Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Serena Chiellino"'
Publikováno v:
Children, Vol 11, Iss 9, p 1126 (2024)
Isolated musculoskeletal infantile myofibroma is a rare tumor of pediatric age. The majority of cases are seen in children under two years old, but it can occur at any age as a painless enlarging mass that involves bone, skin, or soft tissue, typical
Externí odkaz:
https://doaj.org/article/70b5e81375de4f24b91d3a54df9fd6d9
Autor:
Silvia Passantino, Serena Chiellino, Francesca Girolami, Mattia Zampieri, Giovanni Battista Calabri, Gaia Spaziani, Elena Bennati, Giulio Porcedda, Elena Procopio, Iacopo Olivotto, Silvia Favilli
Publikováno v:
Diagnostics, Vol 13, Iss 24, p 3674 (2023)
Background: Cardiac involvement is reported in a significant proportion of patients with classical organic acidurias (OAs), contributing to disability and premature death. Different cardiac phenotypes have been described, among which dilated cardiomy
Externí odkaz:
https://doaj.org/article/fb0ac5bc409e44d3bf1ac5a64cc72c83
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