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1 1H MRS could serve as a sensitive in vivo surrogate indi
2 1H-MRS spectra were collected at baseline and after trea
3 shop participants for the use of DCE-MRI and 1H MRS in the clinical assessment of antitumor therapies
7 tamate and glutamine (Glx), were measured by 1H MRS in the left dorsolateral prefrontal cortex (l-DLP
15 We validated this technique by comparison of 1H-MRS values of creatine with biopsy assays in an anima
16 mance of this test and the potential role of 1H-MRS in the in-vivo assessment of placental function t
17 ny of the metabolites measured by 31P-MRS or 1H-MRS there was a dose-response relationship with aura
18 oxel proton magnetic resonance spectroscopy (1H MRS) has shown abnormalities in patients with tempora
19 ther proton magnetic resonance spectroscopy (1H MRS) measures of the low-field purine resonance, whic
20 sing proton magnetic resonance spectroscopy (1H MRS), this study assessed whether dysregulation of th
22 d single-voxel proton magnetic spectroscopy (1H-MRS) at 4 Tesla to examine GABA relative to total cre
23 not been considered in proton spectroscopy (1H-MRS) studies and it has not been studied in cerebral
24 and proton magnetic resonance spectroscopy (1H-MRS) as standard follow-up after HSCT with cord blood
26 sively with magnetic resonance spectroscopy (1H-MRS) changes in the concentrations of intracellular (
27 ed hydrogen magnetic-resonance spectroscopy (1H-MRS) on a clinical (1.5 T) magnetic-resonance-imaging
29 oxel proton magnetic resonance spectroscopy (1H-MRS) studies of patients with schizophrenia have foun
30 (TE) proton magnetic resonance spectroscopy (1H-MRS) to measure skeletal muscle acetylcarnitine conce
31 used proton magnetic resonance spectroscopy (1H-MRS) to study in vivo the integrity of axonal fibers
35 l proton magnetic resonance spectroscopy (SV 1H-MRS), coupled with supervised pattern recognition (PR
42 tamate ratio, it is not clear which of these 1H-MRS indices of glutamatergic neurotransmission is alt
44 , and 15 MRI-negative TLE patients underwent 1H MRS at an echo time of 30 msec on a 1.5-T GE Signa sc
46 n GABA in similar brain regions in MDD using 1H-MRS suggest a common reduction in cortical GABA among
48 use models of AD that have been studied with 1H MRS, APP-PS1 mice seem to best match the neurochemica
50 easuring acetylcarnitine concentrations with 1H-MRS is feasible on clinical MR scanners and support t
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