Selma A Serra, Noèlia Fernàndez-Castillo, Alfons Macaya, Bru Cormand, Miguel A Valverde, José M Fernández-Fernández. Pflugers Arch 2009
Times Cited: 28
Times Cited: 28
Times Cited
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The S218L familial hemiplegic migraine mutation promotes deinhibition of Ca(v)2.1 calcium channels during direct G-protein regulation.
Norbert Weiss, Alejandro Sandoval, Ricardo Felix, Arn Van den Maagdenberg, Michel De Waard. Pflugers Arch 2008
Norbert Weiss, Alejandro Sandoval, Ricardo Felix, Arn Van den Maagdenberg, Michel De Waard. Pflugers Arch 2008
71
A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.
Arn M J M van den Maagdenberg, Daniela Pietrobon, Tommaso Pizzorusso, Simon Kaja, Ludo A M Broos, Tiziana Cesetti, Rob C G van de Ven, Angelita Tottene, Jos van der Kaa, Jaap J Plomp,[...]. Neuron 2004
Arn M J M van den Maagdenberg, Daniela Pietrobon, Tommaso Pizzorusso, Simon Kaja, Ludo A M Broos, Tiziana Cesetti, Rob C G van de Ven, Angelita Tottene, Jos van der Kaa, Jaap J Plomp,[...]. Neuron 2004
67
The familial hemiplegic migraine mutation R192Q reduces G-protein-mediated inhibition of P/Q-type (Ca(V)2.1) calcium channels expressed in human embryonic kidney cells.
Karim Melliti, Manfred Grabner, Guy R Seabrook. J Physiol 2003
Karim Melliti, Manfred Grabner, Guy R Seabrook. J Physiol 2003
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Enhanced excitatory transmission at cortical synapses as the basis for facilitated spreading depression in Ca(v)2.1 knockin migraine mice.
Angelita Tottene, Rossella Conti, Alessandra Fabbro, Dania Vecchia, Maryna Shapovalova, Mirko Santello, Arn M J M van den Maagdenberg, Michel D Ferrari, Daniela Pietrobon. Neuron 2009
Angelita Tottene, Rossella Conti, Alessandra Fabbro, Dania Vecchia, Maryna Shapovalova, Mirko Santello, Arn M J M van den Maagdenberg, Michel D Ferrari, Daniela Pietrobon. Neuron 2009
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Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.
E E Kors, G M Terwindt, F L Vermeulen, R B Fitzsimons, P E Jardine, P Heywood, S Love, A M van den Maagdenberg, J Haan, R R Frants,[...]. Ann Neurol 2001
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53
Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.
Angelita Tottene, Tommaso Fellin, Stefano Pagnutti, Siro Luvisetto, Joerg Striessnig, Colin Fletcher, Daniela Pietrobon. Proc Natl Acad Sci U S A 2002
Angelita Tottene, Tommaso Fellin, Stefano Pagnutti, Siro Luvisetto, Joerg Striessnig, Colin Fletcher, Daniela Pietrobon. Proc Natl Acad Sci U S A 2002
53
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.
Angelita Tottene, Francesca Pivotto, Tommaso Fellin, Tiziana Cesetti, Arn M J M van den Maagdenberg, Daniela Pietrobon. J Biol Chem 2005
Angelita Tottene, Francesca Pivotto, Tommaso Fellin, Tiziana Cesetti, Arn M J M van den Maagdenberg, Daniela Pietrobon. J Biol Chem 2005
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The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
A Ducros, C Denier, A Joutel, M Cecillon, C Lescoat, K Vahedi, F Darcel, E Vicaut, M G Bousser, E Tournier-Lasserve. N Engl J Med 2001
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Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
R A Ophoff, G M Terwindt, M N Vergouwe, R van Eijk, P J Oefner, S M Hoffman, J E Lamerdin, H W Mohrenweiser, D E Bulman, M Ferrari,[...]. Cell 1996
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High cortical spreading depression susceptibility and migraine-associated symptoms in Ca(v)2.1 S218L mice.
Arn M J M van den Maagdenberg, Tommaso Pizzorusso, Simon Kaja, Nicole Terpolilli, Maryna Shapovalova, Freek E Hoebeek, Curtis F Barrett, Lisa Gherardini, Rob C G van de Ven, Boyan Todorov,[...]. Ann Neurol 2010
Arn M J M van den Maagdenberg, Tommaso Pizzorusso, Simon Kaja, Nicole Terpolilli, Maryna Shapovalova, Freek E Hoebeek, Curtis F Barrett, Lisa Gherardini, Rob C G van de Ven, Boyan Todorov,[...]. Ann Neurol 2010
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Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model.
