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1 l role as a therapeutic agent in early onset torsion dystonia.
2 es dominantly inherited cases of early-onset torsion dystonia.
3 t expressed in mutation carriers for primary torsion dystonia.
4 , and may have implications for the study of torsion dystonia.
5 most cases of autosomal dominant early-onset torsion dystonia.
6 nction in the pathophysiology of early-onset torsion dystonia.
7 is indeed a mutation that causes early-onset torsion dystonia.
8 P1 gene were recently shown to underlie DYT6 torsion dystonia.
9 in the heterozygous state is associated with torsion dystonia-1 (DYT1 or DYT-TOR1A), an early-onset d
10                                              Torsion dystonia-1 (DYT1) dystonia, the most common inhe
11 enes, the candidate disease gene regions for torsion dystonia 3 and two X-linked mental retardation s
12                                  Early-onset torsion dystonia, a CNS-based movement disorder, is usua
13 A is mutated in individuals with early-onset torsion dystonia, a neuromuscular disease.
14 -Mennonite families with mixed-onset primary torsion dystonia (also known as DYT6 dystonia).
15 d now includes three mapped loci for primary torsion dystonia, although other susceptibility genes ar
16                                  Early-onset torsion dystonia, an autosomal dominant disease associat
17 ently arisen Lithuanian mutations, those for torsion dystonia and familial hypercholesterolemia.
18 osome 9q34 in autosomal dominant early-onset torsion dystonia and the detection of linkage for one fo
19                          Adult onset primary torsion dystonia (AOPTD) is a poorly penetrant autosomal
20                    Most cases of early onset torsion dystonia are caused by a 3-bp deletion (GAG) in
21 ese data support that both the wild type and torsion dystonia-associated forms of torsin A are proper
22                 DYT1 early-onset generalized torsion dystonia (DYT1 dystonia) is an inherited movemen
23 tly inherited movement disorder, early onset torsion dystonia (DYT1) are caused by a mutant form of t
24                 The gene causing early-onset torsion dystonia (DYT1) has recently been identified, an
25 tions discussed in detail include idiopathic torsion dystonia (DYT1), focal dystonias (DYT7) and mixe
26 A DeltaE) is the major cause for early-onset torsion dystonia (DYT1).
27 nuclear envelope responsible for early onset torsion dystonia (DYT1).
28 lope, with a mutant form causing early onset torsion dystonia (DYT1).
29                    Most cases of early-onset torsion dystonia (EOTD) are caused by a deletion of one
30                                  Early-onset torsion dystonia (EOTD) is a neurological disorder chara
31  well as the identification of other primary torsion dystonia genes, should help elucidate the mechan
32 mouse models of early-onset DYT1 generalized torsion dystonia; however, the relationship between the
33  common extrapyramidal disorders: idiopathic torsion dystonia, idiopathic Parkinson's disease and Hun
34 be responsible for most cases of early-onset torsion dystonia in both Ashkenazic Jewish (AJ) and non-
35 rsinA cause dominantly inherited early-onset torsion dystonia in humans.
36 ta signaling might also underlie early onset torsion dystonia in humans.
37                           Early onset (DYT1) torsion dystonia is a dominantly inherited movement diso
38                                  Early-onset torsion dystonia is a hereditary movement disorder thoug
39                                  Early-onset torsion dystonia is a hyperkinetic movement disorder cau
40                                  Early-onset torsion dystonia is a movement disorder, characterized b
41                                  Early-onset torsion dystonia is an autosomal dominant hyperkinetic m
42                                              Torsion dystonia is an autosomal dominant movement disor
43                                  Early-onset torsion dystonia is an autosomal dominant movement disor
44                                  Early onset torsion dystonia is characterized by involuntary movemen
45                                      Primary torsion dystonia is one of the most severe types of inhe
46                                  Early-onset torsion dystonia is the most severe heritable form of dy
47 another movement disorder termed early-onset torsion dystonia, is highly expressed in DA neurons and
48 tivation studies on patients with idiopathic torsion dystonia (ITD) have shown overactive striatum an
49       Clinical-genetic studies of idiopathic torsion dystonia (ITD) indicate that the DYT1 gene on ch
50                       Early-onset idiopathic torsion dystonia (ITD) is an autosomal dominant hyperkin
51 ble for most childhood limb-onset idiopathic torsion dystonia (ITD).
52                Study of one of these primary torsion dystonia loci (DYT1) has culminated in the cloni
53 scribe two patients with typical early-onset torsion dystonia of Swiss-Mennonite and non-Jewish Russi
54                                      Primary torsion dystonia (PTD) is a clinically and genetically h
55                 Only three genes for primary torsion dystonia (PTD), TOR1A (DYT1), THAP1 (DYT6) and C
56                 Only three genes for primary torsion dystonia (PTD), TOR1A (DYT1), THAP1 (DYT6) and C
57         The deletion in DYT1 associated with torsion dystonia results in the loss of one of a pair of
58 her mutation in a German family with primary torsion dystonia suggests that THAP1 mutations also caus
59 odevelopmental movement disorder adult-onset torsion dystonia type 6.
60 llular and molecular etiology of early onset torsion dystonia, we have established a Drosophila model
61 n chromosome 9q34 causes early-onset primary torsion dystonia with autosomal dominant inheritance but
62 d in DYT1, the causative gene for idiopathic torsion dystonia with linkage to 9q34.