alterations described in endomyocardial biopsies of transplant patients with reje
207 d RNA sequencing on right ventricular septal endomyocardial biopsies prospectively obtained from pati
208 ionship between MDR1/ABCB1 polymorphisms and endomyocardial biopsy-proven rejection (EBPR) determined
210 ere-derived cells (CDCs) isolated from human endomyocardial biopsies reduce infarct size and improve
215 ith cardiac biomarkers, cardiac imaging, and endomyocardial biopsy represent a pragmatic diagnostic a
216 etection of transplant rejection by repeated endomyocardial biopsy requires catheterization and entai
218 The therapeutic and prognostic benefits of endomyocardial biopsy results have recently been demonst
224 mmunological and histological analyses of an endomyocardial biopsy sample are indicated when inflamma
226 munohistochemical analysis of a conventional endomyocardial-biopsy sample appears to be a highly sens
227 , 101b, 21a) were compared with time-matched endomyocardial biopsy samples (n = 70) in 12 patients to
232 entification of infiltration and fibrosis in endomyocardial biopsy samples to assess transplant rejec
238 tologic and immunofluorescence evaluation of endomyocardial biopsy samples, despite invasiveness and
245 and electroanatomical voltage mapping-guided endomyocardial biopsy showed low endocardial voltages an
247 c right ventricular cardiomyopathy and of an endomyocardial biopsy showing fibro-fatty replacement co
255 as is expressed on myocytes, we investigated endomyocardial biopsy specimens from cardiac transplant
256 okine and receptor gene expression in serial endomyocardial biopsy specimens from heart transplant pa
257 e-transcriptase polymerase chain reaction in endomyocardial biopsy specimens from human heart transpl
261 d percent fibrosis were determined in serial endomyocardial biopsy specimens obtained from 1 month up
262 Immunocytochemistry was performed on serial endomyocardial biopsy specimens to evaluate endothelial
264 to receive CDCs, autologous cells grown from endomyocardial biopsy specimens were infused into the in
265 ologous CDCs (12.5 to 25 x 10(6)) grown from endomyocardial biopsy specimens were infused via the int
271 +/- standard deviation) consecutive routine endomyocardial biopsy surveillance visits during the fir
272 ere positive, concomitantly with a low-grade endomyocardial biopsy, the positive predictive value for
273 ications, the authors do not advocate use of endomyocardial biopsy to diagnose myocarditis in the set
274 icroscope (MMDx) system for heart transplant endomyocardial biopsies used expression of rejection-ass
277 Gal-3 levels and inflammatory cell count on endomyocardial biopsy was observed in patients with iCMP
278 m each patient were examined for AECA and an endomyocardial biopsy was performed at regular intervals
283 To determine whether ischemic changes in endomyocardial biopsies were associated with complement
289 rom transplant recipients undergoing routine endomyocardial biopsies were included in an RNA sequenci
290 Autologous cardiospheres or CDCs grown from endomyocardial biopsies were injected through thoracotom
292 gery (mean follow-up 8.3 months) when repeat endomyocardial biopsies were obtained to correlate trans
293 Serial radionuclide ventriculography and endomyocardial biopsies were performed at baseline, 3, a
294 acute myocarditis typically requires either endomyocardial biopsy (which is invasive) or cardiovascu
295 ognized at autopsy before the application of endomyocardial biopsy, which led to a histopathology-bas
296 methods for the detection of rejection, the endomyocardial biopsy will remain important in the manag
297 inical safety of any such approach, invasive endomyocardial biopsy will remain the gold standard.
298 tegory (1R) appears to have brought together endomyocardial biopsies with different underlying proces
300 ized that the transcriptome obtained from an endomyocardial biopsy would yield clinically relevant an