A 2-Week Course of Enteral Treatment with a Very Low-Calorie Protein-Based Formula for the Management of Severe Obesity

por Castaldo, Giuseppe, Monaco, Luigi, Castaldo, Laura, Sorrentino, Paolo
Publicado en Int J Endocrinol (2015)

An Update on Laboratory Diagnosis of Liver Inherited Diseases

por Zarrilli, Federica, Elce, Ausilia, Scorza, Manuela, Giordano, Sonia, Amato, Felice, Castaldo, Giuseppe
Publicado 2013

Genetic Diseases That Predispose to Early Liver Cirrhosis

por Scorza, Manuela, Elce, Ausilia, Zarrilli, Federica, Liguori, Renato, Amato, Felice, Castaldo, Giuseppe
Publicado 2014

Virtual Screening of Natural Products against Type II Transmembrane Serine Protease (TMPRSS2), the Priming Agent of Coronavirus 2 (SARS-CoV-2)

por Rahman, Noor, Basharat, Zarrin, Yousuf, Muhammad, Castaldo, Giuseppe, Rastrelli, Luca, Khan, Haroon
Publicado en Molecules (2020)

Congenital diarrhoeal disorders: advances in this evolving web of inherited enteropathies

por Canani, Roberto Berni, Castaldo, Giuseppe, Bacchetta, Rosa, Martín, Martín G., Goulet, Olivier
Publicado en Nat Rev Gastroenterol Hepatol (2015)

Gene Mutation in MicroRNA Target Sites of CFTR Gene: A Novel Pathogenetic Mechanism in Cystic Fibrosis?

por Amato, Felice, Seia, Manuela, Giordano, Sonia, Elce, Ausilia, Zarrilli, Federica, Castaldo, Giuseppe, Tomaiuolo, Rossella
Publicado 2013

Different outcome of six homozygotes for prothrombin A20210A gene variant

por Angiolillo Antonella, Quaranta Sandro, Niglio Alferio, Di Fiore Rosanna, Di Micco Pierpaolo, Cardillo Giuseppe, Castaldo Giuseppe
Publicado 2008-07-01

Different outcome of six homozygotes for prothrombin A20210A gene variant

por Di Micco, Pierpaolo, Di Fiore, Rosanna, Niglio, Alferio, Quaranta, Sandro, Angiolillo, Antonella, Cardillo, Giuseppe, Castaldo, Giuseppe
Publicado 2008

Haemophilia A: the consequences of de novo mutations. Two case reports

por Zarrilli, Federica, Coppola, Antonio, Schiavulli, Michele, Cimino, Ernesto, Elce, Ausilia, Rescigno, Giuseppe, Castaldo, Giuseppe, Amato, Felice
Publicado en Blood Transfus (2018)

Impaired Ratio of Unsaturated to Saturated Non-Esterified Fatty Acids in Saliva from Patients with Cystic Fibrosis

por Gelzo, Monica, Iacotucci, Paola, Carnovale, Vincenzo, Castaldo, Alice, Comegna, Marika, Cernera, Gustavo, Corso, Gaetano, Castaldo, Giuseppe
Publicado en Diagnostics (Basel) (2020)

NGS Gene Panel Analysis Revealed Novel Mutations in Patients with Rare Congenital Diarrheal Disorders

por Esposito, Maria Valeria, Comegna, Marika, Cernera, Gustavo, Gelzo, Monica, Paparo, Lorella, Berni Canani, Roberto, Castaldo, Giuseppe
Publicado en Diagnostics (Basel) (2021)

Ex vivo model predicted in vivo efficacy of CFTR modulator therapy in a child with rare genotype

por Terlizzi, Vito, Amato, Felice, Castellani, Chiara, Ferrari, Beatrice, Galietta, Luis J. V., Castaldo, Giuseppe, Taccetti, Giovanni
Publicado en Mol Genet Genomic Med (2021)

Congenital and acquired thrombotic risk factors in lymphoma patients bearing upper extremities deep venous thrombosis: a preliminary report

por Di Micco, Pierpaolo, Niglio, Alferio, De Renzo, Amalia, Lucania, Anna, Di Fiore, Rosanna, Scudiero, Olga, Castaldo, Giuseppe
Publicado 2004

ACE2: The Major Cell Entry Receptor for SARS-CoV-2

por Scialo, Filippo, Daniele, Aurora, Amato, Felice, Pastore, Lucio, Matera, Maria Gabriella, Cazzola, Mario, Castaldo, Giuseppe, Bianco, Andrea
Publicado en Lung (2020)

Anti-CD2 Antibody-Coated Nanoparticles Containing IL-2 Induce NK Cells That Protect Lupus Mice via a TGF-β-Dependent Mechanism

por Horwitz, David A., Liu, Aijing, Bickerton, Sean, Castaldo, Giuseppe, Matarese, Giuseppe, Fahmy, Tarek M., La Cava, Antonio
Publicado en Front Immunol (2020)

A Novel DHPLC-Based Procedure for the Analysis of COL1A1 and COL1A2 Mutations in Osteogenesis Imperfecta

por Fuccio, Antonella, Iorio, Mariangela, Amato, Felice, Elce, Ausilia, Ingino, Rosaria, Filocamo, Mirella, Castaldo, Giuseppe, Salvatore, Francesco, Tomaiuolo, Rossella
Publicado 2011

Congenital Diarrheal Disorders: An Updated Diagnostic Approach

por Terrin, Gianluca, Tomaiuolo, Rossella, Passariello, Annalisa, Elce, Ausilia, Amato, Felice, Di Costanzo, Margherita, Castaldo, Giuseppe, Canani, Roberto Berni
Publicado 2012

S737F is a new CFTR mutation typical of patients originally from the Tuscany region in Italy

por Terlizzi, Vito, Di Lullo, Antonella Miriam, Comegna, Marika, Centrone, Claudia, Pelo, Elisabetta, Castaldo, Giuseppe, Raia, Valeria, Braggion, Cesare
Publicado en Ital J Pediatr (2018)

Two cases of microvillous inclusion disease caused by novel mutations in MYO5B gene

por Comegna, Marika, Amato, Felice, Liguori, Renato, Berni Canani, Roberto, Spagnuolo, Maria Immacolata, Morroni, Manrico, Guarino, Alfredo, Castaldo, Giuseppe
Publicado en Clin Case Rep (2018)

DNA vaccine encoding heat shock protein 90 protects from murine lupus

por Liu, Aijing, Shi, Fu-Dong, Cohen, Irun R., Castaldo, Giuseppe, Matarese, Giuseppe, Quintana, Francisco J., La Cava, Antonio
Publicado en Arthritis Res Ther (2020)