PuSH - Publikationsserver des Helmholtz Zentrums München

Zeitschriften-Browsing

8 Datensätze gefunden.
Zum Exportieren der Ergebnisse bitte einloggen.
▮◀ ◀◀ ▶▶ ▶▮
Alle Publikationen dieser Seite in den Korb legen
1.
Vogel, F.D.* et al.: A de novo missense variant in GABRA4 alters receptor function in an epileptic and neurodevelopmental phenotype. Epilepsia 63, e35-e41 (2022)
2.
Stevelink, R.* et al.: Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations. Epilepsia 62, 1518-1527 (2021)
3.
Vollmar, C.* ; Stredl, I.* ; Heinig, M. ; Noachtar, S.* & Rémi, J.*: Unilateral temporal interictal epileptiform discharges correctly predict the epileptogenic zone in lesional temporal lobe epilepsy. Epilepsia 59, 1577-1582 (2018)
4.
Potschka, H.* et al.: Differential proteome analysis during epileptogenesis: Focus on inflammation. Epilepsia 56, 193-193 (2015)
5.
von Rueden, E.- L.* et al.: Shared pathophysiology of temporal lobe epilepsy and Alzheimer´s disease -  a differential proteomics approach in a post-status epilepticus model. Epilepsia 56, 4-4 (2015)
6.
Lal, D.* et al.: Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy. Epilepsia 54, 265-271 (2013)
7.
Møller, R.S.* et al.: Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy. Epilepsia 54, 256-264 (2013)
8.
Zimprich, F.* et al.: A functional polymorphism in the SCN1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy. Epilepsia 49, 1108-1109 (2008)
▮◀ ◀◀ ▶▶ ▶▮