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1 es, which are dysregulated in HIV-associated neurocognitive disorder.
2 cannot be better explained by a pre-existing neurocognitive disorder.
3 t in this population, such as HIV-associated neurocognitive disorder.
4 HIV-1 pathogenesis including HIV-associated neurocognitive disorder.
5 n of neurological function in HIV-associated neurocognitive disorders.
6 nosis and assessment of neuropsychiatric and neurocognitive disorders.
7 nodeficiency Virus type 1 (HIV-1)-associated neurocognitive disorders.
8 omenon that could lead to the development of neurocognitive disorders.
9 ndromes collectively known as HIV-associated neurocognitive disorders.
10 py of Alzheimer's disease and possibly other neurocognitive disorders.
11 ial therapeutic targets for HIV-1-associated neurocognitive disorders.
12 l as in the pathogenesis of HIV-1-associated neurocognitive disorders.
13 roved design of therapies for HIV-associated neurocognitive disorders.
14 reatment can be developed for HIV-associated neurocognitive disorders.
15 tribute to the development of HIV-associated neurocognitive disorders.
16 an effect has been found for HIV-associated neurocognitive disorders.
17 iates a process that causes HIV-1-associated neurocognitive disorders.
18 al nervous system HIV infection and clinical neurocognitive disorders.
19 ng cardiovascular disease, liver disease, or neurocognitive disorders.
20 -affected individuals, and the potential for neurocognitive disorders.
21 n regions have been implicated in a range of neurocognitive disorders.
22 ons such as delirium and other perioperative neurocognitive disorders.
23 en socioeconomic inequalities and subsequent neurocognitive disorders.
24 naptic transmission proteins associated with neurocognitive disorders.
25 al-task system has a high ability to predict neurocognitive disorders.
26 ving with HIV-1 suffer from mild to moderate neurocognitive disorders.
27 ne dysfunction underlies various cancers and neurocognitive disorders.
28 ions which could be the earliest red flag of neurocognitive disorders.
29 therapeutic strategy against HIV-associated neurocognitive disorders.
30 receptor (mAChR) is a biological target for neurocognitive disorders.
31 given that surgery has been associated with neurocognitive disorders.
32 dache, motor disturbances, seizures and even neurocognitive disorders.
33 roles of cAMP and beta-arrestin pathways in neurocognitive disorders.
34 treatment monitoring of neuropsychiatric and neurocognitive disorders.
35 icity and its deficiency was associated with neurocognitive disorders.
36 ed as a mediating factor of HIV-1 associated neurocognitive disorders.
37 current copy number variants associated with neurocognitive disorders.
38 promising novel targets for the treatment of neurocognitive disorders.
39 esents a novel target against HIV-associated neurocognitive disorders.
40 adaptive immune responses to HIV-associated neurocognitive disorders.
41 ators of neurodegeneration in HIV-associated neurocognitive disorders.
42 may offer protection against HIV-associated neurocognitive disorders.
43 ed as a risk determinant of HIV-1-associated neurocognitive disorders.
44 with HIV, and may exacerbate HIV-associated neurocognitive disorders.
45 ls, approximately 60% develop HIV-associated neurocognitive disorders.
46 the brain early in infection and can lead to neurocognitive disorders.
47 nefit for a CNS-T strategy in HIV-associated neurocognitive disorders.
48 nd oxidative stress has been associated with neurocognitive disorders.
49 role in the pathogenesis of HIV-1-associated neurocognitive disorders.
50 s 30.7% (HIV-associated dementia, 3.2%; mild neurocognitive disorder, 12.6%; and asymptomatic neuroco
51 ocognitive disorder, 12.6%; and asymptomatic neurocognitive disorder, 15.0%; HIV- group: 13.9%; P = .
52 95% CI, 12.4%-16.4%]), neurodevelopmental or neurocognitive disorders (5.7% [95% CI, 4.8%-6.5%] to 13
54 e combination antiretroviral therapy (cART), neurocognitive disorders afflict 30-50% of HIV-infected
55 inhibitors confirmed the diagnosis of major neurocognitive disorders; all use of cholinesterase inhi
56 as used to investigate whether patients with neurocognitive disorder and behavioral disturbance (bvNC
59 injury is thought to underlie HIV-associated neurocognitive disorders and contributes to exaggerated
60 ts output values is limited to screening for neurocognitive disorders and does not extend to estimati
63 e to adjunctive treatment for HIV-associated neurocognitive disorders and/or prevent viral rebound in
64 s indicated a possible association with mild neurocognitive disorder, and a score higher than 27 poin
65 lenging disorders as delirium, perioperative neurocognitive disorder, and the sustained cognitive def
66 nst latent HIV-1 infection, HIV-1 associated neurocognitive disorders, and other HIV-1 comorbidities.
