Zobrazeno 1 - 8
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pro vyhledávání: '"Zacchia M"'
Autor:
Viggiano D, Bruchfeld A, Carriazo S, de Donato A, Endlich N, Ferreira AC, Figurek A, Fouque D, Franssen CFM, Giannakou K, Goumenos D, Hoorn EJ, Nitsch D, Arduan AO, Pešić V, Rastenyté D, Soler MJ, Rroji M, Trepiccione F, Unwin RJ, Wagner CA, Wiecek A, Zacchia M, Zoccali C, Capasso G, CONNECT Action (Cognitive Decline in Nephro-Neurology European Cooperative Target).
Publikováno v:
Nephrology Dialysis Transplantation
Viggiano, Davide; Bruchfeld, Annette; Carriazo, Sol; de Donato, Antonio; Endlich, Nicole; Ferreira, Ana Carina; Figurek, Andreja; Fouque, Denis; Franssen, Casper F M; Giannakou, Konstantinos; Goumenos, Dimitrios; Hoorn, Ewout J; Nitsch, Dorothea; Ortiz, Alberto; Pešić, Vesna; Rastenyté, Daiva; Soler, Maria José; Rroji, Merita; Trepiccione, Francesco; Unwin, Robert J; ... (2021). Brain dysfunction in tubular and tubulointerstitial kidney diseases. Nephrology, dialysis, transplantation, 37(Suppl 2), ii46-ii55. Oxford University Press 10.1093/ndt/gfab276
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Nephrology Dialysis Transplantation, 2021, 37 (Supplement_2), pp.ii46--ii55. ⟨10.1093/ndt/gfab276⟩
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association-European Renal Association, 37(2), ii46-ii55. Oxford University Press
Viggiano, Davide; Bruchfeld, Annette; Carriazo, Sol; de Donato, Antonio; Endlich, Nicole; Ferreira, Ana Carina; Figurek, Andreja; Fouque, Denis; Franssen, Casper F M; Giannakou, Konstantinos; Goumenos, Dimitrios; Hoorn, Ewout J; Nitsch, Dorothea; Ortiz, Alberto; Pešić, Vesna; Rastenyté, Daiva; Soler, Maria José; Rroji, Merita; Trepiccione, Francesco; Unwin, Robert J; ... (2021). Brain dysfunction in tubular and tubulointerstitial kidney diseases. Nephrology, dialysis, transplantation, 37(Suppl 2), ii46-ii55. Oxford University Press 10.1093/ndt/gfab276
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Nephrology Dialysis Transplantation, 2021, 37 (Supplement_2), pp.ii46--ii55. ⟨10.1093/ndt/gfab276⟩
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association-European Renal Association, 37(2), ii46-ii55. Oxford University Press
Funding: This article is published as part of a supplement financially supported by the COST Action CA19127-Cognitive Decline in Nephro-Neurology: European Cooperative Target (CONNECT). Kidney function has two important elements: glomerular filtratio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c45c70edb6bc7e43048ee1bcebe4f439
http://farfar.pharmacy.bg.ac.rs/bitstream/id/9401/Brain_dysfunction_in_pub_2022.pdf
http://farfar.pharmacy.bg.ac.rs/bitstream/id/9401/Brain_dysfunction_in_pub_2022.pdf
Akademický článek
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Akademický článek
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Autor:
Margherita Ruoppolo, Miriam Zacchia, Emanuela Marchese, Giovambattista Capasso, Alessandra F. Perna
Publikováno v:
Kidney International Reports
Kidney International Reports, Vol 5, Iss 9, Pp 1403-1415 (2020)
Kidney International Reports, Vol 5, Iss 9, Pp 1403-1415 (2020)
Bardet–Biedl syndrome (BBS) is a rare pleiotropic inherited disorder known as a ciliopathy. Kidney disease is a cardinal clinical feature; however, it is one of the less investigated traits. This study is a comprehensive analysis of the literature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86e1e4cc51fbf5fcff217687516288d8
http://hdl.handle.net/11591/458955
http://hdl.handle.net/11591/458955
Autor:
Margherita Ruoppolo, Giovambattista Capasso, Miriam Zacchia, Marianna Caterino, Emanuela Marchese, Elena Martina Trani, Alessandra F. Perna, Giovanna Capolongo
The primary cilium (PC) was considered as a vestigial organelle with no significant physiological importance, until the discovery that PC perturbation disturbs several signalling pathways and results in the dysfunction of a variety of organs. Genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c948bd3b46cadb20d4b911a062498cb9
http://hdl.handle.net/11588/755627
http://hdl.handle.net/11588/755627
Publikováno v:
Journal of Nephrology. 26:412-416
Tuberous sclerosis complex (TCS) is a genetic disorder with a variable clinical presentation. It is commonly characterized by seizures, mental retardation and cutaneous angiofibromas. Renal manifestations frequently include angiomyolipomas and cysts