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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.
7 uman Torsin A is mutated in individuals with early-onset torsion dystonia, a neuromuscular disease.
9 ene on chromosome 9q34 in autosomal dominant early-onset torsion dystonia and the detection of linkag
11 the dominantly inherited movement disorder, early onset torsion dystonia (DYT1) are caused by a muta
19 appears to be responsible for most cases of early-onset torsion dystonia in both Ashkenazic Jewish (
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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