269 related articles for article (PubMed ID: 12235360)
41. Late sodium current blocker GS967 inhibits persistent currents induced by familial hemiplegic migraine type 3 mutations of the SCN1A gene.
Barbieri R; Bertelli S; Pusch M; Gavazzo P
J Headache Pain; 2019 Nov; 20(1):107. PubMed ID: 31730442
[TBL] [Abstract][Full Text] [Related]
42. Higher burden of rare frameshift indels in genes related to synaptic transmission separate familial hemiplegic migraine from common types of migraine.
Rasmussen AH; Olofsson I; Chalmer MA; Olesen J; Hansen TF
J Med Genet; 2020 Sep; 57(9):610-616. PubMed ID: 31980564
[TBL] [Abstract][Full Text] [Related]
43. Calcium channels and synaptic transmission in familial hemiplegic migraine type 1 animal models.
Uchitel OD; González Inchauspe C; Di Guilmi MN
Biophys Rev; 2014 Mar; 6(1):15-26. PubMed ID: 28509957
[TBL] [Abstract][Full Text] [Related]
44. Migraine mutations impair hippocampal learning despite enhanced long-term potentiation.
Dilekoz E; Houben T; Eikermann-Haerter K; Balkaya M; Lenselink AM; Whalen MJ; Spijker S; Ferrari MD; van den Maagdenberg AM; Ayata C
J Neurosci; 2015 Feb; 35(8):3397-402. PubMed ID: 25716839
[TBL] [Abstract][Full Text] [Related]
45. [From gene to disease; familial hemiplegic migraine as a result of mutations in a sodium-potassium pump gene].
Kors EE; Vanmolkot KR; Haan J; van den Maagdenberg AM; Frants RR; Ferrari MD
Ned Tijdschr Geneeskd; 2004 Sep; 148(39):1919-20. PubMed ID: 15495990
[TBL] [Abstract][Full Text] [Related]
46. α-Neurexins Together with α2δ-1 Auxiliary Subunits Regulate Ca
Brockhaus J; Schreitmüller M; Repetto D; Klatt O; Reissner C; Elmslie K; Heine M; Missler M
J Neurosci; 2018 Sep; 38(38):8277-8294. PubMed ID: 30104341
[TBL] [Abstract][Full Text] [Related]
47. Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics.
Kraus RL; Sinnegger MJ; Koschak A; Glossmann H; Stenirri S; Carrera P; Striessnig J
J Biol Chem; 2000 Mar; 275(13):9239-43. PubMed ID: 10734061
[TBL] [Abstract][Full Text] [Related]
48. Enhanced Thalamocortical Synaptic Transmission and Dysregulation of the Excitatory-Inhibitory Balance at the Thalamocortical Feedforward Inhibitory Microcircuit in a Genetic Mouse Model of Migraine.
Tottene A; Favero M; Pietrobon D
J Neurosci; 2019 Dec; 39(49):9841-9851. PubMed ID: 31645463
[TBL] [Abstract][Full Text] [Related]
49. Severe and progressive neurotransmitter release aberrations in familial hemiplegic migraine type 1 Cacna1a S218L knock-in mice.
Kaja S; Van de Ven RC; Broos LA; Frants RR; Ferrari MD; Van den Maagdenberg AM; Plomp JJ
J Neurophysiol; 2010 Sep; 104(3):1445-55. PubMed ID: 20631222
[TBL] [Abstract][Full Text] [Related]
50. Abnormal cortical synaptic transmission in CaV2.1 knockin mice with the S218L missense mutation which causes a severe familial hemiplegic migraine syndrome in humans.
Vecchia D; Tottene A; van den Maagdenberg AM; Pietrobon D
Front Cell Neurosci; 2015; 9():8. PubMed ID: 25741235
[TBL] [Abstract][Full Text] [Related]
51. Modeling NaV1.1/SCN1A sodium channel mutations in a microcircuit with realistic ion concentration dynamics suggests differential GABAergic mechanisms leading to hyperexcitability in epilepsy and hemiplegic migraine.
Lemaire L; Desroches M; Krupa M; Pizzamiglio L; Scalmani P; Mantegazza M
PLoS Comput Biol; 2021 Jul; 17(7):e1009239. PubMed ID: 34314446
[TBL] [Abstract][Full Text] [Related]
52. Absence of known familial hemiplegic migraine (FHM) mutations in the CACNA1A gene in patients with common migraine: implications for genetic testing.
Wieser T; Mueller C; Evers S; Zierz S; Deufel T
Clin Chem Lab Med; 2003 Mar; 41(3):272-5. PubMed ID: 12705332
[TBL] [Abstract][Full Text] [Related]
53. Familial hemiplegic migraine: a ion channel disorder.
Carrera P; Stenirri S; Ferrari M; Battistini S
Brain Res Bull; 2001 Oct-Nov 1; 56(3-4):239-41. PubMed ID: 11719257
[TBL] [Abstract][Full Text] [Related]
54. Functional consequences of P/Q-type Ca2+ channel Cav2.1 missense mutations associated with episodic ataxia type 2 and progressive ataxia.
Wappl E; Koschak A; Poteser M; Sinnegger MJ; Walter D; Eberhart A; Groschner K; Glossmann H; Kraus RL; Grabner M; Striessnig J
J Biol Chem; 2002 Mar; 277(9):6960-6. PubMed ID: 11742003
[TBL] [Abstract][Full Text] [Related]
55. Migraine mutations increase stroke vulnerability by facilitating ischemic depolarizations.
Eikermann-Haerter K; Lee JH; Yuzawa I; Liu CH; Zhou Z; Shin HK; Zheng Y; Qin T; Kurth T; Waeber C; Ferrari MD; van den Maagdenberg AM; Moskowitz MA; Ayata C
Circulation; 2012 Jan; 125(2):335-45. PubMed ID: 22144569
[TBL] [Abstract][Full Text] [Related]
56. Enhanced excitatory transmission at cortical synapses as the basis for facilitated spreading depression in Ca(v)2.1 knockin migraine mice.
Tottene A; Conti R; Fabbro A; Vecchia D; Shapovalova M; Santello M; van den Maagdenberg AM; Ferrari MD; Pietrobon D
Neuron; 2009 Mar; 61(5):762-73. PubMed ID: 19285472
[TBL] [Abstract][Full Text] [Related]
57. Gain of function of sporadic/familial hemiplegic migraine-causing SCN1A mutations: Use of an optimized cDNA.
Bertelli S; Barbieri R; Pusch M; Gavazzo P
Cephalalgia; 2019 Apr; 39(4):477-488. PubMed ID: 29986598
[TBL] [Abstract][Full Text] [Related]
58. Spreading depression and the clinical correlates of migraine.
Eikermann-Haerter K; Negro A; Ayata C
Rev Neurosci; 2013; 24(4):353-63. PubMed ID: 23907418
[TBL] [Abstract][Full Text] [Related]
59. TNFα levels and macrophages expression reflect an inflammatory potential of trigeminal ganglia in a mouse model of familial hemiplegic migraine.
Franceschini A; Vilotti S; Ferrari MD; van den Maagdenberg AM; Nistri A; Fabbretti E
PLoS One; 2013; 8(1):e52394. PubMed ID: 23326332
[TBL] [Abstract][Full Text] [Related]
60. Is the CACNA1A gene involved in familial migraine with aura?
Brugnoni R; Leone M; Rigamonti A; Moranduzzo E; Cornelio F; Mantegazza R; Bussone G
Neurol Sci; 2002 Apr; 23(1):1-5. PubMed ID: 12111613
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
