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1 Remodeling During Entresto Therapy for Heart Failure).
2 (<1%) patient in the placebo group (hepatic failure).
3 ameliorate metabolic dysregulation in heart failure.
4 tions of potential drought-induced hydraulic failure.
5 trials for cardiovascular disease and heart failure.
6 tional changes in the heart leading to heart failure.
7 of SDOH in an underserved patient with heart failure.
8 performance and, all too often, spectacular failure.
9 arrhythmogenesis and progression into heart failure.
10 ulmonary vascular resistance and right heart failure.
11 underlie the many different causes of kidney failure.
12 eting cell swelling-induced microcirculatory failure.
13 of ureteral obstruction with eventual kidney failure.
14 s has never been investigated in human heart failure.
15 - and hospital-level factors associated with failure.
16 with survivors at risk for subsequent heart failure.
17 re regulation and reducing the risk of heart failure.
18 mainly contributed to determine a treatment failure.
19 or early toxicity-related death or treatment failure.
20 pattern of occurrence in patients with heart failure.
21 tes and the leading cause of end-stage renal failure.
22 gain better insight into the causes of graft failure.
23 e self-care behaviour in patients with heart failure.
24 d with acute myocardial infarction and heart failure.
25 with excess morbidity and mortality in heart failure.
26 and 15,614 individuals with nonimmune renal failure.
27 intravascular cocaine results in acute heart failure.
28 logic cure and 204 experienced microbiologic failure.
29 immune suppression, and sepsis-related organ failure.
30 ntify the risk factors associated with graft failure.
31 f KEs as a treatment for patients with heart failure.
32 k and may aggravate shock severity and organ failure.
33 haracterized by sepsis and acute respiratory failure.
34 d renal outcomes with empagliflozin in heart failure.
35 ents and not applicable in those with kidney failure.
36 ress, may contribute to pancreatic beta-cell failure.
37 nterstitial pneumonia and severe respiratory failure.
38 patients who had Covid-19 without end-organ failure.
39 via endotracheal tube for acute respiratory failure.
40 4.1% on anticoagulants, and 14.7% with renal failure.
41 cells associated with reduced risk of graft failure.
42 ation with the aim of preventing respiratory failure.
43 disorder characterized by progressive renal failure.
44 -1.3 medications (P = 0.52) in eyes with SLT failure.
45 retrocorneal membranes at the time of graft failure.
46 testinal pathogens and the risk of treatment failures.
47 aintain the information flow under node/link failures.
48 equired in this area to avoid future control failures.
50 rillation, 1.75 (95% CI 1.56-1.97) for heart failure, 1.76 (95% CI 1.51-2.05) for acute myocardial in
51 ion after MI (7% versus 12%), previous heart failure (10% versus 19%), atrial fibrillation (6% versus
52 arge to hospice (37.2% vs 25.3%), extubation failure (12.3% vs 6.1%), tracheostomy (21.6% vs 4.5%), d
54 ficant difference in the incidence of kidney failure (31.7% with intervention vs 27.3% with placebo;
55 sis (Non-ACLF) and in acute-on-chronic liver failure (ACLF) by CCT and ROTEM including agreement of b
56 predict survival and acute-on-chronic liver failure (ACLF) in patients awaiting LT, as well as early
58 = 104, 35.6%) related to sepsis, respiratory failure, acute respiratory distress syndrome, or multipl
60 s hospitalized for acute decompensated heart failure (ADHF) was well-tolerated and led to improved ou
61 n, and the end points of mortality and heart failure admissions in the CASTLE-AF study (Catheter Abla
64 it represents the major cause of acute liver failure (ALF) requiring liver transplantation in USA and
66 us albus) to MeHg also caused early breeding failure and a ~20% reduction in breeding numbers at envi
67 pical cardiovascular diagnoses such as heart failure and acute myocardial infarction, need frequently
69 Exercise intolerance, associated with heart failure and death in general populations, is not well st
70 nary vasculature that results in right heart failure and death, are usually assessed with invasive pr
72 he molecular mechanisms of age-related heart failure and highlight exercise as a valuable experimenta
74 ment of volume status in patients with heart failure and may represent a mechanism contributing to th
