Schrader C - Search Results

1

Identification of a rare SEPT9 variant in a family with autosomal dominant Charcot-Marie-Tooth disease.

Grosse GM, Bauer C, Kopp B, Schrader C, Osmanovic A. Grosse GM, et al. Among authors: schrader c. BMC Med Genet. 2020 Mar 2;21(1):45. doi: 10.1186/s12881-020-0984-7. BMC Med Genet. 2020. PMID: 32122354 Free PMC article.

2

Absence of congruency sequence effects reveals neurocognitive inflexibility in Parkinson's disease.

Rustamov N, Rodriguez-Raecke R, Timm L, Agrawal D, Dressler D, Schrader C, Tacik P, Wegner F, Dengler R, Wittfoth M, Kopp B. Rustamov N, et al. Among authors: schrader c. Neuropsychologia. 2013 Dec;51(14):2976-87. doi: 10.1016/j.neuropsychologia.2013.10.025. Epub 2013 Nov 6. Neuropsychologia. 2013. PMID: 24212103

3

Attention shifting in Parkinson's disease: an analysis of behavioral and cortical responses.

Rustamov N, Rodriguez-Raecke R, Timm L, Agrawal D, Dressler D, Schrader C, Tacik P, Wegner F, Dengler R, Wittfoth M, Kopp B. Rustamov N, et al. Among authors: schrader c. Neuropsychology. 2014 Nov;28(6):929-944. doi: 10.1037/neu0000099. Epub 2014 Jul 28. Neuropsychology. 2014. PMID: 25068668

4

Neural mechanisms underlying cognitive inflexibility in Parkinson's disease.

Lange F, Seer C, Loens S, Wegner F, Schrader C, Dressler D, Dengler R, Kopp B. Lange F, et al. Among authors: schrader c. Neuropsychologia. 2016 Dec;93(Pt A):142-150. doi: 10.1016/j.neuropsychologia.2016.09.021. Epub 2016 Sep 28. Neuropsychologia. 2016. PMID: 27693667

5

Dopaminergic modulation of performance monitoring in Parkinson's disease: An event-related potential study.

Seer C, Lange F, Loens S, Wegner F, Schrader C, Dressler D, Dengler R, Kopp B. Seer C, et al. Among authors: schrader c. Sci Rep. 2017 Jan 24;7:41222. doi: 10.1038/srep41222. Sci Rep. 2017. PMID: 28117420 Free PMC article.

6

Dopaminergic modulation of novelty repetition in Parkinson's disease: A study of P3 event-related brain potentials.

Bertram M, Warren CV, Lange F, Seer C, Steinke A, Wegner F, Schrader C, Dressler D, Dengler R, Kopp B. Bertram M, et al. Among authors: schrader c. Clin Neurophysiol. 2020 Dec;131(12):2841-2850. doi: 10.1016/j.clinph.2020.09.013. Epub 2020 Oct 15. Clin Neurophysiol. 2020. PMID: 33137574

7

Genotype-phenotype correlations in ataxia telangiectasia patients with ATM c.3576G>A and c.8147T>C mutations.

van Os NJH, Chessa L, Weemaes CMR, van Deuren M, Fiévet A, van Gaalen J, Mahlaoui N, Roeleveld N, Schrader C, Schindler D, Taylor AMR, Van de Warrenburg BPC, Dörk T, Willemsen MAAP. van Os NJH, et al. Among authors: schrader c. J Med Genet. 2019 May;56(5):308-316. doi: 10.1136/jmedgenet-2018-105635. Epub 2019 Feb 28. J Med Genet. 2019. PMID: 30819809

8

Severe familial paroxysmal exercise-induced dyskinesia.

Tacik P, Loens S, Schrader C, Gayde-Stephan S, Biskup S, Dressler D. Tacik P, et al. Among authors: schrader c. J Neurol. 2014 Oct;261(10):2009-15. doi: 10.1007/s00415-014-7441-5. Epub 2014 Aug 7. J Neurol. 2014. PMID: 25099510

9

Anti-leucine rich glioma inactivated 1 protein and anti-N-methyl-D-aspartate receptor encephalitis show distinct patterns of brain glucose metabolism in 18F-fluoro-2-deoxy-d-glucose positron emission tomography.

Wegner F, Wilke F, Raab P, Tayeb SB, Boeck AL, Haense C, Trebst C, Voss E, Schrader C, Logemann F, Ahrens J, Leffler A, Rodriguez-Raecke R, Dengler R, Geworski L, Bengel FM, Berding G, Stangel M, Nabavi E. Wegner F, et al. Among authors: schrader c. BMC Neurol. 2014 Jun 20;14:136. doi: 10.1186/1471-2377-14-136. BMC Neurol. 2014. PMID: 24950993 Free PMC article.

10

Impaired Quality of Life and Need for Palliative Care in a German Cohort of Advanced Parkinson's Disease Patients.

Klietz M, Tulke A, Müschen LH, Paracka L, Schrader C, Dressler DW, Wegner F. Klietz M, et al. Among authors: schrader c. Front Neurol. 2018 Mar 6;9:120. doi: 10.3389/fneur.2018.00120. eCollection 2018. Front Neurol. 2018. PMID: 29559949 Free PMC article.

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