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1 atrophy tested, but not in the patients with primary lateral sclerosis.
2 icity recapitulating key aspects of FTLD and primary lateral sclerosis.
3  of the corticospinal tract in patients with primary lateral sclerosis.
4 is (ALS), hereditary spastic paraplegia, and primary lateral sclerosis.
5 r tracts was carried out in 19 patients with primary lateral sclerosis, 18 patients with amyotrophic
6 eral sclerosis, and the relationship between primary lateral sclerosis and amyotrophic lateral sclero
7 coherence values measured from patients with primary lateral sclerosis and control subjects, we estim
8 yotrophic lateral sclerosis (ALS2), juvenile primary lateral sclerosis and infantile-onset ascending
9 ormed to established diagnostic criteria for primary lateral sclerosis and six patients with progress
10 form of amyotrophic lateral sclerosis (ALS), primary lateral sclerosis, and infantile-ascending hered
11 udies have been carried out on patients with primary lateral sclerosis, and the relationship between
12 rrectly classify 95% of ALS cases and 71% of primary lateral sclerosis cases.
13                                              Primary lateral sclerosis differs from amyotrophic later
14                            All patients with primary lateral sclerosis had abnormal motor-evoked pote
15                                              Primary lateral sclerosis is a sporadic disorder charact
16 en and 31 women) (group 2), 10 patients with primary lateral sclerosis (mean age +/- SD, 55.5 +/- 12
17 ith amyotrophic lateral sclerosis and 1 with primary lateral sclerosis met inclusion criteria and wer
18             Brain metabolism between ALS and primary lateral sclerosis patients was nearly identical
19      Amyotrophic lateral sclerosis (ALS) and primary lateral sclerosis (PLS) are neurodegenerative co
20                                          The primary lateral sclerosis (PLS) consensus diagnostic cri
21                           Some patients with primary lateral sclerosis (PLS) have a clinical course s
22                                              Primary lateral sclerosis (PLS) is a motor neuron disord
23                                              Primary lateral sclerosis (PLS) is a neurodegenerative d
24                           On the other hand, primary lateral sclerosis (PLS), a more benign form of M
25 r neuron (UMN) disease, initially resembling primary lateral sclerosis (PLS), and breast cancer.
26 with amyotrophic lateral sclerosis (ALS) and primary lateral sclerosis (PLS).
27  with amyotrophic lateral sclerosis (ALS) or primary lateral sclerosis (PLS).
28 itudinal cohort of patients with ALS (n=82), primary lateral sclerosis (PLS, n=10), ALS-mimic conditi
29 ssified by the revised El Escorial criteria, primary lateral sclerosis, progressive muscular atrophy,
30                                Patients with primary lateral sclerosis showed a similar pattern.
31 g hereditary spastic paraplegia and juvenile primary lateral sclerosis, suggesting prominent upper mo
32                             In patients with primary lateral sclerosis, the greatest loss of fraction
33                                       In the primary lateral sclerosis variant of motor neuron diseas
34              In 7 patients, the diagnosis of primary lateral sclerosis was made; 4 patients had progr
35  sclerosis; progressive muscular atrophy; or primary lateral sclerosis; which met the World Federatio