ライフサイエンスコーパス: levetiracetam

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1 amotrigine) and without proapoptotic action (levetiracetam).

2 nt total synthesis of the antiepileptic drug levetiracetam.

3 ontrol and tolerability with lamotrigine and levetiracetam.

4 e noninducing anticonvulsants lamotrigine or levetiracetam.

5 her patients were switched to lamotrigine or levetiracetam.

6 nteraction is associated with gabapentin and levetiracetam.

7 Lamotrigine (2.31% in 4195 pregnancies) and levetiracetam (1.77% in 817 pregnancies) were associated

8 tamethylene-linked levetiracetam-huprine and levetiracetam-(6-chloro)tacrine hybrids to hit amyloid,

9 identified as the specific binding site for levetiracetam, a second generation antiepileptic drug.

10 Finally, we show that feeding levetiracetam, an anti-epileptic medication, to Abeta-ex

11 Pretreatment of neurons with levetiracetam, an FDA-approved anti-epileptic drug, enha

12 re being used in management of myoclonus are levetiracetam and gamma-hydroxybutyric acid.

13 modern treatment choices include valproate, levetiracetam and lacosamide.

14 wn antiepileptic drugs such as ethosuximide, levetiracetam, and lacosamide.

15 epileptic drugs (AEDs) such as ethosuximide, levetiracetam, and lacosamide.

16 recently been reawakened by the licensing of levetiracetam as a potentially major new antiepileptic d

17 ) or preblocking with the antiepileptic drug levetiracetam at 10 and 30 mg/kg.

18 n, treatment with the atypical antiepileptic levetiracetam at a low dose shown previously to improve

19 The antiepileptic drug, levetiracetam, blocked Kv4.2 depletion.

20 -homoalanine, which is a chiral precursor of levetiracetam, brivaracetam, and ethambutol.

21 By using a low dose of the antiepileptic levetiracetam hippocampal activation in aMCI was reduced

22 ynthesized a series of heptamethylene-linked levetiracetam-huprine and levetiracetam-(6-chloro)tacrin

23 The levetiracetam-huprine hybrid 10 significantly reduced th

24 c drugs (topiramate, lacosamide, pregabalin, levetiracetam), hypothermia, magnesium, pyridoxine, immu

25 Levetiracetam is especially useful for posthypoxic myocl

26 motrigine (LTG) 0.31 (-0.38 to 1.00) p=0.38; levetiracetam (LEV) 1.00 (0.16 to 1.84) p=0.02; sodium v

27 Among the drugs tested, only levetiracetam (LEV) effectively reduced abnormal spike a

28 The antiepileptic drug levetiracetam (LEV) is a potential treatment for alcohol

29 Levetiracetam (LEV) is a prominent antiepileptic drug th

30 le protein SV2A is the brain binding site of levetiracetam (LEV), a new antiepileptic drug with a uni

31 ied as the binding site of the antiepileptic levetiracetam (LEV), making it an interesting therapeuti

32 The same analyses were performed with levetiracetam (LEV).

33 Thus, levetiracetam might be part of a valuable new approach f

34 zepine or phenytoin to the noninducing drugs levetiracetam or lamotrigine produces rapid and clinical

35 Preblocking with 10 and 30 mg/kg of levetiracetam resulted in approximately 60% and 90% occu

36 es appeared to be better for lamotrigine and levetiracetam than for phenytoin.

37 ents such as topiramate, disodium valproate, levetiracetam, the antihistamine cyproheptadine, and the

38 trast, the new AEDs gabapentin, lamotrigine, levetiracetam, tiagabine, topiramate, vigabatrin, and zo

39 ition of the SV2A-binding antiepileptic drug levetiracetam to the medium inhibited the galactose-depe

40 Levetiracetam was discovered to have antiseizure activit

41 Levetiracetam was found not to disrupt synaptic developm

42 Brivaracetam, an analog of levetiracetam, was identified in a medicinal chemistry c

43 iption of antiepileptic drugs, phenytoin and levetiracetam were prescribed most often.

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