Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Di Nuzzi A"'
Autor:
Pietro Vajro, Anna Pia Delli Bovi, Giovanni Scala, Antonella Bisogno, Angelo Colucci, Salvatore Guercio Nuzio, F. Belmonte, Luca Pierri, Pierpaolo Cavallo, Jacopo Troisi, Laura Di Michele, Claudia Mandato, Antonella Di Nuzzi
Publikováno v:
Nutrients
Nutrients, Vol 11, Iss 2, p 274 (2019)
Volume 11
Issue 2
Nutrients, Vol 11, Iss 2, p 274 (2019)
Volume 11
Issue 2
Pediatric obesity-related metabolic syndrome (MetS) and nonalcoholic fatty liver disease (NAFLD) are increasingly frequent conditions with a still-elusive diagnosis and low-efficacy treatment and monitoring options. In this study, we investigated the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::635260ca93f637224d9295081da79dd4
http://europepmc.org/articles/PMC6412994
http://europepmc.org/articles/PMC6412994
Akademický článek
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Autor:
Marco Marano, Alessandro Patriarca, Giuseppe Iulianiello, Luigi Michele Di Nuzzi, Anna D’Amato, Gelsomina Giordano
Publikováno v:
Artificial Organs. 39:960-964
As the name reveals, acetate-free biofiltration (AFB) is featured by lack of acetate and this would seem to allow better hemodynamic stability. However, AFB also has a unique characteristic of carbon dioxide (CO2 )-free dialysate, whereas all other m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01126977d54775194a2c80b96acfbb02
https://doi.org/10.1111/aor.12477
https://doi.org/10.1111/aor.12477
Publikováno v:
Nutrients, Vol 10, Iss 1, p 9 (2017)
Nutrients
Nutrients
Malnutrition in children and adults with advanced liver disease represents a tremendous challenge as the nutritional problems are multifactorial. This Editorial comments the articles appearing in this special issue of Nutrients, “Nutrition and Live
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5177337817d2bf55f13615acd833b5a
https://www.mdpi.com/2072-6643/10/1/9
https://www.mdpi.com/2072-6643/10/1/9
Autor:
Bianca Visciano, Eleonora Riccio, Antonio Pisani, Cristina Marchetiello, Antonio Mancini, Massimo Imbriaco, A. Di Nuzzi
Publikováno v:
Clinical Genetics. 86:301-309
Fabry disease (FD) is an X-linked disease in which mutations of the GLA gene result in a deficiency of the enzyme α-galactosidase A and subsequent progressive, intralysosomal deposition of undegraded glycosphingolipid products, primarily globotriaos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67c497cb094d4478829033f7886b5c97
https://doi.org/10.1111/cge.12386
https://doi.org/10.1111/cge.12386
Akademický článek
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Autor:
Antonino Musumeci, Ivana Capuano, Andrea Memoli, Antonio Pisani, Vincenzo De Falco, Bianca Visciano, Eleonora Riccio, Antonella Di Nuzzi
Publikováno v:
Therapeutic Apheresis and Dialysis. 18:155-161
Color Doppler ultrasonography (CDUS) is a readily available, inexpensive and noninvasive method, which has improved the survival of native arteriovenous fistula (AVF) by increasing the early diagnosis of complications. Although angiography has been c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55c60a7ff8485aa95a715500ffa34108
https://doi.org/10.1111/1744-9987.12073
https://doi.org/10.1111/1744-9987.12073
Publikováno v:
Clinical and experimental nephrology. 19(2)
Low-protein diets have been advocated for many decades as the cornerstone in the treatment of chronic kidney disease. Initially, the low intake of protein was used to reduce uremic symptoms; thereafter, albeit controversial, evidences suggested that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09e59d364c9ffed7378e13770effee31
https://pubmed.ncbi.nlm.nih.gov/25319188
https://pubmed.ncbi.nlm.nih.gov/25319188
Autor:
PISANI, ANTONIO, Visciano B, Di Nuzzi A, Mancini A, Marchetiello C, Riccio E., IMBRIACO, MASSIMO
Publikováno v:
Clinical genetics. 86(4)
Fabry disease (FD) is an X-linked disease in which mutations of the GLA gene result in a deficiency of the enzyme α-galactosidase A and subsequent progressive, intralysosomal deposition of undegraded glycosphingolipid products, primarily globotriaos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::266b3292a29ba8242e4f4b43e5744b27
https://pubmed.ncbi.nlm.nih.gov/24645664
https://pubmed.ncbi.nlm.nih.gov/24645664