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1 rual syndrome, heavy menstrual bleeding, and dysmenorrhea.
2 been adequately characterized in women with dysmenorrhea.
3 ld female who presented with infertility and dysmenorrhea.
4 .11 cm [95% CI, -0.50 to 0.29 cm]; P = .60), dysmenorrhea (-0.09 cm [95% CI, -0.49 to 0.30 cm]; P = .
5 t there was an association between FGM/C and dysmenorrhea (7,349 FGM/C and 4,411 non-FGM/C participan
8 entify genetic variants associated with both dysmenorrhea and depression, followed by colocalization
10 ggests that depression significantly affects dysmenorrhea and identifies key genes and proteins invol
11 2 was a 14-year-old girl who presented with dysmenorrhea and lower abdominal pain since a few months
13 oses of elagolix were effective in improving dysmenorrhea and nonmenstrual pelvic pain during a 6-mon
15 HWW syndrome presenting with regular menses, dysmenorrhea and painful lump in hypogastric region on t
17 n for depression among women presenting with dysmenorrhea and suggest new targeted preventive strateg
18 who had a clinical response with respect to dysmenorrhea and the proportion who had a clinical respo
19 manage, and refer as needed adolescents with dysmenorrhea and/or chronic pelvic pain (CPP) who are su
20 rning the 3 types of pain (noncyclical pain, dysmenorrhea, and dyspareunia) were analyzed separately
21 The most common presentation is pain and dysmenorrhea, and pain and abdominal mass in the lower a
22 s to explore the link between depression and dysmenorrhea by using an integrated and innovative appro
23 onnaire and visual analogue scales (VAS) for dysmenorrhea, chronic pelvic pain, and deep dyspareunia
26 LUNA did not result in improvements in pain, dysmenorrhea, dyspareunia, or quality of life compared w
29 endometriosis report pelvic pain, including dysmenorrhea, nonmenstrual pelvic pain, and dyspareunia,
30 a significant causal effect of depression on dysmenorrhea ['odds ratio' (95% confidence interval) = 1
33 effect on blood pressure, weight management, dysmenorrhea, postoperative nausea, and chemotherapy-ind
34 who had a clinical response with respect to dysmenorrhea was 46.4% in the lower-dose elagolix group
35 ation site reactions, breast discomfort, and dysmenorrhea were significantly more common in the patch