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Entries: 1-6  
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Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
Authors: Horn, D.; Kapeller, J.; Rivera-Brugues, N.; Moog, U.; Lorenz-Depiereux, B.; Eck, S.; Hempel, M.; Wagenstaller, J.; Gawthrope, A.; Monaco, A. P.; Bonin, M.; Riess, O.; Wohlleber, E.; Illig, T.; Bezzina, C. R.; Franke, A.; Spranger, S.; Villavicencio-Lorini, P.; Seifert, W.; Rosenfeld, J.; Klopocki, E.; Rappold, G. A.; Strom, T. M.
Date of Publication (YYYY-MM-DD): 2010-11-01
Title of Journal: Human Mutation
Volume: 31
Issue / Number: 11
Start Page: E1851
End Page: E1860
Document Type: Article
ID: 539476.0
 
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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
Identification of coexpressed gene clusters in a comparative analysis of transcriptome and proteome in mouse tissues
Authors: Mijalski, T.; Harder, A.; Halder, T.; Kersten, M.; Horsch, M.; Strom, T. M.; Liebscher, H. V.; Lottspeich, F.; de Angelis, M. H.; Beckers, J.
Date of Publication (YYYY-MM-DD): 2005-06-14
Title of Journal: Proceedings of the National Academy of Sciences of the United States of America
Volume: 102
Issue / Number: 24
Start Page: 8621
End Page: 8626
Document Type: Article
ID: 261433.0
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
Evidence for genetic heterogeneity in Restless Legs Syndrome
Authors: Winkelmann, J.; Lichtner, P.; Strom, T. M.; Trenkwalder, C.; Meitinger, T.; Müller-Myhsok, B.
Date of Publication (YYYY-MM-DD): 2003-09
Title of Journal: Pharmacopsychiatry
Volume: 36
Issue / Number: 5
Start Page: 273
End Page: 273
Document Type: Article
ID: 121947.0
Mutation analysis of genes regulating the hypothalamo-pituitary adrenal (HPA) axis in patients with depressive syndrome.
Authors: Binder, E. B.; Lichtner, P.; Uhr, M.; Bettecken, T.; Strom, T. M.; Meitinger, T.; Modell, S.; Holsboer, F.
Date of Publication (YYYY-MM-DD): 2002-10
Title of Journal: American Journal of Human Genetics
Volume: 71
Issue / Number: 4 Suppl. Suppl. S
Start Page: 468
End Page: 468
Document Type: Article
ID: 121048.0
Entries: 1-6  
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