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1 using 50% of a remote control segment as the cutoff value.
2 o determine the myocardial enhancement ratio cutoff value.
3 ularly with respect to the aortic valve area cutoff value.
4 ant in 47% with the known FFR, using 0.80 as cutoff value.
5  only, without the requirement of a distance cutoff value.
6 y segments and the FFR value is close to the cutoff value.
7 ecificity of detection to vary with positive cutoff value.
8  are defined with an 83% nucleotide identity cutoff value.
9  are defined with an 84% nucleotide identity cutoff value.
10 e standard, sonographer blinding status, and cutoff value.
11 mV is more accurate than previously reported cutoff values.
12 erating characteristic analysis to calculate cutoff values.
13 erating characteristic analysis to calculate cutoff values.
14 lternative pairs of uniform and sex-specific cutoff values.
15 ty, which can be improved by using optimized cutoff values.
16 curve was used to calculate optimal referral cutoff values.
17 spectively, which is well below the clinical cutoff values.
18 s for each blood marker based on recommended cutoff values.
19 s curves were generated to determine optimal cutoff values.
20 nes of various material and molecular-weight cutoff values.
21  by Cohen's kappa coefficient with different cutoff values.
22                  With the use of the uniform cutoff value, 127 women (14.5%) and 345 men (18.6%) rece
23 value, 42.92 pg/mL), and cathelicidin LL-37 (cutoff value, 3221.01 pg/mL) is presented with a sensiti
24 sed on CSF concentrations of interleukin 13 (cutoff value, 37.26 pg/mL), vascular endothelial growth
25 bited 80.5% sensitivity for the same cohort (cutoff value, 40 mg of antigen-specific antibodies [mgA]
26  pg/mL), vascular endothelial growth factor (cutoff value, 42.92 pg/mL), and cathelicidin LL-37 (cuto
27                                      Numeric cutoff values (5 cm for diameters and 65 cm(3) for volum
28 n) had the best overall predictive accuracy (cutoff value, 50.37; 94.9% sensitivity, 91.7% specificit
29 se in the fraction of CD14(+)/CD16(-) cells (cutoff value, 94.0%).
30                                      Rounded cutoff values above the limit of detection may not have
31  AUROC (pAUROC) >= specificities 90 and 95%, cutoff values and sensitivities at specificities 90 and
32 vised classifier converged with previous PET cutoff values and the established CSF Abeta1-42 cutoff l
33      Tumors were classified using predefined cutoff values, and all were correctly identified in blin
34  for the detection of AVS selectivity at all cutoff values, and for all ratios, the cutoff value of a
35 that are sufficient to reach a predetermined cutoff value are considered invalid and discarded.
36                         Currently applied UV cutoff values are based on studies that lacked epicardia
37 c curve identified >15.5 mm as the best size cutoff value (area under the curve 0.747).
38 ntly higher specificity (P<.0001) than sIgE (cutoff value at 0.35 IU/mL) and the specificity was not
39               For asthma and hay fever, SPT (cutoff value at 3 mm) had a significantly higher specifi
40     Levels of inflammatory markers under the cutoff value between postoperative days 3 and 5 ensure s
41 ponemal signal strength ratio values above a cutoff value can be used in lieu of repeat treponemal te
42  Ideally, the accuracy of our target ROI and cutoff value could be further validated with PET-autopsy
43 LSI clinical breakpoints and epidemiological cutoff value criteria, as appropriate.
44 between CAR and prognosis, regardless of the cutoff value, cutoff value selection, treatment method,
45                                              Cutoff values define low- and high-risk groups and impro
46                                      The PET cutoff values derived from an unsupervised classifier co
47                         Applying the optimal cutoff values, determined from this cohort, to populatio
48 7 ratio of 4.7 was identified as the optimal cutoff value discriminating sensitive and refractory pat
49 es selection of seed alignment sequences and cutoff values during protein family construction.
50                       The calculated optimal cutoff values during the course of disease from the eval
51             This is also the epidemiological cutoff value (ECV) (ie, the end of the wild-type suscept
52                    Using the epidemiological cutoff value (ECV) of 0.12 mug/ml for both caspofungin a
53                    Using the epidemiological cutoff values (ECVs) of 0.12 mug/ml for caspofungin and
54      For these combinations, epidemiological cutoff values (ECVs) provide a methodology for categoriz
55 ithout fluconazole CBPs, the epidemiological cutoff values (ECVs) were used to differentiate wild-typ
56  with >15% of SPTRX3-positive spermatozoa, a cutoff value established by ROC analysis, had their chan
57                               Stratifying by cutoff value for a positive test result or removal of di
58 iagnostic performance of FITs depends on the cutoff value for a positive test result.
