Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Milena Brugnara"'
Autor:
Matteo Guarnaroli, Flavia Padoan, Cristiano Fava, Maria Giulia Benetti, Milena Brugnara, Angelo Pietrobelli, Giorgio Piacentini, Luca Pecoraro
Publikováno v:
Biomedicines, Vol 12, Iss 8, p 1823 (2024)
Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary disorder characterized by the formation of numerous fluid-filled cysts in the kidneys, leading to progressive renal failure and various extrarenal complications, including hypertens
Externí odkaz:
https://doaj.org/article/ef6e3a349daa486f8fe0d83ffe56654d
Autor:
Flavia Padoan, Matteo Guarnaroli, Milena Brugnara, Giorgio Piacentini, Angelo Pietrobelli, Luca Pecoraro
Publikováno v:
Biomedicines, Vol 12, Iss 4, p 911 (2024)
Nutrition management is fundamental for children with chronic kidney disease (CKD). Fluid balance and low-protein and low-sodium diets are the more stressed fields from a nutritional point of view. At the same time, the role of micronutrients is ofte
Externí odkaz:
https://doaj.org/article/07e42363d4214d9eb8f9affefd9a9eec
Autor:
Laura Cesca, Ester Conversano, Federica Alessandra Vianello, Laura Martelli, Chiara Gualeni, Francesca Bassani, Milena Brugnara, Giulia Rubin, Mattia Parolin, Mauro Anselmi, Mara Marchiori, Gianluca Vergine, Elisabetta Miorin, Enrico Vidal, Cristina Milocco, Cecilia Orsi, Giuseppe Puccio, Licia Peruzzi, Giovanni Montini, Roberto Dall’Amico, on the behalf of the Italian Society of Pediatric Nephrology (SINePe)
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-8 (2022)
Abstract Background The first Covid-19 pandemic affected the epidemiology of several diseases. A general reduction in the emergency department (ED) accesses was observed during this period, both in adult and pediatric contexts. Methods This retrospec
Externí odkaz:
https://doaj.org/article/da8e5d47878a49cea921a9c43467d57b
Autor:
Simone Romano, Denise Marcon, Lorella Branz, Angela Tagetti, Giada Monamì, Alice Giontella, Francesca Malesani, Luca Pecoraro, Pietro Minuz, Milena Brugnara, Cristiano Fava
Publikováno v:
Medicina, Vol 59, Iss 10, p 1777 (2023)
Background and Objectives: Hypertension and vascular damage can begin in adolescents affected by Autosomal Dominant Polycystic Kidney Disease (ADPKD). This study aimed to evaluate markers of vascular damage and left ventricular geometry in a sample o
Externí odkaz:
https://doaj.org/article/3cbe69b80bd04b6dab756dba0f1d0e0f
Autor:
Graziana Lella, Luca Pecoraro, Elisa Benetti, Olivia Chapin Arnone, Giorgio Piacentini, Milena Brugnara, Angelo Pietrobelli
Publikováno v:
Medical Sciences, Vol 11, Iss 3, p 47 (2023)
Nephrotic syndrome (NS) is a common pediatric disease characterized by a dysfunction in the glomerular filtration barrier that leads to protein, fluid, and nutrient loss in urine. Corticosteroid therapy is the conventional treatment in children. Long
Externí odkaz:
https://doaj.org/article/202cebefb0fd471f936bdfbadc8c7a47
Autor:
Andrea Puma, Milena Brugnara, Paolo Cavarzere, Marco Zaffanello, Giorgio Piacentini, Rossella Gaudino
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Suprasellar arachnoid cysts represent a rare occurrence in the pediatric population and usually cause symptoms related to mass effect and can occasionally cause endocrine dysfunctions. The association between SAC and the syndrome of inappropriate ant
Externí odkaz:
https://doaj.org/article/00e4a77f9c8e4c2cafc0794360d254b4
Autor:
Paolo Cavarzere, Andrea Gastaldi, Francesca Marta Elli, Rossella Gaudino, Erika Peverelli, Milena Brugnara, Susanne Thiele, Francesca Granata, Giovanna Mantovani, Franco Antoniazzi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/3cd974cfae2041ad8dc03f10d9273e43
Autor:
Marie Morimoto, Clara Myung, Kimberly Beirnes, Kunho Choi, Yumi Asakura, Arend Bokenkamp, Dominique Bonneau, Milena Brugnara, Joel Charrow, Estelle Colin, Amira Davis, Georges Deschenes, Mattia Gentile, Mario Giordano, Andrew K. Gormley, Rajeshree Govender, Mark Joseph, Kory Keller, Evelyne Lerut, Elena Levtchenko, Laura Massella, Christy Mayfield, Behzad Najafian, David Parham, Jurgen Spranger, Peter Stenzel, Uluc Yis, Zhongxin Yu, Jonathan Zonana, Glenda Hendson, Cornelius F. Boerkoel
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 11, Iss 1, Pp 1-12 (2016)
Abstract Background Schimke immuno-osseous dysplasia (SIOD) is a multisystemic disorder caused by biallelic mutations in the SWI/SNF-related matrix-associated actin-dependent regulator of chromatin, subfamily A-like 1 (SMARCAL1) gene. Changes in gene
Externí odkaz:
https://doaj.org/article/3b7ef2c5e2c44cff8f2914c3b624b808
Autor:
Costanza Bruno, Milena Brugnara, Rocco Micciolo, Mariangela Cecchetto, Michele Zuffante, Alessandra Bucci, Marco Zaffanello
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 27, Iss 6, Pp 1139-1147 (2016)
A shear wave velocity (SWV) value obtained by the acoustic radiation force impulse technique depends on tissue elasticity. We investigated the relationship between SWV values and the estimated glomerular filtration rate (eGFR) in children with chroni
Externí odkaz:
https://doaj.org/article/820ce4f0b7614d3c8d8b084b946eedc6
Publikováno v:
The Scientific World Journal, Vol 7, Pp 20-30 (2007)
Although severe kidney involvement in children with Henoch-Shonlein purpura (HSP) is rarer than that in adults, morbidity should not be underevaluated and follow-up is mandatory. Some drugs are introduced as well-defined treatment options, others can
Externí odkaz:
https://doaj.org/article/56858ca82b7d4afcaf13ac862352f91e