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1 ed genes, the majority being associated with advanced age.
2 ate and litter size compared with WT mice at advanced age.
3 isease in different arterial territories and advanced age.
4 ation, a task that is negatively affected by advanced age.
5 rate adherence seemed to fade away with more advanced age.
6  in the prevalence of PAD, CAS, and AAA with advanced age.
7  critical determinants of health status with advanced age.
8 uch as fetal alcohol exposure, seizures, and advanced age.
9 arly adulthood on, and atrophy aggravated in advanced age.
10 cts of AD pathologic changes on cognition in advanced age.
11 hic pulmonary fibrosis [IPF]) increases with advanced age.
12 ned significance in Cox models that included advanced age.
13 ation remains unresolved, in particular with advanced age.
14 adulthood, and including a mild phenotype in advanced age.
15 ults with predisposing chronic conditions or advanced age.
16 in lower muscle protein synthesis rates with advanced age.
17 anges in high-level perceptual processing in advanced age.
18 inclusions increased in number and size with advanced age.
19 ll proliferation was severely decreased with advanced age.
20 ht and developed tumors in various organs at advanced age.
21  reduction of SI change correlated with only advanced age.
22 nd results in elevation of blood pressure at advanced age.
23  for developing carcinoma of the prostate is advanced age.
24        Increasingly, adults are living to an advanced age.
25 ial Alzheimer disease (AD) risk factor after advanced age.
26 nd in population-based cohorts of similar or advanced age.
27 or risk of amyloidosis prior to the onset of advanced age.
28  and was attenuated throughout networks with advanced age.
29 terneurons may be particularly vulnerable in advanced age.
30  of how their functional role is affected by advanced age.
31 ith a history of severe immunosuppression or advanced age.
32 , whereas others remain asymptomatic despite advanced age.
33 in Old, confirming signalling integrity with advanced age.
34 pport consideration of this approach despite advanced age.
35  probably will have more effective impact at advanced ages.
36 nduced cardiac hypertrophy at both young and advanced ages.
37 cantly decreased pathological progression at advanced ages.
38  and causes only mild cardiomyopathy even at advanced ages.
39 re detected in Ppt1-deficient flies, even at advanced ages.
40 mmon markers of neurodegeneration present in advanced aging.
41 ly harboring elevated amyloid burden, and in advanced aging.
42 eport that this maintenance is not random in advanced aging.
43 cal record were poor surgical targets (24%), advanced age (16%), and renal insufficiency (16%).
44                                      At more advanced ages (16-19 months), cognitive deficits progres
45 n p73 KO mice from early embryonic life into advanced age (25 months).
46 development at both early (age 10 weeks) and advanced (age 28 weeks) stages of atherosclerosis in mic
47 vels after active or passive immunization in advanced aged 3xTg-AD mice that contain both amyloid pla
48 gative life events, a higher literacy level, advanced age, a higher educational level, and more time
49 le infection (CDI) are identified, including advanced age, a prolonged hospital stay, and use of acid
50 including 21 within MC who were excluded for advanced age, acquired comorbidities, or refusal and 30
51                                              Advanced age, acute respiratory failure, and sepsis were
52 -deshydrogenase level (P = .0006) and a more advanced age adjusted international prognostic index (P
53                               Whether or not advanced age affects the ability of PRC principal cells
54 ution to cardiac fibrosis, which occurs with advanced age, after acute injury (e.g., myocardial infar
55                                              Advanced age alone does not appear to be a contraindicat
56 thermore, mice that received treatment at an advanced age also showed remarkable preservation of reti
57                              To evaluate how advanced age alters the host immune response to cutaneou
58 operative pulmonary complications, including advanced age, American Society of Anesthesiologists clas
59 frequent but more prevalent in patients with advanced age and a PS of >/= 2, underscoring the need to
60           Patient characteristics, including advanced age and comorbidity, and tumor anatomy are bein
61 or invasive treatments and in the setting of advanced age and complex health status.
