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1 frequently with lopinavir-ritonavir, mainly gastrointestinal disturbance.
2 ith off-target effects, including nausea and gastrointestinal disturbance.
3 icities, peripheral neuropathy, fatigue, and gastrointestinal disturbances.
4 MMF for infection, myelosuppression, and/or gastrointestinal disturbances.
5 MMF for infection, myelosuppression, and/or gastrointestinal disturbances.
6 to further unravel the nature of the chronic gastrointestinal disturbances.
7 tanding of how sleep disturbances arise from gastrointestinal disturbances.
9 most common drug-related adverse events were gastrointestinal disturbances and increased serum creati
11 heral artery disease (nilotinib, ponatinib), gastrointestinal disturbance (bosutinib), or increased a
12 ctors of infection is their association with gastrointestinal disturbances, but this relationship to
13 n in distal extremities including joints and gastrointestinal disturbances, but was absent from an as
14 anemia, 14%; and thrombocytopenia, 23%) and gastrointestinal disturbances (diarrhea, any grade, 72%;
16 ers seeking medical care have a diagnosis of gastrointestinal disturbance in approximately one-third
17 and impaired gut motility) that explains the gastrointestinal disturbances in patients with FOXP1 syn
19 he cause of chronic unexplained diarrhea and gastrointestinal disturbances in transplant patients.
20 ourse involved recurrent febrile illness and gastrointestinal disturbance, lacking an infective cause
21 effects, including anemia, thrombocytopenia, gastrointestinal disturbances, metabolic abnormalities,
22 production (montelukast, n=6; placebo, n=2), gastrointestinal disturbance (montelukast, n=3; placebo,
23 t short shedding events were often linked to gastrointestinal disturbances, our results help explain
24 protease inhibitors currently in use include gastrointestinal disturbances, paraesthesias, hyperbilir
27 ity with azathioprine (five [15%] of 34) and gastrointestinal disturbances (seven [15%] of 48) with m
28 imal performance included these factors plus gastrointestinal disturbance, severe neutropenia, and pr
29 such as bulbar dysfunction, hearing loss and gastrointestinal disturbance should help prioritize gene
31 frequent dosing schedules or elimination of gastrointestinal disturbances, the most common adverse e