ライフサイエンスコーパス: familial hemiplegic migraine

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1 ated disorders is much broader than strictly familial hemiplegic migraine.

2 umber of human neurologic diseases including familial hemiplegic migraine.

3 7) severe myoclonic epilepsy of infancy, and familial hemiplegic migraine.

4 dies, and linkage and association studies of familial hemiplegic migraine.

5 we identified a novel PNKD gene deletion in familial hemiplegic migraine.

6 Familial hemiplegic migraine, a rare Mendelian form of M

7 had episodic ataxia and one PNKD family had familial hemiplegic migraine alone.

8 Studies of linkage between familial hemiplegic migraine and marker 19p13 in 13 exte

9 ly engineered to provide an understanding of familial hemiplegic migraine and possibly, by extrapolat

10 The recent discovery that familial hemiplegic migraine, episodic ataxia type 2, an

11 onal P/Q-type voltage-gated calcium channel (familial hemiplegic migraine, episodic ataxia type 2, sp

12 to cause such human neurological diseases as familial hemiplegic migraine, episodic ataxia-2, and spi

13 ame calcium channel gene are associated with familial hemiplegic migraine, episodic or progressive at

14 s to the genetic susceptibility of both rare familial hemiplegic migraine (FHM) and more common types

15 ldhood (AHC) is typically distinguished from familial hemiplegic migraine (FHM) by infantile onset of

16 Familial hemiplegic migraine (FHM) has been related to m

17 Familial hemiplegic migraine (FHM) is a rare subtype of

18 Familial hemiplegic migraine (FHM) is an autosomal domin

19 Familial hemiplegic migraine (FHM) is an autosomal domin

20 ive and memory difficulties observed in some familial hemiplegic migraine (FHM) patients, we examined

21 Familial hemiplegic migraine (FHM), a migraine subtype t

22 2, and within a candidate region at 1q23 for familial hemiplegic migraine (FHM).

23 linked to several human diseases, including familial hemiplegic migraine (FHM).

24 Familial hemiplegic migraine is associated with at least

25 Familial hemiplegic migraine is caused by mutations in t

26 Familial hemiplegic migraine knock-in mice expressing th

27 g and synaptic transmission resulting from a familial hemiplegic migraine mutation (S218L).

28 Two PRRT2 mutations were in familial hemiplegic migraine or episodic ataxia, one SLC

29 Familial hemiplegic migraine type 1 (FHM1) arises from m

30 Familial hemiplegic migraine type 1 (FHM1) is a subtype

31 Familial hemiplegic migraine type 1 (FHM1) is an autosom

32 Familial hemiplegic migraine type 1 (FHM1), a monogenic

33 e-gated CaV2.1 channels, are associated with familial hemiplegic migraine type 1 (FHM1), a rare monog

34 Familial hemiplegic migraine type 1 (FHM1), a severe mig

35 rare, dominant form of this common disease, familial hemiplegic migraine type 1 (FHM1), arises from

36 g alpha1A mutations that are associated with familial hemiplegic migraine type 1 (FHM1).

37 In familial hemiplegic migraine type 1 mutant mice expressi

38 opagated into subcortical structures in both familial hemiplegic migraine type 1 mutants.

39 ng depolarization in mice carrying the human familial hemiplegic migraine type 1 R192Q missense mutat

40 Familial hemiplegic migraine type 1, a monogenic migrain

41 euron, Tottene et al. study a mouse model of familial hemiplegic migraine type 1, and provide evidenc

42 The neurological disorders familial hemiplegic migraine type 2 (FHM2), alternating

43 s lead to severe human pathologies including Familial Hemiplegic Migraine type 2, Alternating Hemiple

44 Familial hemiplegic migraine type 3 (FHM3) is a severe a

45 The neurological disorder familial hemiplegic migraine type II (FHM2) is caused by

46 isoforms (rapid-onset dystonia parkinsonism, familial hemiplegic migraine type-2), as well as reducti

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