67 alth of offspring in later life, among which neurocognitive disorders are among the best described.
70 d had a higher prevalence of CVS plus (CVS + neurocognitive disorders) as compared to adult-onset CVS
71 cular disease, certain types of cancers, and neurocognitive disorders, as well as leaving them expose
72 icating the Toll-like receptors (TLR) in the neurocognitive disorders associated with NeuroAIDS in th
73 EPA, have shown effects in treating mood and neurocognitive disorders by reducing pro-inflammatory cy
74 nflammatory diseases, such as HIV-associated neurocognitive disorders, cancer, and atherosclerosis.
75 ave shown that HIV-infected patients develop neurocognitive disorders characterized by neuronal dysfu
76 ainst the progression to the early stages of neurocognitive disorders (CIND) and facilitate the poten
78 ilst the inter-rater reliability of the mild neurocognitive disorder criteria was modest, it does app
79 vestigate TBI-related pathology in new-onset neurocognitive disorders, depression, and posttraumatic
87 nflammation and symptoms of HIV-1-associated neurocognitive disorder (HAND) - a significant unmet cha
89 s role in immune response and HIV-associated neurocognitive disorder (HAND) has been widely studied.
92 een HIV-1 RNA discordance and HIV-associated neurocognitive disorder (HAND) may reflect compartmental
93 of HIV+ individuals; however, HIV-associated neurocognitive disorder (HAND) occurrence is increasing
97 nodeficiency virus type-1 (HIV-1)-associated neurocognitive disorder (HAND) remains an important neur
99 mpairment (GDS >/= 0.50), and HIV-associated neurocognitive disorder (HAND) using international crite
100 ins of individuals exhibiting HIV-associated neurocognitive disorder (HAND), likely driven by neuroin
101 tribute to the development of HIV-associated neurocognitive disorder (HAND), the prevalence of which
107 erapy (ART), chronic forms of HIV-associated neurocognitive disorders (HAND) affect an estimated 50%
108 by the rising incidence of HIV-1-associated neurocognitive disorders (HAND) among infected individua
110 rent non-infectious models of HIV-associated neurocognitive disorders (HAND) and reveals a precise co
111 clades differentially induce HIV-associated neurocognitive disorders (HAND) and substance abuse is k
113 uman immunodeficiency virus (HIV)-associated neurocognitive disorders (HAND) are not routinely assess
115 at plays an important role in HIV-associated neurocognitive disorders (HAND) by disrupting neurotrans
116 lia play a pathogenic role in HIV-associated neurocognitive disorders (HAND) by instigating primary d
117 uman immunodeficiency virus (HIV)-associated neurocognitive disorders (HAND) can show variable clinic
118 he most challenging issues in HIV-associated neurocognitive disorders (HAND) caused by HIV-1 virotoxi
119 uman immunodeficiency virus (HIV)-associated neurocognitive disorders (HAND) criteria are frequently
121 rvous system (CNS) and causes HIV-associated neurocognitive disorders (HAND) in about half of the pop
122 discusses current concepts of HIV-associated neurocognitive disorders (HAND) in the era of antiretrov
124 uman immunodeficiency virus (HIV)-associated neurocognitive disorders (HAND) is a significant source
127 however, the prevalence of HIV-1-associated neurocognitive disorders (HAND) is still increasing.
128 ecreased, but milder forms of HIV-associated neurocognitive disorders (HAND) persist along with motor
129 ecreased, but milder forms of HIV-associated neurocognitive disorders (HAND) persist along with motor
130 uman immunodeficiency virus (HIV)-associated neurocognitive disorders (HAND) reflect the spectrum of
