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Entries: 1-10  
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Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1
Authors: Winkelmann, J.; Czamara, D.; Schormair, B.; Knauf, F.; Schulte, E. C.; Trenkwalder, C.; Dauvilliers, Y.; Polo, O.; Högl, B.; Berger, K.; Fuhs, A.; Gross, N.; Stiasny-Kolster, K.; Oertel, W.; Bachmann, C. G.; Paulus, W.; Xiong, L.; Montplaisir, J.; Rouleau, G. A.; Fietze, I.; Vavrova, J.; Kemlink, D.; Sonka, K.; Nevsimalova, S.; Lin, S. C.; Wszolek, Z.; Vilarino-Guell, C.; Farrer, M. J.; Gschliesser, V.; Frauscher, B.; Falkenstetter, T.; Poewe, W.; Allen, R. P.; Earley, C. J.; Ondo, W. G.; Le, W. D.; Spieler, D.; Kaffe, M.; Zimprich, A.; Kettunen, J.; Perola, M.; Silander, K.; Cournu-Rebeix, I.; Francavilla, M.; Fontenille, C.; Fontaine, B.; Vodicka, P.; Prokisch, H.; Lichtner, P.; Peppard, P.; Faraco, J.; Mignot, E.; Gieger, C.; Illig, T.; Wichmann, H. E.; Müller-Myhsok, B.; Meitinger, T.
Date of Publication (YYYY-MM-DD): 2011-07
Title of Journal: PLoS Genetics
Volume: 7
Issue / Number: 7
Sequence Number of Article: e1002171
Document Type: Article
ID: 571350.0
Replication of restless legs syndrome loci in three European populations
Authors: Kemlink, D.; Polo, O.; Frauscher, B.; Gschliesser, V.; Hogl, B.; Poewe, W.; Vodicka, P.; Vavrova, J.; Sonka, K.; Nevsimalova, S.; Schormair, B.; Lichtner, P.; Silander, K.; Peltonen, L.; Gieger, C.; Wichmann, H. E.; Zimprich, A.; Roeske, D.; Müller-Myhsok, B.; Meitinger, T.; Winkelmann, J.
Date of Publication (YYYY-MM-DD): 2009-05
Title of Journal: Journal of Medical Genetics
Volume: 46
Issue / Number: 5
Start Page: 315
End Page: 318
Document Type: Article
ID: 432158.0
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome
Authors: Schormair, B.; Kemlink, D.; Roeske, D.; Eckstein, G.; Xiong, L.; Lichtner, P.; Ripke, S.; Trenkwalder, C.; Zimprich, A.; Stiasny-Kolster, K.; Oertel, W.; Bachmann, C. G.; Paulus, W.; Högl, B.; Frauscher, B.; Gschliesser, V.; Poewe, W.; Peglau, I.; Vodicka, P.; Vavrova, J.; Sonka, K.; Nevsimalova, S.; Montplaisir, J.; Turecki, G.; Rouleau, G.; Gieger, C.; Illig, T.; Wichmann, H. E.; Holsboer, F.; Mueller-Myhsok, B.; Meitinger, T.; Winkelmann, J.
Date of Publication (YYYY-MM-DD): 2008-08
Title of Journal: Nature Genetics
Volume: 40
Issue / Number: 8
Start Page: 946
End Page: 948
Document Type: Article
ID: 379927.0
A functional polymorphism in the SCN1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy
Authors: Zimprich, F.; Stogmann, E.; Bonelli, S.; Baumgartner, C.; Mueller, J. C.; Meitinger, T.; Zimprich, A.; Strom, T. M.
