Zobrazeno 1 - 10 of 24 pro vyhledávání: '"Beatrice, Righi"'
1
Akademický článek
Specific miRNAs Change After 3 Months of GH treatment and Contribute to Explain the Growth Response After 12 Months
Autor: Cecilia Catellani, Gloria Ravegnini, Chiara Sartori, Beatrice Righi, Pietro Lazzeroni, Laura Bonvicini, Silvia Poluzzi, Francesca Cirillo, Barbara Predieri, Lorenzo Iughetti, Paolo Giorgi Rossi, Sabrina Angelini, Maria Elisabeth Street
Publikováno v: Frontiers in Endocrinology, Vol 13 (2022)
ContextThere is growing evidence of the role of epigenetic regulation of growth, and miRNAs potentially play a role.ObjectiveThe aim of this study is to identify changes in circulating miRNAs following GH treatment in subjects with isolated idiopathi
Externí odkaz: https://doaj.org/article/861dc8a365644bbcbddbbb390b03382b
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2
Akademický článek
Overwhelming sepsis in a neonate affected by Zellweger syndrome due to a compound heterozygosis in PEX 6 gene: a case report
Autor: Laura Lucaccioni, Beatrice Righi, Greta Miriam Cingolani, Licia Lugli, Elisa Della Casa, Francesco Torcetta, Lorenzo Iughetti, Alberto Berardi
Publikováno v: BMC Medical Genetics, Vol 21, Iss 1, Pp 1-4 (2020)
Abstract Background Peroxisome biogenesis disorders (PBDs) are a group of metabolic diseases caused by dysfunction of peroxisomes. Different forms of PBDs are described; the most severe one is the Zellweger syndrome (ZS). We report on an unusual pres
Externí odkaz: https://doaj.org/article/0dbb7d4920374543a25b56ec43731bbd
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3
Akademický článek
Precocious Puberty and Covid-19 Into Perspective: Potential Increased Frequency, Possible Causes, and a Potential Emergency to Be Addressed
Autor: Maria E. Street, Chiara Sartori, Cecilia Catellani, Beatrice Righi
Publikováno v: Frontiers in Pediatrics, Vol 9 (2021)
A significant increase in precocious puberty, rapidly progressive puberty and precocious menarche has been reported in Italy since the initial lockdown because of the pandemic, and this could represent a new emergency to be addressed during this pand
Externí odkaz: https://doaj.org/article/b769ea975f134b9abebd4ceab91e54fa
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6
Gut microbiota signatures and clinical manifestations in celiac disease children at onset: a pilot study
Autor: Luigi Colecchia, Lorenzo Iughetti, Federico Ravaioli, Elton Dajti, Antonio Colecchia, Anna Rita Di Biase, Virginia D'Amico, Giovanni Marasco, Beatrice Righi, Davide Festi
Publikováno v: Journal of Gastroenterology and Hepatology. 36:446-454
Background and Aim: Recent researches have shown an altered gut microbiota in celiac disease (CD) patients compared with healthy controls (HCs). This study aims to evaluate the composition of the microbiota of CD children at onset and the relationshi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbeae35ca82678595d6964ad266b8110
https://doi.org/10.1111/jgh.15183
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7
Antitissue transglutaminase antibodies' normalization after starting a gluten-free diet in a large population of celiac children-a real-life experience
Autor: Francesca Sbravati, Paola Sogno Valin, Sara Pagano, P. Alvisi, A.G. Grondona, Annarita Di Biase, Beatrice Righi, Angela Salerno, Anita Cosentino, Michelangelo Fiorentino, Francesca Ambrosi, Laura Bruni, Jacopo Lenzi, Flavio Labriola, Barbara Battistini, S. Brusa
Publikováno v: Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver. 54(3)
Introduction Few data are available regarding the trend of IgA anti-transglutaminase antibodies (TGA-IgA) in children with celiac disease (CD) on a gluten-free diet (GFD). Our aim is to examine the normalization time of CD serology in a large pediatr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae87052d3ae500bb390eafddfe5d09de
https://pubmed.ncbi.nlm.nih.gov/34274255
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10
Overwhelming sepsis in a neonate affected by Zellweger syndrome due to a compound heterozygosis in PEX 6 gene: a case report
Autor: Elisa Della Casa, Greta Cingolani, Lorenzo Iughetti, Beatrice Righi, Alberto Berardi, Francesco Torcetta, Licia Lugli, Laura Lucaccioni
Publikováno v: BMC Medical Genetics, Vol 21, Iss 1, Pp 1-4 (2020)
BMC Medical Genetics
BackgroundPeroxisome biogenesis disorders (PBDs) are a group of metabolic diseases caused by dysfunction of peroxisomes. Different forms of PBDs are described; the most severe one is the Zellweger syndrome (ZS). We report on an unusual presentation o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7071377bba3f27be1fd92d2e70c3c7f4
https://hdl.handle.net/11380/1236618
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