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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.
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
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
16 Seven dogs underwent left L4-S1 dorsal root ganglionectomy (DRG), followed 3 weeks later by transect
18 tely 50%, whereas celiac/superior mesenteric ganglionectomy had no detectable effect on fiber density
24 llel to disease progression, whereas coeliac ganglionectomy led to the disintegration of adventitial
28 s obtained from rats treated with splanchnic ganglionectomy or 6-hydroxydopamine (6-OH-dopamine).
31 nervation was performed by performing celiac ganglionectomy or administration of 6-hydroxydopamine.
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
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