ライフサイエンスコーパス: early-onset torsion dystonia

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1 its potential role as a therapeutic agent in early onset torsion dystonia.

2 onsible for most cases of autosomal dominant early-onset torsion dystonia.

3 aminergic function in the pathophysiology of early-onset torsion dystonia.

4 e DYT1 gene is indeed a mutation that causes early-onset torsion dystonia.

5 ion, underlies dominantly inherited cases of early-onset torsion dystonia.

6 Early-onset torsion dystonia, a CNS-based movement disor

7 uman Torsin A is mutated in individuals with early-onset torsion dystonia, a neuromuscular disease.

8 Early-onset torsion dystonia, an autosomal dominant dise

9 ene on chromosome 9q34 in autosomal dominant early-onset torsion dystonia and the detection of linkag

10 Most cases of early onset torsion dystonia are caused by a 3-bp deleti

11 the dominantly inherited movement disorder, early onset torsion dystonia (DYT1) are caused by a muta

12 nuclear envelope, with a mutant form causing early onset torsion dystonia (DYT1).

13 um (ER) and nuclear envelope responsible for early onset torsion dystonia (DYT1).

14 The gene causing early-onset torsion dystonia (DYT1) has recently been id

15 303 (torsinA DeltaE) is the major cause for early-onset torsion dystonia (DYT1).

16 Most cases of early-onset torsion dystonia (EOTD) are caused by a dele

17 Early-onset torsion dystonia (EOTD) is a neurological di

18 ct in TGF-beta signaling might also underlie early onset torsion dystonia in humans.

19 appears to be responsible for most cases of early-onset torsion dystonia in both Ashkenazic Jewish (

20 ations in torsinA cause dominantly inherited early-onset torsion dystonia in humans.

21 Early onset torsion dystonia is characterized by involun

22 Early-onset torsion dystonia is a hereditary movement di

23 Early-onset torsion dystonia is a hyperkinetic movement

24 Early-onset torsion dystonia is a movement disorder, cha

25 Early-onset torsion dystonia is an autosomal dominant hy

26 Early-onset torsion dystonia is an autosomal dominant mo

27 Early-onset torsion dystonia is the most severe heritabl

28 which cause another movement disorder termed early-onset torsion dystonia, is highly expressed in DA

29 Here we describe two patients with typical early-onset torsion dystonia of Swiss-Mennonite and non-

30 igate the cellular and molecular etiology of early onset torsion dystonia, we have established a Dros

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