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Author/Creator Syrbe, S.

2. V25. Benign familial neonatal seizures and transient neonatal diabetes in a family with a mutation in ABCC8 encoding the SUR1 subunit of the ATP-sensitive potassium (K-ATP) channel. Issue 8 (August 2015)

Authors:
Syrbe, S.; Houghton, J.; Bernhard, M.K.; Lemke, J.; Kapellen, T.M.; Merkenschlager, A.
Journal:
Clinical neurophysiology
Issue:
Volume 126:Issue 8(2015:Aug.)
Page Start:
e78
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. V28. KCNA2 mutations cause epileptic encephalopathy by gain- or loss-of channel function. Issue 8 (August 2015)

Authors:
Hedrich, U.B.S.; Syrbe, S.; Riesch, E.; Djémié, T.; Müller, S.; Møller, R.S.; Maher, B.; Hernandez-Hernandez, L.; Synofzik, M.; Caglayan, H.S.; Arslan, M.; Serratosa, J.; Gonzalez, M.; Züchner, S.; Palotie, A.; Suls, A.; De Jonghe, P.; Helbig, I.; Biskup, S.; Wolff, M.
Journal:
Clinical neurophysiology
Issue:
Volume 126:Issue 8(2015:Aug.)
Page Start:
e80
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