A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes

por Nardello, Rosaria, Antona, Vincenzo, Mangano, Giuseppe Donato, Salpietro, Vincenzo, Mangano, Salvatore, Fontana, Antonina
Publicado 2021

Cancer-Related Cachexia: The Vicious Circle between Inflammatory Cytokines, Skeletal Muscle, Lipid Metabolism and the Possible Role of Physical Training

por Mangano, Giuseppe Donato, Fouani, Malak, D’Amico, Daniela, Di Felice, Valentina, Barone, Rosario
Publicado 2022

Commonalities and distinctions between two neurodevelopmental disorder subtypes associated with SCN2A and SCN8A variants and literature review

por Mangano, Giuseppe Donato, Fontana, Antonina, Antona, Vincenzo, Salpietro, Vincenzo, Mangano, Giuseppa Renata, Giuffrè, Mario, Nardello, Rosaria
Publicado 2022

Two distinct phenotypes, hemiplegic migraine and episodic Ataxia type 2, caused by a novel common CACNA1A variant

por Nardello, Rosaria, Plicato, Giorgia, Mangano, Giuseppe Donato, Gennaro, Elena, Mangano, Salvatore, Brighina, Filippo, Raieli, Vincenzo, Fontana, Antonina
Publicado 2020

Heat Shock Proteins Alterations in Rheumatoid Arthritis

por Fouani, Malak, Basset, Charbel A., Mangano, Giuseppe D., Leone, Lavinia G., Lawand, Nada B., Leone, Angelo, Barone, Rosario
Publicado 2022

Evaluation of Antibacterial, Antifungal, and Antioxidant Activities of Safflower Natural Dyes during Flowering

por Salem, Nidhal, Msaada, Kamel, Elkahoui, Salem, Mangano, Giuseppe, Azaeiz, Sana, Ben Slimen, Imen, Kefi, Sarra, Pintore, Giorgio, Limam, Ferid, Marzouk, Brahim
Publicado 2014

Muscle Histopathological Abnormalities in a Patient With a CCT5 Mutation Predicted to Affect the Apical Domain of the Chaperonin Subunit

por Scalia, Federica, Barone, Rosario, Rappa, Francesca, Marino Gammazza, Antonella, Lo Celso, Fabrizio, Lo Bosco, Giosuè, Barone, Giampaolo, Antona, Vincenzo, Vadalà, Maria, Vitale, Alessandra Maria, Mangano, Giuseppe Donato, Amato, Domenico, Sentiero, Giusy, Macaluso, Filippo, Myburgh, Kathryn H., Conway de Macario, Everly, Macario, Alberto J. L., Giuffrè, Mario, Cappello, Francesco
Publicado 2022

Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders

por Borgia, Paola, Baldassari, Simona, Pedemonte, Nicoletta, Alkhunaizi, Ebba, D’Onofrio, Gianluca, Tortora, Domenico, Calì, Elisa, Scudieri, Paolo, Balagura, Ganna, Musante, Ilaria, Diana, Maria Cristina, Pedemonte, Marina, Vari, Maria Stella, Iacomino, Michele, Riva, Antonella, Chimenz, Roberto, Mangano, Giuseppe D., Mohammadi, Mohammad Hasan, Toosi, Mehran Beiraghi, Ashrafzadeh, Farah, Imannezhad, Shima, Karimiani, Ehsan Ghayoor, Accogli, Andrea, Schiaffino, Maria Cristina, Maghnie, Mohamad, Soler, Miguel Angel, Echiverri, Karl, Abrams, Charles K., Striano, Pasquale, Fortuna, Sara, Maroofian, Reza, Houlden, Henry, Zara, Federico, Fiorillo, Chiara, Salpietro, Vincenzo
Publicado 2022