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1 aims to characterize the evidence regarding cerebrospinal fluid (1,3)-beta-d-glucan measurement to d
3 lyzed associations between PiB retention and cerebrospinal fluid (CSF) Abeta concentrations in 17 M(+
7 ricles, is considered a disease of excessive cerebrospinal fluid (CSF) accumulation and thereby treat
8 xchange between interstitial fluid (ISF) and cerebrospinal fluid (CSF) along the paravascular spaces
9 is a source of secreted signaling factors in cerebrospinal fluid (CSF) and a key barrier between bloo
10 use brain that manifests as pro-inflammatory cerebrospinal fluid (CSF) and accumulation of ChP macrop
11 quencing (scRNA-Seq) was performed on paired cerebrospinal fluid (CSF) and blood from subjects with r
12 as to evaluate the diagnostic performance of cerebrospinal fluid (CSF) and blood KLK8 for AD and mild
15 use brain interstitial fluid (ISF) and human cerebrospinal fluid (CSF) and chronic sleep deprivation
16 1 (CHI3L1), markers of glial activation, in cerebrospinal fluid (CSF) and plasma and determined the
19 n individual HIV-1 polymerase genomes in the cerebrospinal fluid (CSF) and plasma in individuals with
21 tigated a broad set of protein biomarkers in cerebrospinal fluid (CSF) and plasma using a highly sens
26 d for distribution and antiviral activity in cerebrospinal fluid (CSF) as well as neurocognitive (NC)
27 d for distribution and antiviral activity in cerebrospinal fluid (CSF) as well as neurocognitive (NC)
30 ortality, and B cell phenotypes in blood and cerebrospinal fluid (CSF) by flow cytometry in HIV-infec
31 alitis, diagnosed by detection of VZV DNA in cerebrospinal fluid (CSF) by PCR and concomitant symptom
32 contribute to memory consolidation, whereas cerebrospinal fluid (CSF) clears metabolic waste product
34 dy were to determine longitudinal changes in cerebrospinal fluid (CSF) concentrations of MMPs after a
38 gate whether neurodegenerative biomarkers in cerebrospinal fluid (CSF) differentiate patients with su
39 les approach in order to investigate how the cerebrospinal fluid (CSF) enters the brain through a per
42 e intent of this study was to investigate if cerebrospinal fluid (CSF) from autoimmune encephalitis (
43 ed rat hippocampal neurons were treated with cerebrospinal fluid (CSF) from patients with anti-NMDAR
44 with higher cryptococcal antigen levels, the cerebrospinal fluid (CSF) fungal burden by quantitative
45 agenomic next-generation sequencing (NGS) of cerebrospinal fluid (CSF) has the potential to identify
47 uitary morphologic structure, and aqueductal cerebrospinal fluid (CSF) hydrodynamics relative to spac
48 pituitary deformation, augmented aqueductal cerebrospinal fluid (CSF) hydrodynamics, and expansion o
49 horylation in the choroid plexus and reduces cerebrospinal fluid (CSF) hypersecretion in a model of p
50 bound concentrations of bictegravir (BIC) in cerebrospinal fluid (CSF) in 15 asymptomatic, virologica
51 p-tau) and amyloid-beta (Abeta) 42 levels in cerebrospinal fluid (CSF) in the Amsterdam Dementia Coho
52 t microbiologically confirmed bloodstream or cerebrospinal fluid (CSF) infection between 24 h after r
53 -infection influenced clinical presentation, cerebrospinal fluid (CSF) inflammation, and outcome from
54 (GS) hypothesis states that advective driven cerebrospinal fluid (CSF) influx from the perivascular s
55 erivascular spaces that promotes movement of cerebrospinal fluid (CSF) into the brain and clearance o
62 that is released from erythrocytes into the cerebrospinal fluid (CSF) is suggested to cause vasocons
63 led perivascular spaces (PVS), through which cerebrospinal fluid (CSF) is transported from the subara
