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1 , flow, volume, electromyograms of laryngeal abductor and adductor muscles and diaphragm, and, in the
2  HHS and WOMAC scores, rapid recovery of hip abductor and flexor strength, and enhanced limp recovery
3 ally (C5-C7), along with flexors, extensors, abductors and adductors acting on the digits, hand and w
4 chemia changes laryngeal adductor, laryngeal abductor, and diaphragmatic activities, resulting in cen
5 ral spatial segregation between adductor and abductor cell bodies in the spinal cord.
6  but not in the abductor pollicis brevis and abductor digit minimi muscles, was reduced to a similar
7 e was tested in two superficial muscles (the abductor digiti minimi (ADM) and the tibialis anterior (
8 on the size of EMG responses elicited in the abductor digiti minimi (ADM) muscle by a subsequent supr
9 l (MEP) of 1 mV in the resting contralateral abductor digiti minimi (ADM) muscle; the second stimulus
10  (APB), first dorsal interosseous (FDI), and abductor digiti minimi (ADM) muscles.
11  the first dorsal interosseous (FDI) and the abductor digiti minimi (ADM).
12 ence Po2 and pH sensors were inserted in the abductor digiti minimi (V).
13 m first dorsal interosseus muscles (1DI) and abductor digiti minimi brevis (ADMB) muscles for index a
14 ight central motor conduction time (CMCT) to abductor digiti minimi muscle (ADMM) (asymmetry index, 1
15 7 Hz or 40 Hz (control conditions) while the abductor digiti minimi or the tibialis anterior muscle w
16 eus, FDI; abductor pollicis brevis, APB; and abductor digiti minimi, ADM) in order to test its effect
17  muscle action potentials were recorded from abductor digiti minimi, and sensory nerve action potenti
18 different muscles (abductor pollicis brevis, abductor digiti minimi, biceps brachii, tibialis anterio
19  = 0.611/TL: P = 0.011, R = 0.525), and knee abductors during SLL (IC: P = 0.021, R = 0.474) were pos
20 onths old) wild type and mdx mice, and human Abductor Hallucis (AH) and gastrocnemious muscles carryi
21 peak activation of the intrinsic foot muscle abductor hallucis was unchanged (p = 0.31).
22 ii, tibialis anterior, extensor dig. brevis, abductor hallucis) were measured every 3 months on the l
23 s to assess the local fatigue effects of the abductor hip muscles on the functional profile during a
24 al fold paralysis affecting the adductor and abductor laryngeal muscles.
25 ip increased (trading off with decreased hip abductor moment arms).
26 sceptibility, osteolysis, bone marrow edema, abductor muscle or tendon abnormality, and Anderson MR g
27 tage pectoral fins have one adductor and one abductor muscle with an endoskeletal disc between them.
28 motor units recorded from the long and short abductor muscles acting on the same thumb.
29  the anatomy of tendinous attachments of the abductor muscles and the bursal complex of the greater t
30 gnals recorded from the short and long thumb abductor muscles during steady isometric contraction obt
31                        The main adductor and abductor muscles masses of the pectoral system are compl
32  were recorded from the short and long thumb abductor muscles of seventy-five children aged from 4 to
33                    Findings suggest that hip abductor muscles' local fatigue produces a significant e
34 etic horse's respiratory system: as the sole abductors of the airways, they maintain the size of the
35  the interface between familial genotype and abductor phenotype was associated with numerous long-ran
36  motor representations of the right and left abductor pollicis brevis (APB) and flexor carpi radialis
37    We applied low-amplitude vibration to the abductor pollicis brevis (APB) muscle of eight healthy v
38 transcranial magnetic stimulation (TMS) from abductor pollicis brevis (APB), first dorsal interosseou
39 he first dorsal interosseous, but not in the abductor pollicis brevis and abductor digit minimi muscl
40  to evaluate the excitability of the relaxed abductor pollicis brevis muscle (APB) at various interva
41  were the index finger (sensory studies) and abductor pollicis brevis muscle (motor studies).
42 vation of the cortical representation of the abductor pollicis brevis muscle.
43 ompound action potentials were recorded from abductor pollicis brevis muscle.
44                               Median CMCT to abductor pollicis brevis was 14.8 ms (range 8.8-27.4 ms)
45                       Six different muscles (abductor pollicis brevis, abductor digiti minimi, biceps
46 r the strength of first dorsal interosseous, abductor pollicis brevis, anterior tibialis and triceps
47 hand muscles (first dorsal interosseus, FDI; abductor pollicis brevis, APB; and abductor digiti minim
48 ation were assessed while recording from the abductor pollicis brevis, using a paired pulse TMS parad
49  muscle action potentials were recorded from abductor pollicis brevis.
50 pound muscle action potentials recorded from abductor pollicis brevis.
51  muscle action potentials were recorded from abductor pollicis brevis.
52 cle action potentials were recorded from the abductor pollicis brevis.
53 pound muscle action potentials recorded from abductor pollicis brevis.
54 th voice onset after voiceless consonants in abductor SD.
55 od at FRC, during which the PCA, a laryngeal abductor, showed a progressive increase in activity acco
56           DAA had more rapid recovery of hip abductor strength at 1-month (p = 0.03) and hip flexor s
57 7 of 100), effusion (20 of 40 vs 26 of 100), abductor tendon lesion (22 of 40 vs 62 of 100), or bursi
58        The presence of bone marrow edema and abductor tendon tears but not the presence or size of ps
59 m hip-based to knee-based locomotion and hip-abductor to hip-rotator balancing mechanisms inherited b
60 relative weakness (lower MRC score) in thumb abductors versus elbow extensors, for hand extensors ver
61 specificity, 94%; LR, 5.7 [95% CI, 1.6-20]), abductor weakness (sensitivity, 44%; specificity, 90%; L