62                                              Advanced age and complex mitral valve pathologies increa
63                               In conclusion, advanced age and different clinical presentations of the
64 ality of autologous CD34+ cells decline with advanced age and diminished cardiovascular health.
65 n 3 years, reflecting a population with more advanced age and disease than seen in trial populations
66   In contrast, Tg2576 form plaques at a more advanced age and do not show cell death.
67                                     Although advanced age and elevated metabolic syndrome risk were a
68 gher torsion, though the association between advanced age and greater torsion was more pronounced in
69            These responses may increase with advanced age and have been linked to an "immune risk pro
70                                        While advanced age and increased glioma grade reduced SI chang
71 s increased in number and became larger with advanced age and increasing CGG repeat length, supportin
72 ounding tissues, and is associated with both advanced age and joint injury.
73                      Increase in polyp size, advanced age and location in the distal colon were assoc
74 hough risk factors for pulmonary NTM such as advanced age and low BMI are known, the mechanisms under
75 al in patients considered "too ill/old" were advanced age and low functional status.
76 nt predictors for excess DCS mortality, with advanced age and male sex being associated with higher e
77            Mutant cases were associated with advanced age and monosomy 7/deletion 7q (-7/del(7q)) con
78 ne in clinical status that often accompanies advanced age and multimorbidity.
79 ay be a good option among patients with very advanced age and multiple comorbidities.
80 en in brain samples from humans with autism, advanced age and neurodegeneration (Alzheimer's disease
81 should be kept in mind that in patients with advanced age and pain in the left quadrant of the abdome
82  His risk factors for cholecystitis included advanced age and previous abdominal surgeries.
83     AF-TR is not rare and is associated with advanced age and right atrial enlargement.
84                                              Advanced age and severe fibrosis at HCV diagnosis are pr
85                                              Advanced age and severe fibrosis were significant risk f
86                                              Advanced age and splenectomy are risk factors for PAH in
87          The relation between muscle mass in advanced age and telomere length, however, has rarely be
88 s of the world provide care to patients with advanced age and terminal illness at different rates and
89  an elevated risk of CDI simply due to their advanced age and the fact that they are receiving care i
90         Due to the general health condition, advanced age and the large size of the aneurysm we decid
91                               In addition to advanced age and the presence of comorbidities, there ar
92                                              Advanced age and tumor grade do not have a combined effe
93 d endothelial dysfunction can prevail during advanced age and we questioned how calcium signalling ma
94 acroglobulinemia (WM), most of which were of advanced age and with adverse prognostic factors.
95 or potentially curative treatment because of advanced age and/or clinically relevant comorbidities an
96 e study period: 73 for acute disease, 18 for advanced age and/or comorbidities, and 17 to avoid the r
97 ch that the beneficial effects are lost with advanced age and/or with extended hormone deprivation.
98 risk stratification protocol for patients of advanced age and/or with preexisting cardiac disease.
99 104 significantly improves motor function at advanced ages and also mildly extends lifespan.
100  an anatomical breakdown of the MZ occurs in advanced age, and a reduction in frequency of MZM may af
101    Left ventricular size, renal dysfunction, advanced age, and atrial fibrillation/flutter were signi
102 wer lung function, current smoking, obesity, advanced age, and having nonatopic asthma.
103 s age-associated diseases, improve health at advanced age, and increase life span.
104 r mortality were low total lymphocyte count, advanced age, and male sex.
105                  In contrast, female gender, advanced age, and nonwhite race, all risk factors for in
106 ctors for stillbirth, including nulliparity, advanced age, and obesity.
