S
Stefan Evers
Researcher at University of Münster
Publications - 345
Citations - 23282
Stefan Evers is an academic researcher from University of Münster. The author has contributed to research in topics: Migraine & Cluster headache. The author has an hindex of 57, co-authored 330 publications receiving 19515 citations. Previous affiliations of Stefan Evers include University of Michigan.
Papers
More filters
Journal Article
Headache associated with sexual activity: Demography, clinical features, and comorbidity. Commentary
TL;DR: Mean age at onset, a male preponderance, a predominantly bilateral and occipital pain, and a high comorbidity with other primary headaches are in concordance with case reports in the literature.
Journal ArticleDOI
Coronary angiography in migraine patient after subcutaneous sumatriptan
Journal ArticleDOI
Whole body and local cryotherapy in restless legs syndrome: A randomized, single-blind, controlled parallel group pilot study
TL;DR: Whole body cryotherapy at -60°C and, to a less extent, local cryotherapy seem to be a treatment option for RLS in addition to conventional pharmacological treatment, however, the exact mode of cryotherapy needs to be established.
Journal ArticleDOI
Therapie primärer chronischer Kopfschmerzen: Chronische Migräne, chronischer Kopfschmerz vom Spannungstyp und andere chronische tägliche Kopfschmerzen - Evidenzbasierte Empfehlungen der Deutschen Migräne- und Kopfschmerzgesellschaft in Zusammenarbeit m
Andreas Straube,Arne May,Peter Kropp,Zaza Katsarava,Gunther Haag,Christian Lampl,Peter S. Sandor,Hans-Christoph Diener,Stefan Evers +8 more
TL;DR: The IHS-Kriterien definieren vier primare Kopfschmerzerkrankungen, die zu taglichen Dauerkopfschmerszen fuhren konnen: chronische Migrane, 2) KopfsCHmerz vom Spannungstyp, 3) Hemicrania continua, 4) neu aufgetretener Kopfs CHmerz.
No influence of 5-HTTLPR gene polymorphism on migraine symptomatology, comorbid depression, and chronification
Thomas Wieser,Kathrin Dresler,Stefan Evers,Charly Gaul,Dorothea König,Daniela Hölzl,Klaus Berger,Dale R. Nyholt,Thomas Deufel +8 more
TL;DR: In this article, a genetic analysis of the SLC6A4 44 bp insertion/deletion polymorphism (5-HTTLPR) was performed in 293 patients with and without aura.