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1 ycobacterium llatzerense was cultured from a subdiaphragmatic abscess.
2 ar wall of immunodeficient mice (n=11) via a subdiaphragmatic approach.
3 OA) at the thoracic aorta (Zone 1) can limit subdiaphragmatic blood loss and allow for IV fluid resus
4 ls (muCAPs) by electrical stimulation of the subdiaphragmatic branches of the VN.
5                            The volume of the subdiaphragmatic circulation did not increase during con
6 motor neurons that control viscera along the subdiaphragmatic digestive tract, but may also contain n
7                            Ten patients with subdiaphragmatic HD received pelvic and paraaortic RT.
8 gmatic CMAP using a catheter positioned in a subdiaphragmatic hepatic vein seems feasible during cryo
9 d via a quadripolar catheter positioned in a subdiaphragmatic hepatic vein.
10                       The detection rate for subdiaphragmatic nodal metastases on per-region-based an
11  PET/CT detected a higher number of abnormal subdiaphragmatic nodes (P = 0.009).
12 r in magnitude to the inhibition produced by subdiaphragmatic or by coeliac plus coeliac accessory br
13 ical factors, including gravity and negative subdiaphragmatic pressure, carry metastatic cells throug
14 er rates were seen for patients who received subdiaphragmatic radiation therapy (rate ratio [RR], 2.4
15 orectal cancer, which may be associated with subdiaphragmatic radiation therapy and/or alkylating che
16                Patients with HL who received subdiaphragmatic radiotherapy had dose-dependent increas
17 enefits of exposure to both procarbazine and subdiaphragmatic radiotherapy should be weighed carefull
18 oid mesocolon, ileocolic area, and the right subdiaphragmatic space.
19 ate than US (A(z) = 0.86), especially in the subdiaphragmatic spaces and hepatic surfaces.
20 agal afferents regenerate, by 18 weeks after subdiaphragmatic transection, to reinnervate the gut and
21 e if c-FLI expression in the iNTS depends on subdiaphragmatic vagal afferent input to the NTS seconda
22 s potently attenuated by ongoing activity in subdiaphragmatic vagal afferents.
23                 Here, we used a rat model of subdiaphragmatic vagal deafferentation (SDA), the most c
24 for oil was abolished for rats that received subdiaphragmatic vagal deafferentation.
25 ated with CTA expression is not dependent on subdiaphragmatic vagal efferent output or afferent input
26 l baroreceptors, carotid chemo-receptors and subdiaphragmatic vagal inputs eliminated.
27 wall in intact rats or in rats with previous subdiaphragmatic vagal sensory deafferentation.
28                                   Electrical subdiaphragmatic vagal stimulation activated 364 single
29                                      Ventral subdiaphragmatic vagal stimulation elicited frequency-de
30 Sprague-Dawley rats received either complete subdiaphragmatic vagotomies (n = 18) or sham surgeries (
31  male Sprague-Dawley rats underwent complete subdiaphragmatic vagotomies and were injected 18 weeks l
32 l tract, male Sprague-Dawley rats were given subdiaphragmatic vagotomies, sparing only the common hep
33                  Male rats were subjected to subdiaphragmatic vagotomy (or sham surgery) on day 0 and
34 r mesenteric ganglionectomy (CSMG), or total subdiaphragmatic vagotomy (TSV) were exposed to hyperins
35 abeled innervation in nonoperated (control), subdiaphragmatic vagotomy (VAGX), and sham-operated mice
36      Sprague-Dawley rats underwent bilateral subdiaphragmatic vagotomy and were sacrificed 10, 30, or
37                                              Subdiaphragmatic vagotomy blocked the IL-1beta-induced i
38 beta (IL1beta) increases brain IL1beta mRNA; subdiaphragmatic vagotomy blocks this effect.
39                                        Total subdiaphragmatic vagotomy can confound the interpretatio
40                    This study tested whether subdiaphragmatic vagotomy disrupts sickness responses by
41                         It is concluded that subdiaphragmatic vagotomy does not change the rat's ther
42                  We have recently shown that subdiaphragmatic vagotomy enhances bradykinin-induced hy
43                                              Subdiaphragmatic vagotomy has been repeatedly shown to a
44 oeliac branches mimicked the effect of total subdiaphragmatic vagotomy in potentiating the depression
45 in the iNTS by sucrose infusions after total subdiaphragmatic vagotomy in rats with a previously acqu
46                     We studied the effect of subdiaphragmatic vagotomy on plasma ACTH stimulation in
47 , C1-mediated IRI protection persisted after subdiaphragmatic vagotomy or corticosterone receptor blo
48     Adult male Sprague-Dawley rats underwent subdiaphragmatic vagotomy or sham surgery 1 week prior t
49 jection in rats that had undergone bilateral subdiaphragmatic vagotomy or systemic treatment with cap
50 er CTA acquisition, rats underwent bilateral subdiaphragmatic vagotomy or were sham-vagotomized.
51 d by devazepide (0.5 mg kg-1) and by chronic subdiaphragmatic vagotomy performed 10-14 days prior to
52                                              Subdiaphragmatic vagotomy prevented the IL-1-induced inc
53                                              Subdiaphragmatic vagotomy reduced the density of CCK-A r
54 ts (male, Sprague-Dawley) received a partial subdiaphragmatic vagotomy that spared a single branch.
55                 Our results demonstrate that subdiaphragmatic vagotomy triggers transient withdrawal
56                           Here, by combining subdiaphragmatic vagotomy with transcriptomics, chemogen
57 s of the vagus are known to regenerate after subdiaphragmatic vagotomy, but neither the question of w
58                           In rats with acute subdiaphragmatic vagotomy, ghrelin (12 nmol kg(-1) h(-1)
59 oric relaxation was significantly reduced by subdiaphragmatic vagotomy, hexamethonium (20 mg kg(-1))
60                                        Acute subdiaphragmatic vagotomy, intestinal mucosal applicatio
61 ediated sickness responses can be blocked by subdiaphragmatic vagotomy, suggesting that vagal afferen
62                      Fever was unaffected by subdiaphragmatic vagotomy, thus these data provide suppo
63 ateral rhizotomy combined with contralateral subdiaphragmatic vagotomy.
64 ng a unilateral rhizotomy plus contralateral subdiaphragmatic vagotomy.
65 ravasation (PE) that is markedly enhanced by subdiaphragmatic vagotomy.
66 n elicited from both paws was potentiated by subdiaphragmatic vagotomy.
67  pathways have been interrupted by bilateral subdiaphragmatic vagotomy.
68 ted sickness symptoms that can be blocked by subdiaphragmatic vagotomy.
69 ary-adrenal (HPA) axis and is potentiated by subdiaphragmatic vagotomy.
70 m) on gastric contractility was abolished by subdiaphragmatic vagotomy.
71 the motility increase was inhibited by acute subdiaphragmatic vagotomy.
72                   Stimulation of the ventral subdiaphragmatic vagus causes isolated LES relaxation an
73 ls from the ventral and dorsal trunks of the subdiaphragmatic vagus following electrical stimulation
74 d PE was measured in rats with intact or cut subdiaphragmatic vagus nerves.
75 efined, and activated subnuclei with ventral subdiaphragmatic vagus stimulation were detected by c-fo
76 of the afferent and efferent pathways of the subdiaphragmatic vagus to physiology and behavior.
77  of afferent (or efferent) components of the subdiaphragmatic vagus using unilateral rhizotomy combin
78 ectrical stimulation of the ventral trunk of subdiaphragmatic vagus was investigated.
79 oeliac and coeliac accessory branches of the subdiaphragmatic vagus, we tested the hypothesis that th