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1 otions was stronger in control subjects than migraineurs.
2 lved to a greater degree in female than male migraineurs.
3 the interaction of CGRP with its receptor in migraineurs.
4 aine with aura occurs in up to 20-30% of all migraineurs.
5 Severe CA occurred in 20.4% of migraineurs.
6 ormal cerebral cortical energy metabolism in migraineurs.
7 nitroglycerin [glyceryl trinitrate (GTN)] to migraineurs.
8 rmed during spontaneous visual auras in four migraineurs.
9 cribed the general health characteristics of migraineurs.
10 ell as enhanced vulnerability to ischemia in migraineurs.
11 e increased risk for vascular diseases among migraineurs.
12 ance images of the brain were acquired in 63 migraineurs and 18 matched healthy control subjects.
13 n-based genome-wide analysis including 5,122 migraineurs and 18,108 non-migraineurs, rs2651899 (1p36.
14 nt functional differences in male and female migraineurs and a sex-specific pattern of functional con
15 s delayed migraine attacks when infused into migraineurs and also causes iNOS expression and delayed
19 emale age-matched interictal (migraine free) migraineurs and matched healthy controls to determine al
21 rmeability of the blood-brain barrier in six migraineurs and six control subjects at rest and during
24 e affects approximately 50% to 60% of female migraineurs, but knowledge regarding the role of hormone
25 e following thalamic nuclei were observed in migraineurs: central nuclear complex (F(1,233) = 6.79),
26 ons on either interictal or ictal changes in migraineurs compared with controls, largely because of m
31 ine is a subjective phenomenon, and what the migraineur experiences is necessarily inaccessible to ot
32 mes and vibrotactile detection thresholds of migraineurs failed to differentiate them from controls,
35 iting increases in brain NO concentration in migraineurs have not yet been identified, although, anim
39 s including 5,122 migraineurs and 18,108 non-migraineurs, rs2651899 (1p36.32, PRDM16), rs10166942 (2q
41 ons akin to spreading depression predisposes migraineurs to infarction during mild ischemic events, t
43 as used to assess between-group comparisons (migraineurs vs control subjects, the aura effect, the ef
46 l functional and structural abnormalities in migraineurs, which may contribute to hyperexcitability a
49 ce of high noise levels, with performance of migraineurs with aura significantly poorer (P < 0.05) th
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