The Genetics of Migraine, The Lancet Neurology, vol.1, issue.5, pp.285-93, 2002. ,
DOI : 10.1016/S1474-4422(02)00134-5
A gene for familial hemiplegic migraine maps to chromosome 19, Nature Genetics, vol.37, issue.1, pp.40-45, 1993. ,
DOI : 10.1038/359794a0
Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4, Cell, vol.87, issue.3, pp.543-52, 1996. ,
DOI : 10.1016/S0092-8674(00)81373-2
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump ??2 subunit associated with familial hemiplegic migraine type 2, Nature Genetics, vol.33, issue.2, pp.192-198, 2003. ,
DOI : 10.1038/ng1081
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine, The Lancet, vol.366, issue.9483, pp.371-378, 2005. ,
DOI : 10.1016/S0140-6736(05)66786-4
Genetic heterogeneity of familial hemiplegic migraine, Am J Hum Genet, vol.55, pp.1166-72, 1994. ,
The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel, New England Journal of Medicine, vol.345, issue.1, pp.17-24, 2001. ,
DOI : 10.1056/NEJM200107053450103
No Mutations in CACNA1A and ATP1A2 in Probands With Common Types of Migraine, Archives of Neurology, vol.61, issue.6, pp.926-934, 2004. ,
DOI : 10.1001/archneur.61.6.926
Function and dysfunction of synaptic calcium channels: insights from mouse models, Current Opinion in Neurobiology, vol.15, issue.3, pp.257-65, 2005. ,
DOI : 10.1016/j.conb.2005.05.010
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the ??1A-voltage-dependent calcium channel, Nature Genetics, vol.25, issue.1, pp.62-71, 1997. ,
DOI : 10.1038/ng0197-62
Nomenclature of Voltage-Gated Calcium Channels, Neuron, vol.25, issue.3, pp.533-538, 2000. ,
DOI : 10.1016/S0896-6273(00)81057-0
Primary structure and functional expression from complementary DNA of a brain calcium channel, Nature, vol.350, issue.6317, pp.398-402, 1991. ,
DOI : 10.1038/350398a0
Primary structure of a calcium channel that is highly expressed in the rat cerebellum., Proceedings of the National Academy of Sciences, vol.88, issue.13, pp.5621-5626, 1991. ,
DOI : 10.1073/pnas.88.13.5621
Ion channels in presynaptic nerve terminals and control of transmitter release, Physiol Rev, vol.79, pp.1019-88, 1999. ,
A novel ?-conopeptide for the presynaptic localization of calcium channels at the mammalian neuromuscular junction, Journal of Neurocytology, vol.32, issue.1, pp.15-27, 1995. ,
DOI : 10.1007/BF01370157
Calcium-Channel Antibodies in the Lambert???Eaton Syndrome and Other Paraneoplastic Syndromes, New England Journal of Medicine, vol.332, issue.22, pp.1467-74, 1995. ,
DOI : 10.1056/NEJM199506013322203
Subunit interaction sites in voltage-dependent Ca2+ channels: role in channel function, Trends in Neurosciences, vol.21, issue.4, pp.148-54, 1998. ,
DOI : 10.1016/S0166-2236(97)01200-9
X-ray structure of a voltage-dependent K+ channel, Nature, vol.22, issue.6935, pp.33-41, 2003. ,
DOI : 10.1085/JGP.114.4.551
Calcium channel characteristics conferred on the sodium channel by single mutations, Nature, vol.356, issue.6368, pp.441-444, 1992. ,
DOI : 10.1038/356441a0
Structural determinants of fast inactivation of high voltage-activated Ca2+ channels, Trends in Neurosciences, vol.24, issue.3, pp.176-81, 2001. ,
DOI : 10.1016/S0166-2236(00)01738-0
Repositioning of charged I-II loop amino acid residues within the electric field by beta subunit as a novel working hypothesis for the control of fast P/Q calcium channel inactivation, European Journal of Neuroscience, vol.250, issue.7, pp.1759-72, 2004. ,
DOI : 10.1038/372097a0
Nomenclature of Voltage-Gated Sodium Channels, Neuron, vol.28, issue.2, pp.365-373, 2000. ,
DOI : 10.1016/S0896-6273(00)00116-1
