Volltext-Artikel, E-Books und Literaturhinweise aus dem EBSCO Discovery Service
"Artikel & mehr" berücksichtigt nur einen Teil der für die Bibliothek der Frankfurt UAS verfügbaren Datenbanken. Zur Übersicht in DBIS
Ergebnis verändern
- Publikationstyp
Publikationstyp- erschienen in
- Verlag
- Geographic terms
-
1
von Mideksa, K. G. ; Santillan-Guzman, A. ; Japaridze, N. ; et al.
2014 36th Annual International Conference of the IEEE Engineering in Medicine and Biology Society Engineering in Medicine and Biology Society (EMBC), 2014 36th Annual International Conference of the IEEE. :3841-3844 Aug, 2014
-
2
von Berkovic, SF ; Neale, BM ; Zsurka, G ; et al.
Nature Neuroscience , 27 (10) pp. 1864-1879. (2024)
Schlagworte: Humans; Epilepsy; Genetic Predisposition to Disease; Exome Sequencing; Exome; DNA Copy Number Variations; Female; Male; Polymorphism; Single Nucleotide; Risk Factors
-
3
von Japaridze, N. ; Siniatchkin, M. ; Stephani, U. ; et al.
Schlagworte: ddc:004
- 4
-
5
von Friedrichs, P. ; Mitlehner, H. ; Dohnke, K.O. ; et al.
12th International Symposium on Power Semiconductor Devices & ICs. Proceedings (Cat. No.00CH37094) Power semiconductor devices and ICs Power Semiconductor Devices and ICs, 2000. Proceedings. The 12th International Symposium on. :213-216 2000
-
6
von Peters, D. ; Friedrichs, P. ; Mitlehner, H. ; et al.
12th International Symposium on Power Semiconductor Devices & ICs. Proceedings (Cat. No.00CH37094) Power semiconductor devices and ICs Power Semiconductor Devices and ICs, 2000. Proceedings. The 12th International Symposium on. :241-244 2000
-
7
von Mitlehner, H. ; Bartsch, W. ; Dohnke, K.O. ; et al.
11th International Symposium on Power Semiconductor Devices and ICs. ISPSD'99 Proceedings (Cat. No.99CH36312) Power semiconductor devices and ICs Power Semiconductor Devices and ICs, 1999. ISPSD '99. Proceedings., The 11th International Symposium on. :339-342 1999
- 8
-
9
von Mitlehner, H. ; Friedrichs, P. ; Peters, D. ; et al.
Proceedings of the 10th International Symposium on Power Semiconductor Devices and ICs. ISPSD'98 (IEEE Cat. No.98CH36212) Power semiconductor devices and ICs Power Semiconductor Devices and ICs, 1998. ISPSD 98. Proceedings of the 10th International Symposium on. :127-130 1998
- 10
-
11
von Krischel, D. ; Baumgarten, C. ; Geisler, A. ; et al.
IEEE Transactions on Applied Superconductivity IEEE Trans. Appl. Supercond. Applied Superconductivity, IEEE Transactions on. 17(2):2307-2310 Jun, 2007
-
12
von Burgmer, R. ; Klein, H.-U. ; Krischel, D. ; et al.
Proceedings of the 2003 Particle Accelerator Conference Particle accelerator conference Particle Accelerator Conference, 2003. PAC 2003. Proceedings of the. 3:1948-1950 vol.3 2003
-
13
von Jasmine U. Ting ; Maria Carmen S. Tan ; Vincent Antonio S. Ng ; et al.
Crystals, Vol 14, Iss 5, p 438 (2024)
Schlagworte: inflammation; NF-κB; molecular docking; molecular dynamics; p50 inhibitor; Philippine plants; Crystallography; QD901-999
-
14
von Montanucci L. ; Lewis-Smith D. ; Collins R. L. ; et al.
Schlagworte: copy number variant; seizure; genome wide
-
15
von Berkovic S. F. ; Neale B. M. ; Zsurka G. ; et al.
Schlagworte: exome sequencing; epilepsy; genetic risk
-
16
von Baumeister, F.A.M. ; Baethmann, M. ; Schreiber-Gollwitzer, B. ; et al.
In European Journal of Paediatric Neurology November 2016 20(6):874-879
-
17
von Motelow, JE ; Povysil, G ; Dhindsa, RS ; et al.
American Journal of Human Genetics , 108 (6) pp. 965-982. (2021)
Schlagworte: Epilepsy; epileptic encephalopathy; seizures; whole-exome sequencing; focal epilepsy; generalized epilepsy; intolerance; ClinVar; Epi25; Louvain
- 18
- 19
-
20
von Leu C. ; Stevelink R. ; Smith A. W. ; et al.
Schlagworte: Common variant risk; Epilepsy; Genetic generalized epilepsy; Genetic; Cohort Studie; Cost of Illne; Databases; Factual; Epilepsies; Partial; Generalized; European Continental Ancestry Group; Female; Genetic Predisposition to Disease; Genetic Variation; Genome-Wide Association Study; Human; Male; Multifactorial Inheritance; Polymorphism; Single Nucleotide
-
21
- 22
- 23
-
24
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
von Feng, Y-CA ; Howrigan, DP ; Abbott, LE ; et al.
American Journal of Human Genetics , 105 (2) pp. 267-282. (2019)
Schlagworte: epilepsy; seizures; epileptic encephalopathy; exome; sequencing; burden analysis
- 25
Hilfe & Kontakt ǀ Fernleihe | Hilfe zur Fernleihe ǀ Literaturvorschlag| Literaturvorschlag