Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Zacchia M"'
Autor:
Limongelli G, Iucolano S, Monda E, Elefante P, De Stasio C, Lubrano I, Caiazza M, Mazzella M, Fimiani F, Galdo M, De Marchi G, Esposito M, Rubino M, Cirillo A, Fusco A, Esposito A, Trama U, Esposito S, Scarano G, Sepe J, Andria G, Orlando V, Menditto E, Chiodini P, Campania Rare Disease, Iolascon A, Franzese A, Sanduzzi Zamparelli A, Tessitore A, Romano A, Venosa A, Nunzia Olivieri A, Bianco A, La Manna A, Cerbone AM, Spasiano A, Agnese Stanziola A, Colao A, De Bellis A, Gambale A, Toriello A, Tufano A, Ciampa A, Maria Risitano A, Pisani A, Russo A, Volpe A, De Martino B, Amato B, De Fusco C, Piscopo C, Selleri C, Tucci C, Pignata C, Cioffi D, Melis D, Pasquali D, De Brasi D, Spitaleri D, Russo D, Martellotta D, De Michele E, Varricchio E, Miraglia Del Giudice E, Coscioni E, Cimino E, Pane F, Tranfa F, Pollio F, Lonardo F, Nuzzi F, Simonelli F, Trojsi F, Habetswallner F, Valentini G, Cerbone G, Parenti G, Tedeschi G, Capasso G, Battista Rossi G, Gaglione G, Sarnelli G, Argenziano G, Bellastella G, De Michele G, Fiorentino G, Spadaro G, Scala I, Santoro L, Zeppa L, Auricchio L, Elio Adinolfi L, Alessio M, Amitrano M, Savanelli MC, Russo MG, Ferrucci MG, Carbone MT, Pellecchia MT, Salerno M, Melone M, Del Donno M, Vitale M, Triggiani M, Della Monica M, Lo Presti M, Tenuta M, Mignogna MD, Schiavulli M, Zacchia M, Brunetti-Pierri N, Iovino P, Moscato P, Iandoli R, Scarpa R, Russo R, Troisi S, Sbordone S, Perrotta S, Fecarotta S, Sampaolo S, Cicalese V.
Publikováno v:
Journal of Public Health (Oxford, England)
Background The aims of this study were: to investigate the capacity of the rare disease healthcare network in Campania to diagnose patients with rare diseases during the outbreak of Covid-19; and to shed light on problematic diagnoses during this per
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
Autor:
Francesco Trepiccione, Marco Simonini, Paolo Manunta, Angela Bachi, Miriam Zacchia, Vittoria Matafora, Laura Zagato, Chiara Lanzani, Giovambattista Capasso
Publikováno v:
Journal of Nephrology. 34:739-751
Background: Hypertension is a complex disease and is the major cause of cardiovascular complications. In the vast majority of individuals, the aetiology of elevated blood pressure (BP) cannot be determined, thus impairing optimized therapies and prog
Autor:
Tamara Nikuševa Martić, Carmela Errichiello, Albertien M. van Eerde, Anniek Corveleyn, Pascale Hilbert, Rimante Cerkauskiene, Micheel van Geel, Samuela Landini, Concetta Gangemi, Miriam Zacchia, Emma Ashton, Evelien Van Hoof, Valeria Aiello, Martin C. Gregory, Elisabeth Ars, Viviana Palazzo, Constantinos Deltas, Asheeta Gupta, Laura Massella, Susie Gear, Laith Al-Rabadi, Danica Galešić Ljubanović, Louise Hopkinson, Julia Hoefele, Jens Michael Hertz, Peter H. Byers, Elizabeth Watson, Judy Savige, Agnieszka Bierzynska, Francesca Becherucci, Pavlina Plevova, Beata S. Lipska-Ziętkiewicz, Maggie Williams, Adrian Lungu, Ania Koziell, Kathleen Claes, Agne Cerkauskaite, Francesca Mari, Hendica Belge, Alessandra Renieri, Helen Storey, Hansjorg Martin Rothe, Rachel Lennon
Publikováno v:
European Journal of Human Genetics
European journal of human genetics, London : Nature Publishing Group, 2021, vol. 29, no. 8, p. 1186-1197
Savige, J, Storey, H, Watson, E, Hertz, J M, Deltas, C, Renieri, A, Mari, F, Hilbert, P, Plevova, P, Byers, P, Cerkauskaite, A, Gregory, M, Cerkauskiene, R, Ljubanovic, D G, Becherucci, F, Errichiello, C, Massella, L, Aiello, V, Lennon, R, Hopkinson, L, Koziell, A, Lungu, A, Rothe, H M, Hoefele, J, Zacchia, M, Martic, T N, Gupta, A, van Eerde, A, Gear, S, Landini, S, Palazzo, V, al-Rabadi, L, Claes, K, Corveleyn, A, Van Hoof, E, van Geel, M, Williams, M, Ashton, E, Belge, H, Ars, E, Bierzynska, A, Gangemi, C & Lipska-Ziętkiewicz, B S 2021, ' Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome : refining the ACMG criteria ', European Journal of Human Genetics, vol. 29, no. 8, pp. 1186-1197 . https://doi.org/10.1038/s41431-021-00858-1
European Journal of Human Genetics, 29(8), 1186-1197. Nature Publishing Group
European journal of human genetics, London : Nature Publishing Group, 2021, vol. 29, no. 8, p. 1186-1197
