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1 evoked potentials (MEPs) were measured from biceps.
2 s measured by motor evoked potentials in the biceps.
4 aying of the articular aspect of the labrum, biceps anchor avulsion, inferiorly displaced bucket hand
7 ssed between affected and control samples of biceps and deltoid muscle tissues, respectively, with 29
8 genic cells and muscle biopsies derived from biceps and deltoid muscles of FSHD affected subjects and
11 spinal conditioning of the stretch reflex of biceps and quadriceps was abnormal in both hemizygous ma
12 cluded transverse and longitudinal images of biceps and supraspinatus tendons and articular cartilage
17 study, the best directions of SMUs in human biceps (both heads) and deltoid (anterior, medial, and p
18 r (Pmajor) and posterior deltoid (Pdeltoid); biceps brachii (Bi) and Tri brachii (Tri), and linking m
19 e recorded in the surface EMG of contracting biceps brachii (Bi), evoked by taps applied to the tendo
23 e acquired high-density EMG signals from the biceps brachii in 5 male transhumeral amputees who under
25 rected to the motor cortex representation of biceps brachii muscle during the adaptation phase of the
26 same recordings were also performed from the biceps brachii muscle of additional 5 able-bodied indivi
28 hibition (ICI) and facilitation (ICF) to the biceps brachii muscle proximal to the level of deafferen
31 magnetic stimulation (TMS) in small hand and biceps brachii muscles before, during and after INB of t
32 array was used to record surface EMG of the biceps brachii muscles from both impaired and non-impair
34 he rotator interval and the long head of the biceps brachii tendon are anatomically closely associate
37 mous, monosynaptic Group Ia projections from biceps brachii to both the antagonist triceps brachii an
39 scharge characteristics of 53 motor units in biceps brachii were recorded after being recruited durin
41 erent input were observed in the homonymous (biceps brachii) and antagonist (triceps brachii) motor n
42 tor pollicis brevis, abductor digiti minimi, biceps brachii, tibialis anterior, extensor dig. brevis,
43 post-stroke patients with spasticity of the biceps brachii, we found involuntary microscopic contrac
44 ed in the finger and wrist extensors and the biceps, but no response or inhibitory responses were obs
45 before click (Bi-10ms-C); click 25 ms before biceps (C-25ms-Bi); click alone (C only); and biceps alo
46 tion of RVR was seen during 15 s involuntary biceps contractions (engages only muscle reflexes) and L
48 xteen subjects performed 36 elbow flexions ("biceps curls") at one of two submaximal workloads that e
50 re evaluated in the Semimembranosus (SM) and Biceps femoris (BF) muscles of pork legs for composition
51 luate its potential for discrimination among biceps femoris and semimembranosus muscle from two hams,
53 chium and semimembranosus (SM) and conjoined biceps femoris and semitendinosus (BF-ST) tendons and ev
57 branosus, Semitendinosus, Rectus femoris and Biceps femoris muscles of the hams was computed and expr
62 trodes were implanted into vastus lateralis, biceps femoris posterior, lateral gastrocnemius and tibi
65 tivation of erector spinae, gluteus maximus, biceps femoris, soleus and intrinsic foot (toe flexor) m
66 lation elicited responses bilaterally in the biceps femoris, vastus lateralis, rectus femoris, medial
67 0-10 numerical rating scale in an isometric biceps hold-task and was used as a secondary measure of
69 he glenohumeral joint clearly delineates the biceps-labral complex and glenohumeral ligaments, extern
71 The LLSR was significantly enhanced in the biceps muscle (on average by 49%) after the Bi-10ms-C pa
73 uts that drive M1 output was measured in the biceps muscle using a modified twitch interpolation tech
75 s present (in either the cleidobrachialis or biceps muscle) was not significantly different from the
78 xed biopsies of control and FSHD deltoid and biceps muscles, snap-frozen at resting length, were cryo
80 In tests for stationarity the amplitude of biceps phasic stretch reflex varied <10% in the first si
81 ging, but with both methods the magnitude of biceps phasic stretch reflex varied linearly with tap fo
82 I afferents of tibialis posterior, posterior biceps-semitendinosus and gastrocnemius soleus were also
83 s soleus, flexor digitorum longus, posterior biceps-semitendinosus and popliteus (mainly within L7).
84 follows: 0.40 (weight at week 37, kg)+ 0.16 (biceps skinfold thickness at week 37, mm) + 0.15 (thigh
86 6 - (7.34 x sex) + (0.32 x weight) + (0.38 x biceps skinfold) (R2 = 0.84, P < 0.001, SEE = 4.85).
89 ontrolling for chronologic age, was triceps, biceps, subscapular, suprailiac, and thigh (SEE = 2.87),
90 and thigh (SEE = 2.87), and for girls it was biceps, subscapular, suprailiac, thigh, and calf (SEE =
91 ned by DXA, and subcutaneous fat at triceps, biceps, subscapular, suprailiac, thigh, and calf sites w
92 or glenohumeral ligament (SGHL), presence of biceps tendinopathy, and rotator cuff tears adjacent to
93 ed were displacement of the long head of the biceps tendon (LHBT) relative to the subscapularis tendo
95 movement was replaced by stimulation of one biceps tendon with a 50-Hz vibratory stimulus (a selecti
97 glenohumeral joint, acromioclavicular joint, biceps tendon, scapulothoracic articulation, and sternoc
102 iments using vibratory stimuli, vibration of biceps tendons in normal subjects elicited flexion of th
105 rements (i.e., BMI, waist/hip circumference, biceps/triceps/subscapular/suprailiac skinfold thickness
108 analyzed using GeneChip Gene 1.0 ST arrays: biceps, which typically shows an early and severe diseas
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