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1 in the neuronal GlyR alpha or beta subunits (spasmodic and spastic) were shown to be deficient in the
2                                              Spasmodic bursts in particular laryngeal muscles disrupt
3 diffusivity changes and clinical symptoms of spasmodic dysphonia (r = 0.509, P = 0.037).
4                                              Spasmodic dysphonia (SD) is a rare neurological disorder
5  to the clinical and subclinical features of spasmodic dysphonia and may represent the neurochemical
6 YT4 dystonia, a dominantly inherited form of spasmodic dysphonia combined with other focal or general
7                                              Spasmodic dysphonia is a neurological disorder character
8                                              Spasmodic dysphonia is a primary focal dystonia characte
9                       The pathophysiology of spasmodic dysphonia is thought to involve structural and
10  the corticobulbar/corticospinal tract in 20 spasmodic dysphonia patients compared to 20 healthy subj
11 sentences and asymptomatic finger tapping in spasmodic dysphonia patients.
12  abnormalities as well as their relations to spasmodic dysphonia symptoms remain unknown.
13 C DeltaBP measures, while longer duration of spasmodic dysphonia was associated with a decrease in ta
14 n a familial case of segmental dystonia with spasmodic dysphonia.
15 d other mutations in TUBB4 may contribute to spasmodic dysphonia.
16 capacitation, but capacitation of sperm from spasmodic mice for up to 3 h did not result in significa
17 cay of synaptic currents that is observed in spasmodic mice.
18 me the phenotype of a well-known mutant, the spasmodic mouse.
19                                          The spasmodic peptide has a novel disulfide framework and di
20                                        This "spasmodic" peptide has 27 amino acids, including two gam
21 ine at amino acid 52, is responsible for the spasmodic phenotype in mice and alters the ability of gl
22                              A mutant mouse, spasmodic, that has a startle phenotype, has a point mut
23      In this cross-sectional study of ET and spasmodic torticollis (ST) patients (3:1 matching) who h
24 hs postoperatively using the Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS).
25 disease duration >/=3 years, Toronto Western Spasmodic Torticollis Rating Scale [TWSTRS] severity sco
26 muscles was investigated in 24 patients with spasmodic torticollis using small, abrupt 'drops' of the
27                       Cervical dystonia (CD; spasmodic torticollis) can be evoked by inhibition of su
28 n's disease, n = 1 myoclonic dystonia, n = 1 spasmodic torticollis).
29 -collic reflex is disrupted in patients with spasmodic torticollis, a finding which corroborates the

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