Výsledky vyhledávání - "Maria Rosaria Arienzo"

PNPLA3 I148M Polymorphism Influences Renal Function in Children With Obesity and Prediabetes

Autor: Anna Di Sessa, Maria Cecilia Russo, Maria Rosaria Arienzo, Giuseppina Rosaria Umano, Domenico Cozzolino, Grazia Cirillo, Stefano Guarino, Emanuele Miraglia del Giudice, Pierluigi Marzuillo

Publikováno v: Journal of Renal Nutrition. 32:670-676

Objective: Non-alcoholic fatty liver disease (NAFLD) negatively impacts on renal function with the contribution of the I148M variant in the patatin like phospholipase containing domain 3 (PNPLA3) gene. We hypothesized that children with prediabetes p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c17f2ba0ef680357448ccb92847c258a
https://doi.org/10.1053/j.jrn.2022.01.007

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Congenital Solitary Kidney from Birth to Adulthood

Autor: Daniela Capalbo, Salvatore Cappabianca, Pier Francesco Rambaldi, Angela La Manna, Stefano Guarino, Tiziana Esposito, Emanuele Miraglia del Giudice, Giovanna Vacca, Alfonso Reginelli, Carla De Luca Picione, Grazia Cirillo, Maria Rosaria Arienzo, Anna Di Sessa, Cesare Polito, Pierluigi Marzuillo

Publikováno v: Journal of Urology. 205:1466-1475

To evaluate the course of prenatally diagnosed and early-enrolled congenital solitary functioning kidney patients followed until adulthood and to identify risk factors for kidney injury.Among all congenital solitary functioning kidney patients follow

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::123f3f5ec1d33f3ce773ae72a66bd4b8
https://doi.org/10.1097/ju.0000000000001524

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Acute Kidney Injury and Renal Tubular Damage in Children With Type 1 Diabetes Mellitus Onset

Autor: Paolo Montaldo, Angela Zanfardino, Tiziana Esposito, Pierluigi Marzuillo, Daniela Capalbo, Stefano Guarino, Maria Rosaria Arienzo, Emanuele Miraglia del Giudice, Carla De Luca Picione, Grazia Cirillo, Francesca Casaburo, Alessia Piscopo, Maria Ventre, Anna Di Sessa, Dario Iafusco

Publikováno v: The Journal of Clinical Endocrinology & Metabolism. 106:e2720-e2737

Context Acute kidney injury (AKI) and renal tubular damage (RTD), especially if complicated by acute tubular necrosis (ATN), could increase the risk of later chronic kidney disease. No prospective studies on AKI and RTD in children with type1diabetes

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e951cca1134ccccae1d1bdfe7e658968
https://doi.org/10.1210/clinem/dgab090

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Severe Lymphatic Disorder and Multifocal Atrial Tachycardia Treated with Trametinib in a Patient with Noonan Syndrome and SOS1 Mutation

Autor: Michele Lioncino, Adelaide Fusco, Emanuele Monda, Diego Colonna, Michelina Sibilio, Martina Caiazza, Daniela Magri, Angela Carla Borrelli, Barbara D’Onofrio, Maria Luisa Mazzella, Rossella Colantuono, Maria Rosaria Arienzo, Berardo Sarubbi, Maria Giovanna Russo, Giovanni Chello, Giuseppe Limongelli

Publikováno v: Genes. 13:1503

Noonan syndrome (NS) is a multisystemic disorder caused by germline mutations in the Ras/MAPK cascade, causing a broad spectrum of phenotypical abnormalities, including abnormal facies, developmental delay, bleeding diathesis, congenital heart diseas

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1f2525a577a407d962ecd1a45f78a428
https://doi.org/10.3390/genes13091503

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Quando lo scarso accrescimento è (anche) una questione di cuore

Autor: Maria Rosaria Arienzo, Francesca Angrisani

Publikováno v: Medico e Bambino pagine elettroniche. 23:167-167

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3d8d25d107267156350809d8a32619df
https://doi.org/10.53126/mebxxiiil167

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The rs72613567:TA variant in the hydroxysteroid 17-beta dehydrogenase 13 gene reduces liver damage in obese children

Autor: Giuseppina Rosaria Umano, Marcella Pedullà, Emanuele Miraglia del Giudice, Grazia Cirillo, Maria Rosaria Arienzo, Anna Di Sessa, Pierluigi Marzuillo

Publikováno v: Publons

We first investigated in obese children the protective role of the hydroxysteroid 17-beta dehydrogenase 13 (HSD17B13) rs72613567:TA variant in liver damage. Six hundred eighty-five obese children were genotyped for HSD17B13, patatin-like phospholipas

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::156a2a08f4b5a18498fe0f85331d857e
https://publons.com/publon/27083199/