Familial Hemiplegic Migraine Mutations Change ??1ACa2+ Channel Kinetics, Journal of Biological Chemistry, vol.273, issue.10, pp.5586-90, 1998. ,
DOI : 10.1074/jbc.273.10.5586
Three New Familial Hemiplegic Migraine Mutants Affect P/Q-type Ca2+ Channel Kinetics, Journal of Biological Chemistry, vol.275, issue.13, pp.9239-9282, 2000. ,
DOI : 10.1074/jbc.275.13.9239
Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine, J Neurosci, vol.19, pp.1610-1619, 1999. ,
Familial hemiplegic migraine mutations increase Ca2+ influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons, Proceedings of the National Academy of Sciences, vol.99, issue.20, pp.13284-13293, 2002. ,
DOI : 10.1073/pnas.192242399
Specific Kinetic Alterations of Human CaV2.1 Calcium Channels Produced by Mutation S218L Causing Familial Hemiplegic Migraine and Delayed Cerebral Edema and Coma after Minor Head Trauma, Journal of Biological Chemistry, vol.280, issue.18, pp.17678-86, 2005. ,
DOI : 10.1074/jbc.M501110200
Channel Gating, Journal of Biological Chemistry, vol.279, issue.50, pp.51844-50, 2004. ,
DOI : 10.1074/jbc.M408756200
Effects of familial hemiplegic migraine type 1 mutations on neuronal P/Q-type Ca2+ channel activity and inhibitory synaptic transmission, Proceedings of the National Academy of Sciences, vol.102, issue.7, pp.2590-2595, 2005. ,
DOI : 10.1073/pnas.0409896102
Regional expression and cellular localization of the alpha1 and beta subunit of high voltage-activated calcium channels in rat brain A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression, J Neurosci Neuron, vol.17, issue.41, pp.1339-1388, 1997. ,
How do G proteins directly control neuronal Ca2+ channel function?, Trends in Pharmacological Sciences, vol.26, issue.8, pp.427-463, 2005. ,
DOI : 10.1016/j.tips.2005.06.008
URL : https://hal.archives-ouvertes.fr/hal-00145603
2.1) calcium channels expressed in human embryonic kidney cells, The Journal of Physiology, vol.77, issue.2, pp.337-384, 2003. ,
DOI : 10.1113/jphysiol.2002.026716
Neurobiologie de la douleur trig??minale, m??decine/sciences, vol.19, issue.5, pp.567-74, 2003. ,
DOI : 10.1051/medsci/2003195567
Pathophysiology of the migraine aura, Brain, vol.117, issue.1, pp.199-210, 1994. ,
DOI : 10.1093/brain/117.1.199
Spreading and Synchronous Depressions of Cortical Activity in Acutely Injured Human Brain, Stroke, vol.33, issue.12, pp.2738-2781, 2002. ,
DOI : 10.1161/01.STR.0000043073.69602.09
Cortical spreading depression: Its role in migraine pathogenesis and possible therapeutic intervention strategies, Current Pain and Headache Reports, vol.67, issue.5, pp.410-416, 2004. ,
DOI : 10.1007/s11916-996-0016-0
NEUROSCIENCE:Energy on Demand, Science, vol.283, issue.5401, pp.496-503, 1999. ,
DOI : 10.1126/science.283.5401.496
Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine, Annals of Neurology, vol.67, issue.6, pp.753-60, 2001. ,
DOI : 10.1002/ana.1031
A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia, Neurology, vol.53, issue.1, pp.38-43, 1999. ,
DOI : 10.1212/WNL.53.1.38
A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel ??1A-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine, Clinical Genetics, vol.105, issue.1, pp.70-72, 2004. ,
DOI : 10.1111/j..2004.00187.x
CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy, Neurology, vol.55, issue.7, pp.1040-1042, 2000. ,
DOI : 10.1212/WNL.55.7.1040
Genetic heterogeneity in Italian families with familial hemiplegic migraine, Neurology, vol.53, issue.1, pp.26-33, 1999. ,
DOI : 10.1212/WNL.53.1.26
Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation, Neurology, vol.63, issue.6, pp.1136-1143, 2004. ,
DOI : 10.1212/01.WNL.0000138571.48593.FC