Date of Publication (YYYY-MM-DD): 2008-06
Title of Journal: Epilepsia
Volume: 49
Issue / Number: 6
Start Page: 1108
End Page: 1109
Document Type: Article
ID: 410572.0
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
Authors: Winkelmann, J.; Schormair, B.; Lichtner, P.; Ripke, S.; Xiong, L.; Jalilzadeh, S.; Fulda, S.; Pütz, B.; Eckstein, G.; Hauk, S.; Trenkwalder, C.; Zimprich, A.; Stiasny-Kolster, K.; Oertel, W.; Bachmann, C. G.; Paulus, W.; Peglau, I.; Eisensehr, I.; Montplaisir, J.; Turecki, G.; Rouleau, G.; Gieger, C.; Illig, T.; Wichmann, E.; Holsboer, F.; Müller-Myhsok, B.; Meitinger, T.
Date of Publication (YYYY-MM-DD): 2007-08
Title of Journal: Nature Genetics
Volume: 39
Issue / Number: 8
Start Page: 1000
End Page: 1006
Document Type: Article
ID: 334282.0
The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations
Authors: Sharma, M.; Müller, J. C.; Zimprich, A.; Lichtner, P.; Hofer, A.; Leitner, P.; Maass, S.; Berg, D.; Dürr, A.; Bonifati, V.; De Michele, G.; Oostra, B.; Brice, A.; Wood, N. W.; Müller-Myhsok, B.; Gasser, T.
Date of Publication (YYYY-MM-DD): 2006-07
Title of Journal: Journal of Medical Genetics
Volume: 43
Issue / Number: 7
Start Page: 557
End Page: 562
Document Type: Article
ID: 300277.0
Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome
Authors: Asmus, F.; Schoenian, S.; Lichtner, P.; Munz, M.; Mayer, P.; Müller-Myhsok, B.; Zimprich, A.; Remschmidt, H.; Hebebrand, J.; Bandmann, O.; Gasser, T.
Date of Publication (YYYY-MM-DD): 2005-02
Title of Journal: Neurogenetics
Volume: 6
Issue / Number: 1
Start Page: 55
End Page: 56
Document Type: Article
ID: 256752.0
PARK11 is not linked with Parkinson's disease in European families
Authors: Prestel, J.; Sharma, M.; Leitner, P.; Zimprich, A.; Vaughan, J. R.; Dürr, A.; Bonifati, V.; De Michele, G.; Hanagasi, H. A.; Farrer, M.; Hofer, A.; Asmus, F.; Volpe, G.; Meco, G.; Brice, A.; Wood, N. W.; Müller-Myhsok, B.; Gasser, T.
Date of Publication (YYYY-MM-DD): 2005-02
Title of Journal: European Journal of Human Genetics
Volume: 13
Issue / Number: 2
Start Page: 193
End Page: 197
Document Type: Article
ID: 261211.0
Mutations in LRRK2 cause autosomal-dominant Parkinsonism with pleomorphic pathology
Authors: Zimprich, A.; Biskup, S.; Leitner, P.; Lichtner, P.; Farrer, M.; Lincoln, S.; Kachergus, J.; Hulihan, M.; Uitti, R. J.; Calne, D. B.; Stoessl, A. J.; Pfeiffer, R. F.; Patenge, N.; Carbajal, I. C.; Vieregge, P.; Asmus, F.; Müller-Myhsok, B.; Dickson, D. W.; Meitinger, T.; Strom, T. M.; Wszolek, Z. K.; Gasser, T.
Date of Publication (YYYY-MM-DD): 2004-11-18
Title of Journal: Neuron
Volume: 44
Issue / Number: 4
Start Page: 601
End Page: 607
Document Type: Article
ID: 216093.0
Autosomal dominant parkinsonism associated with variable synuclein and tau pathology
Authors: Wszolek, Z. K.; Pfeiffer, R. F.; Tsuboi, Y.; Uitti, R. J.; McComb, R. D.; Stoessl, A. J.; Strongosky, A. J.; Zimprich, A.; Müller-Myhsok, B.; Farrer, M. J.; Gasser, T.; Calne, D. B.; Dickson, D. W.
Date of Publication (YYYY-MM-DD): 2004-05-11
Title of Journal: Neurology
Volume: 62
Issue / Number: 9
Start Page: 1619
End Page: 1622
Document Type: Article
ID: 216081.0
Entries: 1-10  
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