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

per Castaldo, Giuseppe, Monaco, Luigi, Castaldo, Laura, Sorrentino, Paolo
Publicat a Int J Endocrinol (2015)

An Update on Laboratory Diagnosis of Liver Inherited Diseases

per Zarrilli, Federica, Elce, Ausilia, Scorza, Manuela, Giordano, Sonia, Amato, Felice, Castaldo, Giuseppe
Publicat 2013

Genetic Diseases That Predispose to Early Liver Cirrhosis

per Scorza, Manuela, Elce, Ausilia, Zarrilli, Federica, Liguori, Renato, Amato, Felice, Castaldo, Giuseppe
Publicat 2014

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

per Rahman, Noor, Basharat, Zarrin, Yousuf, Muhammad, Castaldo, Giuseppe, Rastrelli, Luca, Khan, Haroon
Publicat a Molecules (2020)

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

per Canani, Roberto Berni, Castaldo, Giuseppe, Bacchetta, Rosa, Martín, Martín G., Goulet, Olivier
Publicat a Nat Rev Gastroenterol Hepatol (2015)

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

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

Different outcome of six homozygotes for prothrombin A20210A gene variant

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

Different outcome of six homozygotes for prothrombin A20210A gene variant

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

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

per Zarrilli, Federica, Coppola, Antonio, Schiavulli, Michele, Cimino, Ernesto, Elce, Ausilia, Rescigno, Giuseppe, Castaldo, Giuseppe, Amato, Felice
Publicat a Blood Transfus (2018)

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

per Gelzo, Monica, Iacotucci, Paola, Carnovale, Vincenzo, Castaldo, Alice, Comegna, Marika, Cernera, Gustavo, Corso, Gaetano, Castaldo, Giuseppe
Publicat a Diagnostics (Basel) (2020)

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

per Esposito, Maria Valeria, Comegna, Marika, Cernera, Gustavo, Gelzo, Monica, Paparo, Lorella, Berni Canani, Roberto, Castaldo, Giuseppe
Publicat a Diagnostics (Basel) (2021)

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

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

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

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

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

per Scialo, Filippo, Daniele, Aurora, Amato, Felice, Pastore, Lucio, Matera, Maria Gabriella, Cazzola, Mario, Castaldo, Giuseppe, Bianco, Andrea
Publicat a Lung (2020)

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

per Horwitz, David A., Liu, Aijing, Bickerton, Sean, Castaldo, Giuseppe, Matarese, Giuseppe, Fahmy, Tarek M., La Cava, Antonio
Publicat a Front Immunol (2020)

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

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

Congenital Diarrheal Disorders: An Updated Diagnostic Approach

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

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

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

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

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

DNA vaccine encoding heat shock protein 90 protects from murine lupus

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