75 les cases, associated with secondary vaccine failure and modified clinical illness, is emerging in Vi
77 ermine whether BDG was associated with organ failure and patient mortality, while accounting for the
78 differentiation is associated with treatment failure and poor outcome in metastatic castration-resist
82 ulant phenotype) could predict midterm graft failure and to investigate potential functional role of
84 to differentiate reinfections from treatment failures and to identify transmission linkages and assoc
89 ovascular death, rehospitalization for heart failure, and pacemaker implantation after a TAVR procedu
91 nt inflammation, history of previous implant failures, and pain/discomfort at the implant site were s
92 s by Glasgow Coma Scale and Sequential Organ Failure Assessment, and central circadian rhythm by mela
93 After adjusting on age and Sequential Organ Failure Assessment, serum CXCL10/IP-10 (P = 0.047) and G
95 ientific cooperation of members of the Heart Failure Association of the ESC, the Heart Failure Societ
98 the ICRS, that is, correlated to an anatomic failure at the site of implantation in an advanced disea
102 literature on the causes of kidney allograft failure, both early and late, both nonimmune and alloimm
103 ne follow-up after hospitalization for heart failure can increase 7-day follow-up and reduce in-perso
104 pair pathways in human cells, how DNA repair failures can lead to human disease, and how PARP inhibit
105 (73.0% versus 78.7%), acute noncardiac organ failure, cardiac arrest (34.3% versus 35.7%), and receiv
106 osteoporosis, non-AIDS cancer, chronic renal failure, cardiovascular and cerebrovascular disease, obe
107 ctor for the progression to end-stage kidney failure, cardiovascular morbidity, and premature death.
110 increased risk of developing incident heart failure compared to a subject at the 10th percentile in
111 ortality are at a higher risk for transplant failure compared with patients with the same duration of
112 available data sets of human and mouse heart failure, demonstrated that EPRS acted as an integrated n
115 ernal causes at the nodal level and external failures due to an adverse environment, and develop a pa
118 P in Patients Stabilized From an Acute Heart Failure Episode), the in-hospital initiation of sacubitr
119 iarrhea and often followed by multiple organ failure, especially of the respiratory and cardiovascula
121 GLT2 inhibition on fatal and non-fatal heart failure events and renal outcomes in all randomly assign
123 ve Remote Monitoring for Prediction of Heart Failure Exacerbation) examined the performance of a pers
124 sis remains poor as many patients with heart failure experience symptoms that negatively impact Quali
125 saving for patients with advanced intestinal failure experiencing complications of parenteral nutriti
126 se of explantation was functional refractive failure followed by spontaneous extrusion of the ICRS, t
127 nonadherence as the major cause of virologic failure for 9 (45%) of 20 highly treatment-experienced p
129 e remains the most common cause of treatment failure for patients with acute myeloid leukemia (AML) w
130 ith a significant increase in reported heart failure from 1.64% (95% CI 0.82-2.65) to 11.72% (3.00-24
131 olled during hospitalisation for acute heart failure from 358 centres in 44 countries on six continen
132 ce of Proteobacteria in the congestive heart failure group (p = 0.014), particularly due to an increa
133 RT-experienced Ugandan adults with virologic failure (>=1000 copies/mL) using leftover plasma after v
135 isk of ESKD, with the highest risk for heart failure (hazard ratio, 11.40; 95% confidence interval, 8
136 are to a large cohort of patients with heart failure, heart transplantation, and left ventricular ass
137 CI, 1.28-2.09, P value = 8.07 x 10-5), heart failure (HF) (OR = 1.61, 95% CI, 1.32-1.95, P value = 1.
138 h New York Heart Association Class III heart failure (HF) and a prior HF hospitalization (HFH) within
139 nsated hypertrophy (CH) until signs of heart failure (HF) are apparent using a trans-aortic pressure
141 leading cause of death and morbidity, heart failure (HF) is responsible for a large portion of healt
142 al Mitral Regurgitation), treatment of heart failure (HF) patients with moderate-severe or severe sec
144 been implicated in the pathogenesis of heart failure (HF) with preserved ejection fraction (HFpEF).
