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1 d the heterogeneous lesion locations causing cervical dystonia.
2 ts, and finally discuss its putative role in cervical dystonia.
3 ervation and/or change in the pattern of the cervical dystonia.
4 the DYT1 gene, as well as for patients with cervical dystonia.
5 search identified 25 cases of lesion-induced cervical dystonia.
6 lly patients with generalized, segmental, or cervical dystonia.
7 han sham stimulation at reducing symptoms of cervical dystonia.
8 pear not to be a common cause of adult-onset cervical dystonia.
9 tation in a family with adult onset, primary cervical dystonia.
10 mal connectivity in patients with idiopathic cervical dystonia.
11 striatal cholinergic interneuron density in cervical dystonia.
12 brain regions in 13 subjects with idiopathic cervical dystonia.
13 cic outlet syndrome, bruxism, spasticity and cervical dystonia.
14 ccessful deep brain stimulation treatment of cervical dystonia.
15 was observed in 50% of blepharospasm, 8% of cervical dystonia, 17% of hand dystonia and 16% of laryn
16 halopathy (n = 4), ocular motor palsies (2), cervical dystonia (2), focal weakness (2), and facial pa
18 ation were enrolled and 87 datasets (43 with cervical dystonia and 44 with generalized dystonia) were
19 A case-control study of 67 patients with cervical dystonia and 67 of their age-matched unaffected
20 sease, one with myoclonic dystonia, two with cervical dystonia and five with primary generalized dyst
22 asians with familial or sporadic adult onset cervical dystonia and matching controls for sequence var
23 obustly associated with dystonic symptoms in cervical dystonia and may be a useful biomarker for adap
24 k (22.4%) for blepharospasm, hand (3.5%) for cervical dystonia and neck for hand (12.8%) and laryngea
26 nths (myoclonic dystonia), 14 and 24 months (cervical dystonia) and 3-24 months (primary generalized
28 report three new phenotypes at presentation: cervical dystonia; autonomic dysfunction and peripheral
29 abismus, blepharospam, hemificial spasm, and cervical dystonia, because of the toxin's tropism for ne
30 ablished therapy for primary generalized and cervical dystonia, but therapeutic success is compromise
31 patterns of head movements in patients with cervical dystonia can be predicted by deficits in a neur
33 thophysiology of arm tremor in patients with cervical dystonia (CD) and its relationship to other typ
35 of selective peripheral denervation (SPD) in cervical dystonia (CD) patients with primary or secondar
36 Sensory trick is a characteristic feature of cervical dystonia (CD), where a light touch on the area
40 matosensory cortex were specific markers for cervical dystonia compared to lesions causing other neur
41 into the causal neuroanatomical substrate of cervical dystonia, demonstrate convergence across idiopa
42 pathway impairment in patients with sporadic cervical dystonia, due to rare coding variation in the e
43 controlled trial, we recruited patients with cervical dystonia from centres in Germany, Norway, and A
46 a appears to increase risk of development of cervical dystonia in genetically predetermined individua
50 rge number of familial and sporadic cases of cervical dystonia led to the identification of a total o
51 ality in families with inherited adult-onset cervical dystonia; linkage to chromosome 18p has been de
53 l ganglia accounted for optimal treatment of cervical dystonia, modulation of pallidothalamic bundles
54 15), benign essential blepharospasm (n = 9), cervical dystonia (n = 10) and in age-matched controls.
55 ons, is abnormal in patients with idiopathic cervical dystonia (n = 39) versus matched controls (n =
56 43) consisting of specific subpopulations of cervical dystonia (N = 45), laryngeal dystonia (N = 49),
57 examining environmental exposure history in cervical dystonia patients and their similarly aged unaf
59 ctive antibodies against toxin from mice and cervical dystonia patients undergoing BoNT/A treatment r
60 The dystonic tremor group included primarily cervical dystonia patients with dystonic head tremor and
62 tions in CIZ1 may cause adult onset, primary cervical dystonia, possibly by precipitating neurodevelo
63 ntrol, as well as a conceptual framework for cervical dystonia that departs considerably from current
64 blepharospasm, oromandibular, laryngeal and cervical dystonia; the sex ratio was reversed in task-sp
65 Caucasian pedigree with adult onset, primary cervical dystonia to identify a cosegregating mutation.
66 es with selective peripheral denervation for cervical dystonia were retrospectively analysed concerni
68 to a novel pathophysiological explanation in cervical dystonia, which proposed that the abnormalities
69 ta oscillations is observed in patients with cervical dystonia who apply effective sensory tricks, su