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1  the posterior dura, peri-occipital skin and neck muscles.
2 lt in hyper-responsiveness to stimulation of neck muscles.
3 ted to be active in our paradigm, and in the neck muscles.
4 e the diaphragmatic, intercostal, spine, and neck muscles.
5 rts of the myocardium and different head and neck muscles.
6 ed after selective peripheral denervation of neck muscles.
7  for the neck, and its activity can contract neck muscles.
8                        Our results show that neck muscle activation increased by 19% when moving the
9                                              Neck muscle activity (p0.1 4.7 vs. 3.0%EMGmax, p0.5 7.4
10 asily applied non-invasive devices assessing neck muscle activity and heart rate (HR) alone could be
11       Here, based on results suggesting that neck muscle activity provides a sensitive indicator of o
12 movement cancellation based on recordings of neck muscle activity while human subjects attempted to c
13 are actively braked by a pulse of antagonist neck muscle activity.
14 rtical activity, eye movements and postural (neck) muscle activity, were disrupted for 3-10 days afte
15 mes.Objectives: To assess the persistence of neck-muscle activity during sleep in patients with COPD
16 cerbation earlier.Conclusions: Sleep-related neck-muscle activity occurs frequently in patients with
17 t neck-muscle activity, those with permanent neck-muscle activity showed more disrupted sleep, had ex
18 mpared with patients with no or intermittent neck-muscle activity, those with permanent neck-muscle a
19 ix of these patients exhibited sleep-related neck-muscle activity, which was intermittent (limited to
20                                   By linking neck muscle and heart development, our findings highligh
21         Very rarely it can affect one of the neck muscles and present as a neck tumor, it can be misd
22 t regions that repress transgene activity in neck muscles and promote differential expression among i
23 applied directly over posterior and anterior neck muscles and tendons.
24                We find that the neck length, neck muscles, and diving speed of the bird predominantly
25 r and lower limbs, torticollis and neck pain/neck muscles, and sialorrhea/parotid and submandibular g
26 re found around the ears, occipital skin and neck muscles; and that administration of inflammatory me
27 th different SHF-derived parts of the heart, neck muscles are clonally distinct from these muscles an
28        The trapezius and sternocleidomastoid neck muscles are formed from progenitor cells that have
29                                              Neck muscles constitute a transition zone between somite
30 e developed a technique to measure posterior neck muscle cross-sectional area (CSA) on volumetric MR
31 ble, valid and reliable method for measuring neck muscle CSA on T1-weighted MR brain scans.
32 principal component explained 72.2% of total neck muscle CSA variance and correlated positively with
33  ICC for between scanner variation for total neck muscle CSA was high at 0.94 (CI 0.86-0.98).
34                                Head and some neck muscles do not derive from somites, but mainly form
35 d hippocampal electroencephalogram (EEG) and neck muscle electromyogram with the electrooculogram and
36  photoactivated in conscious rats while EEG, neck muscle EMG, blood pressure (BP), and breathing were
37 ery had a standardized clinical examination, neck muscle EMG, videofluoroscopic swallow and CT of the
38 rbations.Methods: Video polysomnography with neck-muscle EMG was performed in patients with COPD who
39  preliminary work mapped the distribution of neck muscle fat infiltration (MFI) in the deep cervical
40     This GVS-mediated increased coherence in neck muscles, however, was suppressed during voluntary i
41 ive clonal analysis shows that this group of neck muscles includes laryngeal muscles and a component
42 by spasm or tension of scalp, shoulders, and neck muscles inserted in the occipital region, whereas t
43 ng) stimulus trains was recorded in back and neck muscles, lateral longissimus and splenius before an
44 erature indicates that fat infiltration into neck muscle (MFI) is associated with post-MVC PNPD.
45 F pair of chemosensory neurons and a pair of neck muscle motor neurons, is sufficient to generate rea
46                                          The neck muscles not only stabilize the lovebirds' visual an
47 ses on motoneurons that innervate the flexor neck muscle, rectus capitis anterior (RCA), in the adult
48 bryonic mesoderm populations, the origins of neck muscles remain elusive.
49                             The polysynaptic neck muscle response evoked by TMS of the prefrontal cor
50                                         This neck muscle response resembled that evoked by subsaccadi
51 frequency contributions to vestibular-evoked neck muscle responses could stabilize the head during un
52 nts.SIGNIFICANCE STATEMENT Vestibular-evoked neck muscle responses rely on accurate encoding and tran
53 ed state dependency, with TMS evoking larger neck muscle responses when the stimulated area was activ
54 nformation modulated these vestibular-driven neck muscle responses, we experimentally controlled the
55 nd Tbx1 mutant analysis show that nonsomitic neck muscles share a gene regulatory network with cardia
56  fibres such as the one studied here (bovine neck muscle) show a stack of three or four zigzag layers
57                                              Neck muscles showed increased shared neural drive at res
58                                 Specifically neck muscles showed shared neural drive (intermuscular c
59 tion, velocity, smoothness of neck movement, neck muscle strength, and proprioception (partial correl
60 (NDI), cervical spine range of motion (ROM), neck muscle strength, muscle activation during movement,
61 with earlier studies in the cat hindlimb and neck muscles, these results suggest that the activation
62        Simultaneous measures of behavior and neck muscle tone indicated that bouts of theta occurred
63 tilation compared with high-flow, tachypnea, neck muscle use, abdominal paradox, drowsiness, and inab
64  disordered sensorimotor control of face and neck muscles via ascending and cortical descending proje
65 tromyogram recordings from ocular, face, and neck muscles were also modeled to control for artifacts.
66 ectromyographic activity (EMG) from affected neck muscles were recorded before and immediately after