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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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