Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Luisa Amico"'
Autor:
Giovanni Duro, Carmela Zizzo, Giuseppe Cammarata, Alessandro Burlina, Alberto Burlina, Giulia Polo, Simone Scalia, Roberta Oliveri, Serafina Sciarrino, Daniele Francofonte, Riccardo Alessandro, Antonio Pisani, Giuseppe Palladino, Rosa Napoletano, Maurizio Tenuta, Daniele Masarone, Giuseppe Limongelli, Eleonora Riccio, Andrea Frustaci, Cristina Chimenti, Claudio Ferri, Federico Pieruzzi, Maurizio Pieroni, Marco Spada, Cinzia Castana, Marina Caserta, Ines Monte, Margherita Stefania Rodolico, Sandro Feriozzi, Yuri Battaglia, Luisa Amico, Maria Angela Losi, Camillo Autore, Marco Lombardi, Carmine Zoccali, Alessandra Testa, Maurizio Postorino, Renzo Mignani, Elisabetta Zachara, Antonello Giordano, Paolo Colomba
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 12, p 3726 (2018)
Anderson-Fabry disease (FD) is a rare, progressive, multisystem storage disorder caused by the partial or total deficit of the lysosomal enzyme α-galactosidase A (α-Gal A). It is an X-linked, lysosomal enzymopathy due to mutations in the galactosid
Externí odkaz:
https://doaj.org/article/ffce201584f64d689a7908d067fff010
Fabry disease and multiple sclerosis misdiagnosis: the role of family history and neurological signs
Autor:
Giuseppe Cammarata, Alessandro P. Burlina, Maurizio Pieroni, Paolo Colomba, Luisa Amico, Giovanni Duro, Luigi Sicurella, Riccardo Alessandro, Carmela Zizzo, Antonello Giordano, Simone Scalia
Publikováno v:
Oncotarget
Fabry disease (FD) is an X-linked inherited lysosomal storage disorder caused by a galactosidase A (a-gal A) deficiency. Central nervous system involvement and chronic white matter lesions are observed in both FD and multiple sclerosis (MS), which ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2ecd2b1d6d4d7c10fb6687b62c67703
https://doi.org/10.18632/oncotarget.23970
https://doi.org/10.18632/oncotarget.23970
Autor:
Maria Angela Losi, Riccardo Alessandro, Maurizio Postorino, Federico Pieruzzi, Paolo Colomba, Sandro Feriozzi, Yuri Battaglia, Andrea Frustaci, Alessandra Testa, Ines Monte, Daniele Masarone, Serafina Sciarrino, Antonello Giordano, Antonio Pisani, Cinzia Castana, Carmine Zoccali, Elisabetta Zachara, Giuseppe Limongelli, Eleonora Riccio, Luisa Amico, Claudio Ferri, Alessandro P. Burlina, Renzo Mignani, Margherita Stefania Rodolico, Rosa Napoletano, Marina Caserta, Carmela Zizzo, Simone Scalia, Marco Spada, Roberta Oliveri, Giuseppe Cammarata, Marco Lombardi, Cristina Chimenti, Daniele Francofonte, Giovanni Duro, Maurizio Tenuta, Giuseppe Palladino, Alberto Burlina, Camillo Autore, Giulia Polo, Maurizio Pieroni
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 19, Iss 12, p 3726 (2018)
Volume 19
Issue 12
International Journal of Molecular Sciences, Vol 19, Iss 12, p 3726 (2018)
Volume 19
Issue 12
Anderson-Fabry disease (FD) is a rare, progressive, multisystem storage disorder caused by the partial or total deficit of the lysosomal enzyme &alpha
galactosidase A (&alpha
Gal A). It is an X-linked, lysosomal enzymopathy due to mutations
galactosidase A (&alpha
Gal A). It is an X-linked, lysosomal enzymopathy due to mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf04a9ee9daf738196c14d41bcf6e867
http://europepmc.org/articles/PMC6320967
http://europepmc.org/articles/PMC6320967
Autor:
Laura Giambanco, Giuseppe Calì, F. Forlani, Maria Luisa Amico, Luigi Alio, Mario Vallone, Giuseppe Puccio
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 179:36-41
Objective To evaluate outcomes of women undergoing cesarean hysterectomy for abnormal invasive placenta (AIP) with and without preoperative balloon catheter placement in internal iliac arteries. Study design A prospective observational study of women
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51a2e987f5c98f9ff9729d5ea5b772b9
https://doi.org/10.1016/j.ejogrb.2014.05.007
https://doi.org/10.1016/j.ejogrb.2014.05.007
Autor:
Alberto Noto, Luisa Amico, Giuseppe Costantino, Valeria Chirico, Domenico Ferrara, Luca Visconti, Michele Buemi, Domenico Santoro, Antonio Lacquaniti, Valeria Cernaro, Carmela Aloisi, Antonio David
Publikováno v:
Renal failure. 38(9)
Metformin, belonging to a class of drugs called biguanides, is the recommended first-line treatment for overweight patients with type 2 diabetes mellitus. It has multiple mechanisms of action, such as reduction of gluconeogenesis, increases periphera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f72fbe76327c013e4139fbe9e02dc089
https://pubmed.ncbi.nlm.nih.gov/27686366
https://pubmed.ncbi.nlm.nih.gov/27686366
Autor:
Luca, Visconti, Valeria, Cernaro, Domenico, Ferrara, Viviana, Lacava, Carlo Alberto, Ricciardi, Eleonora, Di Mauro, Luisa, Amico, Domenico, Santoro, Michele, Buemi
Publikováno v:
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia. 32(5)
AL amyloidosis is the most common type of systemic amyloidosis and is caused by the deposition of an amyloidogenic protein composed of immunoglobulin light chains produced by a clonal population of plasma cells.We report the case of a 77-year-old wom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4ffb3d7b21750e595b674bf5fa70ddaf
https://pubmed.ncbi.nlm.nih.gov/26480258
https://pubmed.ncbi.nlm.nih.gov/26480258
Autor:
Luisa, Amico, Giuseppe, Visconti, Antonio, Amato, Vitalba, Azzolina, Adalberto, Sessa, Maurizio, Li Vecchi
Publikováno v:
Journal of nephrology. 18(6)
Anderson-Fabry disease is a rare inborn X-linked glycosphingolipid storage disorder in which the deficient activity of the enzyme alfa-galactosidase A (alfa-gal A) leads to the progressive tissular accumulation of lipidic molecules which, in turn, ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e6d791aabd4581dffc5651e3a6a831e0
https://pubmed.ncbi.nlm.nih.gov/16358237
https://pubmed.ncbi.nlm.nih.gov/16358237