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A gentle introduction to deep learning for graphs.
Bacciu D, Errica F, Micheli A, Podda M. Bacciu D, et al. Among authors: podda m. Neural Netw. 2020 Sep;129:203-221. doi: 10.1016/j.neunet.2020.06.006. Epub 2020 Jun 11. Neural Netw. 2020. PMID: 32559609
Clinical factors associated with death in 3044 COVID-19 patients managed in internal medicine wards in Italy: results from the SIMI-COVID-19 study of the Italian Society of Internal Medicine (SIMI).
Corradini E, Ventura P, Ageno W, Cogliati CB, Muiesan ML, Girelli D, Pirisi M, Gasbarrini A, Angeli P, Querini PR, Bosi E, Tresoldi M, Vettor R, Cattaneo M, Piscaglia F, Brucato AL, Perlini S, Martelletti P, Pontremoli R, Porta M, Minuz P, Olivieri O, Sesti G, Biolo G, Rizzoni D, Serviddio G, Cipollone F, Grassi D, Manfredini R, Moreo GL, Pietrangelo A; SIMI-COVID-19 Collaborators. Corradini E, et al. Intern Emerg Med. 2021 Jun;16(4):1005-1015. doi: 10.1007/s11739-021-02742-8. Epub 2021 Apr 24. Intern Emerg Med. 2021. PMID: 33893976 Free PMC article.
S2k guideline for the treatment of hidradenitis suppurativa / acne inversa - Short version.
Zouboulis CC, Bechara FG, Fritz K, Goebeler M, Hetzer FH, Just E, Kirsten N, Kokolakis G, Kurzen H, Nikolakis G, Pinter A, Podda M, Rosinski K, Schneider-Burrus S, Taube KM, Volz T, Winkler T, Kristandt A, Presser D, Zouboulis VA. Zouboulis CC, et al. Among authors: podda m. J Dtsch Dermatol Ges. 2024 May 21. doi: 10.1111/ddg.15412. Online ahead of print. J Dtsch Dermatol Ges. 2024. PMID: 38770982
Caring for children with cancer evacuated from Ukraine: The patients' perception.
Bolognese M, Massimino M, Cabibbe D, Zecca M, Fornara M, Armiraglio M, Kyzima R, Luksch R, Terenziani M, Casanova M, Spreafico F, Meazza C, Podda M, Biassoni V, Schiavello E, Chiaravalli S, Puma N, Hovsepyan S, Bergamaschi L, Gattuso G, Nigro O, Grampa P, Adduci A, Ferrari A, Clerici CA. Bolognese M, et al. Among authors: podda m. Pediatr Blood Cancer. 2024 May 20:e31087. doi: 10.1002/pbc.31087. Online ahead of print. Pediatr Blood Cancer. 2024. PMID: 38769590
Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project.
Stenton SL, O'Leary MC, Lemire G, VanNoy GE, DiTroia S, Ganesh VS, Groopman E, O'Heir E, Mangilog B, Osei-Owusu I, Pais LS, Serrano J, Singer-Berk M, Weisburd B, Wilson MW, Austin-Tse C, Abdelhakim M, Althagafi A, Babbi G, Bellazzi R, Bovo S, Carta MG, Casadio R, Coenen PJ, De Paoli F, Floris M, Gajapathy M, Hoehndorf R, Jacobsen JOB, Joseph T, Kamandula A, Katsonis P, Kint C, Lichtarge O, Limongelli I, Lu Y, Magni P, Mamidi TKK, Martelli PL, Mulargia M, Nicora G, Nykamp K, Pejaver V, Peng Y, Pham THC, Podda MS, Rao A, Rizzo E, Saipradeep VG, Savojardo C, Schols P, Shen Y, Sivadasan N, Smedley D, Soru D, Srinivasan R, Sun Y, Sunderam U, Tan W, Tiwari N, Wang X, Wang Y, Williams A, Worthey EA, Yin R, You Y, Zeiberg D, Zucca S, Bakolitsa C, Brenner SE, Fullerton SM, Radivojac P, Rehm HL, O'Donnell-Luria A. Stenton SL, et al. Among authors: podda ms. Hum Genomics. 2024 Apr 29;18(1):44. doi: 10.1186/s40246-024-00604-w. Hum Genomics. 2024. PMID: 38685113 Free PMC article.
717 results