131 IV infection is now possible, HIV-associated neurocognitive disorders (HAND) remain intractable.
136 vation better correlates with HIV-associated neurocognitive disorders (HAND) than productive HIV-1 in
137 uman immunodeficiency virus (HIV)-associated neurocognitive disorders (HAND) that result from HIV inf
138 The continued prevalence of HIV-associated neurocognitive disorders (HAND) underscores the need for
139 generative diseases such as HIV-1-associated neurocognitive disorders (HAND), Alzheimer's disease (AD
140 he neurodegenerative syndrome HIV-associated neurocognitive disorders (HAND), for which there is no s
141 uman immunodeficiency virus (HIV) associated neurocognitive disorders (HAND), including memory dysfun
142 ted individuals still develop HIV-Associated Neurocognitive Disorders (HAND), indicating that host in
143 process, now referred to as HIV-1-associated neurocognitive disorders (HAND), provides a range of mol
144 of Parkinson's disease and HIV-1 associated neurocognitive disorders (HAND), requiring an inhibitor
146 1 in the brain often leads to HIV associated neurocognitive disorders (HAND), such as encephalitis an
147 ate abusers and patients with HIV-associated neurocognitive disorders (HAND), which is typically exac
148 ogical complications, such as HIV-associated neurocognitive disorders (HAND), which result in cogniti
149 iduals frequently suffer from HIV-associated neurocognitive disorders (HAND), with about 30% of AIDS
150 he most prevalent features of HIV-associated neurocognitive disorders (HAND), yet their origins are u
171 restorative therapeutic for HIV-1 associated neurocognitive disorders (HAND); its therapeutic utility
172 panied with the prevalence of HIV-associated neurocognitive disorders (HANDs) and risk of comorbiditi
174 uman immunodeficiency virus (HIV)-associated neurocognitive disorders (HANDs) remain among the most c
176 The neuropathology underlying HIV-associated neurocognitive disorders has not been well characterized
178 hanges linked with HIV infection and related neurocognitive disorders; however, group-level compariso
179 ber variants (CNVs) are associated with many neurocognitive disorders; however, these events are typi
181 escribe the manifestations of HIV-associated neurocognitive disorder in the era of effective HIV ther
183 in socioeconomic inequalities in relation to neurocognitive disorders in later life and the potential
188 ing or brain DHA are associated with various neurocognitive disorders including Alzheimer's disease (
189 tance use and psychotic disorders, seizures, neurocognitive disorders (including Alzheimer's disease
191 s in impulse control are observed in several neurocognitive disorders, including attention deficit hy
192 ular diseases, cerebrovascular diseases, and neurocognitive disorders, including current knowledge on
194 f GLP-1RAs for the care of people with major neurocognitive disorders, including their individual bra
195 ular diseases, cerebrovascular diseases, and neurocognitive disorders, including vascular cognitive i
196 munodeficiency Virus type-1 (HIV)-associated neurocognitive disorder is characterized by recruitment
198 f the diagnostic criteria for HIV-associated neurocognitive disorders is a cornerstone of the propose
200 and prevention strategies for HIV-associated neurocognitive disorders likely need to be tailored base
201 atest source of years lived with disability: neurocognitive disorders, major depression, schizophreni
203 her sequelae that include nervous system and neurocognitive disorders, mental health disorders, metab
204 ly being used in clinical practice for minor neurocognitive disorder (MND) as well as HAD, despite un
205 ated with a higher risk of investigation for neurocognitive disorders (n = 25 668 children; adjusted
206 ow certainty) as well as proven or suspected neurocognitive disorders (n = 529 205 children; aHR, 1.1
208 t for preventing and treating HIV-associated neurocognitive disorder; nevertheless, clear cerebrospin
209 eted for regular screening for HIV-associate neurocognitive disorder, particularly with tests referab
210 uman immunodeficiency virus (HIV)-associated neurocognitive disorders persist despite suppressive ant
211 rgery and its contribution to peri-operative neurocognitive disorders (PND) is not well understood.
217 itive impairments, that is, HIV-1-associated neurocognitive disorders remain prevalent potentially du
218 ly relevant HIV-associated dementia and mild neurocognitive disorder sensitivity was 100% and specifi
219 -established as valuable tools for detecting neurocognitive disorders such as mild cognitive impairme
220 t cognitive deficits in neuropsychiatric and neurocognitive disorders that are associated with altera
221 t cognitive deficits in neuropsychiatric and neurocognitive disorders that are associated with altera
222 e findings may have a significant impact for neurocognitive disorders that inhibit memory consolidati
223 iatric Association criteria for psychosis in neurocognitive disorders, the Alzheimer's Association In
225 of Ageing (ELSA, n = 4,815), we ascertained neurocognitive disorders using a recognised consensus cr
226 uman immunodeficiency virus (HIV)-associated neurocognitive disorders, we examined persons with acqui
227 uman immunodeficiency virus (HIV)-associated neurocognitive disorders, we quantified HIV type 1 (HIV-
228 of 109 older adults without a diagnosis of a neurocognitive disorder were enrolled in the study; 44 w
229 uding Alzheimer's disease and HIV-associated neurocognitive disorders where APP misprocessing to amyl
230 nces of cardiometabolic, musculoskeletal and neurocognitive disorders, whereas early puberty is assoc
231 good inter-rater reliability apart from mild neurocognitive disorder which was moderate (k = 0.494).
233 g users have an increased risk of developing neurocognitive disorders with increased progression to d
234 brain health issues associated with HIV (eg, neurocognitive disorders), with specific considerations
235 ought to play a causal role in perioperative neurocognitive disorders, yet the role of these lipids i