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Entries: 1-6  
Genome-wide association analysis identifies susceptibility loci for migraine without aura
Authors: Freilinger, T.; Anttila, V.; de Vries, B.; Malik, R.; Kallela, M.; Terwindt, G. M.; Pozo-Rosich, P.; Winsvold, B.; Nyholt, D. R.; van Oosterhout, W. P. J.; Artto, V.; Todt, U.; Hämäläinen, E.; Fernández-Morales, J.; Louter, M. A.; Kaunisto, M. A.; Schoenen, J.; Raitakari, O.; Lehtimäki, T.; Vila-Pueyo, M.; Göbel, H.; Wichmann, E.; Sintas, C.; Uitterlinden, A. G.; Hofman, A.; Rivadeneira, F.; Heinze, A.; Tronvik, E.; van Duijn, C. M.; Kaprio, J.; Cormand, B.; Wessman, M.; Frants, R. R.; Meitinger, T.; Müller-Myhsok, B.; Zwart, J. A.; Färkkilä, M.; Macaya, A.; Ferrari, M. D.; Kubisch, C.; Palotie, A.; Dichgans, M.; van den Maagdenberg, A. M. J. M.
Date of Publication (YYYY-MM-DD): 2012-07
Title of Journal: Nature Genetics
Volume: 44
Issue / Number: 7
Start Page: 777
End Page: 782
Document Type: Article
ID: 614742.0
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1
Authors: Anttila, V.; Stefansson, H.; Kallela, M.; Todt, U.; Terwindt, G. M.; Calafato, M. S.; Nyholt, D. R.; Dimas, A. S.; Freilinger, T.; Müller-Myhsok, B.; Artto, V.; Inouye, M.; Alakurtti, K.; Kaunisto, M. A.; Hamalainen, E.; de Vries, B.; Stam, A. H.; Weller, C. M.; Heinze, A.; Heinze-Kuhn, K.; Goebel, I.; Borck, G.; Göbel, H.; Steinberg, S.; Wolf, C.; Bjornsson, A.; Gudmundsson, G.; Kirchmann, M.; Hauge, A.; Werge, T.; Schoenen, J.; Eriksson, J. G.; Hagen, K.; Stovner, L.; Wichmann, E.; Meitinger, T.; Alexander, M.; Moebus, S.; Schreiber, S.; Aulchenko, Y. S.; Breteler, M. M. B.; Uitterlinden, A. G.; Hofman, A.; van Duijn, C. M.; Tikka-Kleemola, P.; Vepsalainen, S.; Lucae, S.; Tozzi, F.; Muglia, P.; Barrett, J.; Kaprio, J.; Farkkila, M.; Peltonen, L.; Stefansson, K.; Zwart, J. A.; Ferrari, M. D.; Olesen, J.; Daly, M.; Wessman, M.; van den Maagdenberg, A. M. J. M.; Dichgans, M.; Kubisch, C.; Dermitzakis, E. T.; Frants, R. R.; Palotie, A.
Date of Publication (YYYY-MM-DD): 2010-10
Title of Journal: Nature Genetics
Volume: 42
Issue / Number: 10
Start Page: 869
End Page: 873
Document Type: Article
ID: 519921.0
Genetic Variation in the Lymphotoxin-Alpha Pathway and the Risk of Ischemic Stroke in European Populations
Authors: Freilinger, T.; Bevan, S.; Ripke, S.; Gschwendtner, A.; Lichtner, P.; Müller-Myhsok, B.; Wichmann, H. E.; Markus, H. S.; Meitinger, T.; Dichgans, M.
Date of Publication (YYYY-MM-DD): 2009-03
Title of Journal: Stroke
Volume: 40
Issue / Number: 3
Start Page: 970
End Page: 972
Document Type: Article
ID: 432139.0
Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation
Authors: Freilinger, T.; Bohe, M.; Wegener, B.; Müller-Myhsok, B.; Dichgans, M.; Knoblauch, H.
Date of Publication (YYYY-MM-DD): 2008-04
Title of Journal: Cephalalgia
Volume: 28
Issue / Number: 4
Start Page: 403
End Page: 407
Document Type: Article
ID: 359306.0
Full text / Content available
Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white Europeans
Authors: Gschwendtner, A.; Ripke, S.; Freilinger, T.; Lichtner, P.; Müller-Myhsok, B.; Wichmann, H. E.; Meitinger, T.; Dichgans, M.
Date of Publication (YYYY-MM-DD): 2008
Title of Journal: Stroke
Volume: 39
Start Page: 1593
End Page: 1596
Document Type: Article
ID: 374031.0
H-1-MRS alterations in the cerebellum of patients with familial hemilegic migraine type 1
Authors: Dichgans, M.; Herzog, J.; Freilinger, T.; Wilke, M.; Auer, D. P.
Date of Publication (YYYY-MM-DD): 2005-02-22
Title of Journal: Neurology
Volume: 64
Issue / Number: 4
Start Page: 608
End Page: 613
Document Type: Article
ID: 257124.0
Entries: 1-6  
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