59 ity testing and the biosensor assay when the cutoff value for attenuation of light transmission was 6
60                For prediagnostic cases below cutoff value for CA19-9, the combination with LRG1 and T
61  immunohistochemical staining and generate a cutoff value for differentiation between normal prostate
62 ic curves were used to determine a potential cutoff value for discharge home.
63                                  The optimal cutoff value for face mask-delivered noninvasive mechani
64                                            A cutoff value for global myocardial T2 of >/=60 ms provid
65 ocess was the automated determination of the cutoff value for group separation, which was dependent o
66                                  The optimal cutoff value for HMR was 2.5 mm Hg/cm per second.
67                                          The cutoff value for ICG Ingress was 106.23 AU with sensitiv
68 r operating characteristic analysis with the cutoff value for MA of 65 mm or greater returned area un
69 basis of ROC curves, the most discriminative cutoff value for MTV values was an MTV threshold of 60%
70 tribution, the estimation of the optimal PRU cutoff value for predicting clinical outcome, and the id
71                                      Using a cutoff value for proadrenomedullin taken 6 hours after a
72 aracteristic analysis identified the optimal cutoff value for proven meningitis to be 66 pg/ml (sensi
73 n splines were used to determine the optimal cutoff value for separating transcripts with high and lo
74 ered with histology to determine the optimal cutoff value for strut coverage by OCT which was defined
75 election of a region of interest (ROI) and a cutoff value for the automated classification of subject
76 g characteristic curve analysis, the optimal cutoff value for the composite endpoint was PRU >/=234 (
77 ction of mortality, assessed the appropriate cutoff value for the dichotomized score, and compared th
78                                          The cutoff value for the extensively validated 30% of positi
79                                          The cutoff value for the highest SUVmax of (18)F-FDG aiming
80                                A data-driven cutoff value for the ratio of septal apical to basal LSs
81 n of an optimal target ROI and an associated cutoff value for the separation of subjects into the Abe
82 elded an optimal mean fluorescence intensity cutoff value for tumor detection of 5,775 (sensitivity o
83  intermediate-, or high-risk groups based on cutoff values for 2 of the following: NAFLD fibrosis sco
84 ensitivity for CRC improved with lower assay cutoff values for a positive test result (for example, 0
85      The goal of this study was to determine cutoff values for absolute MBF and to evaluate the diagn
86 ties were used to identify treatment-related cutoff values for cerebellar ICH.
87                                     The best cutoff values for circulating BMP-9 to predict MetS was
88 akpoints and, more recently, epidemiological cutoff values for clinically relevant fungal pathogens.
89 (SPE based method), which are lower than the cutoff values for confirmative conclusions regarding coc
90 analysis to determine the best symptom score cutoff values for detection of remission.
91                                sCD48 optimal cutoff values for differentiating asthma from health wer
92                                      Optimal cutoff values for distinguishing advanced fibrosis were
93 ults in a large data set define and optimize cutoff values for early diagnosis of molecular relapse.
94                                       Youden cutoff values for F>=F2, F>=F3, and F=F4 were 8.2 kPa, 9
95                                              Cutoff values for fibrosis stages >/=F1, >/=F2, >/=F3, a
96                                              Cutoff values for FISH with the pancreatobiliary probes
97 e terms, but there are no uniformly accepted cutoff values for hemodynamically significant CAD.
98 ularization decisions based on either binary cutoff values for iFR and Pd/Pa or hybrid strategies inc
99                                       Binary cutoff values for iFR and Pd/Pa result in misclassificat
100 uction >/=1.4%LV were identified as the best cutoff values for MACE prediction.
101                                           T1 cutoff values for oedematous versus necrotic myocardium
102                                          The cutoff values for optimal identification of significant
103                                              Cutoff values for patient outcome were determined using
104                                              Cutoff values for RA area were significantly different i
105 rees of unreliability, instead of relying on cutoff values for reliability indices.
106                                       Youden cutoff values for S>=S1, S>=S2, and S>=S3 were 302 dB/m,
107 ETATION: Our findings challenge the proposed cutoff values for spirometry, the order in which the lun
108                                          The cutoff values for SSI and FibroScan for staging fibrosis
109                                    Optimized cutoff values for subclinical keratoconus increased the
110 max (bSUVmax) and HT risk was assessed using cutoff values for SUVmax >10 and >20.
