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1 lity-of-life questionnaire for patients with chemotherapy-induced peripheral neuropathy.
2 re no known effective treatments for painful chemotherapy-induced peripheral neuropathy.
3 tment protocols has the potential to prevent chemotherapy-induced peripheral neuropathy.
4 cularly bortezomib, have significant risk of chemotherapy-induced peripheral neuropathy.
5 ead of VPT measurements in future studies of chemotherapy-induced peripheral neuropathy.
6 independent predictors of the development of chemotherapy-induced peripheral neuropathy.
9 Research and Treatment of Cancer (EORTC) QLQ-chemotherapy-induced peripheral neuropathy-20 (CIPN20) i
10 urotoxicity of cisplatin in rodent models of chemotherapy-induced peripheral neuropathy and explored
12 no effective disease-modifying therapies for chemotherapy-induced peripheral neuropathies, but these
13 for Research and Treatment of Cancer (EORTC) Chemotherapy-Induced Peripheral Neuropathy (CIPN) -20 in
15 e an understanding of the pathophysiology of chemotherapy-induced peripheral neuropathy (CIPN) and ma
16 enotype in a preclinical model of bortezomib chemotherapy-induced peripheral neuropathy (CIPN) and to
29 v1.7 are increased in a preclinical model of chemotherapy-induced peripheral neuropathy (CIPN), the m
30 be useful in the prevention and treatment of chemotherapy-induced peripheral neuropathy in humans.
34 r, axon loss in most neuropathies, including chemotherapy-induced peripheral neuropathy, is the resul
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