107 iring the perirhinal cortex are disrupted in advanced age, and suggest that at least some of these im
108  we uncover in CRPS does not break down with advanced age, and surprisingly, remains stable across su
109  (DRIs) are not specific for women living to advanced ages, and little research has been conducted sp
110 xposure, such as in early development and at advanced age; and, second, the potential of stress-induc
111                                              Advanced age appeared to be of advantage for both bindin
112 k factors of family history, black race, and advanced age are associated with increased risk for POAG
113 who have substantial comorbidities or are of advanced age are at high risk of both relapse and nonrel
114 as cholangiocarcinoma (n = 594); patients of advanced age at diagnosis had an increased incidence com
115 ia and its presence has been associated with advanced age at diagnosis, higher hemoglobin and leukocy
116 etween young and old mice via alphaARs; with advanced age, attenuated dilatation of upstream branches
117 iated with higher readmission rates included advanced age, body mass index, cardiovascular/pulmonary
118                               Outcomes using advanced age brain-dead or cardiac-dead donor kidneys ar
119 for atrial fibrillation were associated with advanced age but were fairly infrequent.
120 elief, prolongation of ovarian function into advanced age by Bax deficiency did not lead to an increa
121 Thus, microvascular endothelium can adapt to advanced age by reducing Ca(2+) influx during elevated o
122  Hindlimb ischemia was surgically induced in advanced-age C57/BL6 mice.
123      These patients were more likely to have advanced age, cardiac disease, chronic obstructive pulmo
124  predictors of DNR status at enrollment were advanced age, chronic obstructive pulmonary disease, pre
125                   In multivariable analyses, advanced age, comorbidities, and disease severity were s
126                                     However, advanced age, comorbidities, and myocardial injury in pa
127 lack race (odds ratio [OR], 0.76; P < .001), advanced age, comorbidity, and Medicare insurance.
128                                           In advanced age, decreased CD8(+) cytotoxic T-lymphocyte (C
129 duals with a variety of conditions including advanced age, dementia, and cancer.
130 ity score adjustment for surgery showed that advanced age, diabetes mellitus, health care-associated
131 redictors of ranolazine intolerance, such as advanced age, diabetes, poor exercise tolerance, or hist
132 the hypothesis that "exceptional agers" with advanced ages do not have significant ADP because they h
133                                              Advanced age does not impair bone marrow engraftment, th
134 independent baseline predictors (female sex, advanced age, elevated serum creatinine and white blood
135    Cognitive decline is commonly observed in advanced aging even in the absence of disease.
136 x gene, which sustains ovarian lifespan into advanced age, extends fertile potential and minimizes ma
137                                              Advanced age, features of the metabolic syndrome, and ch
138 ndependent predictors of major bleeding were advanced age, female gender, diabetes, hypertension, ren
139          Clinical features of AF-TR included advanced age, female sex, greater right atrial than left
140                      Screening patients with advanced age for HIV is economically attractive in many
141  feature of insulin-resistant states such as advanced age, genetic diabetes, and diet-induced obesity
142  of more hypomethylated DNA sequences in the advanced age group.
143    For CVG, multivariate analysis identified advanced age (&gt; 70 years), concomitant coronary artery s
144              Participants were stratified by advanced age (&gt;/=70 years), sex, and diagnosed hypertens
145  death, severe comorbidity, refusal of care, advanced age (&gt;/=80 years), or prior malignancy.
146                               In our cohort, advanced age (&gt;67) was the strongest predictor of overal
147                                Patients with advanced age (&gt;74 years) had a higher risk of extraction
148 fluenced by limited education (<8 years) and advanced age (&gt;80 years, P < 0.001).
149   Patients with ischaemic stroke who were of advanced age, had increased neurological impairment, or
150                     Whether patients of more advanced age harbor similar risks is unresolved, often c
151                                              Advanced age has repeatedly been identified as an indepe
152 ly associated with 1-year mortality included advanced age (hazard ratio [HR] for >/=95 vs <75 years,
153                               Because of his advanced age, he is not considered a candidate for lung
154 antation risk score, based on combination of advanced age, high HCT-CI, very poor-risk cytogenetic an
155                                        Thus, advanced age, high-fat diet, and decreased CFH induce su
156 nt cardiovascular disease, heart failure, or advanced age (higher risk).
