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Page 1
Long-term effects on growth, development, and metabolism of ALL treatment in childhood.
Expert Rev Endocrinol Metab. 2019 Jan;14(1):49-61. doi: 10.1080/17446651.2019.1561271. Epub 2018 Dec 31.
Expert Rev Endocrinol Metab. 2019.
PMID: 30596296
Review.
Pyomyositis associated with abscess formation caused by streptococcus pneumoniae in children: a case report and review of literature.
Barchi L, Fastiggi M, Bassoli I, Bonvicini F, Silvotti M, Iughetti L, De Fanti A.
Barchi L, et al. Among authors: bonvicini f.
Ital J Pediatr. 2023 Jun 14;49(1):73. doi: 10.1186/s13052-023-01472-1.
Ital J Pediatr. 2023.
PMID: 37316947
Free PMC article.
Review.
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Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients.
Garavelli L, Ivanovski I, Caraffi SG, Santodirocco D, Pollazzon M, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Baldo C, Bayat A, Belligni E, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, Devriendt K, Dinulos MB, Djuric O, Epifanio R, Faravelli F, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Lacombe D, Maggi M, Malbora B, Mammi I, Moutton S, Møller R, Muschke P, Napoli M, Pantaleoni C, Pascarella R, Pellicciari A, Poch-Olive ML, Raviglione F, Rivieri F, Russo C, Savasta S, Scarano G, Selicorni A, Silengo M, Sorge G, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zollino M, Dobyns WB, Paciorkowski AR.
Garavelli L, et al. Among authors: bonvicini f.
Genet Med. 2017 Jun;19(6):691-700. doi: 10.1038/gim.2016.176. Epub 2016 Nov 10.
Genet Med. 2017.
PMID: 27831545
Free PMC article.
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Tick-Borne Encephalitis in a 6-Year-Old Patient: A Case Report.
Cesaroni CA, Frattini D, Lecis M, Bonvicini F, Bartolomeo D, Rizzi S, Spagnoli C, Napoli M, Pascarella R, De Fanti A, Fusco C.
Cesaroni CA, et al. Among authors: bonvicini f.
Neurohospitalist. 2024 Jan;14(1):64-68. doi: 10.1177/19418744231205626. Epub 2023 Oct 9.
Neurohospitalist. 2024.
PMID: 38235031
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Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care.
Ivanovski I, Djuric O, Caraffi SG, Santodirocco D, Pollazzon M, Rosato S, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Ajmone PF, Badura-Stronka M, Baldo C, Baldi M, Bayat A, Bigoni S, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, De Brasi D, Devriendt K, Dinulos MB, Hjortshøj TD, Epifanio R, Faravelli F, Fiumara A, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Kuburovic V, Kutkowska-Kazmierczak A, Lacombe D, Lo Rizzo C, Luchetti A, Malbora B, Mammi I, Mari F, Montorsi G, Moutton S, Møller RS, Muschke P, Nielsen JEK, Obersztyn E, Pantaleoni C, Pellicciari A, Pisanti MA, Prpic I, Poch-Olive ML, Raviglione F, Renieri A, Ricci E, Rivieri F, Santen GW, Savasta S, Scarano G, Schanze I, Selicorni A, Silengo M, Smigiel R, Spaccini L, Sorge G, Szczaluba K, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zenker M, Conidi A, Zollino M, Rauch A, Zweier C, Garavelli L.
Ivanovski I, et al. Among authors: bonvicini f.
Genet Med. 2018 Sep;20(9):965-975. doi: 10.1038/gim.2017.221. Epub 2018 Jan 4.
Genet Med. 2018.
PMID: 29300384
Free article.
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