ライフサイエンスコーパス: primary lateral sclerosis

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1 icity recapitulating key aspects of FTLD and primary lateral sclerosis.

2 of the corticospinal tract in patients with primary lateral sclerosis.

3 atrophy tested, but not in the patients with primary lateral sclerosis.

4 r tracts was carried out in 19 patients with primary lateral sclerosis, 18 patients with amyotrophic

5 eral sclerosis, and the relationship between primary lateral sclerosis and amyotrophic lateral sclero

6 coherence values measured from patients with primary lateral sclerosis and control subjects, we estim

7 yotrophic lateral sclerosis (ALS2), juvenile primary lateral sclerosis and infantile-onset ascending

8 ormed to established diagnostic criteria for primary lateral sclerosis and six patients with progress

9 form of amyotrophic lateral sclerosis (ALS), primary lateral sclerosis, and infantile-ascending hered

10 udies have been carried out on patients with primary lateral sclerosis, and the relationship between

11 rrectly classify 95% of ALS cases and 71% of primary lateral sclerosis cases.

12 Primary lateral sclerosis differs from amyotrophic later

13 All patients with primary lateral sclerosis had abnormal motor-evoked pote

14 Primary lateral sclerosis is a sporadic disorder charact

15 en and 31 women) (group 2), 10 patients with primary lateral sclerosis (mean age +/- SD, 55.5 +/- 12

16 Brain metabolism between ALS and primary lateral sclerosis patients was nearly identical

17 Amyotrophic lateral sclerosis (ALS) and primary lateral sclerosis (PLS) are neurodegenerative co

18 Some patients with primary lateral sclerosis (PLS) have a clinical course s

19 Primary lateral sclerosis (PLS) is a motor neuron disord

20 r neuron (UMN) disease, initially resembling primary lateral sclerosis (PLS), and breast cancer.

21 with amyotrophic lateral sclerosis (ALS) and primary lateral sclerosis (PLS).

22 with amyotrophic lateral sclerosis (ALS) or primary lateral sclerosis (PLS).

23 Patients with primary lateral sclerosis showed a similar pattern.

24 g hereditary spastic paraplegia and juvenile primary lateral sclerosis, suggesting prominent upper mo

25 In patients with primary lateral sclerosis, the greatest loss of fraction

26 In the primary lateral sclerosis variant of motor neuron diseas

27 In 7 patients, the diagnosis of primary lateral sclerosis was made; 4 patients had progr

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