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De novo mutations in HCN1 cause early infantile epileptic encephalopathy.
Nat Genet. 2014 Jun;46(6):640-5. doi: 10.1038/ng.2952. Epub 2014 Apr 20.
Nat Genet. 2014.
PMID: 24747641
Seizure semiology in autosomal dominant epilepsy with auditory features, due to novel LGI1 mutations.
Sadleir LG, Agher D, Chabrol E, Elkouby L, Leguern E, Paterson SJ, Harty R, Bellows ST, Berkovic SF, Scheffer IE, Baulac S.
Sadleir LG, et al. Among authors: agher d.
Epilepsy Res. 2013 Dec;107(3):311-7. doi: 10.1016/j.eplepsyres.2013.09.008. Epub 2013 Oct 8.
Epilepsy Res. 2013.
PMID: 24206907
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Decision Support System for Selection of e-Health Interventions.
Agher D, Fouque M, Brandi M, Sedki K, Tsopra R, Meneton P, Despres S, Jaulent MC.
Agher D, et al.
Stud Health Technol Inform. 2020 Jun 26;272:326-329. doi: 10.3233/SHTI200561.
Stud Health Technol Inform. 2020.
PMID: 32604668
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Influence of Connected Health Interventions for Adherence to Cardiovascular Disease Prevention: A Scoping Review.
Agher D, Sedki K, Tsopra R, Despres S, Jaulent MC.
Agher D, et al.
Appl Clin Inform. 2020 Aug;11(4):544-555. doi: 10.1055/s-0040-1715649. Epub 2020 Aug 19.
Appl Clin Inform. 2020.
PMID: 32814353
Free PMC article.
Review.
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Encouraging Behavior Changes and Preventing Cardiovascular Diseases Using the Prevent Connect Mobile Health App: Conception and Evaluation of App Quality.
Agher D, Sedki K, Despres S, Albinet JP, Jaulent MC, Tsopra R.
Agher D, et al.
J Med Internet Res. 2022 Jan 20;24(1):e25384. doi: 10.2196/25384.
J Med Internet Res. 2022.
PMID: 35049508
Free PMC article.
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