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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 tered by lowering blood pressure with celiac ganglionectomy.
8 s recorded in rats with bilateral trigeminal ganglionectomy, arguing against a trigeminally mediated
9 a variety of interventions including celiac ganglionectomy as well as open, laparoscopic, or robotic
10 emptying was partially antagonized by celiac ganglionectomy but not by atropine or N(G)-nitro-l-argin
12 on via capsaicin, celiac-superior mesenteric ganglionectomy (CSMG), or total subdiaphragmatic vagotom
13 e of reinnervation and mLTD expression after ganglionectomy, demonstrate that the autonomic-driven ch
15 Seven dogs underwent left L4-S1 dorsal root ganglionectomy (DRG), followed 3 weeks later by transect
17 tely 50%, whereas celiac/superior mesenteric ganglionectomy had no detectable effect on fiber density
25 s obtained from rats treated with splanchnic ganglionectomy or 6-hydroxydopamine (6-OH-dopamine).
29 ation, neonatal unilateral superior cervical ganglionectomy, or unilateral ganglionectomy on postnata
30 superior cervical ganglia because unilateral ganglionectomy, performed when cholinergic reinnervation
31 nervation of the adrenal gland by suprarenal ganglionectomy prevented vagotomy-induced decrease in ba
32 ation of hippocampus (Medial septal lesion + ganglionectomy; SAP + Gx) but also in hippocampal sympat
34 ected to either unilateral superior cervical ganglionectomy (SCGectomy), unilateral transection of th
35 are prevented by bilateral superior cervical ganglionectomy, which also prevents the noradrenergic sy
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