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Cognitive training with and without additional physical activity in healthy older adults: cognitive effects, neurobiological mechanisms, and prediction of training success.
Rahe J, Becker J, Fink GR, Kessler J, Kukolja J, Rahn A, Rosen JB, Szabados F, Wirth B, Kalbe E. Rahe J, et al. Among authors: wirth b. Front Aging Neurosci. 2015 Oct 13;7:187. doi: 10.3389/fnagi.2015.00187. eCollection 2015. Front Aging Neurosci. 2015. PMID: 26528177 Free PMC article.
Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta.
Becker J, Semler O, Gilissen C, Li Y, Bolz HJ, Giunta C, Bergmann C, Rohrbach M, Koerber F, Zimmermann K, de Vries P, Wirth B, Schoenau E, Wollnik B, Veltman JA, Hoischen A, Netzer C. Becker J, et al. Among authors: wirth b. Am J Hum Genet. 2011 Mar 11;88(3):362-71. doi: 10.1016/j.ajhg.2011.01.015. Epub 2011 Feb 25. Am J Hum Genet. 2011. PMID: 21353196 Free PMC article.
A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callus.
Semler O, Garbes L, Keupp K, Swan D, Zimmermann K, Becker J, Iden S, Wirth B, Eysel P, Koerber F, Schoenau E, Bohlander SK, Wollnik B, Netzer C. Semler O, et al. Among authors: wirth b. Am J Hum Genet. 2012 Aug 10;91(2):349-57. doi: 10.1016/j.ajhg.2012.06.011. Epub 2012 Aug 2. Am J Hum Genet. 2012. PMID: 22863195 Free PMC article.
Effects of a Cognitive Training With and Without Additional Physical Activity in Healthy Older Adults: A Follow-Up 1 Year After a Randomized Controlled Trial.
Kalbe E, Roheger M, Paluszak K, Meyer J, Becker J, Fink GR, Kukolja J, Rahn A, Szabados F, Wirth B, Kessler J. Kalbe E, et al. Among authors: wirth b. Front Aging Neurosci. 2018 Dec 18;10:407. doi: 10.3389/fnagi.2018.00407. eCollection 2018. Front Aging Neurosci. 2018. PMID: 30618714 Free PMC article.
Discrepancy in redetermination of SMN2 copy numbers in children with SMA.
Schorling DC, Becker J, Pechmann A, Langer T, Wirth B, Kirschner J. Schorling DC, et al. Among authors: wirth b. Neurology. 2019 Aug 6;93(6):267-269. doi: 10.1212/WNL.0000000000007836. Epub 2019 Jun 24. Neurology. 2019. PMID: 31235659 No abstract available.
VPS13D: One Family, Same Mutations, Two Phenotypes.
Petry-Schmelzer JN, Keller N, Karakaya M, Wirth B, Fink GR, Wunderlich G. Petry-Schmelzer JN, et al. Among authors: wirth b. Mov Disord Clin Pract. 2021 May 5;8(5):803-806. doi: 10.1002/mdc3.13232. eCollection 2021 Jul. Mov Disord Clin Pract. 2021. PMID: 34307758 Free PMC article. No abstract available.
PLS3 Overexpression Delays Ataxia in Chp1 Mutant Mice.
Janzen E, Wolff L, Mendoza-Ferreira N, Hupperich K, Delle Vedove A, Hosseinibarkooie S, Kye MJ, Wirth B. Janzen E, et al. Among authors: wirth b. Front Neurosci. 2019 Sep 19;13:993. doi: 10.3389/fnins.2019.00993. eCollection 2019. Front Neurosci. 2019. PMID: 31607845 Free PMC article.
Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders.
Michalk A, Stricker S, Becker J, Rupps R, Pantzar T, Miertus J, Botta G, Naretto VG, Janetzki C, Yaqoob N, Ott CE, Seelow D, Wieczorek D, Fiebig B, Wirth B, Hoopmann M, Walther M, Körber F, Blankenburg M, Mundlos S, Heller R, Hoffmann K. Michalk A, et al. Among authors: wirth b. Am J Hum Genet. 2008 Feb;82(2):464-76. doi: 10.1016/j.ajhg.2007.11.006. Am J Hum Genet. 2008. PMID: 18252226 Free PMC article.
358 results