111                       Therefore, 2 different cutoff values for the age groups 4-10 and 11-18 were cal
112 tic curves were used to identify the optimal cutoff values for the textural features and TLG.
113 r studies are needed to evaluate the correct cutoff values for these ages.
114 ation is needed of new age- and sex-specific cutoff values for this assay.
115 nfections to validate the test and determine cutoff values for use in a cascading diagnostic algorith
116 r curve analysis was used to select critical cutoff values for use in clinical settings in which a ba
117  After successful internal validation of the cutoff values generated by the training cohort for DFS (
118                        Use of a fat fraction cutoff value greater than 1.8% yielded a sensitivity of
119 lysis indicated that the NCAR cylinder test (cutoff value &gt;/= 0.875 D) was the best test for screenin
120 dictive value for both tests was 95% using a cutoff value &gt;/=1 ISU/l with poor corresponding sensitiv
121                     Using the manufacturer's cutoff value (&gt;/=80 pg/ml), the sensitivity and specific
122 esponse to TMVR after 6 months of follow-up (cutoff value, &gt;/= 6.4%; area under the curve, 0.81; P =
123                                              Cutoff values, guidelines, and clinical recommendations
124                           All higher rounded cutoff values had sensitivities less than 98.0%.
125 iac arrest, but the relevance of recommended cutoff values has been questioned due to the lack of a s
126                                    Optimized cutoff values identified subjects with celiac disease on
127                      The use of an optimized cutoff value improved pneumococcal etiology determinatio
128 ls of hs-cTnT were already above the uniform cutoff value in 427 patients (sensitivity, 91.3% [95% CI
129 of 5.95 mo were determined to be the optimal cutoff values in the prediction of a positive (11)C-chol
130 ategorical measure using the 85th percentile cutoff value) in controls and rates of cognitive decline
131  These parameters need to be considered when cutoff values indicating the need for treatment or even
132 rebrospinal fluid (CSF), and the appropriate cutoff value is unknown.
133 t (for example, 0.89 [CI, 0.80 to 0.95] at a cutoff value less than 20 microg/g vs. 0.70 [CI, 0.55 to
134 best predictive value for ICU mortality with cutoff values less than or equal to 1.25 arbitrary perfu
135 wice: once using the uniform 99th percentile cutoff value level of 14 ng/L and once using sex-specifi
136              When assessed using categorical cutoff values, LNR had a somewhat better prognostic perf
137 ve value to discriminate patients with LVNC (cutoff value &lt;5.8 degrees ; sensitivity, 82%; specificit
138 revalence, negative predictive values of CLQ cutoff values (men, 0.99 [573 of 582]; women, 0.97 [745
139                                 However, new cutoff values might be needed to differentiate subclinic
140 ns (16%; P = 0.78) by pyrosequencing using a cutoff value of >/= 2.0%, and at 125 codons (28%; P < 0.
141                                Using a score cutoff value of >/=1.8, the Biotyper correctly identifie
142 6% specificity for SPA incompleteness with a cutoff value of >10 seconds and a 59% sensitivity and 60
143                                            A cutoff value of >40 sfu/2.5 x 10(5) cells for either IE-
144 a 59% sensitivity and 60% specificity with a cutoff value of >5 seconds.
145 ed for elevated versus normal levels using a cutoff value of >7.0 mmol/l.
146                      Of 3 cutoff values, the cutoff value of >=40 mum yielded the best sensitivity (9
147 estionnaire (RBDSQ) and dichotomized using a cutoff value of >=6.
148  Detection of a carbapenemase gene at a C(T) cutoff value of </=35 was culture confirmed in 23/24 (96
149                          Using a higher C(T) cutoff value of <=40, 90% sensitivity was achieved for u
150                                     A TAG320 cutoff value of -15.1 HU/10 mm as previously described w
151  a weight for length z score (WLZ) below the cutoff value of -3 SDs from the median as per the WHO 20
152                                            A cutoff value of -47 provided sensitivity of 92.0%, speci
153                                     Use of a cutoff value of -80 to differentiate edematous vertebral
154                                      Using a cutoff value of 0.3 ng/mL for PCT and 20 mg/L for CRP, n
155                                        A PCI cutoff value of 0.32 had 100% sensitivity and 45% specif
156 The ROC curve analysis identified an optimal cutoff value of 0.334/min for K(trans) to predict HT ris
157 cocaine in hair was found to comply with the cutoff value of 0.5 ng/mg recommended by the Society of
158 ount [HC] and low-count [LC]-MBL) based on a cutoff value of 0.5 x 10(9)/L clonal B cells.
