Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/31971
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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