Teaching molecular genetics: chapter 4—positional cloning of genetic disorders

por Puliti, Aldamaria, Caridi, Gianluca, Ravazzolo, Roberto, Ghiggeri, Gian Marco
Publicado 2007

Molecular and Cellular Mechanisms for Proteinuria in Minimal Change Disease

por Bertelli, Roberta, Bonanni, Alice, Caridi, Gianluca, Canepa, Alberto, Ghiggeri, G. M.
Publicado 2018

Familial forms of nephrotic syndrome

por Caridi, Gianluca, Trivelli, Antonella, Sanna-Cherchi, Simone, Perfumo, Francesco, Ghiggeri, Gian Marco
Publicado 2010

Recurrent Hypoglycemia in a Case of Congenital Analbuminemia

por Litzel, Martin, Caridi, Gianluca, Lugani, Francesca, Campagnoli, Monica, Minchiotti, Lorenzo, Fischli, Stefan
Publicado 2020

Variations in the Human Serum Albumin Gene: Molecular and Functional Aspects

por Caridi, Gianluca, Lugani, Francesca, Angeletti, Andrea, Campagnoli, Monica, Galliano, Monica, Minchiotti, Lorenzo
Publicado 2022

Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia

por Minchiotti, Lorenzo, Caridi, Gianluca, Campagnoli, Monica, Lugani, Francesca, Galliano, Monica, Kragh-Hansen, Ulrich
Publicado 2019

Renal involvement and Strømme syndrome

por Caridi, Gianluca, Lugani, Francesca, Lerone, Margherita, Divizia, Maria Teresa, Ghiggeri, Gian Marco, Verrina, Enrico
Publicado 2020

Vaccines and nephrotic syndrome: efficacy and safety

por Angeletti, Andrea, Lugani, Francesca, La Porta, Edoardo, Verrina, Enrico, Caridi, Gianluca, Ghiggeri, Gian Marco
Publicado 2022

Molecular Diagnosis of Analbuminemia: A New Case Caused by a Nonsense Mutation in the Albumin Gene

por Dagnino, Monica, Caridi, Gianluca, Haenni, Ueli, Duss, Adrian, Aregger, Fabienne, Campagnoli, Monica, Galliano, Monica, Minchiotti, Lorenzo
Publicado 2011

A rare 3q13.31 microdeletion including GAP43 and LSAMP genes

por Gimelli, Stefania, Leoni, Massimiliano, Di Rocco, Maja, Caridi, Gianluca, Porta, Simona, Cuoco, Cristina, Gimelli, Giorgio, Tassano, Elisa
Publicado 2013

A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family

por Caridi, Gianluca, Gulec, Elif Yilmaz, Campagnoli, Monica, Lugani, Francesca, Onal, Hasan, Kilic, Duzgun, Galliano, Monica, Minchiotti, Lorenzo
Publicado 2016

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

por Sanna-Cherchi, Simone, Caridi, Gianluca, Weng, Patricia L., Scolari, Francesco, Perfumo, Francesco, Gharavi, Ali G., Ghiggeri, Gian Marco
Publicado 2007

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

por Sanna-Cherchi, Simone, Caridi, Gianluca, Weng, Patricia L., Scolari, Francesco, Perfumo, Francesco, Gharavi, Ali G., Ghiggeri, Gian Marco
Publicado 2007

Randomised controlled trial comparing rituximab to mycophenolate mofetil in children and young adults with steroid-dependent idiopathic nephrotic syndrome: study protocol

por Lugani, Francesca, Angeletti, Andrea, Ravani, Pietro, Vivarelli, Marina, Colucci, Manuela, Caridi, Gianluca, Verrina, Enrico, Emma, Francesco, Ghiggeri, Gian Marco
Publicado 2021

Congenital Analbuminemia in Unrelated Algerian and Turkish Families is Caused by the Same Molecular Defect in the Albumin Gene

por Caridi, Gianluca, Maout, Abdelbasset, Artan, Reha, Campagnoli, Monica, Lugani, Francesca, Abada, Mohamed El Amine, Sayar, Ersin, Galliano, Monica, Minchiotti, Lorenzo
Publicado 2018

Biologics in steroid resistant nephrotic syndrome in childhood: review and new hypothesis-driven treatment

por Angeletti, Andrea, Bruschi, Maurizio, Kajana, Xhuliana, La Porta, Edoardo, Spinelli, Sonia, Caridi, Gianluca, Lugani, Francesca, Verrina, Enrico Eugenio, Ghiggeri, Gian Marco
Publicado 2023

Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene

por Caridi, Gianluca, Dagnino, Monica, Erdeve, Omer, Di Duca, Marco, Yildiz, Duran, Alan, Serdar, Atasay, Begum, Arsan, Saadet, Campagnoli, Monica, Galliano, Monica, Minchiotti, Lorenzo
Publicado 2014

Refractory Minimal Change Disease and Focal Segmental Glomerular Sclerosis Treated With Anakinra

por Angeletti, Andrea, Magnasco, Alberto, AntonellaTrivelli, Degl’Innocenti, Ludovica M., Piaggio, Giorgio, Lugani, Francesca, Caridi, Gianluca, Verrina, Enrico, Cravedi, Paolo, Ghiggeri, Gian Marco
Publicado 2021

Autosomal Dominant Tubulointerstitial Kidney Disease with Adult Onset due to a Novel Renin Mutation Mapping in the Mature Protein

por Schaeffer, Céline, Izzi, Claudia, Vettori, Andrea, Pasqualetto, Elena, Cittaro, Davide, Lazarevic, Dejan, Caridi, Gianluca, Gnutti, Barbara, Mazza, Cinzia, Jovine, Luca, Scolari, Francesco, Rampoldi, Luca
Publicado 2019

Circulating Anti-Rituximab Antibodies Do Not Affect Response to Rituximab in Steroid-Dependent Nephrotic Syndrome

por Angeletti, Andrea, Bruschi, Maurizio, Colucci, Manuela, Kajana, Xhuliana, La Porta, Edoardo, Caridi, Gianluca, Lugani, Francesca, Ravani, Pietro, Vivarelli, Marina, Cravedi, Paolo, Ghiggeri, Gian Marco
Publicado 2022