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|Title:||Rare. The importance of research, analysis, reporting and education in 'solving' the genetic epilepsies: A perspective from the European patient advocacy group for EpiCARE.||Austin Authors:||Nott, E;Behl, K E;Brambilla, I;Green, T E;Lucente, M;Vavassori, R;Watson, A;Dalla Bernardina, B;Hildebrand, M S||Affiliation:||Murdoch Children's Research Institute, The Royal Children's Hospital, Parkville, Victoria, 3052, Australia.
Hope for Hypothalamic Hamartomas and Hope for Hypothalamic Hamartomas-UK, UK; Epilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, Heidelberg, Victoria, 3084, Australia
Epilepsy Research Centre
European Patient Advocacy Group (ePAG) EpiCARE, France; Hope for Hypothalamic Hamartomas and Hope for Hypothalamic Hamartomas-UK, UK.
Alternating Hemiplegia of Childhood UK (AHCUK) and Alternating Hemiplegia of Childhood Federation of Europe (AHCFE), UK.
Dravet Italia Onlus; Research Center for Pediatric Epilepsies Verona, Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Italy.
|Issue Date:||6-Jan-2023||Date:||2023||Publication information:||European Journal of Medical Genetics 2023; 66(3)||URI:||https://ahro.austin.org.au/austinjspui/handle/1/31971||DOI:||10.1016/j.ejmg.2022.104680||ORCID:||Journal:||European Journal of Medical Genetics||Start page:||104680||PubMed URL:||36623768||ISSN:||1878-0849||Type:||Journal Article|
|Appears in Collections:||Journal articles|
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checked on Dec 7, 2023
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