ライフサイエンスコーパス: hemiplegic migraine

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

2 mechanism for enhanced CSD susceptibility in hemiplegic migraine.

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

4 rders is much broader than strictly familial 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 teral sclerosis, parkinsonism, epilepsy, 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 -subunit, have been associated with familial hemiplegic migraine (ATP1A2), alternating hemiplegia of

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

22 e ion pump alpha2-Na/K ATPase cause familial hemiplegic migraine, but the mechanisms by which alpha2-

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

24 gical and developmental disorders, including hemiplegic migraine, epilepsy, developmental delay, and

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

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

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

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

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

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

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

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

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

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

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

36 ortical synapses in mouse models of familial hemiplegic migraine (FHM) suggested the hypothesis that

37 neurons (FS INs) in mouse models of familial hemiplegic migraine (FHM) suggested the hypothesis that

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

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

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

41 Familial hemiplegic migraine is an episodic neurological disorder

42 Familial hemiplegic migraine is associated with at least 13 diffe

43 Familial hemiplegic migraine is caused by mutations in the calciu

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

45 and has previously been related to familial hemiplegic migraine (MIM#602481) and alternating hemiple

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

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

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

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

50 3 patients with familial episodic ataxia and hemiplegic migraine to investigate the mutation frequenc

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

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

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

54 Patients suffering from familial hemiplegic migraine type 1 (FHM1) may have a disproporti

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

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

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

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

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

60 -gated calcium channels can lead to familial hemiplegic migraine type 1 (FHM1).

61 se Episodic Ataxia type 2 (EA2) and Familial Hemiplegic Migraine type 1 (FHM1).

62 tation analogous to the one causing familial hemiplegic migraine type 1 in humans, showed markedly re

63 In familial hemiplegic migraine type 1 mice, olcegepant 1mg/kg incre

64 In familial hemiplegic migraine type 1 mutant mice expressing human

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

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

67 Familial hemiplegic migraine type 1, a monogenic migraine variant

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

69 (NTG)-induced rat migraine model, a familial hemiplegic migraine type 2 (FHM2) mouse model, and a tra

70 we show that awake mice carrying a familial hemiplegic migraine type 2 (FHM2) mutation have slower c

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

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

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

74 enic subtype of migraine with aura, familial hemiplegic migraine type 3 (FHM3).

75 3V) missense mutation, which causes familial hemiplegic migraine type 3 in heterozygous family member

76 sistent with mild gain of function, familial hemiplegic migraine type 3 variants induce a larger effe

77 tional studies of both epilepsy and familial hemiplegic migraine type 3 variants reveal alterations o

78 were related to Dravet syndrome and familial hemiplegic migraine type 3 variants.

79 between SCN1A-related epilepsy and familial hemiplegic migraine type 3, and identifies sodium channe

80 SCN1A variants are associated with familial hemiplegic migraine type 3.

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

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

83 n mutations of NaV1.1 (SCN1A) cause familial hemiplegic migraine type-3 (FHM3), a subtype of migraine

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