147 porter 2 inhibitors reduce the risk of heart failure hospitalization and cardiovascular death in pati
148 nsporter-2 (SGLT-2) inhibitors reduced heart failure hospitalization and end-stage renal disease.
149 es and presented an increased risk for heart failure hospitalization that warrants further study.
150 ent MI or coronary revascularization), heart failure hospitalization, and all-cause mortality (Medica
152 agliflozin reduced the total number of heart failure hospitalizations that required intensive care (H
153 shown to contribute to HE during acute liver failure; however, TGFbeta1 must be activated to bind its
154 eriencing HP had a marginally higher risk of failure (HR = 1.16, 95% CI = 0.6-2.1), but this relation
157 patients who had Covid-19 without end-organ failure in a 1:1 ratio to receive either LY-CoV555 or ma
160 ) would serve as a predictive tool for graft failure in patients (n = 181) who received a kidney tran
163 e management acute or acute on chronic liver failure in the ICU, related to five groups (cardiovascul
165 proposes a novel nonlinear model of cascade failure in weighted complex networks considering overloa
166 yopathies, which are a common cause of heart failure in young people, have increased during the last
168 rceived by many to be expensive and prone to failure, in part explaining its low rates of implementat
170 to target macrophage metabolism during heart failure, including antidiabetic therapies, anti-inflamma
171 Factors that predicted death-censored graft failure independent of both donor and recipient clinical
174 during sympathetic activation, and in heart failure is a major determinant of cardiac physiology and
178 lity of human organs for patients with organ failure-is limited by molecular incompatibilities betwee
179 the OptiLink HF trial (Optimization of Heart Failure Management Using OptiVol(TM) Fluid Status Monito
181 sepsis, pneumonia, pneumothorax, respiratory failure, myocardial infarction, thyrotoxicosis, alcohol,
184 le dopamine D2 receptor (D2R) levels and the failure of antipsychotic drugs to rescue adult behaviora
185 preclinical models of HCC with the clinical failure of AR antagonists in patients with advanced HCC
186 ver, the molecular mechanisms underlying the failure of beta-cells to respond to glucose in T2D remai
188 , rebleeding from both adhesive and cohesive failure of clots decreases survival from hemorrhage in v
190 ppointing in treating UTI, likely due to the failure of infused antibiotics to penetrate the bladder
191 haracterized by insulin resistance with late failure of insulin production, severe hyperglycemia/diab
192 or to treatment is associated with long-term failure of integrase inhibitor-containing first-line reg
193 y significantly contribute to the success or failure of MSC-based virotherapy as well as generate new
194 severe congenital malformations caused by a failure of neural tube closure during early embryonic de
195 These findings may explain the persistent failure of NK cell therapy in patients with solid tumors
196 l subcellular mechanism for the maturational failure of oligodendrocytes and offers a potential thera
197 ls between humans and mice, and explains the failure of potent biotin biosynthesis inhibitors in stan
199 s in a deterioration of these functions, and failure of RA signaling is perhaps associated with norma
200 apilla morphology could be a risk factor for failure of selective biliary cannulation (SBC) and post
205 ariant, showing that the change results in a failure of the polymerisation of alpha/beta/gamma lamini
206 t health and scientific investigation is the failure of these cells to achieve full functional maturi
208 s bacteriocin limitations, the successes and failures of this technology thus far, the challenges tha
210 ned risk of death, hospitalization for heart failure or an emergent/urgent heart failure visit requir
211 eased mortality vulnerability, but hydraulic failure or biotic attack may dominate the process during
212 older, presented with acute congestive heart failure or non-ST-segment-elevation myocardial infarctio
216 the MitraClip Percutaneous Therapy for Heart Failure Patients with Functional Mitral Regurgitation) t
217 the MitraClip Percutaneous Therapy for Heart Failure Patients With Functional Mitral Regurgitation),
223 during long-term follow-up with a low graft failure rate: 5% class 1, vs 30% class 2, vs 50% class 3
226 red to generate evidence about UAS lifespan, failure rates, and performance under different weather c
227 veloping the outcomes of mortality and heart failure remained similar across years, although the diff
232 rt study, prediction models of acute ovarian failure risk were developed using eligible female US and
235 Meta-Analysis Global Group in Chronic Heart Failure score, genotype, level of BB exposure, and BB pr
238 rt Failure Association of the ESC, the Heart Failure Society of America and the Japanese Heart Failur
240 was associated with a similar risk of graft failure (subdistribution hazard ratio [sHR] 0.74; 95% co
241 renal and liver injury or/and multiple organ failure, suggesting a spread of the SARS-CoV-2 in blood.
