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Case Report: short stature, kidney anomalies, and cerebral aneurysms in a novel homozygous mutation in the PCNT gene associated with microcephalic osteodysplastic primordial dwarfism type II.
Petraroli M, Percesepe A, Piane M, Ormitti F, Castellone E, Gnocchi M, Messina G, Bernardi L, Patianna VD, Esposito SMR, Street ME. Petraroli M, et al. Among authors: castellone e. Front Endocrinol (Lausanne). 2023 May 10;14:1018441. doi: 10.3389/fendo.2023.1018441. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37234811 Free PMC article.
SARS-CoV-2 infection in children in Parma.
Dodi I, Castellone E, Pappalardo M, Rubini M, Veronese P, Ruberto C, Bianchi L, Iovane B, Maffini V. Dodi I, et al. Among authors: castellone e. Acta Biomed. 2020 May 11;91(2):214-215. doi: 10.23750/abm.v91i2.9563. Acta Biomed. 2020. PMID: 32420948 Free PMC article.