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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
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
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.
328 results