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1 1H MRS could serve as a sensitive in vivo surrogate indi
2 1H-MRS of the medial prefrontal cortex was obtained in 2
3 1H-MRS scans were acquired to assess pgACC glutamate lev
4 1H-MRS showed adequate discriminant validity, but limite
5 1H-MRS spectra were collected at baseline and after trea
6 shop participants for the use of DCE-MRI and 1H MRS in the clinical assessment of antitumor therapies
11 tamate and glutamine (Glx), were measured by 1H MRS in the left dorsolateral prefrontal cortex (l-DLP
23 We validated this technique by comparison of 1H-MRS values of creatine with biopsy assays in an anima
24 mance of this test and the potential role of 1H-MRS in the in-vivo assessment of placental function t
25 ny of the metabolites measured by 31P-MRS or 1H-MRS there was a dose-response relationship with aura
26 oxel proton magnetic resonance spectroscopy (1H MRS) has shown abnormalities in patients with tempora
27 ther proton magnetic resonance spectroscopy (1H MRS) measures of the low-field purine resonance, whic
28 sing proton magnetic resonance spectroscopy (1H MRS), this study assessed whether dysregulation of th
30 d single-voxel proton magnetic spectroscopy (1H-MRS) at 4 Tesla to examine GABA relative to total cre
31 not been considered in proton spectroscopy (1H-MRS) studies and it has not been studied in cerebral
32 and proton magnetic resonance spectroscopy (1H-MRS) as standard follow-up after HSCT with cord blood
34 sively with magnetic resonance spectroscopy (1H-MRS) changes in the concentrations of intracellular (
35 ard, proton magnetic resonance spectroscopy (1H-MRS) has been used as a non-invasive alternative to q
37 ed hydrogen magnetic-resonance spectroscopy (1H-MRS) on a clinical (1.5 T) magnetic-resonance-imaging
40 r of proton magnetic resonance spectroscopy (1H-MRS) studies in patients with first-episode psychosis
41 oxel proton magnetic resonance spectroscopy (1H-MRS) studies of patients with schizophrenia have foun
42 for proton magnetic resonance spectroscopy (1H-MRS) studies reporting glutamate, glutamine or Glx in
43 (TE) proton magnetic resonance spectroscopy (1H-MRS) to measure skeletal muscle acetylcarnitine conce
44 used proton magnetic resonance spectroscopy (1H-MRS) to study in vivo the integrity of axonal fibers
48 l proton magnetic resonance spectroscopy (SV 1H-MRS), coupled with supervised pattern recognition (PR
51 tudy used a cross-sectional design using 3-T 1H-MRS in participants not taking MDD medication recruit
57 tamate ratio, it is not clear which of these 1H-MRS indices of glutamatergic neurotransmission is alt
59 , and 15 MRI-negative TLE patients underwent 1H MRS at an echo time of 30 msec on a 1.5-T GE Signa sc
60 olerant control subjects (n = 128) underwent 1H-MRS to measure IMCL and muscle volume, whole-body ins
64 n GABA in similar brain regions in MDD using 1H-MRS suggest a common reduction in cortical GABA among
68 use models of AD that have been studied with 1H MRS, APP-PS1 mice seem to best match the neurochemica
70 easuring acetylcarnitine concentrations with 1H-MRS is feasible on clinical MR scanners and support t