157  to worsen over time and was associated with advanced age, higher baseline insulin level, and hemodyn
158                        Among those with more advanced age, higher pulse pressure was also associated
159      Multivariate analysis demonstrated that advanced age, history of coronary artery disease, prolon
160 sk factors for BI/NAP1/027 infection include advanced age, hospitalization, and exposure to specific
161 mal lipid synthesis in humans and in mice of advanced age (i.e., >75 years in human or >18-24 months
162 combination of a poor performance status and advanced age identified a group of patients with a very
163 w here that CMA activity is maintained until advanced ages if the decrease in the receptor abundance
164 eterminants of poor outcome are factors such advanced age; impaired premorbid health status, especial
165 h in 2 individuals compared with survival to advanced age in 6 individuals).
166 dial infarction was increased in patients of advanced age in both CEA and CAS (OR, 1.64; 95% CI, 1.57
167 ffect the gammadelta T cell compartment with advanced age in humans.
168 lts indicate a decline in whole body EE with advanced age in mice, independent of changes in body wei
169 ll proliferation is severely restricted with advanced age in mice, whether stimulated by partial panc
170 ly associated with increased creatinine, and advanced age in PMF (P < .001) and hemoglobin less than
171 e prophylactic defibrillator implantation at advanced ages in HCM.
172 , and it was driven by positive selection at advanced ages in the presence of microenvironmental decl
173 s, characteristics that are observed only at advanced ages in WT flies.
174 ease in Alpl (-/-) mice prevents analysis at advanced ages, including studies to target rescue of den
175 ty of patients with heart failure presenting advanced age, infirmity, and impaired regenerative capac
176                                              Advanced age is a predictor of death and ventricular dil
177                                              Advanced age is a risk factor for development of and dea
178                                              Advanced age is an important risk factor for discharge t
179                                              Advanced age is associated with a breakdown of the epith
180                                              Advanced age is associated with alterations in innate an
181                                              Advanced age is associated with an increased risk of vas
182                                              Advanced age is associated with immune system deficits t
183       Surprisingly, even though selection at advanced age is expected to be weak, a CD33 allele prote
184 ome progressively impaired with age and that advanced age is itself a significant risk factor for car
185                                              Advanced age is known to impair neovascularization.
186 he hypothesis that attenuation of ROV during advanced age is most effective in proximal branches of m
187 resistance networks, attenuation of ROV with advanced age is most effective in proximal branches via
188         Outcome of treatment for patients of advanced age is often compromised by comorbid conditions
189                                              Advanced age is related to left ventricular (LV) remodel
190                                              Advanced age is the greatest risk factor for neurodegene
191                                              Advanced age is the main risk factor for most chronic di
192                                              Advanced age is the most important risk factor for atria
193 ether this function is impaired in humans of advanced age is unknown.
