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1 , flow, volume, electromyograms of laryngeal abductor and adductor muscles and diaphragm, and, in the
2 ally (C5-C7), along with flexors, extensors, abductors and adductors acting on the digits, hand and w
3 chemia changes laryngeal adductor, laryngeal abductor, and diaphragmatic activities, resulting in cen
5 but not in the abductor pollicis brevis and abductor digit minimi muscles, was reduced to a similar
6 e was tested in two superficial muscles (the abductor digiti minimi (ADM) and the tibialis anterior (
7 on the size of EMG responses elicited in the abductor digiti minimi (ADM) muscle by a subsequent supr
8 l (MEP) of 1 mV in the resting contralateral abductor digiti minimi (ADM) muscle; the second stimulus
11 m first dorsal interosseus muscles (1DI) and abductor digiti minimi brevis (ADMB) muscles for index a
12 ight central motor conduction time (CMCT) to abductor digiti minimi muscle (ADMM) (asymmetry index, 1
13 eus, FDI; abductor pollicis brevis, APB; and abductor digiti minimi, ADM) in order to test its effect
14 muscle action potentials were recorded from abductor digiti minimi, and sensory nerve action potenti
15 different muscles (abductor pollicis brevis, abductor digiti minimi, biceps brachii, tibialis anterio
16 onths old) wild type and mdx mice, and human Abductor Hallucis (AH) and gastrocnemious muscles carryi
17 ii, tibialis anterior, extensor dig. brevis, abductor hallucis) were measured every 3 months on the l
19 sceptibility, osteolysis, bone marrow edema, abductor muscle or tendon abnormality, and Anderson MR g
20 tage pectoral fins have one adductor and one abductor muscle with an endoskeletal disc between them.
22 the anatomy of tendinous attachments of the abductor muscles and the bursal complex of the greater t
23 gnals recorded from the short and long thumb abductor muscles during steady isometric contraction obt
24 were recorded from the short and long thumb abductor muscles of seventy-five children aged from 4 to
25 the interface between familial genotype and abductor phenotype was associated with numerous long-ran
26 motor representations of the right and left abductor pollicis brevis (APB) and flexor carpi radialis
27 We applied low-amplitude vibration to the abductor pollicis brevis (APB) muscle of eight healthy v
28 transcranial magnetic stimulation (TMS) from abductor pollicis brevis (APB), first dorsal interosseou
29 he first dorsal interosseous, but not in the abductor pollicis brevis and abductor digit minimi muscl
30 to evaluate the excitability of the relaxed abductor pollicis brevis muscle (APB) at various interva
35 r the strength of first dorsal interosseous, abductor pollicis brevis, anterior tibialis and triceps
36 hand muscles (first dorsal interosseus, FDI; abductor pollicis brevis, APB; and abductor digiti minim
37 ation were assessed while recording from the abductor pollicis brevis, using a paired pulse TMS parad
44 od at FRC, during which the PCA, a laryngeal abductor, showed a progressive increase in activity acco
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