ライフサイエンスコーパス: POMA

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1 POMA disease antisera (6/6) recognize the third KH domai

2 e associations with POMA balance (P = 0.02), POMA gait scores (P < 0.01), and IADL (P < 0.01).

3 paraneoplastic opsoclonus-myoclonus ataxia (POMA) antigen.

4 Paraneoplastic opsoclonus myoclonus ataxia (POMA) is a neurologic disorder thought to be mediated by

5 paraneoplastic opsoclonus myoclonus ataxia (POMA) patients with latent cancer, reduced inhibitory co

6 paraneoplastic opsoclonus myoclonus ataxia (POMA), a disorder associated with breast cancer and moto

7 paraneoplastic opsoclonus myoclonus ataxia (POMA), an autoimmune neurologic disease characterized by

8 paraneoplastic opsoclonus myoclonus ataxia (POMA), Nova-1 and Nova-2 proteins are present as auto-an

9 paraneoplastic opsoclonus-myoclonus ataxia (POMA).

10 [paraneoplastic opsoclonus-myoclonus ataxia (POMA)].

11 paraneoplastic opsoclonus-myoclonus-ataxia (POMA).

12 in vitro, and this binding can be blocked by POMA antisera.

13 However, POMA antisera recognize antigens that are widely express

14 l for understanding the motor dysfunction in POMA.

15 to the cause of abnormal motor inhibition in POMA.

16 m for the loss of motor function observed in POMA patients.

17 ults demonstrate that the immune response in POMA targets a family of highly related sequence-specifi

18 A may underlie the motor dysfunction seen in POMA.

19 ate with the predominantly motor symptoms in POMA.

20 Thus, a cardinal feature of POMA is the production of antibodies that inhibit Nova-1

21 One POMA disease antigen, termed Nova-1, has been identified

22 A antisera to clone a cDNA encoding a second POMA disease antigen termed Nova-2.

23 he development of cognitive deficits in some POMA patients.

24 We have used POMA antisera to clone a cDNA encoding a second POMA dis

25 howed significant negative associations with POMA balance (P = 0.02), POMA gait scores (P < 0.01), an

26 a significant positive association only with POMA balance scores (P < 0.045).

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