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3 ally, perivascular adipose tissue (PVAT) and perirenal adipose tissue (PRAT) depots influence cardiov
4 -beta, -gamma; and GR in female but not male perirenal adipose tissue and in male but not female live
5 c responsiveness becomes desensitized in the perirenal adipose tissue of IUGR fetuses and lambs by me
10 ly communicated with each other and with the perirenal and anterior and posterior pararenal spaces of
11 vel by 11.4% and 12.4%, respectively, in the perirenal and epididymal white adipose tissue (PWAT, EWA
12 ntralipid elicited mild inflammation in both perirenal and omental fat by increasing the expression o
13 sity include kidney compression by visceral, perirenal and renal sinus fat; increased renal sympathet
16 of interest (ROIs), automated elliptical and perirenal background ROIs and no background correction a
18 653 for 5 days, preadipocytes from the human perirenal depot accumulated lipid, and a proportion of c
19 human pre-adipocytes, particularly from the perirenal depot, showed a marked increase in UCP-1 expre
21 d in adipose tissues including perivascular, perirenal, epididymal, subcutaneous and brown adipose ti
22 ed (P<0.05) subcutaneous, intramuscular, and perirenal fat deposition, and induced hyperglycemia, hyp
23 chow diet from weaning, exhibited increased perirenal fat pad mass relative to body weight and adipo
26 abolic syndrome related to liver, heart, and perirenal fat volume; fat content in subcutaneous fat in
28 nal amplitudes of the thermal ablation zone, perirenal fat, and normal renal cortex on the MR images.
32 lem with the interpretation of the images of perirenal haematoma is their ability to change in time.
33 the renal parenchyma, who were suspected of perirenal haematoma, underwent a CE-US examination after
34 gnificant, difference in the echogenicity of perirenal haematomas compared to the routine examination
35 s to assess the echogenicity and the size of perirenal haematomas in patients after kidney transplant
37 sion from urinothorax and late effusion from perirenal lymphocele years after kidney transplantation.
38 Immunohistochemical analysis of perigonadal, perirenal, mesenteric, and subcutaneous adipose tissue r
39 located in the psoas (n = 25, 55.3%), renal-perirenal (n = 7, 14.8%), and pararenal (n = 14, 29.7%)
41 associated with the lateral, elliptical and perirenal ROIs were not significantly different from zer
42 n the mouse WAT depots examined (epididymal, perirenal, s.c., and mammary gland) and in interscapular
43 ight anterior pararenal space (n = 8), right perirenal space (n = 7), right posterior pararenal space
46 assessment of the size of haematomas in the perirenal space that appeared during early post-operativ
47 thway to the free spread of disease from the perirenal space to the central retroperitoneum or from t
52 tion, perfusion index, regional cerebral and perirenal tissue oxygenation, heart rate, transcutaneous
53 sectioned from proximal to distal including perirenal tissues and examined after paraffin embedding,