159 its/(final-initial hematocrit+0.01)), with a cutoff value of 0.75.
160                                 Using an FFR cutoff value of 0.80, the sensitivity, specificity, and
161 predicting pressure wire-derived FFR using a cutoff value of 0.80.
162                        An [18F]-AV-1451 SUVR cutoff value of 1.19 (sensitivity, 100%; specificity, 86
163            The use of an initial cholesterol cutoff value of 1.35 MoM (95th percentile) plus a mutati
164 pecificity were 67% and 77% (p=0.003) at the cutoff value of 1.5 for b=600 s/mm(2), and 79% and 62% (
165        The use of a prespecified cholesterol cutoff value of 1.53 multiples of the median (MoM, corre
166 lammatory response syndrome criteria average cutoff value of 1.72 had 51% sensitivity and 77% specifi
167                                            A cutoff value of 1.8 D for ACA had 90.2% sensitivity and
168 00 s/mm(2), and 79% and 62% (p=0.004) at the cutoff value of 1.99 for b=1000 s/mm(2) as regards the d
169 Against the composite diagnostic standard, a cutoff value of 10,000 copies/ml for good-quality sputum
170                                      An LTB4 cutoff value of 11 pg/mL EBC provides 100% sensitivity a
171 al = 0.996-1.000, p < 0.001) with an optimal cutoff value of 11.5%.
172                                            A cutoff value of 138 pg/mL provided 100% sensitivity and
173                               Using GAM, the cutoff value of 14.7 mug/L for pi-GST showed the best pe
174 on of relapse in 77% of patients exceeding a cutoff value of 150 RUNX1-RUNX1T1 TLs in BM, and in 84%
175 d difference of calcium volume score, with a cutoff value of 2.5.
176                                            A cutoff value of 2.7 ng/mL separated the 2 groups.
177 00 s/mm(2), and 86% and 61% (p=0.003) at the cutoff value of 2.9 for b=1000 s/mm(2) as regrads the di
178  The incidence of malignancy was 88% above a cutoff value of 20 HU in the ten (18)F-FDG-equivocal lym
179                                            A cutoff value of 20 points identified patients in remissi
180                                         At a cutoff value of 22.3 kPa, sensitivity, specificity, posi
181 ghest agreement (kappa=.44) was found with a cutoff value of 3 and 5 mm for SPT, and 3.5 IU/mL for sI
182                                       At the cutoff value of 3 mm for SPT and 0.35 IU/mL for sIgE, SP
183 a were also reviewed according to a clinical cutoff value of 3 mug/mL.
184                       At the model-predicted cutoff value of 3,000 ng/mL, sensitivity was 100%, speci
185 pecificity were 78% and 79% (p=0.001) at the cutoff value of 3.1 for b=600 s/mm(2), and 86% and 61% (
186                             T SUV max with a cutoff value of 3.2 is the best prognostic indicator.
187                             T SUV max with a cutoff value of 3.2 was the most significant prognostic
188 g prostate cancer development, identifying a cutoff value of 3.25 ng/mL with a sensitivity and a spec
189 OMA-IR values as a continuous variable and a cutoff value of 3.8 confirmed the association between re
190 al right ventricular scar, an endocardial UV cutoff value of 3.9 mV is more accurate than previously
191 ejection proportional regression analysis, a cutoff value of 33.7% was optimal, with a sensitivity of
192  liver transplantation, we identified an SMI cutoff value of 48 cm/m to predict post-transplant morta
193 ith CLL, from which it is discriminated by a cutoff value of 5 x 10(9)/L circulating clonal B cells.
194 esion revascularization at 1-year follow-up (cutoff value of 5.1 mm(2); P=0.05).
195                                            A cutoff value of 50 points identified patients in remissi
196                                            A cutoff value of 51.0 kPa at 4 cm proximal to the medial
197         With application of a low troponin I cutoff value of 6 ng/L, the rule-out algorithm showed a
198                                      Thus, a cutoff value of 600 U/L was utilized.
199 ormed similarly to the previously identified cutoff value of 8,000 copies/ml for NP swab lytA rtPCR (
200                                      A TLF10 cutoff value of 8,000 discriminated survivors from nonsu
201                                       With a cutoff value of 84% on day 4 for the diagnosis of alloge
202                     Considering %NVQ only, a cutoff value of 90% correctly categorized 28 of 30 patie
203 5% CI, 0.73-0.95]; P < .001) revealed, for a cutoff value of 91.13 milliseconds, a sensitivity of 78.
