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1 0 mg or 40 mg of hyoscine butylbromide or no spasmolytic.
2 ly, the five tested ITCs exerted significant spasmolytic activity (on rat distal colon), with PhPeITC
5 ared with control subjects, patients given a spasmolytic had odds of 6.49 for clinically adequate dis
6 refoil family factor 2 (TFF2), also known as spasmolytic peptide, is a low-molecular-weight protein t
10 trefoil auto- and cross-induction, and both spasmolytic polypeptide (SP) and ITF stimulation of gast
11 r (ITF, 59 residues), pS2 (60 residues), and spasmolytic polypeptide (SP, 106 residues) form a small
14 adenocarcinoma are intestinal metaplasia and spasmolytic polypeptide expressing metaplasia (SPEM), de
15 broblasts, loss of parietal and chief cells, spasmolytic polypeptide expressing metaplasia, and dyspl
16 family (pS2, intestinal trefoil factor, and spasmolytic polypeptide) are produced in the mammalian g
17 e described a trefoil factor family 2 (TFF2; spasmolytic polypeptide) expressing metaplasia (SPEM) as
18 refoil factor family 2 (TFF2), also known as spasmolytic polypeptide, is a member of the trefoil fami
19 ntified cellular and molecular mechanisms in spasmolytic polypeptide-expressing (pseudopyloric) metap
22 differentiation factor that correlates with spasmolytic polypeptide-expressing metaplasia (SPEM) in
24 velops in the context of parietal cell loss, spasmolytic polypeptide-expressing metaplasia (SPEM), an
25 emergence of a type of metaplasia designated spasmolytic polypeptide-expressing metaplasia (SPEM).
26 MBT1, were validated as specific markers for spasmolytic polypeptide-expressing metaplasia and intest
28 yntic atrophy, mucous neck cell hyperplasia, spasmolytic polypeptide-expressing metaplasia, dysplasia
30 with DMP-777 leads to the rapid emergence of spasmolytic polypeptide/trefoil factor family 2 (TFF2)-e
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