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Erratum zu: Konsensusstatement der Migräne- und Kopfschmerzgesellschaften (DMKG, ÖKSG & SKG) zur Therapiedauer der medikamentösen Migräneprophylaxe.
- Published in:
- 2023
- By:
- Publication type:
- Correction Notice
Konsensusstatement der Migräne- und Kopfschmerzgesellschaften (DMKG, ÖKSG & SKG) zur Therapiedauer der medikamentösen Migräneprophylaxe.
- Published in:
- Der Nervenarzt, 2023, v. 94, n. 4, p. 306, doi. 10.1007/s00115-022-01403-1
- By:
- Publication type:
- Article
Hypoglossal nerve palsy due to internal carotid artery dissection.
- Published in:
- Vascular Medicine, 2010, v. 15, n. 5, p. 435, doi. 10.1177/1358863X10378789
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- Publication type:
- Article
Computed tomography angiography vs 3 T black-blood cardiovascular magnetic resonance for identification of symptomatic carotid plaques.
- Published in:
- Journal of Cardiovascular Magnetic Resonance (BioMed Central), 2014, v. 16, p. 1, doi. 10.1186/s12968-014-0084-y
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- Publication type:
- Article
Comparison of symptomatic and asymptomatic atherosclerotic carotid plaques using parallel imaging and 3 T black-blood in vivo CMR.
- Published in:
- Journal of Cardiovascular Magnetic Resonance (BioMed Central), 2013, v. 15, n. 1, p. 44, doi. 10.1186/1532-429X-15-44
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- Publication type:
- Article
Prevalence of complicated carotid atherosclerotic plaques ispilateral to ischemic cryptogenic stroke using high-resolution mri.
- Published in:
- 2011
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- Publication type:
- Abstract
Neurologic manifestations of COVID-19 in critically ill patients: results of the prospective multicenter registry PANDEMIC.
- Published in:
- Critical Care, 2022, v. 26, n. 1, p. 1, doi. 10.1186/s13054-022-04080-3
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- Publication type:
- Article
Neurologic manifestations of COVID-19 in critically ill patients: results of the prospective multicenter registry PANDEMIC.
- Published in:
- 2022
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- Publication type:
- journal article
Migraine without aura: genome-wide association analysis identifies several novel susceptibility.
- Published in:
- 2013
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- Publication type:
- Abstract
Genome-wide association analysis identifies susceptibility loci for migraine without aura.
- Published in:
- Nature Genetics, 2012, v. 44, n. 7, p. 777, doi. 10.1038/ng.2307
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- Publication type:
- Article
Genome-wide association study reveals three susceptibility loci for common migraine in the general population.
- Published in:
- Nature Genetics, 2011, v. 43, n. 7, p. 695, doi. 10.1038/ng.856
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- Publication type:
- Article
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.
- Published in:
- Nature Genetics, 2010, v. 42, n. 10, p. 869, doi. 10.1038/ng.652
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- Publication type:
- Article
Erratum zu: Konsensusstatement der Migräne- und Kopfschmerzgesellschaften (DMKG, ÖKSG & SKG) zur Therapiedauer der medikamentösen Migräneprophylaxe.
- Published in:
- 2023
- By:
- Publication type:
- Correction Notice
Konsensusstatement der Migräne- und Kopfschmerzgesellschaften (DMKG, ÖKSG & SKG) zur Therapiedauer der medikamentösen Migräneprophylaxe.
- Published in:
- Der Schmerz, 2023, v. 37, n. 1, p. 5, doi. 10.1007/s00482-022-00671-9
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- Publication type:
- Article
Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas.
- Published in:
- Human Genetics, 2016, v. 135, n. 4, p. 425, doi. 10.1007/s00439-016-1638-x
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- Publication type:
- Article
Minimal important difference of the Migraine Disability Assessment (MIDAS): Longitudinal data from the DMKG Headache Registry.
- Published in:
- Cephalalgia, 2024, v. 44, n. 7, p. 1, doi. 10.1177/03331024241261077
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- Publication type:
- Article
Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants.
- Published in:
- PLoS ONE, 2017, v. 12, n. 9, p. 1, doi. 10.1371/journal.pone.0185663
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- Publication type:
- Article
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies.
- Published in:
- Human Mutation, 2007, v. 28, n. 5, p. 522, doi. 10.1002/humu.9486
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- Publication type:
- Article
Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia—a comment.
- Published in:
- Brain: A Journal of Neurology, 2005, v. 128, n. 6, p. E32, doi. 10.1093/brain/awh440
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- Publication type:
- Article
Herpes simplex virus type 2 meningitis and symptomatic migraine.
- Published in:
- 2011
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- Publication type:
- Letter
Ischemic stroke of the cortical “hand knob” area: stroke mechanisms and prognosis.
- Published in:
- Journal of Neurology, 2009, v. 256, n. 7, p. 1146, doi. 10.1007/s00415-009-5104-8
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- Publication type:
- Article
Assessing the Enrichment Performance in Targeted Resequencing Experiments.
- Published in:
- Human Mutation, 2012, v. 33, n. 4, p. 635, doi. 10.1002/humu.22036
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- Publication type:
- Article
Triptan non-response in specialized headache care: cross-sectional data from the DMKG Headache Registry.
- Published in:
- Journal of Headache & Pain, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s10194-023-01676-0
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- Publication type:
- Article
Causal relationships between migraine and microstructural white matter: a Mendelian randomization study.
- Published in:
- Journal of Headache & Pain, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s10194-023-01550-z
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- Publication type:
- Article
Two novel families with hemiplegic migraine caused by recurrent SCN1A mutation p.F1499L.
- Published in:
- 2018
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- Publication type:
- letter
Early-onset familial hemiplegic migraine due to a novel SCN1A mutation.
- Published in:
- 2016
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- Publication type:
- journal article
Gene-based pleiotropy across migraine with aura and migraine without aura patient groups.
- Published in:
- 2016
- By:
- Publication type:
- journal article
The migraine-stroke connection: A genetic perspective.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Involvement of astrocyte and oligodendrocyte gene sets in migraine.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies.
- Published in:
- Cephalalgia, 2015, v. 35, n. 6, p. 489, doi. 10.1177/0333102414547784
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- Publication type:
- Article
Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene.
- Published in:
- Cephalalgia, 2014, v. 34, n. 3, p. 183, doi. 10.1177/0333102413506128
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- Publication type:
- Article
Decreased Autonomic Reactivity and Psychiatric Comorbidities in Neurological Patients With Medically Unexplained Sensory Symptoms: A Case-Control Study.
- Published in:
- Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.713391
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- Publication type:
- Article