Hayrunnisa Bolay, Uwe Reuter, Andrew K Dunn, Zhihong Huang, David A Boas, Michael A Moskowitz. Nat Med 2002
Hayrunnisa Bolay, Uwe Reuter, Andrew K Dunn, Zhihong Huang, David A Boas, Michael A Moskowitz. Nat Med 2002
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Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects.
Carmen Müllner, Ludo A M Broos, Arn M J M van den Maagdenberg, Jörg Striessnig. J Biol Chem 2004
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Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine.
M Hans, S Luvisetto, M E Williams, M Spagnolo, A Urrutia, A Tottene, P F Brust, E C Johnson, M M Harpold, K A Stauderman,[...]. J Neurosci 1999
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Genetic and hormonal factors modulate spreading depression and transient hemiparesis in mouse models of familial hemiplegic migraine type 1.
Katharina Eikermann-Haerter, Ergin Dileköz, Chiho Kudo, Sean I Savitz, Christian Waeber, Michael J Baum, Michel D Ferrari, Arn M J M van den Maagdenberg, Michael A Moskowitz, Cenk Ayata. J Clin Invest 2009
Katharina Eikermann-Haerter, Ergin Dileköz, Chiho Kudo, Sean I Savitz, Christian Waeber, Michael J Baum, Michel D Ferrari, Arn M J M van den Maagdenberg, Michael A Moskowitz, Cenk Ayata. J Clin Invest 2009
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Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
Martin Dichgans, Tobias Freilinger, Gertrud Eckstein, Elena Babini, Bettina Lorenz-Depiereux, Saskia Biskup, Michel D Ferrari, Jürgen Herzog, Arn M J M van den Maagdenberg, Michael Pusch,[...]. Lancet 2005
Martin Dichgans, Tobias Freilinger, Gertrud Eckstein, Elena Babini, Bettina Lorenz-Depiereux, Saskia Biskup, Michel D Ferrari, Jürgen Herzog, Arn M J M van den Maagdenberg, Michael Pusch,[...]. Lancet 2005
35
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.
Maurizio De Fusco, Roberto Marconi, Laura Silvestri, Luigia Atorino, Luca Rampoldi, Letterio Morgante, Andrea Ballabio, Paolo Aridon, Giorgio Casari. Nat Genet 2003
Maurizio De Fusco, Roberto Marconi, Laura Silvestri, Luigia Atorino, Luca Rampoldi, Letterio Morgante, Andrea Ballabio, Paolo Aridon, Giorgio Casari. Nat Genet 2003
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Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics.
R L Kraus, M J Sinnegger, A Koschak, H Glossmann, S Stenirri, P Carrera, J Striessnig. J Biol Chem 2000
R L Kraus, M J Sinnegger, A Koschak, H Glossmann, S Stenirri, P Carrera, J Striessnig. J Biol Chem 2000
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Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics.
R L Kraus, M J Sinnegger, H Glossmann, S Hering, J Striessnig. J Biol Chem 1998
R L Kraus, M J Sinnegger, H Glossmann, S Hering, J Striessnig. J Biol Chem 1998
35
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
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Immunochemical identification and subcellular distribution of the alpha 1A subunits of brain calcium channels.
R E Westenbroek, T Sakurai, E M Elliott, J W Hell, T V Starr, T P Snutch, W A Catterall. J Neurosci 1995
R E Westenbroek, T Sakurai, E M Elliott, J W Hell, T V Starr, T P Snutch, W A Catterall. J Neurosci 1995
32
Presynaptic Ca2+ channels compete for channel type-preferring slots in altered neurotransmission arising from Ca2+ channelopathy.
Yu-Qing Cao, Erika S Piedras-Rentería, Geoffrey B Smith, Gong Chen, Nobutoshi C Harata, Richard W Tsien. Neuron 2004
Yu-Qing Cao, Erika S Piedras-Rentería, Geoffrey B Smith, Gong Chen, Nobutoshi C Harata, Richard W Tsien. Neuron 2004
32
Ca(V)2.1 P/Q-type calcium channel alternative splicing affects the functional impact of familial hemiplegic migraine mutations: implications for calcium channelopathies.
