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Page 1
Improving paediatric movement disorders care: Insights on rating scales utilization and clinical practice.
Amato ME, Darling A, Stovickova L, Attard S, Eggink H, Engelen M, Freilinger M, Grosso S, Hadzsiev K, Moroni I, Nardocci N, Neubauer D, Nicita F, Pagliano E, Siegert S, Soler D, van de Pol LA, Vasco G, Vidailhet M, Willemsen MA, Zibordi F, Zorzi G, Zumrova A, Reinhard C, Sevin C, Wolf N, Rodriguez-Blazquez C, Sival DA, Ortigoza-Escobar JD; Pediatric issues working group of the European Reference Network for Rare Neurological Diseases (ERN-RND). Amato ME, et al. Eur J Paediatr Neurol. 2024 Sep;52:10-19. doi: 10.1016/j.ejpn.2024.06.011. Epub 2024 Jun 29. Eur J Paediatr Neurol. 2024. PMID: 38970889
Developmental and epileptic encephalopathy 56 due to YWHAG variants: 12 new cases and review of the literature.
Amato ME, Balsells S, Martorell L, Alcalá San Martín A, Ansell K, Børresen ML, Johnson H, Korff C, Garcia-Tarodo S, Lefranc J, Denommé-Pichon AS, Sarrazin E, Szabo NZ, Saraiva JM, Wicher D, Goverde A, Bindels-de Heus KGCB, Barakat TS, Ortigoza-Escobar JD. Amato ME, et al. Eur J Paediatr Neurol. 2024 Oct 9;53:63-72. doi: 10.1016/j.ejpn.2024.10.005. Online ahead of print. Eur J Paediatr Neurol. 2024. PMID: 39413657
Genetic heritage of the Baphuthi highlights an over-ethnicized notion of "Bushman" in the Maloti-Drakensberg, southern Africa.
Daniels RJ, D'Amato ME, Lesaoana M, Kasu M, Ehlers K, Chauke PA, Lecheko P, Challis S, Rockett K, Montinaro F, González-Santos M, Capelli C. Daniels RJ, et al. Among authors: d amato me. Am J Hum Genet. 2023 May 4;110(5):880-894. doi: 10.1016/j.ajhg.2023.03.018. Epub 2023 Apr 26. Am J Hum Genet. 2023. PMID: 37105174 Free PMC article.
The genetic landscape of South African males: A Y-STR perspective.
Kasu M, Cloete KW, Pitere R, Tsiana KJ, D'Amato ME. Kasu M, et al. Among authors: d amato me. Forensic Sci Int Genet. 2022 May;58:102677. doi: 10.1016/j.fsigen.2022.102677. Epub 2022 Feb 11. Forensic Sci Int Genet. 2022. PMID: 35228005
Predicting haplogroups using a versatile machine learning program (PredYMaLe) on a new mutationally balanced 32 Y-STR multiplex (CombYplex): Unlocking the full potential of the human STR mutation rate spectrum to estimate forensic parameters.
Bouakaze C, Delehelle F, Saenz-Oyhéréguy N, Moreira A, Schiavinato S, Croze M, Delon S, Fortes-Lima C, Gibert M, Bujan L, Huyghe E, Bellis G, Calderon R, Hernández CL, Avendaño-Tamayo E, Bedoya G, Salas A, Mazières S, Charioni J, Migot-Nabias F, Ruiz-Linares A, Dugoujon JM, Thèves C, Mollereau-Manaute C, Noûs C, Poulet N, King T, D'Amato ME, Balaresque P. Bouakaze C, et al. Among authors: d amato me. Forensic Sci Int Genet. 2020 Sep;48:102342. doi: 10.1016/j.fsigen.2020.102342. Epub 2020 Jun 29. Forensic Sci Int Genet. 2020. PMID: 32818722
DNA commission of the International Society of Forensic Genetics (ISFG): Recommendations on the interpretation of Y-STR results in forensic analysis.
Roewer L, Andersen MM, Ballantyne J, Butler JM, Caliebe A, Corach D, D'Amato ME, Gusmão L, Hou Y, de Knijff P, Parson W, Prinz M, Schneider PM, Taylor D, Vennemann M, Willuweit S. Roewer L, et al. Among authors: d amato me. Forensic Sci Int Genet. 2020 Sep;48:102308. doi: 10.1016/j.fsigen.2020.102308. Epub 2020 Jun 4. Forensic Sci Int Genet. 2020. PMID: 32622324
52 results