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39 results on '"Sander, T."'

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1. GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

6. Effectiveness of different types of masks in aerosol dispersion in SARS-CoV-2 infection

7. Distinct gene-set burden patterns underlie common generalized and focal epilepsies

9. Effectiveness of different types of masks in aerosol dispersion in SARS-CoV-2 infection

10. Early detection of marine non-indigenous species on Svalbard by DNA metabarcoding of sediment

11. No evidence for a BRD2 promoter hypermethylation inblood leukocytes of Europeans with juvenile myoclonic epilepsy

12. The fluid membrane determines mechanics of erythrocyte extracellular vesicles and is softened in hereditary spherocytosis

13. Rare gene deletions in genetic generalized and Rolandic epilepsies

14. The fluid membrane determines mechanics of erythrocyte extracellular vesicles and is softened in hereditary spherocytosis

15. Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

16. The fluid membrane determines mechanics of erythrocyte extracellular vesicles and is softened in hereditary spherocytosis

17. The fluid membrane determines mechanics of erythrocyte extracellular vesicles and is softened in hereditary spherocytosis

18. Analysis of shared heritability in common disorders of the brain

19. Rare gene deletions in genetic generalized and Rolandic epilepsies

22. Calibration of dosemeters used in mammography with different X ray qualities: Euromet Project No. 526

23. Evaluation of presumably disease causing SCN1A variants in a cohort of common epilepsy syndromes

24. Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes

25. Wurtzite silicon as a potential absorber in photovoltaics : Tailoring the optical absorption by applying strain

26. CHD2 variants are a risk factor for photosensitivity in epilepsy

27. Functional characterization of the c.462delA mutation in the NDUFS4 subunit gene of mitochondrial complex I

28. Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy

29. Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy

30. Functional characterization of the c.462delA mutation in the NDUFS4 subunit gene of mitochondrial complex I

31. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

32. KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes

33. Taeniasis in Mongolia, 2002–2006

36. Application of Spontaneous Raman Scattering to the Flowfield in a Scramjet Combustor

37. Nonlinear time series analysis of human alpha rhythm

38. Nonlinear time series analysis of human alpha rhythm

39. Calibration of dosemeters used in mammography with different X ray qualities: Euromet Project No. 526

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