Paul J Adams, Esperanza Garcia, Laurence S David, Kirk J Mulatz, Sian D Spacey, Terrance P Snutch. Channels (Austin) 2009
Paul J Adams, Esperanza Garcia, Laurence S David, Kirk J Mulatz, Sian D Spacey, Terrance P Snutch. Channels (Austin) 2009
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Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel.
Sandrine Cestèle, Paolo Scalmani, Raffaella Rusconi, Benedetta Terragni, Silvana Franceschetti, Massimo Mantegazza. J Neurosci 2008
Sandrine Cestèle, Paolo Scalmani, Raffaella Rusconi, Benedetta Terragni, Silvana Franceschetti, Massimo Mantegazza. J Neurosci 2008
28
Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes.
E Cuenca-León, R Corominas, N Fernàndez-Castillo, V Volpini, M Del Toro, M Roig, A Macaya, B Cormand. Cephalalgia 2008
E Cuenca-León, R Corominas, N Fernàndez-Castillo, V Volpini, M Del Toro, M Roig, A Macaya, B Cormand. Cephalalgia 2008
28
Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia.
Paola Imbrici, Stephen L Jaffe, Louise H Eunson, Nicholas P Davies, Colin Herd, Robert Robertson, Dimitri M Kullmann, Michael G Hanna. Brain 2004
Paola Imbrici, Stephen L Jaffe, Louise H Eunson, Nicholas P Davies, Colin Herd, Robert Robertson, Dimitri M Kullmann, Michael G Hanna. Brain 2004
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Suppression of cortical spreading depression in migraine prophylaxis.
Cenk Ayata, Hongwei Jin, Chiho Kudo, Turgay Dalkara, Michael A Moskowitz. Ann Neurol 2006
Cenk Ayata, Hongwei Jin, Chiho Kudo, Turgay Dalkara, Michael A Moskowitz. Ann Neurol 2006
25
Mechanisms of migraine aura revealed by functional MRI in human visual cortex.
N Hadjikhani, M Sanchez Del Rio, O Wu, D Schwartz, D Bakker, B Fischl, K K Kwong, F M Cutrer, B R Rosen, R B Tootell,[...]. Proc Natl Acad Sci U S A 2001
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25
25
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Mechanisms of spreading depression and hypoxic spreading depression-like depolarization.
G G Somjen. Physiol Rev 2001
G G Somjen. Physiol Rev 2001
25
Androgenic suppression of spreading depression in familial hemiplegic migraine type 1 mutant mice.
Katharina Eikermann-Haerter, Michael J Baum, Michel D Ferrari, Arn M J M van den Maagdenberg, Michael A Moskowitz, Cenk Ayata. Ann Neurol 2009
Katharina Eikermann-Haerter, Michael J Baum, Michel D Ferrari, Arn M J M van den Maagdenberg, Michael A Moskowitz, Cenk Ayata. Ann Neurol 2009
25
Function and dysfunction of synaptic calcium channels: insights from mouse models.
Daniela Pietrobon. Curr Opin Neurobiol 2005
Daniela Pietrobon. Curr Opin Neurobiol 2005
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Gating deficiency in a familial hemiplegic migraine type 1 mutant P/Q-type calcium channel.
Curtis F Barrett, Yu-Qing Cao, Richard W Tsien. J Biol Chem 2005
Curtis F Barrett, Yu-Qing Cao, Richard W Tsien. J Biol Chem 2005
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Calcium channel regulation and presynaptic plasticity.
William A Catterall, Alexandra P Few. Neuron 2008
William A Catterall, Alexandra P Few. Neuron 2008
25
Genome-wide association study reveals three susceptibility loci for common migraine in the general population.
Daniel I Chasman, Markus Schürks, Verneri Anttila, Boukje de Vries, Ulf Schminke, Lenore J Launer, Gisela M Terwindt, Arn M J M van den Maagdenberg, Konstanze Fendrich, Henry Völzke,[...]. Nat Genet 2011
Daniel I Chasman, Markus Schürks, Verneri Anttila, Boukje de Vries, Ulf Schminke, Lenore J Launer, Gisela M Terwindt, Arn M J M van den Maagdenberg, Konstanze Fendrich, Henry Völzke,[...]. Nat Genet 2011
25
Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2.