194  be predicted by clinical factors, including advanced age, ischemic cardiomyopathy, more severe heart
195 ia donor, high Kidney Donor Profile Index or advanced age kidneys are poorer than those with standard
196 ew of outcomes of expanded criteria donor or advanced age kidneys, we assessed the value of the Kidne
197 tically significant recurrence risk factors: advanced age, largest basal diameter, and the use of adj
198 ith a higher revascularization rate, whereas advanced age, left main disease, and smoking were associ
199                                              Advanced age, length of stay, and duration of life suppo
200                                         With advanced age, loss of dilatory signalling mediated throu
201 tients with atrial fibrillation and isolated advanced age, low body weight, or renal dysfunction have
202                      Among baseline factors, advanced age, lower body mass index, poorer performance
203 d in symptomatic heart failure patients with advanced age, male gender, baseline hyperkalemia, renal
204                     Among patients with SVR, advanced age, male gender, cirrhosis, decreased platelet
205                Studies have established that advanced age, male sex, and European ancestry are promin
206                      In prognostic analyses, advanced age, male sex, poorer PS, increasing ratio of p
207 fusal in patients considered "too well" were advanced age, male sex, university hospital admission, c
208 sk factors for complications of GERD include advanced age, male sex, white race, abdominal obesity, a
209 ophagus include chronic GERD, hiatal hernia, advanced age, male sex, white race, cigarette smoking, a
210                                              Advanced age may act as a partial surrogate for conditio
211                  Microvascular adaptation to advanced age may protect endothelial cells during elevat
212 ified 248 patients with Bcc BSI, who were of advanced age (mean, 68 years), chronically ill, and had
213        Patients with class 2 tumors had more advanced age (mean: 64 years vs 57 years; P = .001), had
214 , a similar relationship was present only at advanced ages (men aged > or = 80 years and women aged >
215 ons not meeting enrollment criteria included advanced age, noncardiovascular comorbidities, discharge
216 ring to interval appointments were having an advanced age (odds ratio, 1.02; 95% CI, 1.01-1.04) and k
217 rimordial follicle stage to ensure SCC up to advanced age of mice.
218                        To assess the role of advanced age on survival and dialysis dependency after i
219  the major regionally distributed effects of advanced age on the brain involve reductions in prefront
220    Uncertainty exists about the influence of advanced age on the outcomes of carotid revascularizatio
221 nd is precluded for many patients because of advanced age or comorbidities.
222 or invasive treatments and in the setting of advanced age or complex health status.
223 rse diastolic and longitudinal function with advanced age or elevated load in both sexes, a significa
224                     Each of these groups had advanced age or increased injury severity.
225 tients are poor surgical candidates owing to advanced age or medical comorbidities.
226 ith a limited life expectancy as a result of advanced age or severe comorbidity for whom dialysis wil
227 whether to perform colonoscopy in persons of advanced age or those with comorbid conditions.
228 logy and Chronic Health Evaluation II score, advanced age, or presence of nonrenal organ failures.
229 ndividuals--eg, those with comorbidities, of advanced age, or receiving immunosuppressive treatment--
230 ere demonstrated between SRSF2 mutations and advanced age (P < .01), IDH mutations (P < .01), and hig
231                    On multivariate analysis, advanced age (P = 0.0021), extended resection (P = 0.000
232                                Patients with advanced age (p = 0.01) and descending aorta grafting (p
233                                              Advanced age (P = 0.012), extended resection (P = 0.012)
234 tatistically significant decline of CCT with advanced age (P = 0.02).
235  follow-up was poor, which may be related to advanced age, poor initial VA, and the high incidence of
236 e the ADT Alzheimer's disease association in advanced age populations given the greater potential cli
237 s shared common clinical features, including advanced age, predominantly motor involvement, aggressiv
238 d propensity toward morbidity and mortality (advanced age, presence of cardiovascular risk factors, m
239 matologists frequently encounter patients of advanced age presenting with chronic eczematous eruption
240 ctive therapies is hampered by the fact that advanced age, primary age-related tauopathy or comorbidi
241                We tested the hypothesis that advanced age protects microvascular endothelium by atten
242 to date where hearing loss begins at such an advanced age, providing an opportunity to study both pro
243 ross the genome increased significantly with advanced age (r = 0.224, P =8 x 10(-30)).
244                                              Advanced age, radiographic pneumonia, requirement for ve
245 upheld in other human tissues and reveals an advanced aging rate in tumor tissue.
246                                         With advanced age, rats show deficits on PER-dependent behavi
247 patients with ARVC spans from adolescence to advanced age, reaching its peak between ages 21 and 40 y
248   Nineteen subjects, 12 with intermediate or advanced age-related macular degeneration (AMD) (AREDS c
249 betes (T2D), myocardial infarction (MI), and advanced age-related macular degeneration (AMD) as examp
250 inc supplementation decreases progression to advanced age-related macular degeneration (AMD) in patie
251  vitamins and minerals on the development of advanced age-related macular degeneration (AMD) in perso
252                                              Advanced age-related macular degeneration (AMD) is the l
253                                              Advanced age-related macular degeneration (AMD) is the l
254       To define the role of rare variants in advanced age-related macular degeneration (AMD) risk, we
255 mentation in reducing the risk of developing advanced age-related macular degeneration (AMD).
