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1 minutive thoracic or lumbar rib, os centrale carpi and bipartite scaphoid, tripartite patella, left f
2 and surface EMGs were recorded from extensor carpi radialis (ECR) and flexor carpi radialis (FCR) mus
3 the flexor carpi radialis (FCR) and extensor carpi radialis (ECR) muscles of right human forearm was
4 cuted voluntary contractions of the extensor carpi radialis (ECR), and attempted motions in the flexo
6 y of corticospinal projections to the flexor carpi radialis (FCR) and extensor carpi radialis (ECR) m
8 rom extensor carpi radialis (ECR) and flexor carpi radialis (FCR) muscles during motor tasks that eli
9 ft abductor pollicis brevis (APB) and flexor carpi radialis (FCR) muscles in nine normal subjects (th
10 ditioned responses were recorded from flexor carpi radialis (FCR) when the wrist was passively moving
12 erve: thickened leading edge of the extensor carpi radialis brevis (n = 4), prominent radial recurren
13 ae, a thickened leading edge of the extensor carpi radialis brevis, or prominent radial recurrent ves
15 pping of the motor neuron pool of the flexor carpi radialis muscle showed precise re-innervation afte
16 re was no effect on H reflexes in the flexor carpi radialis muscle, even though the amplitude of the
18 ointense to muscle just medial to the flexor carpi radialis tendon (in the expected location of the p
19 motor threshold were recorded from extensor carpi radialis using transcranial magnetic stimulation,
20 with long fibres (brachioradialis, extensor carpi radialis) closely matched patterns of overall fore
21 o the tendon of an antagonist muscle (flexor carpi radialis) during the course of the movement have b
25 ders, with De Quervain syndrome and extensor carpi ulnaris tendon disorders being the most common amo
27 ed RNA-protein interaction detection method (CARPID), which leverages CRISPR-CasRx-based RNA targetin