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Susanne Blichfeldt

Showing results (1-10 of 6) with videos related to

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Ugeskrift for Laeger|May 21, 2008
[Children with commotio cerebri at paediatric departments in Denmark]Gitte Rønde, Susanne Blichfeldt
Ugeskrift for Laeger|April 25, 2008
[Ten practical, theory-based tips for clinical course planners]Thomas Balslev, Ian Westphall, Susanne Blichfeldt, et al.
Ugeskrift for Laeger|January 29, 2009
[Valproate treatment during pregnancy: description of four cases with foetal valproate syndrome]Anne Sabers, Katja Larsen, Susanne Blichfeldt, et al.
Epilepsia|November 6, 2015
The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndromeJan Larsen, Katrine Marie Johannesen, Jakob Ek, et al.
Neurology|January 6, 2017
Mutations in GABRB3: From febrile seizures to epileptic encephalopathiesRikke S Møller, Thomas V Wuttke, Ingo Helbig, et al.
Epilepsia|April 11, 2019
The spectrum of intermediate SCN8A-related epilepsyKatrine M Johannesen, Elena Gardella, Alejandra C Encinas, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Ugeskrift for Laeger|May 21, 2008
[Children with commotio cerebri at paediatric departments in Denmark]Gitte Rønde, Susanne Blichfeldt
Ugeskrift for Laeger|April 25, 2008
[Ten practical, theory-based tips for clinical course planners]Thomas Balslev, Ian Westphall, Susanne Blichfeldt, et al.
Ugeskrift for Laeger|January 29, 2009
[Valproate treatment during pregnancy: description of four cases with foetal valproate syndrome]Anne Sabers, Katja Larsen, Susanne Blichfeldt, et al.
Epilepsia|November 6, 2015
The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndromeJan Larsen, Katrine Marie Johannesen, Jakob Ek, et al.
Neurology|January 6, 2017
Mutations in GABRB3: From febrile seizures to epileptic encephalopathiesRikke S Møller, Thomas V Wuttke, Ingo Helbig, et al.
Epilepsia|April 11, 2019
The spectrum of intermediate SCN8A-related epilepsyKatrine M Johannesen, Elena Gardella, Alejandra C Encinas, et al.
Pageof 1