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1 ilities of end points (e.g., death or system failure).
2 cute respiratory failure, and cardiovascular failure).
3 s (or prior, in the event of early treatment failure).
4 s on human spermatogenesis and spermatogenic failure.
5 t-tubule organization and accelerated heart failure.
6 ion, stroke, or hospital admission for heart failure.
7 er time, these chronic loads can cause heart failure.
8 ities, including pericardial edema and heart failure.
9 ther improve outcomes in patients with heart failure.
10 1 and 2014 to determine risk factors for FMT failure.
11 spiratory and autonomic dysfunction in heart failure.
12 included death and death-censored allograft failure.
13 sed grafts to treat patients with intestinal failure.
14 pertrophic cardiomyopathy and advanced heart failure.
15 e CpGs novel epigenetic biomarkers for heart failure.
16 GATA3 function could lead to early pregnancy failure.
17 ane oxygenation for severe acute respiratory failure.
18 rdial infarction, ischemic stroke, and heart failure.
19 ABMR) is a leading cause of kidney allograft failure.
20 frequently associated with multisystem organ failure.
21 prerenal and intrinsic acute renal allograft failure.
22 in system inhibitors for patients with heart failure.
23 ty remains unresolved in patients with heart failure.
24 yopathy (DCM) is an important cause of heart failure.
25 ions, including stroke, eclampsia, and organ failure.
26 singly used in the management of respiratory failure.
27 n the kidney, it predicts the onset of renal failure.
28 that regulates FGF23 expression during renal failure.
29 rtension, obstructive sleep apnoea and heart failure.
30 ocandin therapy altered the risk of clinical failure.
31 iretroviral therapy and to prevent virologic failure.
32 rget in a number of diseases including heart failure.
33 it is the second most common cause of liver failure.
34 on cause of childhood hypertension and renal failure.
35 n unselected patients with acute respiratory failure.
36 including cardiovascular mortality and heart failure.
37 ed, but suggested an increased risk of renal failure.
38 ses, including cardiac hypertrophy and heart failure.
39 ations were investigated in the AL treatment failures.
40 nearly all (70 [89%] of 79) XR-NTX induction failures.
41 ents (CVEs) including 281 (23.8%) with heart failure, 109 (9.2%) with atrial fibrillation, 89 (8%) wi
43 iting photosynthesis and promoting hydraulic failure, (2) increases carbon costs during periods of ca
44 reatment), pneumonia (27 [11%]), acute renal failure (25 [10%]; five related to treatment), pyrexia (
45 ounts in the highest 50% had a risk of graft failure 3.59 times as high (95% confidence interval, 1.1
46 ough week 24 were anaemia (10 [5%]), cardiac failure (5 [2%]), pyrexia (4 [2%]), and pneumonia (4 [2%
47 d cBIN1 level decreased in humans with heart failure, a condition with reduced cardiac muscle cBIN1,
50 71, and 1 125 231 hospitalizations for heart failure, acute myocardial infarction, and pneumonia, res
52 ith dihydroartemisinin-piperaquine treatment failure after adjusting for the presence of amplified pl
53 ged as the most important cause of treatment failure after allogeneic hematopoietic stem cell transpl
54 composite outcome of incident ASCVD or heart failure after further stratifying by CAC (0, 1-100, or >
63 iovascular events may be enhanced when heart failure and glucose intolerance coexist and may be atten
66 in a pig model with features of human heart failure and preserved ejection fraction with sternum int
68 athophysiology of aortic stenosis with heart failure and reduced ejection fraction and summarizes the
69 y patients' characteristics that may predict failure and removal of the Linx sphincter augmentation d
70 ated significantly later with comorbid heart failure and renal failure, with absence of fever or hypo
71 inary sepsis in one patient, and acute renal failure and respiratory failure in one patient) were sus
72 brane oxygenation in adults with respiratory failure and sepsis is steadily increasing, but the knowl
76 iliary strictures as a risk factor for graft failure, and does not validate other risk factors for IC
78 r nonfatal stroke, hospitalization for heart failure, and hospitalization for acute coronary syndrome
79 for both groups older age, congestive heart failure, and increased left ventricular end-systolic dim
80 bling substantial catch-up from early growth failure, and leveraging improved learning from concomita
83 lass III or IV, previous admission for heart failure, and valve disease) and non-cardiac variables (b
84 roup [coronary artery disease and multiorgan failure] and three in the trastuzumab emtansine group [m
85 05 [1.02-1.09]; p = 0.003), Sequential Organ Failure Assessment (relative risk = 1.09 [1.00-1.18]; p
86 ement in the cardiovascular Sequential Organ Failure Assessment (SOFA) score (scores range from 0 to
87 nts in the Sequential [Sepsis-related] Organ Failure Assessment (SOFA) score, introduced quick SOFA (
88 The sensitivity of quick Sequential Organ Failure Assessment for predicting critical care interven
89 Accuracy of the quick Sepsis-related Organ Failure Assessment score, Sepsis-related Organ Failure A
90 ilure Assessment score, Sepsis-related Organ Failure Assessment score, systemic inflammatory response
91 Response Syndrome and quick Sequential Organ Failure Assessment scores were calculated, and their rel
93 l samples from patients with end-stage heart failure at time of transplant, with or without diabetes
94 yocardial infarction, new or worsening heart failure, atrial fibrillation, stroke, deep venous thromb
95 cant difference in the rate of target-vessel failure between the patients who received a bioresorbabl
97 heat treatment, is known to cause disastrous failure, but its mechanism is still not completely clear
98 unction (CVpef) is associated with treatment failure, but the pattern of change in self-similarity le
99 as associated with all-cause death and heart failure, but the result was not significant (P=0.051).
