戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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
17 l deformities (97%), limb dystonia (55%) and cervical dystonia (31%).
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
21               A total of 15 individuals with cervical dystonia and good outcome after pallidal deep b
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
25 nding insight into the brain regions causing cervical dystonia and possible treatment targets.
26 nths (myoclonic dystonia), 14 and 24 months (cervical dystonia) and 3-24 months (primary generalized
27                                Most cases of cervical dystonia are idiopathic, with no obvious cause,
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
32                     However, lesions causing cervical dystonia can occur in multiple different brain
33 thophysiology of arm tremor in patients with cervical dystonia (CD) and its relationship to other typ
34 's disease patients without dyskinesia (PD), cervical dystonia (CD) and writer's cramp.
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
37 euvres (AM), also called 'sensory tricks' in cervical dystonia (CD).
38                                              Cervical dystonia (CD; spasmodic torticollis) can be evo
39 ography in four PD participants and one with cervical dystonia (clinical trial: NCT03582891).
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
44                                   Idiopathic cervical dystonia (ICD) is the most common form of adult
45       Screening in subjects with adult-onset cervical dystonia identified 2 additional CIZ1 missense
46 a appears to increase risk of development of cervical dystonia in genetically predetermined individua
47                                              Cervical dystonia is a neurological disorder characteriz
48                                              Cervical dystonia is a non-degenerative movement disorde
49                                              Cervical dystonia is managed mainly by repeated botulinu
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
52 00) to test whether lesion locations causing cervical dystonia map to a common brain network.
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
58                                              Cervical dystonia patients had a history, prior to sympt
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
61                      By univariate analysis, cervical dystonia patients, compared to their unaffected
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
67 emains a surgical option in the treatment of cervical dystonia when conservative measures fail.
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