ライフサイエンスコーパス: hemiplegic migraine

1 mechanism for enhanced CSD susceptibility in hemiplegic migraine.

2 ified a novel PNKD gene deletion in familial hemiplegic migraine.

3 rders is much broader than strictly familial hemiplegic migraine.

4 teral sclerosis, parkinsonism, epilepsy, and hemiplegic migraine.

5 human neurologic diseases including familial hemiplegic migraine.

6 myoclonic epilepsy of infancy, and familial hemiplegic migraine.

7 cium channel gene associated with ataxia and hemiplegic migraine.

8 linkage and association studies of familial hemiplegic migraine.

9 ns included a high frequency of migraine and hemiplegic migraine.

10 Familial hemiplegic migraine, a rare Mendelian form of MA, can be

11 odic ataxia and one PNKD family had familial hemiplegic migraine alone.

12 med on 7 family members, 5 with a history of hemiplegic migraine and 2 without history of migraine.

13 variant was identified in two families with hemiplegic migraine and in one patient with migraine wit

14 h controls the PCr/Pi ratio in patients with hemiplegic migraine and in patients with persistent aura

15 Studies of linkage between familial hemiplegic migraine and marker 19p13 in 13 extended fami

16 a gain-of-function and associated with both hemiplegic migraine and migraine with aura in patients.

17 rare monogenic migraine syndromes, in which hemiplegic migraine and non-hemiplegic migraine with or

18 ered to provide an understanding of familial hemiplegic migraine and possibly, by extrapolation, may

19 with neurological disorders, such as ataxia, hemiplegic migraine, and epilepsy.

20 We suggest that the hemiplegic migraine attacks and the cerebellar degenerat

21 Of these, hemiplegic migraine emerges as a novel PRRT2-associated

22 The recent discovery that familial hemiplegic migraine, episodic ataxia type 2, and spinoce

23 type voltage-gated calcium channel (familial hemiplegic migraine, episodic ataxia type 2, spinocerebe

24 such human neurological diseases as familial hemiplegic migraine, episodic ataxia-2, and spinocerebel

25 um channel gene are associated with familial hemiplegic migraine, episodic or progressive ataxia, com

26 genetic susceptibility of both rare familial hemiplegic migraine (FHM) and more common types of migra

27 HC) is typically distinguished from familial hemiplegic migraine (FHM) by infantile onset of the char

28 Familial hemiplegic migraine (FHM) has been related to mutations

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

30 Familial hemiplegic migraine (FHM) is an autosomal dominant disor

31 Familial hemiplegic migraine (FHM) is an autosomal dominant subty

32 emory difficulties observed in some familial hemiplegic migraine (FHM) patients, we examined hippocam

33 Familial hemiplegic migraine (FHM), a migraine subtype that also

34 thin a candidate region at 1q23 for familial hemiplegic migraine (FHM).

35 o several human diseases, including familial hemiplegic migraine (FHM).

36 Familial hemiplegic migraine is associated with at least 13 diffe

37 Familial hemiplegic migraine is caused by mutations in the calciu

38 Familial hemiplegic migraine knock-in mice expressing the S218L o

39 aptic transmission resulting from a familial hemiplegic migraine mutation (S218L).

40 venous sinus thrombosis and seizure (n = 3), hemiplegic migraine (n = 1), and hyperacute arterial inf

41 Two PRRT2 mutations were in familial hemiplegic migraine or episodic ataxia, one SLC2A1 famil

42 and was significantly lower in patients with hemiplegic migraine than in patients with non-motor aura

43 3 patients with familial episodic ataxia and hemiplegic migraine to investigate the mutation frequenc

44 Familial hemiplegic migraine type 1 (FHM1) arises from missense m

45 Familial hemiplegic migraine type 1 (FHM1) is a subtype of migrai

46 Familial hemiplegic migraine type 1 (FHM1) is an autosomal domina

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

48 aV2.1 channels, are associated with familial hemiplegic migraine type 1 (FHM1), a rare monogenic subt

49 Familial hemiplegic migraine type 1 (FHM1), a severe migraine wit

50 minant form of this common disease, familial hemiplegic migraine type 1 (FHM1), arises from missense

51 mutations that are associated with familial hemiplegic migraine type 1 (FHM1).

52 In familial hemiplegic migraine type 1 mutant mice expressing human

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

54 rization in mice carrying the human familial hemiplegic migraine type 1 R192Q missense mutation as we

55 Familial hemiplegic migraine type 1, a monogenic migraine variant

56 ttene et al. study a mouse model of familial hemiplegic migraine type 1, and provide evidence for the

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

58 severe human pathologies including Familial Hemiplegic Migraine type 2, Alternating Hemiplegia of Ch

59 Familial hemiplegic migraine type 3 (FHM3) is a severe autosomal

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

61 (rapid-onset dystonia parkinsonism, familial hemiplegic migraine type-2), as well as reduction in Na,

62 dromes, in which hemiplegic migraine and non-hemiplegic migraine with or without aura are part of a w