Savige, J, Storey, H, Watson, E, Hertz, J M, Deltas, C, Renieri, A, Mari, F, Hilbert, P, Plevova, P, Byers, P, Cerkauskaite, A, Gregory, M, Cerkauskiene, R, Ljubanovic, D G, Becherucci, F, Errichiello, C, Massella, L, Aiello, V, Lennon, R, Hopkinson, L, Koziell, A, Lungu, A, Rothe, H M, Hoefele, J, Zacchia, M, Martic, T N, Gupta, A, van Eerde, A, Gear, S, Landini, S, Palazzo, V, al-Rabadi, L, Claes, K, Corveleyn, A, Van Hoof, E, van Geel, M, Williams, M, Ashton, E, Belge, H, Ars, E, Bierzynska, A, Gangemi, C & Lipska-Ziętkiewicz, B S 2021, ' Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome : refining the ACMG criteria ', European Journal of Human Genetics, vol. 29, no. 8, pp. 1186-1197 . https://doi.org/10.1038/s41431-021-00858-1
European Journal of Human Genetics, 29(8), 1186-1197. Nature Publishing Group
The recent Chandos House meeting of the Alport Variant Collaborative extended the indications for screening for pathogenic variants in the COL4A5, COL4A3 and COL4A4 genes beyond the classical Alport phenotype (haematuria, renal failure; family histor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96ba1d946479e3486070f5e6a820f420
https://lirias.kuleuven.be/handle/123456789/675238
https://lirias.kuleuven.be/handle/123456789/675238
Autor:
Mariadelina Simeoni, Miriam Zacchia, Davide Viggiano, Pietro Anastasio, Ida Molfino, Cristina Masella, Giovanna Capolongo
Publikováno v:
Kidney & Blood Pressure Research, Pp 1-13 (2019)
Background: Diuretic resistance is among the most challenging problems that the cardio-nephrologist must address in daily clinical practice, with a considerable burden on hospital admissions and health care costs. Indeed, loop diuretics are the first
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
Autor:
Aldo Filosa, Amerigo Beneduci, Giuseppina De Luca, Giovanna Capolongo, Patrizia Cinque, Miriam Zacchia, Giovambattista Capasso, Francesco Trepiccione, Silvia Costantini, Anna Spasiano, Maria Enrica Di Pietro, Paolo Ricchi
Publikováno v:
Kidney & Blood Pressure Research, Vol 45, Iss 3, Pp 455-466 (2020)
Introduction: Renal dysfunction is a frequent complication in patients suffering from β-thalassemia major (β-TM). The aim of this study was to analyze the renal function and urine metabolomic profile of β-TM patients undergoing transfusions and de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a58a56ea33348101048d6b118337426
http://hdl.handle.net/11591/435720
http://hdl.handle.net/11591/435720
Autor:
Giuliana Bruno, Giovambattista Capasso, Maria Fiorella Mazzeo, Margherita Ruoppolo, Rosa Anna Siciliano, Davide Arcaniolo, Francesco Trepiccione, Miriam Zacchia, Marianna Caterino, Michele Costanzo
Publikováno v:
Kidney & blood pressure research 43 (2018): 389–405. doi:10.1159/000488096
info:cnr-pdr/source/autori:Caterino M.; Zacchia M.; Costanzo M.; Bruno G.; Arcaniolo D.; Trepiccione F.; Sicilianog R.A.; Mazzeo M.F.; Ruoppolo M.; Capasso G./titolo:Urine proteomics revealed a significant correlation between urine-Fibronectin abundance and estimated-GFR decline in patients with bardet-Biedl syndrome/doi:10.1159%2F000488096/rivista:Kidney & blood pressure research/anno:2018/pagina_da:389/pagina_a:405/intervallo_pagine:389–405/volume:43
Kidney & Blood Pressure Research, Vol 43, Iss 2, Pp 389-405 (2018)
info:cnr-pdr/source/autori:Caterino M.; Zacchia M.; Costanzo M.; Bruno G.; Arcaniolo D.; Trepiccione F.; Sicilianog R.A.; Mazzeo M.F.; Ruoppolo M.; Capasso G./titolo:Urine proteomics revealed a significant correlation between urine-Fibronectin abundance and estimated-GFR decline in patients with bardet-Biedl syndrome/doi:10.1159%2F000488096/rivista:Kidney & blood pressure research/anno:2018/pagina_da:389/pagina_a:405/intervallo_pagine:389–405/volume:43
Kidney & Blood Pressure Research, Vol 43, Iss 2, Pp 389-405 (2018)
Background:/Aims: Renal disease is a common cause of morbidity in patients with Bardet-Biedl syndrome (BBS), however the severity of kidney dysfunction is highly variable. To date, there is little information on the pathogenesis, the risk and predict
Autor:
Francesco Trepiccione, Gabriella Pinto, Carolina Fontanarosa, Miriam Zacchia, Alessandra F. Perna, Francesca Pane, Evgeniya Anishchenko, Diego Ingrosso, Angela Amoresano, Piero Pucci, Nunzio Sepe
Publikováno v:
Methods in Molecular Biology ISBN: 9781493995271
In the context of the vascular effects of hydrogen sulfide (H2S), it is known that this gaseous endogenous biological modulator of inflammation, oxidative stress, etc. is a potent vasodilator. Chronic renal failure, a common disease affecting the agi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74724556a70557c1708d182b79de85e7
https://doi.org/10.1007/978-1-4939-9528-8_2
https://doi.org/10.1007/978-1-4939-9528-8_2