Related references
Note: Only part of the references are listed.Cortical Excitability in Chronic Migraine
Gianluca Coppola et al.
CURRENT PAIN AND HEADACHE REPORTS (2012)
Heritability and genome-wide linkage analysis of migraine in the genetic isolate of Norfolk Island
Hannah C. Cox et al.
GENE (2012)
Genetics of migraine in the age of genome-wide association studies
Markus Schuerks
JOURNAL OF HEADACHE AND PAIN (2012)
Genome-wide association analysis identifies susceptibility loci for migraine without aura
Tobias Freilinger et al.
NATURE GENETICS (2012)
Pharmacogenomics in neurology: Current state and future steps
Andrew Chan et al.
ANNALS OF NEUROLOGY (2011)
New directions in migraine
Greg A. Weir et al.
BMC MEDICINE (2011)
Association of a Notch 3 gene polymorphism with migraine susceptibility
S. Menon et al.
CEPHALALGIA (2011)
A new Italian FHM2 family: Clinical aspects and functional analysis of the disease-associated mutation
Lucio Santoro et al.
CEPHALALGIA (2011)
Gene polymorphisms involved in triptans pharmacokinetics and pharmacodynamics in migraine therapy
Giovanna Gentile et al.
EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY (2011)
Identification of molecular genetic factors that influence migraine
Bridget H. Maher et al.
MOLECULAR GENETICS AND GENOMICS (2011)
Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype
P. Kaufmann et al.
NEUROLOGY (2011)
Prophylaxis of migraine: general principles and patient acceptance
Domenico D'Amico et al.
Neuropsychiatric Disease and Treatment (2011)
Role of 2 Common Variants of 5HT2A Gene in Medication Overuse Headache
Salvatore Terrazzino et al.
HEADACHE (2010)
Lack of association between five serotonin metabolism-related genes and medication overuse headache
Sabina Cevoli et al.
JOURNAL OF HEADACHE AND PAIN (2010)
Genetic polymorphisms related to efficacy and overuse of triptans in chronic migraine
Giovanna Gentile et al.
JOURNAL OF HEADACHE AND PAIN (2010)
Energetics, epigenetics, mitochondrial genetics
Douglas C. Wallace et al.
MITOCHONDRION (2010)
A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura
Ronald G. Lafreniere et al.
NATURE MEDICINE (2010)
Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays
Radoje Drmanac et al.
SCIENCE (2010)
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)
Molecular genetics of migraine
Boukje de Vries et al.
HUMAN GENETICS (2009)
Drug consumption in medication overuse headache is influenced by brain-derived neurotrophic factor Val66Met polymorphism
Cherubino Di Lorenzo et al.
JOURNAL OF HEADACHE AND PAIN (2009)
The Epidemiology, Burden, and Comorbidities of Migraine
Marcelo E. Bigal et al.
NEUROLOGIC CLINICS (2009)
Elicited repetitive daily blindness A new phenotype associated with hemiplegic migraine and SCN1A mutations
K. Vahedi et al.
NEUROLOGY (2009)
Mitochondrial DNA haplogroups influence the therapeutic response to riboflavin in migraineurs
C. Di Lorenzo et al.
NEUROLOGY (2009)
Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes Basic Concepts, Clinical Phenotype, and Therapeutic Management of MELAS Syndrome
Douglas M. Sproule et al.
YEAR IN NEUROLOGY 2008 (2008)
Angiotensin-converting enzyme gene insertion/deletion polymorphism in migraine patients
Erling Tronvik et al.
BMC NEUROLOGY (2008)
Animal models of migraine headache and aura
Katharina Eikermann-Haerter et al.
CURRENT OPINION IN NEUROLOGY (2008)
Epilepsy as part of the phenotype associated with ATP1A2 mutations
Liesbet Deprez et al.
EPILEPSIA (2008)
A high-density association screen of 155 ion transport genes for involvement with common migraine
Dale R. Nyholt et al.
HUMAN MOLECULAR GENETICS (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)
Stepwise Developmental Regression Associated With Novel CACNA1A Mutation
Andrea A. Guerin et al.
PEDIATRIC NEUROLOGY (2008)
The wolframin His611Arg polymorphism influences medication overuse headache
C. Di Lorenzo et al.
NEUROSCIENCE LETTERS (2007)
Mapping the chromosomal targets of STAT1 by Sequence Tag Analysis of Genomic Enrichment (STAGE)
Akshay A. Bhinge et al.
GENOME RESEARCH (2007)
Electrocardiogram in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy patients without any clinical evidence of coronary artery disease - A case-control study
R Cumurciuc et al.
STROKE (2006)
A novel ATP1A2 mutation in a family with FHM type II
F Pierelli et al.
CEPHALALGIA (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)
Familial basilar migraine associated with a new mutation in the ATP1A2 gene
A Ambrosini et al.
NEUROLOGY (2005)
Rare missense variants in ATP1A2 in families with clustering of common forms of migraine
U Todt et al.
HUMAN MUTATION (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)
Sodium channel mutations in epilepsy and other neurological disorders
MH Meisler et al.
JOURNAL OF CLINICAL INVESTIGATION (2005)
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine
M Dichgans et al.
LANCET (2005)
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
A Tottene et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Neurologic symptoms are common during gestation and puerperium in CADASIL
S Roine et al.
NEUROLOGY (2005)
Retinal vascular abnormalities in CADASIL
C Haritoglou et al.
NEUROLOGY (2004)
A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression
AMJM van den Maagdenberg et al.
NEURON (2004)
Novel splice site CACNA1A mutation causing episodic ataxia type 2
MA Kaunisto et al.
NEUROGENETICS (2004)
Migraine as a risk factor for subclinical brain lesions
MC Kruit et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2004)
A G301R Na+/K+-ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs
M Spadaro et al.
NEUROGENETICS (2004)
Elicited repetitive daily blindness - A new familial disorder related to migraine and epilepsy
D Le Fort et al.
NEUROLOGY (2004)
Alternating hemiplegia of childhood or familial hemiplegic migraine?:: A novel ATP1A2 mutation
KJ Swoboda et al.
ANNALS OF NEUROLOGY (2004)
Kinetic alterations due to a missense mutation in the Na,K-ATPase α2 subunit cause familial hemiplegic migraine type 2
L Segall et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants
K Jurkat-Rott et al.
NEUROLOGY (2004)
Novel mutations in the Na+,K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions
KRJ Vanmolkot et al.
ANNALS OF NEUROLOGY (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)
Sporadic hemiplegic migraine is an aetiologically heterogeneous disorder
LL Thomsen et al.
CEPHALALGIA (2003)
A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria
LL Thomsen et al.
BRAIN (2002)
Share Paper