204 t all cutoff values, and for all ratios, the cutoff value of at least 2 has the best sensitivity for
205 0 to 14 mL/min per kg were dichotomized by a cutoff value of BNP of 506 pg/mL, those with BNP<506 pg/
206                                            A cutoff value of CAP of 249 dB/m rules in liver steatosis
207          In addition, we aimed to identify a cutoff value of Cn for outcome prediction in this settin
208                                          The cutoff value of DT for prediction of 1-y survival was 55
209 e CRYSTAL and OPUS trials, respectively, the cutoff value of ETS >/= 20% (v < 20%) identified patient
210 teristic analysis indicated that the optimal cutoff value of FFR for demonstrating reversible ischemi
211 7] at 24 hours after inclusion by applying a cutoff value of greater than or equal to 0.6 (ng/mL)/1,0
212 activator receptor performed best by using a cutoff value of greater than or equal to 8.53 ng/mL (sen
213  with cfDNA at 24 h concentrations above the cutoff value of healthy patients (>850 ng/ml) had a sign
214 assess the clinical implications and optimal cutoff value of high platelet reactivity (HPR) in patien
215                                      Using a cutoff value of IP-10 >/=44.2 pg/mL, the model identifie
216 idence interval [CI]: 1.302-25.543), and the cutoff value of level of serum LDL-C was 3.08 mmol/l.
217  present study was to assess the appropriate cutoff value of neointimal thickness of stent strut cove
218 an accuracy of 0.79 (0.66-0.93), the optimal cutoff value of pre-LT BNP serum level to predict ICU mo
219 6 (CI 0.91-1.0) for gland distortion, with a cutoff value of six distorted glands yielding a sensitiv
220                                  The optimal cutoff value of these parameters was defined using a rec
221                                            A cutoff value of urinary CCL2: Cr 34.8 ng/mmol yielded a
222                                  The optimal cutoff value of water uptake distinguishing stroke onset
223 was based upon a standard normal transformed cutoff value of z = 3 for chromosome 21 and z = 3.95 for
224 rsus FFR </=0.80 was calculated using binary cutoff values of </=0.90 for iFR and </=0.92 for Pd/Pa,
225 . 68%, respectively, P = 0.02), with optimal cutoff values of 1.86 mL/min/g and 2.30, respectively.
226                                   Additional cutoff values of 15 and 40 optimized sensitivity (>0.80)
227 urately classified ATB and LTBI status, with cutoff values of 18%, 60%, and 5% for CD38+IFN-gamma+, H
228 isk score weighted by the OR was built using cutoff values of 2.2 or greater for international normal
229 n 20 microg/g vs. 0.70 [CI, 0.55 to 0.81] at cutoff values of 20 to 50 microg/g) but with a correspon
230 n and were dichotomized with 80th percentile cutoff values of 268 and 1703, respectively.
231             sBT measurements higher than the cutoff values of 5.7 and 14.5 were associated with 50% a
232                                    Screening cutoff values of 8-OHdG >50 ng/mg of creatinine or urine
233 alysis, demographic factors, glycohemoglobin cutoff values of 8.0%, 8.5%, and 9.0%, and mean glycohem
234 icity (area under the curve [AUC] of 1) with cutoff values of 80 and 60, respectively.
235      The sensitivity and specificity for the cutoff values of at least 3, at least 2, and at least 1.
236 teristic curve analysis evidenced predictive cutoff values of bronchial neutrophils and nasal/bronchi
237                                      Optimal cutoff values of CTCA-derived parameters were determined
238                                          The cutoff values of LSM were selected based on the accuracy
239 antibody (multiple regression analysis), and cutoff values of measures for 2 titers of anti-Dsg with
240          Second, to identify age-appropriate cutoff values of ONSD to be used in the diagnosis of int
241  We investigated whether two widely accepted cutoff values of PaO2/FIO2 and positive end-expiratory p
242                                     The best cutoff values of PET-derived parameters discriminating b
243                                  The optimal cutoff values of SUVmax and TNR were 4.8 and 2.0, respec
244                                     The best cutoff values of the absolute change in pulse pressure v
245                                    Different cutoff values of the degree of circumferential angle clo
246 operating characteristic (ROC) curve optimal cutoff value (P = .001, P = .018, P = .032, P = .008, an
247 for combined ratios (sensitivity at the >/=2 cutoff value: P < .0001 for combined ratio vs Ca/Cp rati
248                                         This cutoff value performed similarly to the previously ident
249  the range from 0 to 50 ng/mL, covering most cutoff values proposed in previous studies.
