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[Formal genetic findings in attention-deficit/hyperactivity-disorder].
Smidt J, Heiser P, Dempfle A, Konrad K, Hemminger U, Kathöfer A, Halbach A, Strub J, Grabarkiewicz J, Kiefl H, Linder M, Knölker U, Warnke A, Remschmidt H, Herpertz-Dahlmann B, Hebebrand J. Smidt J, et al. Among authors: dempfle a. Fortschr Neurol Psychiatr. 2003 Jul;71(7):366-77. doi: 10.1055/s-2003-40561. Fortschr Neurol Psychiatr. 2003. PMID: 12858257 Review. German.
Evolution of E. coli in a mouse model of inflammatory bowel disease leads to a disease-specific bacterial genotype and trade-offs with clinical relevance.
Unni R, Andreani NA, Vallier M, Heinzmann SS, Taubenheim J, Guggeis MA, Tran F, Vogler O, Künzel S, Hövener JB, Rosenstiel P, Kaleta C, Dempfle A, Unterweger D, Baines JF. Unni R, et al. Among authors: dempfle a. Gut Microbes. 2023 Dec;15(2):2286675. doi: 10.1080/19490976.2023.2286675. Epub 2023 Dec 7. Gut Microbes. 2023. PMID: 38059748 Free PMC article.
Nectin-4 as Blood-Based Biomarker Enables Detection of Early Ovarian Cancer Stages.
Rogmans C, Feuerborn J, Treeck L, Tribian N, Flörkemeier I, Arnold N, Weimer JP, Maass N, Jansen P, Lieb W, Dempfle A, Bauerschlag DO, Hedemann N. Rogmans C, et al. Among authors: dempfle a. Cancers (Basel). 2022 Nov 29;14(23):5867. doi: 10.3390/cancers14235867. Cancers (Basel). 2022. PMID: 36497350 Free PMC article.
Mutation screen of the brain derived neurotrophic factor gene (BDNF): identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention-deficit/hyperactivity disorder.
Friedel S, Horro FF, Wermter AK, Geller F, Dempfle A, Reichwald K, Smidt J, Brönner G, Konrad K, Herpertz-Dahlmann B, Warnke A, Hemminger U, Linder M, Kiefl H, Goldschmidt HP, Siegfried W, Remschmidt H, Hinney A, Hebebrand J. Friedel S, et al. Among authors: dempfle a. Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):96-9. doi: 10.1002/ajmg.b.30090. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15457498
Molecular genetic aspects of attention-deficit/hyperactivity disorder.
Heiser P, Friedel S, Dempfle A, Konrad K, Smidt J, Grabarkiewicz J, Herpertz-Dahlmann B, Remschmidt H, Hebebrand J. Heiser P, et al. Among authors: dempfle a. Neurosci Biobehav Rev. 2004 Oct;28(6):625-41. doi: 10.1016/j.neubiorev.2004.09.010. Neurosci Biobehav Rev. 2004. PMID: 15527867 Review.
Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder.
Walitza S, Renner TJ, Dempfle A, Konrad K, Wewetzer Ch, Halbach A, Herpertz-Dahlmann B, Remschmidt H, Smidt J, Linder M, Flierl L, Knölker U, Friedel S, Schäfer H, Gross C, Hebebrand J, Warnke A, Lesch KP. Walitza S, et al. Among authors: dempfle a. Mol Psychiatry. 2005 Dec;10(12):1126-32. doi: 10.1038/sj.mp.4001734. Mol Psychiatry. 2005. PMID: 16116490 Clinical Trial.
132 results