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1 acterized by ataxia, oculomotor apraxia, and choreoathetosis.
2 8.7%; n = 560) and infantile convulsions and choreoathetosis (14.3%; n = 206) constitute the vast maj
3 ement disorder comprising dystonia (84%) and choreoathetosis (52%).
4 nfantile epilepsy, infantile convulsions and choreoathetosis and paroxysmal kinesigenic dyskinesia, c
5 cluding early-onset dystonia with dysphagia, choreoathetosis, and T2-hyperintense lesions in striatum
6                             Three syndromes (choreoathetosis, anti-NMDAR-like encephalitis and behavi
7 , two major movement disorders, dystonia and choreoathetosis, are present together most of the time.
8 logical disorder with epilepsy and prominent choreoathetosis caused by biallelic pathogenic variants
9 n, she was alert and communicative, but with choreoathetosis, dysarthria, and an unsteady gait.
10 ntellectual disability, epilepsy, scoliosis, choreoathetosis, dysmorphic facial features and altered
11         Patients present with hyperuricemia, choreoathetosis, dystonia, and aggressive and self-injur
12 movement disorders (present in 44%) included choreoathetosis, dystonia, and ataxia.
13 ile-onset seizures, psychomotor retardation, choreoathetosis, dystonia, and ataxia.
14 rder that is characterized by hyperuricemia, choreoathetosis, dystonia, and compulsive self-injury.
15 on chromosome 4p; 2) the paroxysmal dystonic choreoathetosis gene at 2q34; 3) the dentatorubral-palli
16 nown as infantile convulsions and paroxysmal choreoathetosis (ICCA)-are related autosomal dominant di
17 le for 'infantile convulsions and paroxysmal choreoathetosis' (ICCA).
18 t 1-4 h and consist of dramatic dystonia and choreoathetosis in the limbs, trunk and face.
19 ystonia, chorea encephalopathy, and dystonic choreoathetosis occurring as sequelae of streptococcal i
20 dromes: paroxysmal kinesigenic dyskinesia or choreoathetosis, paroxysmal exercise-induced dyskinesia,
21                          Paroxysmal dystonic choreoathetosis (PDC) is characterized by attacks of inv
22                          Paroxysmal dystonic choreoathetosis (PDC) is characterized by attacks of inv
23                       Paroxysmal kinesigenic choreoathetosis (PKC) is a rare paroxysmal movement diso
24 pallidoluysian atrophy gene at 12p13; 4) the choreoathetosis/spasticity disease locus on 1p that lies
25 nia is often more pronounced and severe than choreoathetosis, with a major effect on daily activity,