64 ctivity (EFA) of Cryptococcus clearance from cerebrospinal fluid (CSF) is used as a surrogate endpoin
65 neither the relationship between plasma and cerebrospinal fluid (CSF) KP metabolites nor their assoc
71 volume, cortical surface area and thickness, cerebrospinal fluid (CSF) levels of amyloid-beta (Abeta(
72 ing the A/T/N classification, relying on the cerebrospinal fluid (CSF) levels of beta-amyloid peptide
75 ogression from normal aging to early AD, and cerebrospinal fluid (CSF) miR-195 levels of MCI subjects
77 lobin-haptoglobin complexes were measured in cerebrospinal fluid (CSF) of 44 patients with aSAH and r
78 d examined the immune cell profiles from the cerebrospinal fluid (CSF) of Neuro-COVID patients compar
80 e blood as well as on ventricular and lumbar cerebrospinal fluid (CSF) of pediatric patients treated
81 lf-lives and permeability into the brain and cerebrospinal fluid (CSF) of recombinant human (rh) proS
83 medications, coexisting medical conditions, cerebrospinal fluid (CSF) opening pressure, treatments,
84 ociated with increased NFL concentrations in cerebrospinal fluid (CSF) or plasma in MCI Abeta+ and AD
85 fied two miR-298 SNPs associated with higher cerebrospinal fluid (CSF) p-tau and lower CSF Abeta42 le
87 ut not significantly different compared with cerebrospinal fluid (CSF) P-tau217, CSF P-tau181, and ta
88 >=100 cells/muL by clinical characteristics, cerebrospinal fluid (CSF) parameters, and 18-week surviv
91 of multiple sclerosis (MS), but whether the cerebrospinal fluid (CSF) profile can help to identify p
93 t genome-wide association study (GWAS) of 59 cerebrospinal fluid (CSF) proteins with a connection to
94 oimaging Initiative (ADNI) participants with cerebrospinal fluid (CSF) Ptau collected at baseline, di
95 h diagnostic value of a second generation of cerebrospinal fluid (CSF) Real-Time Quaking-Induced Conv
97 gadoteric acid (Gd-DOTA) administration into cerebrospinal fluid (CSF) requires pre-contrast data for
98 r change in profile and concentration in the cerebrospinal fluid (CSF) resulted from fluctuations in
99 te the diagnostic accuracy of NAA tests with cerebrospinal fluid (CSF) samples against that of cultur
100 ament light (NFL) chain in serum, plasma and cerebrospinal fluid (CSF) samples collected over 12 mont
102 erial diseases in The Gambia where blood and cerebrospinal fluid (CSF) samples of hospitalized partic
103 tive viral load assays of plasma, semen, and cerebrospinal fluid (CSF) samples to detect HIV-1 RNA.
104 e, and neurologic examination, with elective cerebrospinal fluid (CSF) sampling, brain diffusion tens
105 re used: (1) regression of white matter (WM)/cerebrospinal fluid (CSF) signals only (BASE); (2) WM/CS
106 outcome was the change from baseline in the cerebrospinal fluid (CSF) SOD1 concentration at day 85.
107 Among suspected cases, 16 885 (92.5%) had a cerebrospinal fluid (CSF) specimen collected, 13 625 (80
109 disease (AD) has been suggested in GWASs of cerebrospinal fluid (CSF) tau levels and longitudinal ch
116 t cohorts to identify protein alterations in cerebrospinal fluid (CSF), a proximal site to pathology.
117 beta-amyloid(42) and tau were quantified in cerebrospinal fluid (CSF), and white matter hyperintensi
122 e and is characterized by enlargement of the cerebrospinal fluid (CSF)-filled brain ventricles result
133 rylated at threonine 181 (p-tau), and NFL in cerebrospinal fluid (CSF); and one or more of PET with (
134 rkers of neuroinflammation and injury in the cerebrospinal fluid (tumor necrosis factor-alpha, kynure
139 ersons who underwent lumbar puncture and had cerebrospinal fluid analysis (January 1, 2008-December 3
144 tracranial air (ICA)], water-filled balloon (cerebrospinal fluid and blood) and agarose gel (brain).