Loredana Leo, Lisa Gherardini, Virginia Barone, Maurizio De Fusco, Daniela Pietrobon, Tommaso Pizzorusso, Giorgio Casari. PLoS Genet 2011
Loredana Leo, Lisa Gherardini, Virginia Barone, Maurizio De Fusco, Daniela Pietrobon, Tommaso Pizzorusso, Giorgio Casari. PLoS Genet 2011
25
Molecular genetics of migraine.
Boukje de Vries, Rune R Frants, Michel D Ferrari, Arn M J M van den Maagdenberg. Hum Genet 2009
Boukje de Vries, Rune R Frants, Michel D Ferrari, Arn M J M van den Maagdenberg. Hum Genet 2009
25
Cerebellar ataxia by enhanced Ca(V)2.1 currents is alleviated by Ca2+-dependent K+-channel activators in Cacna1a(S218L) mutant mice.
Zhenyu Gao, Boyan Todorov, Curtis F Barrett, Stijn van Dorp, Michel D Ferrari, Arn M J M van den Maagdenberg, Chris I De Zeeuw, Freek E Hoebeek. J Neurosci 2012
Zhenyu Gao, Boyan Todorov, Curtis F Barrett, Stijn van Dorp, Michel D Ferrari, Arn M J M van den Maagdenberg, Chris I De Zeeuw, Freek E Hoebeek. J Neurosci 2012
25
Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation.
Yee-Cheun Chan, Jean-Marc Burgunder, Einar Wilder-Smith, Soh-Eng Chew, Karen M J Lam-Mok-Sing, Vijay Sharma, Benjamin K C Ong. J Clin Neurosci 2008
Yee-Cheun Chan, Jean-Marc Burgunder, Einar Wilder-Smith, Soh-Eng Chew, Karen M J Lam-Mok-Sing, Vijay Sharma, Benjamin K C Ong. J Clin Neurosci 2008
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Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.
A Ducros, C Denier, A Joutel, K Vahedi, A Michel, F Darcel, M Madigand, D Guerouaou, F Tison, J Julien,[...]. Am J Hum Genet 1999
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21
Diverse functional consequences of mutations in the Na+/K+-ATPase alpha2-subunit causing familial hemiplegic migraine type 2.
Neslihan N Tavraz, Thomas Friedrich, Katharina L Dürr, Jan B Koenderink, Ernst Bamberg, Tobias Freilinger, Martin Dichgans. J Biol Chem 2008
Neslihan N Tavraz, Thomas Friedrich, Katharina L Dürr, Jan B Koenderink, Ernst Bamberg, Tobias Freilinger, Martin Dichgans. J Biol Chem 2008
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Migraine--current understanding and treatment.
Peter J Goadsby, Richard B Lipton, Michel D Ferrari. N Engl J Med 2002
Peter J Goadsby, Richard B Lipton, Michel D Ferrari. N Engl J Med 2002
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Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop.
F Cricchi, C Di Lorenzo, G S Grieco, C Rengo, A Cardinale, M Racaniello, F M Santorelli, G Nappi, F Pierelli, C Casali. J Neurol Sci 2007
F Cricchi, C Di Lorenzo, G S Grieco, C Rengo, A Cardinale, M Racaniello, F M Santorelli, G Nappi, F Pierelli, C Casali. J Neurol Sci 2007
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Specificity in the interaction of HVA Ca2+ channel types with Ca2+-dependent AHPs and firing behavior in neocortical pyramidal neurons.
J C Pineda, R S Waters, R C Foehring. J Neurophysiol 1998
J C Pineda, R S Waters, R C Foehring. J Neurophysiol 1998
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Gene dosage-dependent transmitter release changes at neuromuscular synapses of CACNA1A R192Q knockin mice are non-progressive and do not lead to morphological changes or muscle weakness.
S Kaja, R C G van de Ven, L A M Broos, H Veldman, J G van Dijk, J J G M Verschuuren, R R Frants, M D Ferrari, A M J M van den Maagdenberg, J J Plomp. Neuroscience 2005
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21
Effects of familial hemiplegic migraine type 1 mutations on neuronal P/Q-type Ca2+ channel activity and inhibitory synaptic transmission.
Yu-Qing Cao, Richard W Tsien. Proc Natl Acad Sci U S A 2005
Yu-Qing Cao, Richard W Tsien. Proc Natl Acad Sci U S A 2005
21
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.