Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Letizia Sabatini"'
Autor:
Sergio Ghirardo, Letizia Sabatini, Alessandro Onofri, Maria Beatrice Chiarini Testa, Maria Giovanna Paglietti, Daria Diodato, Lorena Travaglini, Fabrizia Stregapede, Marta Luisa Ciofi degli Atti, Claudio Cherchi, Renato Cutrera
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-4 (2022)
Abstract Background Breathing disturbances are often a primary clinical concern especially during wakefulness of the classic form of Rett syndrome, but data for atypical forms are lacking. Case presentation We report the case of a 20-month-old female
Externí odkaz:
https://doaj.org/article/4fd327885e6d417784a818f981cc379f
Autor:
Silvio Marchesani, Valentina Bertaina, Olivia Marini, Matilde Cossutta, Margherita Di Mauro, Gioacchino Andrea Rotulo, Paolo Palma, Letizia Sabatini, Maria Isabella Petrone, Giacomo Frati, Giulia Monteleone, Giuseppe Palumbo, Giulia Ceglie
Publikováno v:
Frontiers in Molecular Biosciences, Vol 9 (2023)
Introduction: The mutation of the beta-globin gene that causes sickle cell disease (SCD) results in pleiotropic effects, such as hemolysis and vaso-occlusive crisis that can induce inflammatory mechanisms with deleterious consequences on the organism
Externí odkaz:
https://doaj.org/article/1386bf603b004d1081e4a6c584365c85
Autor:
Laura Papetti, Maria Elisa Amodeo, Letizia Sabatini, Melissa Baggieri, Alessandro Capuano, Federica Graziola, Antonella Marchi, Paola Bucci, Emilio D’Ugo, Maedeh Kojouri, Silvia Gioacchini, Carlo Efisio Marras, Carlotta Ginevra Nucci, Fabiana Ursitti, Giorgia Sforza, Michela Ada Noris Ferilli, Gabriele Monte, Romina Moavero, Federico Vigevano, Massimiliano Valeriani, Fabio Magurano
Publikováno v:
Viruses, Vol 14, Iss 4, p 733 (2022)
Subacute sclerosing panencephalitis (SSPE) is a late complication of measles virus infection that occurs in previously healthy children. This disease has no specific cure and is associated with a high degree of disability and mortality. In recent yea
Externí odkaz:
https://doaj.org/article/dc2eff4760ae46428c1cd6ce21f43fa0
Autor:
Francesco Nicita, Letizia Sabatini, Viola Alesi, Giulia Lucignani, Ester Sallicandro, Antonella Sferra, Enrico Bertini, Ginevra Zanni, Giuseppe Palumbo
Publikováno v:
Brain Sciences, Vol 12, Iss 2, p 182 (2022)
Recessive hereditary methemoglobinemia (RHM) due to NADH-cytochrome b5 reductase deficiency is a rare disease caused by pathogenic variants in CYB5R3. Unlike type I, in RHM type II (RHM2), the enzymatic defect affects erythrocytes and all body tissue
Externí odkaz:
https://doaj.org/article/51680d3a2bc640778fd125aab9e0adc3
Autor:
Letizia Sabatini, Marcello Chinali, Alessio Franceschini, Margherita Di Mauro, Silvio Marchesani, Francesca Fini, Giorgia Arcuri, Mariachiara Lodi, Giuseppe Palumbo, Giulia Ceglie
Publikováno v:
Journal of Clinical Medicine; Volume 12; Issue 1; Pages: 7
Cardiovascular involvement has a great impact on morbidity and mortality in sickle cell disease (SCD). Currently, few studies are available regarding the paediatric setting and, moreover, current guidelines for the echocardiogram screening program in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64f8683f0676602e439ab4f4e694c26b
https://pubmed.ncbi.nlm.nih.gov/36614810
https://pubmed.ncbi.nlm.nih.gov/36614810
Autor:
Silvio Marchesani, Letizia Sabatini, Valentina Bertaina, Olivia Marini, Michela Ambrosi, Margherita Di Mauro, Matilde Cossutta, Livia Schettini, Mariachiara Lodi, Gioacchino Andrea Rotulo, Paolo Palma, Giuseppe Palumbo, Giulia Ceglie
Publikováno v:
Blood cells, moleculesdiseases. 98
Spherocytosis is a hereditary disease caused by the deficiencies of different membrane proteins of red blood cells. Currently, splenectomy is the main therapeutic strategy available, although it is accompanied by an increased risk of sepsis. Several
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfa7d5e33a94d8de1bbbbc6dda69ac00
https://pubmed.ncbi.nlm.nih.gov/36055084
https://pubmed.ncbi.nlm.nih.gov/36055084
Autor:
Sergio Ghirardo, Letizia Sabatini, Alessandro Onofri, Maria Beatrice Chiarini Testa, Maria Giovanna Paglietti, Daria Diodato, Lorena Travaglini, Fabrizia Stregapede, Marta Luisa Ciofi degli Atti, Claudio Cherchi, Renato Cutrera
Publikováno v:
Italian journal of pediatrics. 48(1)
Background Breathing disturbances are often a primary clinical concern especially during wakefulness of the classic form of Rett syndrome, but data for atypical forms are lacking. Case presentation We report the case of a 20-month-old female affected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e672088f154bd333989c5e98974b8cd5
https://pubmed.ncbi.nlm.nih.gov/36071486
https://pubmed.ncbi.nlm.nih.gov/36071486