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1 ected to chronic bilateral superior cervical ganglionectomy.
2  and during reinnervation following neonatal ganglionectomy.
3 ignificantly attenuated by superior cervical ganglionectomy.
4 tion fields ipsilateral to unilateral nodose ganglionectomy.
5 patients undergoing arthrodesis surgery with ganglionectomy.
6 tered by lowering blood pressure with celiac ganglionectomy.
7                            Superior cervical ganglionectomy and sympathetic decentralization signific
8 oscopic, or robotic ligament release; celiac ganglionectomy; and celiac artery revascularization.
9 s recorded in rats with bilateral trigeminal ganglionectomy, arguing against a trigeminally mediated
10  a variety of interventions including celiac ganglionectomy as well as open, laparoscopic, or robotic
11 emptying was partially antagonized by celiac ganglionectomy but not by atropine or N(G)-nitro-l-argin
12       This staining disappeared after nodose ganglionectomy, consistent with a presynaptic function.
13 on via capsaicin, celiac-superior mesenteric ganglionectomy (CSMG), or total subdiaphragmatic vagotom
14 e of reinnervation and mLTD expression after ganglionectomy, demonstrate that the autonomic-driven ch
15                Sympathetic superior cervical ganglionectomy did not abolish label in the SCN after in
16  Seven dogs underwent left L4-S1 dorsal root ganglionectomy (DRG), followed 3 weeks later by transect
17 tphal nucleus ablation and superior cervical ganglionectomy eliminated infection of the SCN.
18 tely 50%, whereas celiac/superior mesenteric ganglionectomy had no detectable effect on fiber density
19          Lowering blood pressure with celiac ganglionectomy in SHRs did not alter the increased CK2al
20          Lowering blood pressure with celiac ganglionectomy in SHRs did not alter the increased level
21           Using unilateral superior cervical ganglionectomy in wild-type C57BL/6 mice, we showed that
22                     In addition, sympathetic ganglionectomy increases meal frequency and lowers satie
23                           Following neonatal ganglionectomy, intracranial fibers of contralateral ori
24 llel to disease progression, whereas coeliac ganglionectomy led to the disintegration of adventitial
25                               Neither nodose ganglionectomy nor vagotomy altered the CB1 receptor ter
26 erior cervical ganglionectomy, or unilateral ganglionectomy on postnatal day 30.
27                          Second, using L6-S1 ganglionectomies or L6-S1 ventral root rhizotomies we li
28 s obtained from rats treated with splanchnic ganglionectomy or 6-hydroxydopamine (6-OH-dopamine).
29 s obtained from rats treated with splanchnic ganglionectomy or 6-OH-dopamine.
30 s obtained from rats treated with splanchnic ganglionectomy or 6-OH-dopamine.
31 nervation was performed by performing celiac ganglionectomy or administration of 6-hydroxydopamine.
32             We further show that sympathetic ganglionectomy or pharmacological blockade of beta2-adre
33 ation, neonatal unilateral superior cervical ganglionectomy, or unilateral ganglionectomy on postnata
34 superior cervical ganglia because unilateral ganglionectomy, performed when cholinergic reinnervation
35 nervation of the adrenal gland by suprarenal ganglionectomy prevented vagotomy-induced decrease in ba
36 ation of hippocampus (Medial septal lesion + ganglionectomy; SAP + Gx) but also in hippocampal sympat
37 renergic fibers (Medial septal lesion + sham ganglionectomy; SAP + IG).
38 ected to either unilateral superior cervical ganglionectomy (SCGectomy), unilateral transection of th
39 are prevented by bilateral superior cervical ganglionectomy, which also prevents the noradrenergic sy