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Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women.
Domschke K, Freitag CM, Kuhlenbäumer G, Schirmacher A, Sand P, Nyhuis P, Jacob C, Fritze J, Franke P, Rietschel M, Garritsen HS, Fimmers R, Nöthen MM, Lesch KP, Stögbauer F, Deckert J. Domschke K, et al. Among authors: schirmacher a. Int J Neuropsychopharmacol. 2004 Jun;7(2):183-8. doi: 10.1017/S146114570400416X. Epub 2004 Mar 5. Int J Neuropsychopharmacol. 2004. PMID: 15009906 Free article.
Human nuclear transcription factor gene CREM: genomic organization, mutation screening, and association analysis in panic disorder.
Domschke K, Kuhlenbäumer G, Schirmacher A, Lorenzi C, Armengol L, DiBella D, Gratacos M, Garritsen HS, Nöthen MM, Franke P, Sand P, Fritze J, Perez G, Maier W, Sibrowski W, Estivill X, Bellodi L, Ringelstein EB, Arolt V, Martin-Santos R, Catalano M, Stögbauer F, Deckert J. Domschke K, et al. Among authors: schirmacher a. Am J Med Genet B Neuropsychiatr Genet. 2003 Feb;117B(1):70-8. doi: 10.1002/ajmg.b.10018. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12555239
Autosomal dominant striatal degeneration (ADSD): clinical description and mapping to 5q13-5q14.
Kuhlenbäumer G, Lüdemann P, Schirmacher A, De Vriendt E, Hünermund G, Young P, Hund-Georgiadis M, Schuierer G, Möller H, Ringelstein EB, Van Broeckhoven C, Timmerman V, Stögbauer F. Kuhlenbäumer G, et al. Among authors: schirmacher a. Neurology. 2004 Jun 22;62(12):2203-8. doi: 10.1212/01.wnl.0000130485.89814.10. Neurology. 2004. PMID: 15210883
Cholecystokinin- and cholecystokinin-B-receptor gene polymorphisms in panic disorder.
Hösing VG, Schirmacher A, Kuhlenbäumer G, Freitag C, Sand P, Schlesiger C, Jacob C, Fritze J, Franke P, Rietschel M, Garritsen H, Nöthen MM, Fimmers R, Stögbauer F, Deckert J. Hösing VG, et al. Among authors: schirmacher a. J Neural Transm Suppl. 2004;(68):147-56. doi: 10.1007/978-3-7091-0579-5_17. J Neural Transm Suppl. 2004. PMID: 15354400
Norepinephrine transporter (NET) promoter and 5'-UTR polymorphisms: association analysis in panic disorder.
Lee YJ, Hohoff C, Domschke K, Sand P, Kuhlenbäumer G, Schirmacher A, Freitag CM, Meyer J, Stöber G, Franke P, Nöthen MM, Fritze J, Fimmers R, Garritsen HS, Stögbauer F, Deckert J. Lee YJ, et al. Among authors: schirmacher a. Neurosci Lett. 2005 Mar 22;377(1):40-3. doi: 10.1016/j.neulet.2004.11.063. Epub 2004 Dec 15. Neurosci Lett. 2005. PMID: 15722184
Mutations in SEPT9 cause hereditary neuralgic amyotrophy.
Kuhlenbäumer G, Hannibal MC, Nelis E, Schirmacher A, Verpoorten N, Meuleman J, Watts GD, De Vriendt E, Young P, Stögbauer F, Halfter H, Irobi J, Goossens D, Del-Favero J, Betz BG, Hor H, Kurlemann G, Bird TD, Airaksinen E, Mononen T, Serradell AP, Prats JM, Van Broeckhoven C, De Jonghe P, Timmerman V, Ringelstein EB, Chance PF. Kuhlenbäumer G, et al. Among authors: schirmacher a. Nat Genet. 2005 Oct;37(10):1044-6. doi: 10.1038/ng1649. Epub 2005 Sep 25. Nat Genet. 2005. PMID: 16186812
58 results