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pro vyhledávání: '"Giovan Battista Calabri"'
Autor:
Luciano De Simone, Serena Chiellino, Gaia Spaziani, Giulio Porcedda, Giovan Battista Calabri, Sergio Berti, Silvia Favilli, Laura Stefani, Giuseppe Santoro
Publikováno v:
Children, Vol 10, Iss 3, p 526 (2023)
Hutchinson–Gilford progeria syndrome is an extremely rare genetic disease caused by a de novo mutation in the LMNA gene, leading to an accumulation of a form of Lamin A, called Progerin, which results in a typical phenotype and a marked decrease in
Externí odkaz:
https://doaj.org/article/f41d35970fcc46e99a0c917ec042c627
Autor:
Gabriele Simonini, Giovan Battista Calabri, Francesca Grisolia, Sandra Trapani, Fernanda Falcini
Publikováno v:
Università degli studi di Firenze-IRIS
To assess the frequency and types of cancer found in children presenting to our Unit with musculoskeletal symptoms over a 10-year period.The medical records of patients with musculoskeletal symptoms and a final diagnosis of cancer were reviewed. In e