242 f (1) death; (2) rehospitalization for heart failure symptoms and valve prosthesis complication; or (
247 risingly, the simultaneous loss of RAP80 and failure therein of BRCA1 PARsylation results in the dysr
248 elomere biology genes leading to bone-marrow failure, these data provide evidence that genetically in
250 ss of human beta-cell maturity and beta-cell failure through activation of the BMP/SMAD signaling pat
252 of TAVR versus SAVR durability in which TAVR failure times were varied to determine the impact of TAV
254 ciated with each hour until antibiotics, and failure to control for large potential confounders inclu
256 er patients (52%) developed refractory heart failure to disabling New York Heart Association function
257 phorylation of the SAF-A DNA-binding domain; failure to execute this pathway leads to accumulation of
258 rgued that psychosis may emerge because of a failure to learn sensory statistics, resulting in an imp
259 this study were to: (1) measure the rate of failure to provide defect-free postoperative venous thro
260 ) chemoprophylaxis, (2) identify reasons for failure to provide defect-free VTE chemoprophylaxis, and
261 ic derangement, and human factors, including failure to recognize and reluctance to manage the failed
262 this review, we discuss the consequences of failure to reprogram histone methylation during three cr
263 stent and accurate dose monitoring; however, failure to return one or both badges, reversal of badges
265 tematic processes in formulating guidelines, failure to state conflicts of interest, and lack of cons
268 were predictive of distinct types of errors: failures-to-stop, failures-to-go, and incorrect choices.
269 -HF (Baroreflex Activation Therapy for Heart Failure) trial was a multicenter, prospective, randomize
270 , every 4 weeks group) confirmed virological failures (two sequential measures >=200 copies per mL).
272 TAVR, and disease symptoms (congestive heart failure, unstable angina, non-ST-elevation myocardial in
273 or heart failure or an emergent/urgent heart failure visit requiring intravenous treatment (415 versu
277 l infarction, or rehospitalization for heart failure was not different between the 2 groups (odds rat
281 re recently hospitalized for worsening heart failure were randomly assigned to receive sotagliflozin
283 secutive anaesthetic weans (23 successes, 24 failures) were identified from a single-centre cohort of
284 Engineered genetic systems are prone to failure when their genetic parts contain repetitive sequ
286 mes of fluid removal in patients with kidney failure who are treated with intermittent haemodialysis,
287 e able to identify those patients with heart failure who have a cardio-inflammatory phenotype and wil
289 yocardial infarction, because of respiratory failure with hypoxia and hemodynamic instability in crit
294 cohort of Medicare beneficiaries with heart failure with reduced ejection fraction and existing qual
296 with reduced ejection fraction (HFrEF; heart failure with reduced left ventricular ejection fraction
297 ession showed increasing odds of respiratory failure with sC5b-9 (odds ratio 31.9, 95% CI 1.4 to 746,
299 utcomes, including hospitalization for heart failure, with this benefit extending to patients without