Binkofski F - Search Results

1

Neural correlates of impaired emotion processing in manifest Huntington's disease.

Dogan I, Saß C, Mirzazade S, Kleiman A, Werner CJ, Pohl A, Schiefer J, Binkofski F, Schulz JB, Shah NJ, Reetz K. Dogan I, et al. Among authors: binkofski f. Soc Cogn Affect Neurosci. 2014 May;9(5):671-80. doi: 10.1093/scan/nst029. Epub 2013 Mar 11. Soc Cogn Affect Neurosci. 2014. PMID: 23482620 Free PMC article.

2

Neural activity in human primary motor cortex areas 4a and 4p is modulated differentially by attention to action.

Binkofski F, Fink GR, Geyer S, Buccino G, Gruber O, Shah NJ, Taylor JG, Seitz RJ, Zilles K, Freund HJ. Binkofski F, et al. J Neurophysiol. 2002 Jul;88(1):514-9. doi: 10.1152/jn.2002.88.1.514. J Neurophysiol. 2002. PMID: 12091573 Free article.

3

A fronto-parietal circuit for tactile object discrimination: an event-related fMRI study.

Stoeckel MC, Weder B, Binkofski F, Buccino G, Shah NJ, Seitz RJ. Stoeckel MC, et al. Among authors: binkofski f. Neuroimage. 2003 Jul;19(3):1103-14. doi: 10.1016/s1053-8119(03)00182-4. Neuroimage. 2003. PMID: 12880836 Clinical Trial.

4

Left and right superior parietal lobule in tactile object discrimination.

Stoeckel MC, Weder B, Binkofski F, Choi HJ, Amunts K, Pieperhoff P, Shah NJ, Seitz RJ. Stoeckel MC, et al. Among authors: binkofski f. Eur J Neurosci. 2004 Feb;19(4):1067-72. doi: 10.1111/j.0953-816x.2004.03185.x. Eur J Neurosci. 2004. PMID: 15009154

5

Morphometric fingerprint of asymptomatic Parkin and PINK1 mutation carriers in the basal ganglia.

Binkofski F, Reetz K, Gaser C, Hilker R, Hagenah J, Hedrich K, van Eimeren T, Thiel A, Büchel C, Pramstaller PP, Siebner HR, Klein C. Binkofski F, et al. Neurology. 2007 Aug 28;69(9):842-50. doi: 10.1212/01.wnl.0000267844.72421.6c. Neurology. 2007. PMID: 17724286

6

Limbic and frontal cortical degeneration is associated with psychiatric symptoms in PINK1 mutation carriers.

Reetz K, Lencer R, Steinlechner S, Gaser C, Hagenah J, Büchel C, Petersen D, Kock N, Djarmati A, Siebner HR, Klein C, Binkofski F. Reetz K, et al. Among authors: binkofski f. Biol Psychiatry. 2008 Aug 1;64(3):241-7. doi: 10.1016/j.biopsych.2007.12.010. Epub 2008 Feb 7. Biol Psychiatry. 2008. PMID: 18261714

7

Structural findings in the basal ganglia in genetically determined and idiopathic Parkinson's disease.

Reetz K, Gaser C, Klein C, Hagenah J, Büchel C, Gottschalk S, Pramstaller PP, Siebner HR, Binkofski F. Reetz K, et al. Among authors: binkofski f. Mov Disord. 2009 Jan 15;24(1):99-103. doi: 10.1002/mds.22333. Mov Disord. 2009. PMID: 18823048

8

Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype.

van Nuenen BF, Weiss MM, Bloem BR, Reetz K, van Eimeren T, Lohmann K, Hagenah J, Pramstaller PP, Binkofski F, Klein C, Siebner HR. van Nuenen BF, et al. Among authors: binkofski f. Neurology. 2009 Mar 24;72(12):1041-7. doi: 10.1212/01.wnl.0000338699.56379.11. Epub 2008 Nov 26. Neurology. 2009. PMID: 19038850 Free PMC article.

9

ATP13A2 variants in early-onset Parkinson's disease patients and controls.

Djarmati A, Hagenah J, Reetz K, Winkler S, Behrens MI, Pawlack H, Lohmann K, Ramirez A, Tadić V, Brüggemann N, Berg D, Siebner HR, Lang AE, Pramstaller PP, Binkofski F, Kostić VS, Volkmann J, Gasser T, Klein C. Djarmati A, et al. Among authors: binkofski f. Mov Disord. 2009 Oct 30;24(14):2104-11. doi: 10.1002/mds.22728. Mov Disord. 2009. PMID: 19705361

10

Structural changes associated with progression of motor deficits in spinocerebellar ataxia 17.

Reetz K, Lencer R, Hagenah JM, Gaser C, Tadic V, Walter U, Wolters A, Steinlechner S, Zühlke C, Brockmann K, Klein C, Rolfs A, Binkofski F. Reetz K, et al. Among authors: binkofski f. Cerebellum. 2010 Jun;9(2):210-7. doi: 10.1007/s12311-009-0150-4. Cerebellum. 2010. PMID: 20016963

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