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1 l open probability, an event associated with chemotherapy-induced peripheral neuropathy.
2 independent predictors of the development of chemotherapy-induced peripheral neuropathy.
3 lity-of-life questionnaire for patients with chemotherapy-induced peripheral neuropathy.
4 re no known effective treatments for painful chemotherapy-induced peripheral neuropathy.
5 tment protocols has the potential to prevent chemotherapy-induced peripheral neuropathy.
6 cularly bortezomib, have significant risk of chemotherapy-induced peripheral neuropathy.
7 ead of VPT measurements in future studies of chemotherapy-induced peripheral neuropathy.
8 s shown to protect axons in animal models of chemotherapy-induced peripheral neuropathy.
9 se effects, in particular nephrotoxicity and chemotherapy-induced peripheral neuropathy.
10 improved the tactile response in a model of chemotherapy-induced peripheral neuropathy.
11 bition has analgesic properties in models of chemotherapy-induced peripheral neuropathy.
12 mechanical and cold allodynia in a model of chemotherapy-induced peripheral neuropathy.
13 eral sclerosis, and neuronal injury, such as chemotherapy-induced peripheral neuropathy.
14 DJ-1 also plays a role in the progression of chemotherapy-induced peripheral neuropathies.
18 Research and Treatment of Cancer (EORTC) QLQ-chemotherapy-induced peripheral neuropathy-20 (CIPN20) i
19 function and this effect is known to mediate chemotherapy-induced peripheral neuropathy and cognitive
20 urotoxicity of cisplatin in rodent models of chemotherapy-induced peripheral neuropathy and explored
21 peutic strategy for the treatment of cancer, chemotherapy-induced peripheral neuropathy, and neurodeg
23 no effective disease-modifying therapies for chemotherapy-induced peripheral neuropathies, but these
25 for Research and Treatment of Cancer (EORTC) Chemotherapy-Induced Peripheral Neuropathy (CIPN) -20 in
28 erapy may be correlated with the severity of chemotherapy-induced peripheral neuropathy (CIPN) after
29 e an understanding of the pathophysiology of chemotherapy-induced peripheral neuropathy (CIPN) and ma
30 enotype in a preclinical model of bortezomib chemotherapy-induced peripheral neuropathy (CIPN) and to
33 and reversed neuropathic pain in a model of chemotherapy-induced peripheral neuropathy (CIPN) in wil
42 tment of CIPN.SIGNIFICANCE STATEMENT Painful chemotherapy-induced peripheral neuropathy (CIPN) is a d
47 uced neuropathic pain.SIGNIFICANCE STATEMENT Chemotherapy-induced peripheral neuropathy (CIPN) is a m
50 hanisms are warranted.SIGNIFICANCE STATEMENT Chemotherapy-induced peripheral neuropathy (CIPN) is a p
63 ancer therapy have improved remission rates, chemotherapy-induced peripheral neuropathy (CIPN) remain
64 ed massage therapy for symptomatic relief of chemotherapy-induced peripheral neuropathy (CIPN) to det
65 n of patients with acute and chronic painful chemotherapy-induced peripheral neuropathy (CIPN), a ser
66 oth prevent and reverse pain associated with chemotherapy-induced peripheral neuropathy (CIPN), a sev
68 e (HRQoL) and alleviate symptoms of fatigue, chemotherapy-induced peripheral neuropathy (CIPN), and g
71 v1.7 are increased in a preclinical model of chemotherapy-induced peripheral neuropathy (CIPN), the m
72 er survivors suffer from intractable painful chemotherapy-induced peripheral neuropathy (CIPN), which
73 y drug paclitaxel (PTX) causes dose-limiting chemotherapy-induced peripheral neuropathy (CIPN), which
77 be useful in the prevention and treatment of chemotherapy-induced peripheral neuropathy in humans.
80 eting of mitochondria.SIGNIFICANCE STATEMENT Chemotherapy-induced peripheral neuropathy is a major, d
85 r, axon loss in most neuropathies, including chemotherapy-induced peripheral neuropathy, is the resul
86 nstellation of neurologic disorders known as chemotherapy-induced peripheral neuropathy, mechanistic
87 fe Questionnaire Core 30 [EORTC QLQ-C30] and Chemotherapy-Induced Peripheral Neuropathy Module [CIPN2
88 tem disorders, particularly those related to chemotherapy-induced peripheral neuropathies or CNS dise
90 ssociated with CFA injection, skin incision, chemotherapy induced peripheral neuropathy, sickle cell
92 t the role of histone deacetylase (HDAC)6 in chemotherapy-induced peripheral neuropathy, through mech