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

بواسطة Castaldo, Giuseppe, Monaco, Luigi, Castaldo, Laura, Sorrentino, Paolo
الحاوية / القاعدة Int J Endocrinol (2015)

An Update on Laboratory Diagnosis of Liver Inherited Diseases

بواسطة Zarrilli, Federica, Elce, Ausilia, Scorza, Manuela, Giordano, Sonia, Amato, Felice, Castaldo, Giuseppe
منشور في 2013

Genetic Diseases That Predispose to Early Liver Cirrhosis

بواسطة Scorza, Manuela, Elce, Ausilia, Zarrilli, Federica, Liguori, Renato, Amato, Felice, Castaldo, Giuseppe
منشور في 2014

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

بواسطة Rahman, Noor, Basharat, Zarrin, Yousuf, Muhammad, Castaldo, Giuseppe, Rastrelli, Luca, Khan, Haroon
الحاوية / القاعدة Molecules (2020)

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

بواسطة Canani, Roberto Berni, Castaldo, Giuseppe, Bacchetta, Rosa, Martín, Martín G., Goulet, Olivier
الحاوية / القاعدة Nat Rev Gastroenterol Hepatol (2015)

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

بواسطة Amato, Felice, Seia, Manuela, Giordano, Sonia, Elce, Ausilia, Zarrilli, Federica, Castaldo, Giuseppe, Tomaiuolo, Rossella
منشور في 2013

Different outcome of six homozygotes for prothrombin A20210A gene variant

بواسطة Angiolillo Antonella, Quaranta Sandro, Niglio Alferio, Di Fiore Rosanna, Di Micco Pierpaolo, Cardillo Giuseppe, Castaldo Giuseppe
منشور في 2008-07-01

Different outcome of six homozygotes for prothrombin A20210A gene variant

بواسطة Di Micco, Pierpaolo, Di Fiore, Rosanna, Niglio, Alferio, Quaranta, Sandro, Angiolillo, Antonella, Cardillo, Giuseppe, Castaldo, Giuseppe
منشور في 2008

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

بواسطة Zarrilli, Federica, Coppola, Antonio, Schiavulli, Michele, Cimino, Ernesto, Elce, Ausilia, Rescigno, Giuseppe, Castaldo, Giuseppe, Amato, Felice
الحاوية / القاعدة Blood Transfus (2018)

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

بواسطة Gelzo, Monica, Iacotucci, Paola, Carnovale, Vincenzo, Castaldo, Alice, Comegna, Marika, Cernera, Gustavo, Corso, Gaetano, Castaldo, Giuseppe
الحاوية / القاعدة Diagnostics (Basel) (2020)

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

بواسطة Esposito, Maria Valeria, Comegna, Marika, Cernera, Gustavo, Gelzo, Monica, Paparo, Lorella, Berni Canani, Roberto, Castaldo, Giuseppe
الحاوية / القاعدة Diagnostics (Basel) (2021)

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

بواسطة Terlizzi, Vito, Amato, Felice, Castellani, Chiara, Ferrari, Beatrice, Galietta, Luis J. V., Castaldo, Giuseppe, Taccetti, Giovanni
الحاوية / القاعدة Mol Genet Genomic Med (2021)

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

بواسطة Di Micco, Pierpaolo, Niglio, Alferio, De Renzo, Amalia, Lucania, Anna, Di Fiore, Rosanna, Scudiero, Olga, Castaldo, Giuseppe
منشور في 2004

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

بواسطة Scialo, Filippo, Daniele, Aurora, Amato, Felice, Pastore, Lucio, Matera, Maria Gabriella, Cazzola, Mario, Castaldo, Giuseppe, Bianco, Andrea
الحاوية / القاعدة Lung (2020)

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

بواسطة Horwitz, David A., Liu, Aijing, Bickerton, Sean, Castaldo, Giuseppe, Matarese, Giuseppe, Fahmy, Tarek M., La Cava, Antonio
الحاوية / القاعدة Front Immunol (2020)

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

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

Congenital Diarrheal Disorders: An Updated Diagnostic Approach

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

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

بواسطة Terlizzi, Vito, Di Lullo, Antonella Miriam, Comegna, Marika, Centrone, Claudia, Pelo, Elisabetta, Castaldo, Giuseppe, Raia, Valeria, Braggion, Cesare
الحاوية / القاعدة Ital J Pediatr (2018)

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

بواسطة Comegna, Marika, Amato, Felice, Liguori, Renato, Berni Canani, Roberto, Spagnuolo, Maria Immacolata, Morroni, Manrico, Guarino, Alfredo, Castaldo, Giuseppe
الحاوية / القاعدة Clin Case Rep (2018)

DNA vaccine encoding heat shock protein 90 protects from murine lupus

بواسطة Liu, Aijing, Shi, Fu-Dong, Cohen, Irun R., Castaldo, Giuseppe, Matarese, Giuseppe, Quintana, Francisco J., La Cava, Antonio
الحاوية / القاعدة Arthritis Res Ther (2020)