145 uencing (mNGS) of RNA and DNA extracted from cerebrospinal fluid and brain tissue now offers another
146 , soluble TREM2 (sTREM2), is abundant in the cerebrospinal fluid and its levels positively correlate
148 able to monitor the changes in DA levels in cerebrospinal fluid and plasma of a mouse model of PD an
149 effector C3 were present at higher levels in cerebrospinal fluid and plasma(8,9) in men than in women
150 cleavage product of TREM2, is elevated in AD cerebrospinal fluid and positively correlates with cogni
155 the recognition of oligoclonal bands in the cerebrospinal fluid as a possible marker of disseminatio
156 She was ultimately found to have sterile cerebrospinal fluid ascites which was treated successful
157 r's disease are accessible only via invasive cerebrospinal fluid assays, and reactive oxygen species
158 In vivo tauopathy has been measured using cerebrospinal fluid assays, but these do not provide inf
159 heir phase II metabolites permeate the blood-cerebrospinal fluid barrier (B-CSF-B) of sheep and to pr
161 luding the blood brain barrier and the blood cerebrospinal fluid barrier, protect the CNS from extern
162 Additional analyses included continuous cerebrospinal fluid biomarker levels to examine the effe
163 to investigate the cognitive impairment and cerebrospinal fluid biomarkers in a follow-up study of p
165 can result in very low folate levels in the cerebrospinal fluid causing childhood neurodegenerative
167 ated tau concentrations in serial samples of cerebrospinal fluid collected from participants who were
170 sed of amyloid beta (Abeta) peptides and the cerebrospinal fluid concentrations of those peptides are
174 nifesting in abnormal cerebral perfusion and cerebrospinal fluid convection, present observation pres
175 ics of the alpha-synuclein aggregates in the cerebrospinal fluid could be used to readily distinguish
176 ositive participants, 3 of whom had negative cerebrospinal fluid CrAg tests from lumbar punctures (LP
179 gh titers of IgG autoantibodies in serum and cerebrospinal fluid directed against the nuclei of Purki
181 in vivo biomarkers of AD, whether by serum, cerebrospinal fluid examination or PET, have transformed
182 atic system, a brain-wide interstitial fluid-cerebrospinal fluid exchange described in rodents, exist
184 athological, clinical, molecular imaging and cerebrospinal fluid features of the most common neurodeg
188 CA assay can discriminate between samples of cerebrospinal fluid from patients diagnosed with Parkins
190 sis secreted higher levels of glutamate, and cerebrospinal fluid glutamine levels were increased.
191 brain ventricular system reported to govern cerebrospinal fluid homeostasis [13, 14], neurogenesis [
192 an adaptive immune response in the blood and cerebrospinal fluid in Alzheimer's disease and provide e
194 es in ratios comparable to those secreted to cerebrospinal fluid in human, however the protocol to ac
195 chemosensitive glial cells that contact the cerebrospinal fluid in the third ventricle and send proc
196 NMDAR antibody seropositive have coexisting cerebrospinal fluid inflammatory changes or other paracl
197 mmune, the presence of GAD antibodies in the cerebrospinal fluid is sufficient to confirm a pathogeni
202 tate at multiple sites of the tau protein in cerebrospinal fluid markers across four decades of disea
203 l cut point, 1.55 SUVR), and comparison with cerebrospinal fluid measures of amyloid-beta (optimal cu
204 ussian mixture modeling, and comparison with cerebrospinal fluid measures of amyloid-beta, specifical
206 ses the technical advantages and pitfalls of cerebrospinal fluid mNGS in the context of patients with
207 c during head and neck movements and promote cerebrospinal fluid motion; however, their role in neuro
209 impairment, and increased protein content in cerebrospinal fluid occurred in anti-Drebrin-seropositiv
210 ens from the brains of people with AD and in cerebrospinal fluid of individuals diagnosed with AD.
212 specificity of clonally expanded TCRs in the cerebrospinal fluid of patients with Alzheimer's disease
213 lonally expanded CD8(+) T(EMRA) cells in the cerebrospinal fluid of patients with Alzheimer's disease
217 he endocannabinoid anandamide is elevated in cerebrospinal fluid of patients with schizophrenia.
