Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Maria Amicone"'
Autor:
Oriana De Marco, Jessica Gambardella, Antonio Bianco, Antonella Fiordelisi, Federica Andrea Cerasuolo, Antonietta Buonaiuto, Roberta Avvisato, Ivana Capuano, Maria Amicone, Teodolinda Di Risi, Eleonora Riccio, Letizia Spinelli, Antonio Pisani, Guido Iaccarino, Daniela Sorriento
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
Fabry disease (FD), also known as Anderson-Fabry disease, is a hereditary disorder of glycosphingolipid metabolism, caused by a deficiency of the lysosomal alpha-galactosidase A enzyme. This causes a progressive accumulation of glycosphingolipids in
Externí odkaz:
https://doaj.org/article/c946a08cf9ab4942b405442ef45de95c
Autor:
Ersilia Nigro, Daniela D’Arco, Fiorenzo Moscatelli, Antonio Pisani, Maria Amicone, Eleonora Riccio, Ivana Capuano, Francesca Argentino, Marcellino Monda, Giovanni Messina, Aurora Daniele, Rita Polito
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 11, p 6243 (2024)
Orexin-A is a neuropeptide product of the lateral hypothalamus that acts on two receptors, OX1R and OX2R. The orexinergic system is involved in feeding, sleep, and pressure regulation. Recently, orexin-A levels have been found to be negatively correl
Externí odkaz:
https://doaj.org/article/33f492687293416fbecb2b882a37fa17
Autor:
Ersilia Nigro, Marta Mallardo, Maria Amicone, Daniela D’Arco, Eleonora Riccio, Maurizio Marra, Fabrizio Pasanisi, Antonio Pisani, Aurora Daniele
Publikováno v:
Genes, Vol 15, Iss 4, p 484 (2024)
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a common monogenic disorder characterized by renal cysts and progressive renal failure. In kidney diseases, adipose tissue undergoes functional changes that have been associated with increased i
Externí odkaz:
https://doaj.org/article/03e512826ef044b69a7e51df7bc175b3
Autor:
Giovanna Muscogiuri, Oriana De Marco, Tonia Di Lorenzo, Maria Amicone, Ivana Capuano, Eleonora Riccio, Guido Iaccarino, Antonio Bianco, Teodolinda Di Risi, Antonio Pisani
Publikováno v:
Nutrients, Vol 16, Iss 7, p 1061 (2024)
Fabry disease (FD) is caused by mutations in the galactosidase alpha (GLA) gene which lead to the accumulation of globotriaosylceramide (Gb-3). Enzyme replacement therapy (ERT) and oral chaperone therapy are the current pharmacological treatments for
Externí odkaz:
https://doaj.org/article/f91409285f7f4b37aeda135c7120e79c
Autor:
Ersilia Nigro, Maria Amicone, Daniela D’Arco, Gina Sellitti, Oriana De Marco, Maria Guarino, Eleonora Riccio, Antonio Pisani, Aurora Daniele
Publikováno v:
Genes, Vol 14, Iss 6, p 1236 (2023)
Polycystic Kidney Diseases (PKDs) consist of a genetically and phenotypically heterogeneous group of inherited disorders characterized by numerous renal cysts. PKDs include autosomal dominant ADPKD, autosomal recessive ARPKD and atypical forms. Here,
Externí odkaz:
https://doaj.org/article/4d506f608ed849e3912b75538e147d1a
Autor:
Eleonora Riccio, Ivana Capuano, Pasquale Buonanno, Michele Andreucci, Michele Provenzano, Maria Amicone, Manuela Rizzo, Antonio Pisani
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
Hyperkalemia is common in patients treated with renin–angiotensin–aldosterone system inhibitors (RAASis), and it represents the main cause of the large gap reported between guideline recommendations and real-world practice in chronic kidney disea
Externí odkaz:
https://doaj.org/article/e8e687ec0d8f48c69f7cdf7c260255d8
Autor:
Eleonora Riccio, Mario Zanfardino, Monica Franzese, Ivana Capuano, Pasquale Buonanno, Lucia Ferreri, Maria Amicone, Antonio Pisani
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 5, Pp n/a-n/a (2021)
Abstract Background Although enzyme replacement therapy with agalsidase beta resulted in a variety of clinical benefits, life‐long biweekly intravenous infusion may impact on patients’ quality of life. Moreover, regular infusions are time‐consu
Externí odkaz:
https://doaj.org/article/baa073ea254e4ba89f823d4c32a034cd
Autor:
Livia Maria Sorrentino, Luigi Annicchiarico Petruzzelli, Angela Maria Pellegrino, Cristina Marchetiello, Maria Amicone, Eleonora Riccio, Antonio Pisani
Publikováno v:
Giornale di Clinica Nefrologia e Dialisi, Vol 29, Iss 2 (2017)
Abstract non disponibile
Externí odkaz:
https://doaj.org/article/ea4cd5cfbd0a42289d2f8917dd03af7d
Publikováno v:
Giornale di Clinica Nefrologia e Dialisi, Vol 28, Iss 4 (2016)
Abstract non disponibile
Externí odkaz:
https://doaj.org/article/9f4813712cea472d84384aa385b75345
Autor:
Daniele, Ersilia Nigro, Maria Amicone, Daniela D’Arco, Gina Sellitti, Oriana De Marco, Maria Guarino, Eleonora Riccio, Antonio Pisani, Aurora
Publikováno v:
Genes; Volume 14; Issue 6; Pages: 1236
Polycystic Kidney Diseases (PKDs) consist of a genetically and phenotypically heterogeneous group of inherited disorders characterized by numerous renal cysts. PKDs include autosomal dominant ADPKD, autosomal recessive ARPKD and atypical forms. Here,