Prevalence of migraine in persons with the 3243A>G mutation in mitochondrial DNA

Author:

Guo S.1,Esserlind A.-L.1,Andersson Z.1,Frederiksen A. L.2,Olesen J.1,Vissing J.3,Ashina M.1

Affiliation:

1. Department of Neurology; Danish Headache Center; Rigshospitalet Glostrup; Faculty of Health and Medical Sciences; University of Copenhagen; Copenhagen Denmark

2. Department of Clinical Genetics; Odense University Hospital; Odense Denmark

3. Department of Neurology; Copenhagen Neuromuscular Center; Rigshospitalet Blegdamsvej; Faculty of Health and Medical Sciences; University of Copenhagen; Copenhagen Denmark

Funder

Novo Nordisk Foundation

Independent Research − Medical Sciences (FSS)

Lundbeck Foundation

FP7-EUROHEADPAIN

Biostatistical Department at Copenhagen University

Genzyme/Sanofi, Novartis

Reata Pharmaceuticals

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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1. Migräne und mitochondriale Erkrankungen;Der Nervenarzt;2024-01-26

2. Behavioral Aspects of Migraine: A Focus on the Response to Visual Phenomenon;Handbook of the Behavior and Psychology of Disease;2024

3. Migraine and mitochondrial diseases;Der Schmerz;2023-11-03

4. Mitochondrial metabolism related markers GDF‐15, FGF‐21, and HIF‐1α are elevated in pediatric migraine attacks;Headache: The Journal of Head and Face Pain;2023-08-19

5. Genetics of migraine: where are we now?;The Journal of Headache and Pain;2023-02-20

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