220 e screening tool than the currently approved cerebrospinal fluid or amyloid beta positron emission to
222 to amyloid-beta or tau pathology measured in cerebrospinal fluid or by positron emission tomography(2
224 ance imaging or computed tomography imaging, cerebrospinal fluid parameters and clinical endpoints.
225 inical improvement along with a reduction of cerebrospinal fluid parameters was observed after high-d
227 n the processes of notochord development and cerebrospinal fluid physiology, and how defects in those
230 jury biomarker soluble PDGFRbeta(7,8) in the cerebrospinal fluid predicted future cognitive decline i
232 ura mater-surround the CNS, encompassing the cerebrospinal fluid produced by the choroid plexus epith
238 n this study of >2,000 brains and nearly 400 cerebrospinal fluid samples by quantitative proteomics,
239 kynurenine (Kyn) and tryptophan (Trp) in 221 cerebrospinal fluid samples from patients with bacterial
241 metagenomic sequencing testing requested on cerebrospinal fluid samples submitted to an outside refe
245 oton imaging in rodents to show instead that cerebrospinal fluid surrounding the brain enters the tis
247 novel protein changes in Parkinson's disease cerebrospinal fluid that may be exploited for understand
249 source of miR-204 that is released into the cerebrospinal fluid to control number of NSCs within the
251 lammation, and increase AD biomarkers in the cerebrospinal fluid to similar levels observed in patien
252 faster in female youths than in male youths; cerebrospinal fluid volume expanded faster in most cereb
253 mian white matter expansion, and accelerated cerebrospinal fluid volumes expansion of anterior lobule
256 s of aggregates that were amplified from the cerebrospinal fluid were similar to those of aggregates
258 ect alpha-synuclein aggregates in samples of cerebrospinal fluid with high sensitivity and specificit
260 ion of T cells, B cells, and blinatumomab in cerebrospinal fluid, (iv) blinatumomab-induced T-cell ro
261 e chimeric antigen receptor T cells into the cerebrospinal fluid, alone or in combination with azacyt
262 whether nilotinib is safe, and detectable in cerebrospinal fluid, and alters biomarkers and clinical
263 e Mini-Mental Status Exam, protein levels in cerebrospinal fluid, and genotype at the APOE and MAPT l
269 ry of alpha-glucan material in healthy human cerebrospinal fluid, establishing a novel methodological
270 h nonscintigraphic biomarkers from blood and cerebrospinal fluid, have provided an opportunity to inv
271 ll polymeric micelles exhibited stability in cerebrospinal fluid, highlighting the potential for loca
272 cords were excluded, as they did not examine cerebrospinal fluid, included animals, or focused on non
273 Cs) for testing postmortem specimens (blood, cerebrospinal fluid, lung tissue, respiratory tract swab
274 We observed neither SARS-CoV-2 RNA in the cerebrospinal fluid, nor intrathecal IgG synthesis, but
275 as are located adjacent to and bathed by the cerebrospinal fluid, presenting an opportunity for locor
276 ase of levels of neurofilaments in patients' cerebrospinal fluid, suggest that IgLON5 IgG, unlike oth
277 ical microbiology laboratory testing data of cerebrospinal fluid, the expected August/September/Octob
278 tetrameric carrier of thyroxine in blood and cerebrospinal fluid, the pathogenic aggregation of which
279 ut mice have low levels of circulating OT in cerebrospinal fluid, which can be corrected by the oral
280 n of phosphorylated tau and amyloid in their cerebrospinal fluid, yielding neurotypical and preclinic
281 study, we assessed the levels of ventricular cerebrospinal fluid-cfmtDNA (vCSF-cfmtDNA) in a diverse
283 tion of human ChP organoids, which produce a cerebrospinal fluid-like secretion and recapitulate barr
296 The first comprises an interconnected set of cerebrospinal-fluid-contacting DA nuclei surrounding the
297 eding activities in patient biosamples, e.g. cerebrospinal fluids (CSF), and study their correlation
300 ithin the cingulum bundle of hippocampus and cerebrospinal tracts were the most robust deficits in in