100 stimulation have been reported in left heart failure, but whether it would be beneficial for pulmonar
102 virus (HIV)-infected patients with end organ failure can safely receive an organ transplant from an H
103 valuation of congenital heart disease, heart failure, cardiac masses, pericardial disease, and corona
104 ploy in harsh reservoir conditions and where failures cause material aggregation and sticking to rock
107 tegies for Management of Patients with Heart failure) clinical cohort study, 496 patients with acute
108 llitus) are characteristic features of heart failure; conversely, neurohormonal systems activated in
109 l cure, defined as absence of these clinical failure criteria at follow-up visits: fever; increase in
112 RATIONALE: In patients with chronic heart failure, daytime oscillatory breathing at rest is associ
113 higher rate of hospital admission for heart failure decompensation in follow-up (HR, 1.66; 95% CI, 1
115 vasive telemonitoring in patients with heart failure does not reduce mortality or hospitalizations, l
116 rapy for toxic ingestion or idiopathic liver failure (DT) in a level 1 trauma center and large transp
117 ciated with an increased risk of virological failure during treatment with NNRTI-containing regimens.
118 30% to 40% of patients with congestive heart failure eligible for cardiac resynchronization therapy (
120 s the only available option after first-line failure for the majority of individuals living with huma
123 tal quartile of ICU use for congestive heart failure had a sensitivity of 50-60% and specificity of 7
126 ciated with increased hazards of virological failure (hazard ratio [HR] 2.6, 95% CI 2.5-2.8; p<0.0001
127 ycline chemotherapy is associated with heart failure (HF) among survivors of non-Hodgkin lymphoma (NH
131 perfused hearts from control (CTL) and heart failure (HF) mice (HF induced by transaortic constrictio
134 ole of ischemic heart disease (IHD) in heart failure (HF) with reduced ejection fraction (HFrEF; EF <
136 Atrial fibrillation (AF) is common in heart failure (HF), but the outcome by type of AF is largely u
137 ers increase survival in patients with heart failure (HF), the mechanisms behind this protection are
143 CI: 0.07 to 0.75), total mortality or heart failure hospitalization (aHR: 0.32; 95% CI: 0.12 to 0.82
144 point or day-30 all-cause mortality or heart failure hospitalization rate differed between the 2 grou
145 range) showed strong associations with heart failure (HR: 2.04; 95% confidence interval [CI]: 1.82 to
147 er limb ischemia - diabetes, end-stage renal failure, hyperparathyroidism, or even symptoms of left u
148 e mortality at 1 year in patients with heart failure in Africa, China, India, the Middle East, southe
149 cardiac hypertrophy and progression to heart failure in both vitamin D deficient and normal mice with
154 ent, and acute renal failure and respiratory failure in one patient) were suspected to be related to
155 be a major contributing factor in treatment failure in patients with atopic dermatitis, yet it has b
157 entification and stratification of induction failure in patients with pediatric acute lymphoblastic l
162 s a key reason for the frequent regeneration failures in humans, the transcriptional mechanisms that
167 4.1 years, surgery patients had lower heart failure incidence than lifestyle modification patients (
169 h short bowel syndrome (SBS) with intestinal failure, increasing intestinal wet weight absorption and
170 on drug recently approved for treating heart failure, inhibits stretch-induced hypertrophy, and predi
171 Here, in the International Congestive Heart Failure (INTER-CHF) study, we aimed to measure mortality
172 Specifically, the risk of developing heart failure is higher in patients with diabetes or obesity,
175 he cause of nutritional dyshomeostasis (oral failure, malabsorption, or both), and to quantify the ef
177 ad persisting symptoms compatible with heart failure (median of 13 [range 0-76] in the Minnesota Livi
178 cotherapies for African Americans (eg, heart failure medications), disease management is less effecti
180 endpoint were age, anemia, congestive heart failure, multivessel disease, number of stents implanted
182 Conclusion In the absence of known renal failure, neonates receiving standard inpatient care do n
183 ly, neurohormonal systems activated in heart failure (norepinephrine, angiotensin II, aldosterone, an
187 as associated with a significant risk of FMT failure (odds ratio, 0.15; 95% confidence interval, .007
190 k of a known correlate of protection and the failure of a neutralizing antibody to correlate with pro
191 al health community can judge the success or failure of a Trump presidency, based on a selection of t
194 -Saharan Africa in patients with virological failure of first-line combination antiretroviral therapy
195 cell fusion assays show a strain-independent failure of fusion pore enlargement among H2 (A/Japan/305
197 was defined as symptomatic congestive heart failure of New York Heart Association class III or IV, c
