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A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemia.
Torraco A, Bianchi M, Verrigni D, Gelmetti V, Riley L, Niceta M, Martinelli D, Montanari A, Guo Y, Rizza T, Diodato D, Di Nottia M, Lucarelli B, Sorrentino F, Piemonte F, Francisci S, Tartaglia M, Valente EM, Dionisi-Vici C, Christodoulou J, Bertini E, Carrozzo R. Torraco A, et al. Among authors: sorrentino f. Clin Genet. 2017 Mar;91(3):441-447. doi: 10.1111/cge.12790. Epub 2016 May 25. Clin Genet. 2017. PMID: 27102574
Screening of metabolic syndrome in obese children: a primary care concern.
Viggiano D, De Filippo G, Rendina D, Fasolino A, D'Alessio N, Avellino N, Verga MC, Prisco AG, Sorrentino FA, Sabatini P, Chiarelli F; O.Si.M.E. Study Group. Viggiano D, et al. Among authors: sorrentino fa. J Pediatr Gastroenterol Nutr. 2009 Sep;49(3):329-34. doi: 10.1097/MPG.0b013e31819b54b7. J Pediatr Gastroenterol Nutr. 2009. PMID: 19590449
New frontiers in retinal transplantation.
Sorrentino FS, Di Terlizzi P, De Rosa F, Salati C, Spadea L, Gagliano C, Musa M, Zeppieri M. Sorrentino FS, et al. World J Transplant. 2024 Dec 18;14(4):97690. doi: 10.5500/wjt.v14.i4.97690. World J Transplant. 2024. PMID: 39697450 Free PMC article. Review.
Genetic Features of Uveal Melanoma.
Sorrentino FS, Culiersi C, Florido A, De Nadai K, Adamo GG, Nasini F, Vivarelli C, Mura M, Parmeggiani F. Sorrentino FS, et al. Genes (Basel). 2024 Oct 22;15(11):1356. doi: 10.3390/genes15111356. Genes (Basel). 2024. PMID: 39596556 Free PMC article. Review.
Telemedicine for hearing-impaired patients in Italy.
Ghiselli S, Sorrentino F, Lazzerini F, Rabito C, Murri A, Scimemi P. Ghiselli S, et al. Among authors: sorrentino f. Acta Otorhinolaryngol Ital. 2024 Oct;44(5):342-345. doi: 10.14639/0392-100X-N3116. Acta Otorhinolaryngol Ital. 2024. PMID: 39526771 Free PMC article. No abstract available.
413 results