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Page 1
Clinical Characteristics of Inpatients with Childhood vs. Adolescent Anorexia Nervosa.
Jaite C, Bühren K, Dahmen B, Dempfle A, Becker K, Correll CU, Egberts KM, Ehrlich S, Fleischhaker C, von Gontard A, Hahn F, Kolar D, Kaess M, Legenbauer T, Renner TJ, Schulze U, Sinzig J, Thomae E, Weber L, Wessing I, Antony G, Hebebrand J, Föcker M, Herpertz-Dahlmann B. Jaite C, et al. Among authors: dempfle a. Nutrients. 2019 Oct 28;11(11):2593. doi: 10.3390/nu11112593. Nutrients. 2019. PMID: 31661861 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.
A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs.
Hebebrand J, Dempfle A, Saar K, Thiele H, Herpertz-Dahlmann B, Linder M, Kiefl H, Remschmidt H, Hemminger U, Warnke A, Knölker U, Heiser P, Friedel S, Hinney A, Schäfer H, Nürnberg P, Konrad K. Hebebrand J, et al. Among authors: dempfle a. Mol Psychiatry. 2006 Feb;11(2):196-205. doi: 10.1038/sj.mp.4001761. Mol Psychiatry. 2006. PMID: 16222334 Clinical Trial.
Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample.
Heiser P, Dempfle A, Friedel S, Konrad K, Hinney A, Kiefl H, Walitza S, Bettecken T, Saar K, Linder M, Warnke A, Herpertz-Dahlmann B, Schäfer H, Remschmidt H, Hebebrand J. Heiser P, et al. Among authors: dempfle a. J Neural Transm (Vienna). 2007;114(4):513-21. doi: 10.1007/s00702-006-0584-5. Epub 2006 Nov 10. J Neural Transm (Vienna). 2007. PMID: 17093889
No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD.
Schimmelmann BG, Friedel S, Dempfle A, Warnke A, Lesch KP, Walitza S, Renner TJ, Romanos M, Herpertz-Dahlmann B, Linder M, Schäfer H, Seitz C, Palmason H, Freitag C, Meyer J, Konrad K, Hinney A, Hebebrand J. Schimmelmann BG, et al. Among authors: dempfle a. J Neural Transm (Vienna). 2007;114(4):523-6. doi: 10.1007/s00702-006-0616-1. Epub 2007 Jan 15. J Neural Transm (Vienna). 2007. PMID: 17219016
132 results