Epilepsi og utviklingshemming
Sist oppdatert: Sist revidert:
Sist revidert av:Karl Otto Nakken, spesialist i nevrologi
- Dixit A, Suri M.. When the face says it all: dysmorphology in identifying syndromic causes of epilepsy.. Pract Neurol 2016. pmid:26864574 PubMed
- Brodtkorb E. Management of epilepsy in people with learning disability. In: Shorvon S, Perucca E, Engel J, editors. The treatment of Epilepsy, p. 219-400.. Chichester: Wiley-Blackwell, 2009.
- Faulkner MA, Singh SP. Neurogenetic disorders and treatment of associated seizures. Pharmacotherapy. 2013; 33(3): 330-43. pmid:23400943 PubMed
- Johannesen KM et al. Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications. Brain. 2021 Aug 25:awab321. doi: 10.1093/brain/awab321. Epub ahead of print. PMID: 34431999 PubMed
- De Maria B, Balestrini S, Mei D, Melani F, Pellacani S, Pisano T, Rosati A, Scaturro GM, Giordano L, Cantalupo G, Fontana E, Zammarchi C, Said E, Leuzzi V, Mastrangelo M, Galosi S, Parrini E, Guerrini R. Expanding the genetic and phenotypic spectrum of CHD2-related disease: From early neurodevelopmental disorders to adult-onset epilepsy. Am J Med Genet A. 2021 Oct 29. doi: 10.1002/ajmg.a.62548. Epub ahead of print. PMID: 34713950. PubMed
- Karl Otto Nakken, spesialist i nevrologi, dr med
- Eylert Brodtkorb, spesialist i nevrologi, professor dr med
- Unn Ljøstad, spesialist i nevrologi, professor PhD
- Åse Mygland, spesialist i nevrologi, professor dr med