256 n shown to reduce the risk of progression to advanced age-related macular degeneration (AMD).
257 ciated with progression from intermediate to advanced age-related macular degeneration (AMD).
258 ntermediate and large drusen usually precede advanced age-related macular degeneration (AMD).
259  found to be associated with reduced risk of advanced age-related macular degeneration (AMD).
260 rmediate age-related macular degeneration or advanced age-related macular degeneration (neovascular o
261  successful in preventing the development of advanced age-related macular degeneration by 25%.
262 s and zinc can reduce the risk of developing advanced age-related macular degeneration by about a qua
263 c and antioxidants slowed the progression of advanced age-related macular degeneration in high-risk p
264 etina as well as reducing the progression to advanced age-related macular degeneration in higher risk
265  risk of age-related macular degeneration or advanced age-related macular degeneration in one eye are
266 d 50 to 85 years, at risk for progression to advanced age-related macular degeneration.
267 cts on the primary outcome of progression to advanced age-related macular degeneration.
268 axanthin are associated with a lower risk of advanced age-related macular degeneration.
269 are also associated with a decreased risk of advanced age-related macular degeneration.
270 ay vary in conferred risk for progression to advanced age-related macular disease.
271 hether they induce chronic inflammation with advanced age remains unclear.
272                                     Males of advanced age represent a rapidly growing population at r
273                                Patients with advanced age represent a substantial subgroup of patient
274                                      Because advanced age represents a risk factor for complications
275 obic exercise training, initiated even at an advanced age, restores muscle blood flow distribution pa
276           Exercise training, initiated at an advanced age, reverses age-related diastolic and microva
277                                              Advanced age should not be used as an independent contra
278 to the patient (ie, poor performance status, advanced age, significant weight loss, severe comorbid d
279 inked to coronary artery disease and include advanced age, smoking, diabetes mellitus, hyperlipidemia
280             Independent risk factors include advanced age, smoking, peripheral arterial disease, high
281  neurodegeneration were not observed even at advanced ages, supporting the hypothesis that RNA foci a
282                                              Advanced age, systolic blood pressure, and diabetes were
283 e exhibit a higher fat to lean mass ratio at advanced ages than age-matched wild type mice.
284  IAV-specific CD8(+) T-cell populations with advanced age that parallel age-associated changes in the
285 est that these brain regions are affected by advanced age, the extent to which aging alters appetitiv
286                                         With advanced age, the loss of sensory nerve function and dim
287        Together these data suggest that with advanced age there may be reduced afferent drive from ex
288                                Despite their advanced age, these clones are euglycaemic, insulin sens
289              Among risk factors for CDI, the advanced age threshold was younger for Chinese patients
290 ROV) in skeletal muscle is attenuated during advanced age via alpha-adrenoreceptor (alphaAR) activati
291                                              Advanced age was a major risk factor for all adverse out
292                                              Advanced age was associated with a significantly greater
293                                              Advanced age was associated with greater LV concentricit
294                                              Advanced age was significantly associated with increased
295                                              Advanced age was the strongest risk factor for uterine c
296       As Alzheimer's disease is a disease of advanced age, we hypothesize that older individuals on A
297  addition, multivariable analysis identified advanced age, weight loss, anemia, thrombocytopenia, hyp
298  York Heart Association class IV status, and advanced age were powerful adjusted predictors of poor o
299 l degeneration relative to wild-type mice at advanced ages, when bred on the light-sensitive BALB/c b
300 th concomitant coronary artery disease, with advanced age, with chronic kidney disease, or with valvu

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