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Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe.
Garnier N, Berghout J, Zygmunt A, Singh D, Huang KA, Kantz W, Blankart CR, Gillner S, Zhao J, Roettger R, Saier C, Kirschner J, Schenk J, Atkins L, Ryan N, Zarakowska K, Zschüntzsch J, Zuccolo M, Müllenborn M, Man YS, Goodman L, Trad M, Chalandon AS, Sansen S, Martinez-Fresno M, Badger S, Walther van Olden R, Rothmann R, Lehner P, Tschohl C, Baillon L, Gumus G, Gross E, Stefanov R, Iskrov G, Raycheva R, Kostadinov K, Mitova E, Einhorn M, Einhorn Y, Schepers J, Hübner M, Alves F, Iskandar R, Mayer R, Renieri A, Piperkova A, Gut I, Beltran S, Matthiesen ME, Poetz M, Hansson M, Trollmann R, Agolini E, Ottombrino S, Novelli A, Bertini E, Selvatici R, Farnè M, Fortunato F, Ferlini A. Garnier N, et al. Among authors: kostadinov k. PLoS One. 2023 Nov 22;18(11):e0293503. doi: 10.1371/journal.pone.0293503. eCollection 2023. PLoS One. 2023. PMID: 37992053 Free PMC article.
Socio-Economic Burden of Myasthenia Gravis: A Cost-of-Illness Study in Bulgaria.
Ignatova V, Kostadinov K, Vassileva E, Muradyan N, Stefanov G, Iskrov G, Stefanov R. Ignatova V, et al. Among authors: kostadinov k. Front Public Health. 2022 Mar 3;10:822909. doi: 10.3389/fpubh.2022.822909. eCollection 2022. Front Public Health. 2022. PMID: 35309194 Free PMC article.
Trauma Informed Interventions to Reduce Seclusion, Restraint and Restrictive Practices Amongst Staff Caring for Children and Adolescents with Challenging Behaviours: A Systematic Review.
Kelly P, Saab MM, Hurley EJ, Heffernan S, Goodwin J, Mulud ZA, O Malley M, O Mahony J, Curtin M, Groen G, Ivanova S, Jörns-Presentati A, Korhonen J, Kostadinov K, Lahti M, Lalova V, Petrova G, O Donovan A. Kelly P, et al. Among authors: kostadinov k. J Child Adolesc Trauma. 2023 Mar 15;16(3):629-647. doi: 10.1007/s40653-023-00524-2. eCollection 2023 Sep. J Child Adolesc Trauma. 2023. PMID: 37593061 Free PMC article.
Landscape analysis of available European data sources amenable for machine learning and recommendations on usability for rare diseases screening.
Raycheva R, Kostadinov K, Mitova E, Iskrov G, Stefanov G, Vakevainen M, Elomaa K, Man YS, Gross E, Zschüntzsch J, Röttger R, Stefanov R. Raycheva R, et al. Among authors: kostadinov k. Orphanet J Rare Dis. 2024 Apr 6;19(1):147. doi: 10.1186/s13023-024-03162-5. Orphanet J Rare Dis. 2024. PMID: 38582900 Free PMC article.