Changing the diagnostic approach to diabetes insipidus: role of copeptin

por Grandone, Anna, Marzuillo, Pierluigi, Patti, Giuseppa, Perrotta, Silverio, Maghnie, Mohamad
Publicado en Ann Transl Med (2019)

Iron chelating properties of Eltrombopag: Investigating its role in thalassemia-induced osteoporosis

por Punzo, Francesca, Tortora, Chiara, Argenziano, Maura, Casale, Maddalena, Perrotta, Silverio, Rossi, Francesca
Publicado en PLoS One (2018)

Arg(1809) substitution in neurofibromin: further evidence of a genotype–phenotype correlation in neurofibromatosis type 1

por Santoro, Claudia, Maietta, Anna, Giugliano, Teresa, Melis, Daniela, Perrotta, Silverio, Nigro, Vincenzo, Piluso, Giulio
Publicado en Eur J Hum Genet (2015)

From Gardner fibroma diagnosis to constitutional APC mutation detection: a one‐way street

por Santoro, Claudia, Giugliano, Teresa, Bifano, Delfina, D'Anna, Carolina, D'Onofrio, Vittoria, Perrotta, Silverio
Publicado en Clin Case Rep (2017)

Acute kidney injury in children hospitalized for acute gastroenteritis: prevalence and risk factors

por Marzuillo, Pierluigi, Baldascino, Maria, Guarino, Stefano, Perrotta, Silverio, Miraglia del Giudice, Emanuele, Nunziata, Felice
Publicado en Pediatr Nephrol (2021)

Tyrosine kinase inhibitors and mesenchymal stromal cells: effects on self-renewal, commitment and functions

por Borriello, Adriana, Caldarelli, Ilaria, Bencivenga, Debora, Stampone, Emanuela, Perrotta, Silverio, Oliva, Adriana, Ragione, Fulvio Della
Publicado en Oncotarget (2016)

Organizing national responses for rare blood disorders: the Italian experience with sickle cell disease in childhood

por Colombatti, Raffaella, Perrotta, Silverio, Samperi, Piera, Casale, Maddalena, Masera, Nicoletta, Palazzi, Giovanni, Sainati, Laura, Russo, Giovanna
Publicado en Orphanet J Rare Dis (2013)

A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity

por Roberti, Domenico, Conforti, Renata, Giugliano, Teresa, Brogna, Barbara, Tartaglione, Immacolata, Casale, Maddalena, Piluso, Giulio, Perrotta, Silverio
Publicado en Front Genet (2018)

An Autosomal Dominant Thrombocytopenia Gene Maps to Chromosomal Region 10p

por Savoia, Anna, Del Vecchio, Maria, Totaro, Antonio, Perrotta, Silverio, Amendola, Giovanni, Moretti, Arcangela, Zelante, Leopoldo, Iolascon, Achille
Publicado 1999

The Endocannabinoid/Endovanilloid System in Bone: From Osteoporosis to Osteosarcoma

por Rossi, Francesca, Tortora, Chiara, Punzo, Francesca, Bellini, Giulia, Argenziano, Maura, Di Paola, Alessandra, Torella, Marco, Perrotta, Silverio
Publicado en Int J Mol Sci (2019)

Evaluation of Browning Agents on the White Adipogenesis of Bone Marrow Mesenchymal Stromal Cells: A Contribution to Fighting Obesity

por Di Maio, Girolamo, Alessio, Nicola, Demirsoy, Ibrahim Halil, Peluso, Gianfranco, Perrotta, Silverio, Monda, Marcellino, Di Bernardo, Giovanni
Publicado en Cells (2021)

The Tyrosine Kinase Inhibitor Dasatinib Induces a Marked Adipogenic Differentiation of Human Multipotent Mesenchymal Stromal Cells

por Borriello, Adriana, Caldarelli, Ilaria, Basile, Maria Assunta, Bencivenga, Debora, Tramontano, Annunziata, Perrotta, Silverio, Ragione, Fulvio Della, Oliva, Adriana
Publicado 2011

Very early onset of autoimmune thyroiditis in a toddler with severe hypothyroidism presentation: a case report

por Marzuillo, Pierluigi, Grandone, Anna, Perrotta, Silverio, Ruggiero, Laura, Capristo, Carlo, Luongo, Caterina, Miraglia del Giudice, Emanuele, Perrone, Laura
Publicado en Ital J Pediatr (2016)

Juvenile erythrocytosis in children after liver transplantation: prevalence, risk factors and outcome

por Casale, Maddalena, Roberti, Domenico, Mandato, Claudia, Iorio, Raffaele, Caropreso, Maria, Scianguetta, Saverio, Picariello, Stefania, Perrotta, Silverio, Vajro, Pietro
Publicado en Sci Rep (2020)

p27Kip1 serine 10 phosphorylation determines its metabolism and interaction with cyclin-dependent kinases

por Bencivenga, Debora, Tramontano, Annunziata, Borgia, Alessia, Negri, Aide, Caldarelli, Ilaria, Oliva, Adriana, Perrotta, Silverio, Della Ragione, Fulvio, Borriello, Adriana
Publicado en Cell Cycle (2014)

Unusual association of non-anaplastic Wilms tumor and Cornelia de Lange syndrome: case report

por Santoro, Claudia, Apicella, Andrea, Casale, Fiorina, La Manna, Angela, Di Martino, Martina, Di Pinto, Daniela, Indolfi, Cristiana, Perrotta, Silverio
Publicado en BMC Cancer (2016)

Medullary unidentified bright objects in Neurofibromatosis type 1: a case series

por D’Amico, Alessandra, Mazio, Federica, Ugga, Lorenzo, Cuocolo, Renato, Cirillo, Mario, Santoro, Claudia, Perrotta, Silverio, Melis, Daniela, Brunetti, Arturo
Publicado en BMC Pediatr (2018)

CB2 Receptor Stimulation and Dexamethasone Restore the Anti-Inflammatory and Immune-Regulatory Properties of Mesenchymal Stromal Cells of Children with Immune Thrombocytopenia

por Rossi, Francesca, Tortora, Chiara, Palumbo, Giuseppe, Punzo, Francesca, Argenziano, Maura, Casale, Maddalena, Di Paola, Alessandra, Locatelli, Franco, Perrotta, Silverio
Publicado en Int J Mol Sci (2019)

Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship

por Iolascon, Achille, Russo, Roberta, Esposito, Maria Rosaria, Asci, Roberta, Piscopo, Carmelo, Perrotta, Silverio, Fénéant-Thibault, Madeleine, Garçon, Loïc, Delaunay, Jean
Publicado 2010

LEOPARD syndrome: clinical dilemmas in differential diagnosis of RASopathies

por Santoro, Claudia, Pacileo, Giuseppe, Limongelli, Giuseppe, Scianguetta, Saverio, Giugliano, Teresa, Piluso, Giulio, Ragione, Fulvio Della, Cirillo, Mario, Mirone, Giuseppe, Perrotta, Silverio
Publicado 2014