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1 al sensorineural hearing loss and vestibular areflexia.
2 scending neural paralysis, hyporeflexia, and areflexia.
3 tis pigmentosa (RP), and variable vestibular areflexia.
4 e, and the presence or absence of vestibular areflexia.
5  syndrome, characterized by ophthalmoplegia, areflexia and ataxia.
6                                      Stretch areflexia and gait ataxia, for example, emerge from a co
7 toimmune neuropathy characterized by ataxia, areflexia and ophthalmoplegia, and in the majority of ca
8 4 clinical phenotypes (typical GSS, GSS with areflexia and paresthesia, pure dementia GSS, and Creutz
9 travenous gammaglobulin (IVGG) his pupillary areflexia and severe hypotension resolved.
10 the brain stem, resulting in coma, brainstem areflexia, and apnea in the setting of an adequate stimu
11 H1) is characterized by deafness, vestibular areflexia, and progressive retinal degeneration.
12  disorder marked by hearing loss, vestibular areflexia, and retinitis pigmentosa.
13 ic neuropathy with marked sensory ataxia and areflexia, and with relatively preserved motor function
14 ensory neuronopathy and bilateral vestibular areflexia coexist.
15                                      Bladder areflexia developed in both operated groups, but NRP/GRP
16     Motivated by the likelihood that stretch areflexia is related to problems with sensing and contro
17                       The cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural h
18 t dystonia-parkinsonism or cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing
19 set dystonia-parkinsonism, cerebellar ataxia-areflexia-progressive optic atrophy, and relapsing encep
20 The classic phenotype, early onset myopathy, areflexia, respiratory distress and dysphagia, is severe
21  from individuals with early onset myopathy, areflexia, respiratory distress and dysphagia.
22 antile myopathy with diaphragmatic weakness, areflexia, respiratory distress and dysphagia.
23 ations in MEGF10 cause early onset myopathy, areflexia, respiratory distress, and dysphagia (EMARDD),
24 ns in humans result in early-onset myopathy, areflexia, respiratory distress, and dysphagia (EMARDD).
25 of cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS) and a major cause of late on
26 ed cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS) include the characteristic c
27 Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS) is a progressive late-onset,
28 xia with neuropathy and bilateral vestibular areflexia syndrome (CANVAS) is a recently recognized neu
29 bellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS) is a recessively inherited n
30 Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS) is an autosomal recessive ne
31 erebellar ataxia, neuropathy, and vestibular areflexia syndrome (CANVAS) is known, the contributions
32 cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS) RR = 1.34, P < 0.001; larger
33 bellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS), caused by biallelic expansi
34 erebellar ataxia, neuropathy, and vestibular areflexia syndrome (CANVAS), respectively.
35 ensory ganglionopathy, or SG) and vestibular areflexia syndrome (CANVAS).
36 erebellar ataxia, neuropathy, and vestibular areflexia syndrome (CANVAS).
37 cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS).
38 xia with neuropathy and bilateral vestibular areflexia syndrome (CANVAS).
39 ed cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS).
40 C1 cerebellar ataxia, neuropathy, vestibular areflexia syndrome, we speculated that RFC1 expansions c
41  stretch reflexes, extending observations of areflexia to a second species.