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1 e, n = 1 myoclonic dystonia, n = 1 spasmodic torticollis).
2 nificant improvement in ocular alignment and torticollis.
3 ective, or necessary, in congenital muscular torticollis.
4 more resistant cases of congenital muscular torticollis.
5 t to differentiate muscular from nonmuscular torticollis.
6 controlling head position may contribute to torticollis.
7 ure distinguishing dystonic from psychogenic torticollis.
8 12 Hz, which was absent in all patients with torticollis.
9 eticular and corticospinal drive in dystonic torticollis.
10 nd C4/C5 vertebrae in a 5-year-old girl with torticollis.
11 SD, interval between onset of arm tremor and torticollis 0 +/- 2.9 years) whereas it began much earli
12 flex is disrupted in patients with spasmodic torticollis, a finding which corroborates the patients'
13 L) muscles of eight patients with rotational torticollis and eight age-matched controls, and analysed
16 periodic syndromes include benign paroxysmal torticollis, benign paroxysmal vertigo, abdominal migrai
17 age 14 years +/- 6 SD) and preceded onset of torticollis by a longer interval (21.6 +/- 17.5 years) i
20 ate and simultaneous onset of arm tremor and torticollis (group A), and another with an early onset o
27 The pathophysiology of idiopathic dystonic torticollis is unclear and there is no simple test that
28 ients in group A started simultaneously with torticollis (mean onset age of arm tremor 40 years +/- 2
32 ration >/=3 years, Toronto Western Spasmodic Torticollis Rating Scale [TWSTRS] severity score >/=15 p
35 is cross-sectional study of ET and spasmodic torticollis (ST) patients (3:1 matching) who had head tr
36 ugh retrocollis and anterocollis, as well as torticollis to the right, were significantly more common
37 s investigated in 24 patients with spasmodic torticollis using small, abrupt 'drops' of the head.
38 better understand the spectrum of disease in torticollis, which is the third most common pediatric or
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