Genotype-phenotype correlation in migraine without aura focusing on the rs1835740 variant on 8q22.1.

scientific article published on October 2011

Genotype-phenotype correlation in migraine without aura focusing on the rs1835740 variant on 8q22.1. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1007/S10194-011-0386-5
P932PMC publication ID3253151
P698PubMed publication ID21964821
P5875ResearchGate publication ID51688336

P50authorJes OlesenQ29643374
P2093author name stringHan Le
Malene Kirchmann
Anne Francke Christensen
P2860cites workClinical characteristics of 362 patients with familial migraine with aura.Q53288456
Migraine without aura and migraine with aura are distinct disorders. A population-based twin survey.Q53314169
Migraine without aura: A population-based twin studyQ57024768
THE COMMON MIGRAINE ATTACK MAY NOT BE INITIATED BY CEREBRAL ISCHAEMIAQ57025408
Focal hyperemia followed by spreading oligemia and impaired activation of rcbf in classic migraineQ57025417
Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entitiesQ57268943
Neuroexcitatory amino acid levels in plasma and cerebrospinal fluid during migraine attacksQ72219165
Therapeutic potential of novel glutamate receptor antagonists in migraineQ83791701
Pharmacogenomics in migraine: catching biomarkers for a predictable disease control [corrected]Q84576284
Ionotropic and metabotropic glutamate receptor structure and pharmacologyQ36054635
Migraine pathophysiologyQ36099504
Increased familial risk and evidence of genetic factor in migraineQ36904792
Migraine with and without aura: a single entity?Q37188617
Glutamate-immunoreactivity in the trigeminal and dorsal root ganglia, and intraspinal neurons and fibres in the dorsal horn of the ratQ42464930
Co-localization of 5-HT(1B/1D/1F) receptors and glutamate in trigeminal ganglia in ratsQ43642832
Evidence of a genetic factor in migraine with aura: a population-based Danish twin studyQ43798765
Cerebrospinal fluid glutamate levels in chronic migraineQ45021407
Objective assessment of cortical excitability in migraine with and without aura.Q48495941
Quantitative autoradiographic distribution of L-[3H]glutamate-binding sites in rat central nervous systemQ48642305
Migraine without aura and migraine with aura are distinct clinical entities: a study of four hundred and eighty-four male and female migraineurs from the general population.Q51011775
Inheritance of migraine investigated by complex segregation analysis.Q51049481
Migraine with aura and migraine without aura are not distinct entities: further evidence from a large Dutch population study.Q51810828
Mechanisms of migraine aura revealed by functional MRI in human visual cortexQ24635174
The International Classification of Headache Disorders: 2nd editionQ29547231
Extracellular glutamate, aspartate and arginine increase in the ventral posterolateral thalamic nucleus during nociceptive stimulationQ30778937
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.Q34023677
The inheritance of migraine with aura estimated by means of structural equation modellingQ34503071
The relative role of genetic and environmental factors in migraine without auraQ34505089
Prevalence and sex-ratio of the subtypes of migraine.Q34721342
Pathophysiology of the migraine aura. The spreading depression theoryQ34724476
Cerebrospinal fluid analyses in migraine patients and controlsQ34733869
Molecular genetics of migraineQ34981965
Glutamate receptor functions in sensory relay in the thalamusQ35081259
P275copyright licenseCreative Commons Attribution 2.0 GenericQ19125117
P6216copyright statuscopyrightedQ50423863
P433issue1
P921main subjectmigraine without auraQ3724157
migraineQ133823
genotype-phenotype correlationQ108687160
P304page(s)21-27
P577publication date2011-10-01
P1433published inThe journal of headache and pain : official journal of the Italian Society for the Study of HeadachesQ26842211
P1476titleGenotype-phenotype correlation in migraine without aura focusing on the rs1835740 variant on 8q22.1.
P478volume13