200 e the efficacy, safety, and risk factors for failure of standalone ab interno gelatin microstent impl
201 that dwell time was the only risk factor for failure of standard retrieval technique (odds ratio, 1.0
202 bility criteria included measurable disease, failure of standard therapy, and Eastern Cooperative Onc
203 reactivation which is likely linked with the failure of the monocytes to differentiate to a DC phenot
209 collaboration who had locally defined viral failure on first-line therapy with tenofovir plus a cyto
210 ent-related (pneumonia, two [2%]; multiorgan failure, one [1%]; and sepsis, one [1%], all in the 10-d
211 ) who received placebo experienced treatment failure or disease recurrence, or died (absolute risk di
214 robability of corneal transplantation, graft failure, or both were calculated based on data from publ
215 k of dying from myocardial infarction, heart failure, or stroke, respectively, than members of the ge
221 mprovement of patient health status in heart failure patients with low self-reported hrQoL, but not i
222 with left bundle branch block (LBBB), heart failure patients with narrow QRS and nonspecific intrave
224 -scale technology needed to treat intestinal failure patients.There is a need for humanised grafts to
226 but no RASs were associated with ledipasvir failure, pointing to a limited efficacy of ledipasvir in
228 nge 0-76] in the Minnesota Living with Heart Failure Questionnaire) and cardiac limitation on exercis
232 ded by partner drug resistance, causing high failure rates of artemisinin combination therapies in so
234 or interstitial nephritis, as cause of renal failure, represented the only predictive factor for MGUS
237 s of all ages had significantly higher graft failure risks than males (adjusted hazard ratios 0-14 ye
238 ssociated with a 58% increased risk of heart failure (RR 1.58; 95% CI, 1.46 to 1.72) and a 40% increa
241 kg/m(2)), worse Minnesota Living With Heart Failure score (48 versus 40), higher median N-terminal p
243 cally, at times be the source of performance failures.SIGNIFICANCE STATEMENT The performance-monitori
244 of patients of black race, those with heart failure signs at admission, and bleeding complications i
245 ise from interventional cardiologists, heart failure specialists, cardiac surgeons, and cardiac anest
246 , nonfatal myocardial infarction [MI], heart failure, stroke, transient ischemic attack, peripheral a
249 l help identify, and eventually correct, the failures that lead to the deterioration of this importan
253 ted with outcomes of remission and treatment failure to CBT and antidepressant medication and survive
256 accumulated bystander mutations indicating a failure to express their products at the cell surface in
257 of Hsp104 function in yeast cells leads to a failure to generate new propagons, the molecular entitie
261 ts effectiveness is frequently undermined by failure to obtain follow-up colonoscopy after positive t
263 .70 vs 2.77 instances per hour, P = .03) and failure to progress (mean, 1.20 vs 0.13 instances per ho
264 cal dynein inhibition in zebrafish result in failure to properly distribute mbp mRNA in oligodendrocy
265 EGFR-TKI use, EGFR-TKI resistance mutation, failure to receive EGFR-TKI after WBRT/SRS, or insuffici
267 of repair cells and regeneration tracks, and failure to sustain expression of repair cell markers, in
270 e S187A mutant died in the first week due to failure to undergo the peroxisome proliferator-activated
271 sis genes prominently in RP-mediated DBA and failure to upregulate components of the translational ap
275 rubinemia and/or Encephalopathy and/or Renal Failure trial by applying the recently introduced Chroni
276 ar Improvements With MV-ASV Therapy in Heart Failure) trial investigated whether minute ventilation (
277 t on Global Mortality and Morbidity in Heart Failure) trial randomly assigned 8399 patients with chro
280 An index that is derived to predict graft failure using donor and recipient factors, based on loca
282 bably due to immunosenescence, because heart failure was associated with increased senescent CD4+ T c
291 A demonstrated elevated risks of early graft failure, whereas those with de novo DSA experienced acce
292 therapy (CRRT) benefits patients with renal failure who are too hemodynamically unstable for intermi
293 in Patients Hospitalized for Worsening Heart Failure With Challenging Volume Management [SECRET of CH
294 ODS AND We randomized 12 subjects with heart failure with preserved ejection fraction to oral KNO3 (n
296 irst study to evaluate elamipretide in heart failure with reduced ejection fraction and demonstrates
298 under investigation for patients with heart failure with reduced left ventricular ejection fraction.
299 treating malaria patients with uncomplicated failures with the same ACT used for the primary episode,
300 later with comorbid heart failure and renal failure, with absence of fever or hypotension, and in in
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