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Author/Creator Korenke, G.C.

1. Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome. (1st June 2021)

Authors:
Vornweg, J.; Gläser, S.; Ahmad‐Anwar, M.; Zimmer, A.D.; Kuhn, M.; Hörer, S.; Korenke, G.C.; Grothaus, J.; Ott, H.; Fischer, J.
Journal:
British journal of dermatology
Issue:
Volume 184:Number 6(2021)
Page Start:
1190
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome. (3rd March 2021)

Authors:
Vornweg, J.; Gläser, S.; Ahmad‐Anwar, M.; Zimmer, A.D.; Kuhn, M.; Hörer, S.; Korenke, G.C.; Grothaus, J.; Ott, H.; Fischer, J.
Journal:
British journal of dermatology
Issue:
Volume 184:Number 6(2021)
Page Start:
1190
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Retrospective evaluation of low long-term efficacy of antiepileptic drugs and ketogenic diet in 39 patients with CDKL5-related epilepsy. (January 2016)

Authors:
Müller, A.; Helbig, I.; Jansen, C.; Bast, T.; Guerrini, R.; Jähn, J.; Muhle, H.; Auvin, S.; Korenke, G.C.; Philip, S.; Keimer, R.; Striano, P.; Wolf, N.I.; Püst, B.; Thiels, Ch.; Fogarasi, A.; Waltz, S.; Kurlemann, G.; Kovacevic-Preradovic, T.; Ceulemans, B.
Journal:
European journal of paediatric neurology
Issue:
Volume 20:Number 1(2016:Jan.)
Page Start:
147
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