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NEUROLOGY (2010)
Defective membrane expression of the Na+-HCO3- cotransporter NBCe1 is associated with familial migraine
Masashi Suzuki et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Next generation tools for the annotation of human SNPs
Rachel Karchin
BRIEFINGS IN BIOINFORMATICS (2009)
Migraine and genetic and acquired vasculopathies
A. H. Stam et al.
CEPHALALGIA (2009)
Association of the C677T polymorphism in the MTHFR gene with migraine: a meta-analysis
E. Rubino et al.
CEPHALALGIA (2009)
First mutation in the voltage-gated NaV1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy
M-J Castro et al.
CEPHALALGIA (2009)
Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutation identified in sporadic or familial hemiplegic migraine
Neslihan N. Tavraz et al.
CHANNELS (2009)
Molecular genetics of migraine
Boukje de Vries et al.
HUMAN GENETICS (2009)
Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing
R. W. Labrum et al.
JOURNAL OF MEDICAL GENETICS (2009)
Enhanced Excitatory Transmission at Cortical Synapses as the Basis for Facilitated Spreading Depression in Cav2.1 Knockin Migraine Mice
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NEURON (2009)
Epilepsy as part of the phenotype associated with ATP1A2 mutations
Liesbet Deprez et al.
EPILEPSIA (2008)
Diverse Functional Consequences of Mutations in the Na+/K+-ATPase α2-Subunit Causing Familial Hemiplegic Migraine Type 2
Neslihan N. Tavraz et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Self-limited hyperexcitability:: Functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel
Sandrine Cestele et al.
JOURNAL OF NEUROSCIENCE (2008)
Divergent sodium channel defects in familial hemiplegic migraine
Kristopher M. Kahlig et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant Cav2.1 channels
Kei Watase et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
TRESK two-pore-domain K+ channels constitute a significant component of background potassium currents in murine dorsal root ganglion neurones
Tina Dobler et al.
JOURNAL OF PHYSIOLOGY-LONDON (2007)
Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine
B. de Vries et al.
NEUROLOGY (2007)
G protein β3 polymorphism and triptan response in cluster headache
M. Schuerks et al.
CLINICAL PHARMACOLOGY & THERAPEUTICS (2007)
Brainstem dysfunction in chronic migraine as evidenced by neurophysiological and positron emission tomography studies
Sheena K. Aurora et al.
HEADACHE (2007)
Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons:: A circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation
Ikuo Ogiwara et al.
JOURNAL OF NEUROSCIENCE (2007)
Modeling of a human circadian mutation yields insights into clock regulation by PER2
Y. Xu et al.
CELL (2007)
Testing of variants of the MTHFR and ESR1 genes in 1798 Finnish individuals fails to confirm the association with migraine with aura
M. A. Kaunisto et al.
CEPHALALGIA (2006)
MTHFR C677T polymorphism and migraine with aura
Unda Todt et al.
ANNALS OF NEUROLOGY (2006)
Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy
Frank H. Yu et al.
NATURE NEUROSCIENCE (2006)
TREK-2 (K2P10.1) and TRESK (K2P18.1) are major background K+ channels in dorsal root ganglion neurons
Dawon Kang et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2006)
Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation
KRJ Vanmolkot et al.
ANNALS OF NEUROLOGY (2006)
Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly
G. Breedveld et al.
JOURNAL OF MEDICAL GENETICS (2006)
ATP1A2 Mutations in 11 Families With Familial Hemiplegic Migraine
Florence Riant et al.
HUMAN MUTATION (2005)
Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures
JC Jen et al.
NEUROLOGY (2005)
Alterations in the α2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2
L Segall et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine
M Dichgans et al.
LANCET (2005)
Na,K-ATPase mutations in familial hemiplegic migraine lead to functional inactivation
JB Koenderink et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES (2005)
Functional consequences of a CKIδ mutation causing familial advanced sleep phase syndrome
Y Xu et al.
NATURE (2005)
Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities
DR Nyholt et al.
GENETIC EPIDEMIOLOGY (2004)
A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression
AMJM van den Maagdenberg et al.
NEURON (2004)
A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood
MT Bassi et al.
JOURNAL OF MEDICAL GENETICS (2004)
The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway
HY Lee et al.
HUMAN MOLECULAR GENETICS (2004)
Elicited repetitive daily blindness - A new familial disorder related to migraine and epilepsy
D Le Fort et al.
NEUROLOGY (2004)
Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosis
S Rainier et al.
ARCHIVES OF NEUROLOGY (2004)
Hyperexcitability of the primary somatosensory cortex in migraine -: a magnetoencephalographic study
E Lang et al.
BRAIN (2004)
Functional effects of Na+,K+-ATPase gene mutations linked to familial hemiplegic migraine
O Capendeguy et al.
NEUROMOLECULAR MEDICINE (2004)
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants
K Jurkat-Rott et al.
NEUROLOGY (2004)
Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation
EE Kors et al.
ARCHIVES OF NEUROLOGY (2003)
Population stratification and spurious allelic association
LR Cardon et al.
LANCET (2003)
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump α2 subunit associated with familial hemiplegic migraine type 2
M De Fusco et al.
NATURE GENETICS (2003)
Familial hemiplegic migraine mutations increase Ca2+ influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons
A Tottene et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
An epidemiological survey of hemiplegic migraine
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CEPHALALGIA (2002)
Migraine without aura and migraine with aura are distinct disorders. A population-based twin survey
MB Russell et al.
HEADACHE (2002)
Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model
H Bolay et al.
NATURE MEDICINE (2002)
Clinical and molecular correlations in spinocerebellar ataxia type 6 - A study of 24 Dutch families
RJ Sinke et al.
ARCHIVES OF NEUROLOGY (2001)
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
A Ducros et al.
NEW ENGLAND JOURNAL OF MEDICINE (2001)
Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine
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ANNALS OF NEUROLOGY (2001)
From ionic currents to molecular mechanisms: The structure and function of voltage-gated sodium channels
WA Catterall
NEURON (2000)
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