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Entries: 1-10  
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Post-stroke cogntive decline: An update and perspectives for clinical research
Authors: Brainin, Michael; Tuomilehto, Jaakko; Heiss, Wolf-Dieter; Bornstein, Natan M.; Bath, P. M. W.; Teuschi, Y.; Richard, E.; Guekht, A.; Quinn, T.; Auer, S.; Dachenhausen, M. A.; Pinter, M.; Dichgans, M.; Fazekas, F.; Lees, K.; Matz, K.; Reiter, M.
Date of Publication (YYYY-MM-DD): 2015
Title of Journal: European Journal of Neurology
Volume: 22
Issue / Number: 2
Start Page: 229
End Page: 238
Document Type: Article
ID: 698865.0
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 identifies a variant in HDAC9 associated with large vessel ischemic stroke
Authors: Bellenguez, C.; Bevan, S.; Gschwendtner, A.; Spencer, C. C. A.; Burgess, A. I.; Pirinen, M.; Jackson, C. A.; Traylor, M.; Strange, A.; Su, Z.; Band, G.; Syme, P. D.; Malik, R.; Pera, J.; Norrving, B.; Lemmens, R.; Freeman, C.; Schanz, R.; James, T.; Poole, D.; Murphy, L.; Segal, H.; Cortellini, L.; Cheng, Y. C.; Woo, D.; Nalls, M. A.; Müller-Myhsok, B.; Meisinger, C.; Seedorf, U.; Ross-Adams, H.; Boonen, S.; Wloch-Kopec, D.; Valant, V.; Slark, J.; Furie, K.; Delavaran, H.; Langford, C.; Deloukas, P.; Edkins, S.; Hunt, S.; Gray, E.; Dronov, S.; Peltonen, L.; Gretarsdottir, S.; Thorleifsson, G.; Thorsteinsdottir, U.; Stefansson, K.; Boncoraglio, G. B.; Parati, E. A.; Attia, J.; Holliday, E.; Levi, C.; Franzosi, M. G.; Goel, A.; Helgadottir, A.; Blackwell, J. M.; Bramon, E.; Brown, M. A.; Casas, J. P.; Corvin, A.; Duncanson, A.; Jankowski, J.; Mathew, C. G.; Palmer, C. N. A.; Plomin, R.; Rautanen, A.; Sawcer, S. J.; Trembath, R. C.; Viswanathan, A. C.; Wood, N. W.; Worrall, B. B.; Kittner, S. J.; Mitchell, B. D.; Kissela, B.; Meschia, J. F.; Thijs, V.; Lindgren, A.; Macleod, M. J.; Slowik, A.; Walters, M.; Rosand, J.; Sharma, P.; Farrall, M.; Sudlow, C. L. M.; Rothwell, P. M.; Dichgans, M.; Donnelly, P.; Markus, H. S.
Date of Publication (YYYY-MM-DD): 2012-03
Title of Journal: Nature Genetics
Volume: 44
Issue / Number: 3
Start Page: 328
End Page: 333
Document Type: Article
ID: 596923.0
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
Polymorphisms in the receptor for GDNF (RET) are not associated with Parkinson's disease in Southern Germany
Authors: Luecking, C. B.; Lichtner, P.; Kramer, E. R.; Gieger, C.; Illig, T.; Dichgans, M.; Berg, D.; Gasser, T.
Date of Publication (YYYY-MM-DD): 2010-01
Title of Journal: Neurobiology of Aging
Volume: 31
Issue / Number: 1
Start Page: 167
End Page: 168
Document Type: Article
ID: 440939.0
Sequence Variants on Chromosome 9p21.3 Confer Risk for Atherosclerotic Stroke
Authors: Gschwendtner, A.; Bevan, S.; Cole, J. W.; Plourde, A.; Matarin, M.; Ross-Adams, H.; Meitinger, T.; Wichmann, E.; Mitchell, B. D.; Furie, K.; Slowik, A.; Rich, S. S.; Syme, P. D.; MacLeod, M. J.; Meschia, J. F.; Rosand, J.; Kittner, S. J.; Markus, H. S.; Müller-Myhsok, B.; Dichgans, M.
Date of Publication (YYYY-MM-DD): 2009-05
Title of Journal: Annals of Neurology
Volume: 65
Issue / Number: 5
Start Page: 531
End Page: 539
Document Type: Article
ID: 432147.0
Sequence Variants on Chromosome 9p21 Confer Risk of Large Vessel Stroke.
Authors: Dichgans, M.; Bevan, S.; Cole, J. W.; Plourde, A.; Matarin, M.; Ross-Adams, H.; Meitinger, T.; Wichmann, E.; Mitchel, B. D.; Furie, K.; Rich, S. S.; MacLeod, M. J.; Meschia, J.; Rosand, J.; Kittner, S. J.; Markus, H. S.; Müller-Myhsok, B.; Gschwendtner, A.
Date of Publication (YYYY-MM-DD): 2009-04
Title of Journal: Stroke
Volume: 40
Issue / Number: 4
Start Page: E109
End Page: E109
Document Type: Article
ID: 429205.0
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
Measurement of brain atrophy in subcortical vascular disease: A comparison of different approaches and the impact of ischaemic lesions
Authors: O'Sullivan, M.; Jouvent, E.; Sämann, P. G.; Mangin, J. F.; Viswanathan, A.; Gschwendtner, A.; Bracoud, L.; Pachai, C.; Chabriat, H.; Dichgans, M.
Date of Publication (YYYY-MM-DD): 2008-11-01
Title of Journal: NeuroImage
Volume: 43
Issue / Number: 2
Start Page: 312
End Page: 320
Document Type: Article
ID: 395631.0
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
 
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