250 , Aa/Ap ratio, and combined ratios for three cutoff values reported in the literature.
251    The AUC, sensitivity, specificity and the cutoff value, respectively, for differentiating low- fro
252 d prognosis, regardless of the cutoff value, cutoff value selection, treatment method, country, sampl
253                               For MBF, these cutoff values showed a sensitivity, specificity, and acc
254    We further identified a saliva viral load cutoff value that reliably distinguished between true-po
255                                         Of 3 cutoff values, the cutoff value of >=40 mum yielded the
256  then determined goodness-of-fit and optimal cutoff values through receiver operator characteristic a
257 alue increased above 95% when increasing the cutoff value to 5.41 kUA /l.
258                                     The best cutoff value to differentiate between asymptomatic volun
259 group over miR-22/29a group could serve as a cutoff value to distinguish normal cervix from CIN and f
260 ss >=40 mum by OCT yielded the most accurate cutoff value to identify stent strut coverage validated
261 ysis identified 0.65 mmol/L cFFA as the best cutoff value to predict adequate (18)F-FDG uptake suppre
262 racteristic analysis showed that the optimal cutoff value to predict lung tissue recruitment for the
263  ability of the proposed endoscopic response cutoff value to predict midterm CFREM should be validate
264                                              Cutoff values to distinguish between physiologic and pat
265                                      Optimal cutoff values to predict flow-limiting coronary lesion w
266  the new method is superior to the 300 ng/mL cutoff values used by the only other portable analysis s
267    This study aimed to define endocardial UV cutoff values using computed tomography-derived fat info
268                                      The CLQ cutoff value was 0.16 for men and 0.56 for women.
269                                          The cutoff value was 15.0% for EW and 3.7% for OVM.
270      To dichotomize the population, an hENT1 cutoff value was defined using primary PDAC samples from
271 mor detection, a mean fluorescence intensity cutoff value was determined from the formalin-fixed tiss
272                               The so-derived cutoff value was validated in a prospective cohort from
273                     Under different coverage cutoff values, we compare four algorithms and calculate
274 and 60% decrease from baseline at week 10 as cutoff values, we determined that the respective sensiti
275                                  The optimal cutoff values were 2.3 and 2.5 for hyperemic MBF and myo
276 the same method was applied to SUVrange, the cutoff values were 5.8 for (18)F-FDG (specificity, 71%)
277                    For HER2 GCN, the optimal cutoff values were 9.4, 10.0, and 9.5, respectively (P =
278                                   When lower cutoff values were applied, it appeared that subjects at
279 g the resolution of OCT is 10 to 20 mum, the cutoff values were assessed at >=20, >=40, and >=60 mum.
280                                The following cutoff values were associated with low BDI: biliary bica
281                              Epidemiological cutoff values were calculated and determined to be 256 m
282                              Laboratory test cutoff values were calculated based on receiver operatin
283                 For this reason, 2 different cutoff values were calculated for age groups 4-10 and 11
284                                    Burn size cutoff values were determined for mortality, burn wound
285                                              Cutoff values were determined using the receiver-operati
286                                      The PET cutoff values were established using a mixture-modeling
287                               No significant cutoff values were found for SUVmax or SUVmean at univar
288                                  Optimal PSV cutoff values were less than 67 cm/sec and 39 cm/sec for
289                               Antibody assay cutoff values were selected to provide 100% diagnostic s
290                                    Different cutoff values were set for endoscopic response based on
291                                              Cutoff values were then determined by using Youden's Ind
292 ession tree analysis, combined LV EF and LAS cutoff values were used to stratify patients into three
293  for quantitative lesion differentiation and cutoff values were validated in an independent data set.
294 ach study (mean vitamin B-12 insufficiency / cutoff value), which internally corrected for geographic
295 n index, 30 was determined to be the optimal cutoff value with a sensitivity 0.62 and specificity of
296 ed likelihood ratios of result intervals and cutoff values with 100% negative (NPV) and positive (PPV
297                                              Cutoff values with 100% positive and negative predictive
298                                     High NSE cutoff values with false positive rates </=5% and tight
299  most of the changes took place close to the cutoff values, with only few exceptions of overall left
300 on provided the following optimum diagnostic cutoff values: women 0.36 U/ml (area under curve [AUC]:

 
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