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1 sponsible for the crotamine-induced skeletal muscle spasm.
2 SCI restoration of neuronal excitability and muscle spasms.
3 mished by maladaptive changes that can cause muscle spasms.
5 drug-related adverse effects, most commonly muscle spasms (12 patients), weight loss (10), dysgeusia
6 y, patients receiving etelcalcetide had more muscle spasms (12.0% and 11.1% vs 7.1% and 6.2% with pla
7 differences between arms (PAG v AG) included muscle spasms (13% v 1%), neutropenia (29% v 18%), and m
8 ients), hypertension (22 [12%] vs six [3%]), muscle spasms (22 [12%] vs seven [4%]), acne (20 [11%] v
9 e events reported with teprotumumab included muscle spasms (25%), nausea (17%), alopecia (13%), diarr
10 se events (AEs) of diarrhea (34.7% v 22.8%), muscle spasms (28.6% v 11.9%), hypertension (25.5% v 14.
11 in 491 (98%) patients; the most common were muscle spasms (317 [64%]), alopecia (307 [62%]), dysgeus
12 reported adverse events with bimagrumab were muscle spasms (32 [51%] in the bimagrumab 10 mg/kg group
14 most common grade 1 or 2 complications were muscle spasm (76%), followed by dysgeusia (57%), alopeci
15 adelpar 50 mg and one on seladelpar 200 mg), muscle spasms (8%; three patients on seladelpar 200 mg),
18 nes are used for treating anxiety, epilepsy, muscle spasm, alcohol withdrawal, palliation, insomnia,
19 occurring in more than 30% of patients were muscle spasms, alopecia, dysgeusia (taste disturbance),
20 CT scanning to minimize the degree of smooth-muscle spasm and peristalsis and to reduce the patient's
21 ctomy would create a prolonged inhibition of muscle spasm and postoperative pain, facilitating tissue
24 m Clostridium tetani and is characterised by muscle spasms and autonomic nervous system dysfunction.
25 assisted ventilation and of drugs to control muscle spasms and cardiovascular instability within the
28 ions of cannabis in the treatment of painful muscle spasms and other symptoms of multiple sclerosis a
29 3-20 Hz correlated with the strength of the muscle spasms and preceded them by approximately 320 ms.
30 use/facial muscles, migraine/facial and head muscles, spasms and spasticity/upper and lower limbs, to
32 hralgia, urinary tract infection, back pain, muscle spasms, and dyspepsia were higher with ibrutinib,
34 ion, diarrhea, peripheral edema, hemorrhage, muscle spasms, and pneumonia, as well as adverse events
37 s also useful for treatment of spasticity or muscle spasms associated with several clinical condition
38 worse treatment-related adverse events were muscle spasms (four [4%] patients in treatment group A v
39 aemia, and strokes with anastrozole and more muscle spasm, gynaecological cancers and symptoms, vasom
40 s characterized by muscle rigidity, episodic muscle spasms, high titers of antibodies against glutami
42 e as free doxorubicin injections in reducing muscle spasms in blepharospasm patients but with increas
43 ion, anxiety, mood swings, severe headaches, muscle spasms, interphalangeal joint stiffness, decrease
47 hototherapeutic applications to safely treat muscle spasms, pain, anxiety, sleep disorders, and epile
48 s in the placebo group), with hypocalcaemia, muscle spasm, paraesthesias, headache, and nausea being
49 s (muscle stiffness, pain and discomfort and muscle spasms,), physical impact (activities of daily li
50 the number of injections needed for patient muscle spasm relief, decreasing the risk of negative sid
51 f baclofen on spasticity (e.g. management of muscle spasms that may otherwise hinder movement or soci
53 ith uncontrolled falls, and episodic painful muscle spasms triggered by anxiety, task-specific phobia