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1 ed with healthy control individuals, whereas homovanillic acid (17 studies; SMD, -0.26; 95% CI, -0.39
4 ns of dopamine, and the dopamine metabolites homovanillic acid (HVA) and dihydroxyphenylacetic acid (
5 , 3-4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) and in the DOPAC/dopamine ratio
6 uorescein molecules as the model analyte and Homovanillic acid (HVA) as the target bioanalyte within
7 3, 4-dihydroxyphenylacetic acid (DOPAC), and homovanillic acid (HVA) by 76%, 53% and 40%, respectivel
8 s 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) in caudate nucleus resulting fro
10 kg i.p.) 15 min prior to sacrifice increased homovanillic acid (HVA) levels in the left medial prefro
11 of greater than 10 points and an increase in homovanillic acid (HVA) or 5-hydroxyindoleacetic acid (5
14 SF concentrations of the dopamine metabolite homovanillic acid (HVA) were determined in 30 recently a
15 ne (DA), dihydroxyphenylacetic acid (DOPAC), homovanillic acid (HVA), 5-hydroxyindoleacetic acid (5-H
17 triatal tissue punches were analyzed for DA, homovanillic acid (HVA), and DA activity (HVA/DA) using
18 sma levels of fenfluramine, norfenfluramine, homovanillic acid (HVA), cortisol, and prolactin were de
19 SF) concentration of the dopamine metabolite homovanillic acid (HVA), in an extended inbred vervet mo
20 ions of 5-hydroxyindoleacetic acid (5-HIAA), homovanillic acid (HVA), or 3-methoxy-4-hydroxyphenylgyc
21 , 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA), were elevated over the same tim
22 , 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA), were found to be decreased by >
26 ites, 3,4-dihydroxyphenylalanine (DOPAC) and homovanillic acid (HVA); norepinephrine (NE) and its met
27 [3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA)] levels and tyrosine hydroxylase
29 alyzed cerebrospinal fluid concentrations of homovanillic acid (the major catabolite of dopamine) and
31 ydroxyindoleacetic acid [5-HIAA]), dopamine (homovanillic acid [HVA]), and norepinephrine (3-methoxy-
33 of tetrahydrobiopterin (BH4), neopterin, and homovanillic acid and low levels of tyrosine hydroxylase
34 30, 1994, were eligible for urinary assay of homovanillic acid and vanillylmandelic acid at 3 weeks a
36 of dopamine, 3,4-dihydroxybenzoic acid, and homovanillic acid in GSHPx knock-out mice than those see
38 stored the decreased content of dopamine and homovanillic acid in the nigrostriatal neurons of the ag
43 ograms and urinary vanillylmandelic acid and homovanillic acid measurements were performed during a 9
44 ystonia during treatment, growth hormone and homovanillic acid measures, psychotic symptom activation
46 f tyrosine-metabolizing bacteria to reducing homovanillic acid production, triggered neuroinflammatio
48 catecholamine values, or an increase in the homovanillic acid to vanillylmandelic acid ratio greater
50 of D-cycloserine, relevant amino acids, and homovanillic acid were assayed at baseline and at weeks
51 dopamine, 3,4-dihydroxyphenylacetic acid and homovanillic acid were comparable in the young and aged
52 ine metabolites (5-hydroxyindoleacetic acid, homovanillic acid, and 3-methoxy-4-hydroxyphenethylenegl
53 acetic acid, 3,4-dihydroxyphenylacetic acid, homovanillic acid, and 3-methoxytyramine in addition to
54 the metabolites 3,4-deoxyphenylacetic acid, homovanillic acid, and 5-hydroxyindoleacetic acid were m
55 Aspects of the interaction among thiols, homovanillic acid, and peroxidase are discussed which li
58 CSF measures of 5-hydroxyindoleacetic acid, homovanillic acid, dehydroepiandrosterone, or pregnenolo
60 metabolites, dihydroxyphenylacetic acid and homovanillic acid, increased in the auditory forebrain b
61 bolism to 3,4-dihydroxyphenylacetic acid and homovanillic acid, our results indicate that Met homozyg
62 gamma-aminobutyric acid, 3-methoxytyramine, homovanillic acid, serotonin, histamine, amino acids, an
63 ds (PCLCs): vanillic acid, isovanillic acid, homovanillic acid, syringic acid, syringaldehyde, feruli