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Comorbidities of Rare Epilepsies: Results from the Rare Epilepsy Network.
Ho NT, Kroner B, Grinspan Z, Fureman B, Farrell K, Zhang J, Buelow J, Hesdorffer DC; Rare Epilepsy Network Steering Committee. Ho NT, et al. J Pediatr. 2018 Dec;203:249-258.e5. doi: 10.1016/j.jpeds.2018.07.055. Epub 2018 Sep 5. J Pediatr. 2018. PMID: 30195559
Phelan-McDermid syndrome data network: Integrating patient reported outcomes with clinical notes and curated genetic reports.
Kothari C, Wack M, Hassen-Khodja C, Finan S, Savova G, O'Boyle M, Bliss G, Cornell A, Horn EJ, Davis R, Jacobs J, Kohane I, Avillach P. Kothari C, et al. Among authors: bliss g. Am J Med Genet B Neuropsychiatr Genet. 2018 Oct;177(7):613-624. doi: 10.1002/ajmg.b.32579. Epub 2017 Sep 1. Am J Med Genet B Neuropsychiatr Genet. 2018. PMID: 28862395 Free PMC article.
The Carmarthen audit project.
Bliss G, Martin P. Bliss G, et al. J Nurs Manag. 1994 May;2(3):111-4. doi: 10.1111/j.1365-2834.1994.tb00139.x. J Nurs Manag. 1994. PMID: 7952699
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