Zobrazeno 1 - 10
of 118
pro vyhledávání: '"Natascia di Iorgi"'
Autor:
Giampiero I. Baroncelli, Pasquale Comberiati, Tommaso Aversa, Federico Baronio, Alessandra Cassio, Mariangela Chiarito, Mirna Cosci o di Coscio, Luisa De Sanctis, Natascia Di Iorgi, Maria Felicia Faienza, Danilo Fintini, Roberto Franceschi, Mila Kalapurackal, Silvia Longhi, Michela Mariani, Marco Pitea, Andrea Secco, Daniele Tessaris, Francesco Vierucci, Malgorzata Wasniewska, Giovanna Weber, Stefano Mora
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Rickets results from impaired mineralization of growing bone due to alterations in calcium and phosphate homeostasis. Clinical signs of rickets are related to the age of the patient, the duration of the disease, and the underlying disorder. The most
Externí odkaz:
https://doaj.org/article/4f680e033815480ba82d6dae0a6f7336
Autor:
Patrizia Bruzzi, Silvia Vannelli, Emanuela Scarano, Natascia Di Iorgi, Maria Parpagnoli, MariaCarolina Salerno, Marco Pitea, Maria Elisabeth Street, Andrea Secco, Adolfo Andrea Trettene, Malgorzata Wasniewska, Nicola Corciulo, Gianluca Tornese, Maria Felicia Faienza, Maurizio Delvecchio, Simona Filomena Madeo, Lorenzo Iughetti
Publikováno v:
Endocrine Connections, Vol 12, Iss 7, Pp 1-10 (2023)
Objective: This Italian survey aims to evaluate real-life long-term efficac y and safety of recombinant human growth hormone (rhGH) therapy in children wit h short stature homeobox-containing gene deficiency disorders (SHOX-D) and to id entify potent
Externí odkaz:
https://doaj.org/article/82d6fe2bd57c403b9090fe00f9ba81ab
Autor:
Giuseppa Patti, Marco Scaglione, Nadia Gabriella Maiorano, Giulia Rosti, Maria Teresa Divizia, Tiziana Camia, Elena Lucia De Rose, Alice Zucconi, Emilio Casalini, Flavia Napoli, Natascia Di Iorgi, Mohamad Maghnie
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundNoonan syndrome (NS) is a genetic multisystem disorder characterised by variable clinical manifestations including dysmorphic facial features, short stature, congenital heart disease, renal anomalies, lymphatic malformations, chest deformit
Externí odkaz:
https://doaj.org/article/72330c4209af431b938af2d047b796b9
Autor:
Laura Chioma, Carla Bizzarri, Martina Verzani, Daniela Fava, Mariacarolina Salerno, Donatella Capalbo, Chiara Guzzetti, Laura Penta, Luigi Di Luigi, Natascia di Iorgi, Mohamad Maghnie, Sandro Loche, Marco Cappa
Publikováno v:
Endocrine Connections, Vol 11, Iss 2, Pp 1-10 (2022)
Objective: This retrospective study aimed to evaluate children observed for suspected precocious puberty in five Italian centers of Pediatric Endocrin ology during the first wave of coronavirus disease 2019 pandemic (March–September 2020), compared
Externí odkaz:
https://doaj.org/article/94e6b599936a4b6b904541980a790e56
Autor:
Giuseppa Patti, Federica Malerba, Maria Grazia Calevo, Maurizio Schiavone, Marco Scaglione, Emilio Casalini, Silvia Russo, Daniela Fava, Marta Bassi, Flavia Napoli, Anna Elsa Maria Allegri, Giuseppe D’Annunzio, Roberto Gastaldi, Mohamad Maghnie, Natascia Di Iorgi
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/2157d110a282474c99eb73597a384b3f
Autor:
Jenneke E. vanAtteveld, Iris E. Verhagen, Marry M. van denHeuvel‐Eibrink, Hanneke M. vanSanten, Inge M. van derSluis, Natascia Di Iorgi, Jill H. Simmons, Leanne M. Ward, Sebastian J.C.M.M. Neggers
Publikováno v:
Cancer Medicine, Vol 10, Iss 13, Pp 4177-4194 (2021)
Abstract Background Prevalent vitamin D deficiency (VDD) and low bone mineral density (BMD) have led to vitamin D supplementation for children with cancer, regardless vitamin D status. However, it remains unsettled whether this enhances bone strength
Externí odkaz:
https://doaj.org/article/4ad1db9965ac49629a2a322c382d7397
Autor:
Giuseppa Patti, Federica Malerba, Maria Grazia Calevo, Maurizio Schiavone, Marco Scaglione, Emilio Casalini, Silvia Russo, Daniela Fava, Marta Bassi, Flavia Napoli, Anna Elsa Maria Allegri, Giuseppe D’Annunzio, Roberto Gastaldi, Mohamad Maghnie, Natascia Di Iorgi
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
ContextData on pubertal timing in Silver Russell syndrome (SRS) are limited.Design and methodsRetrospective observational study including twenty-three SRS patients [11p15 loss of methylation, (11p15 LOM, n=10) and maternal uniparental disomy of chrom
Externí odkaz:
https://doaj.org/article/6d3d40a3253d447497bb22f2eb81f286
Autor:
Natascia Di Iorgi, Giovanni Morana, Marco Cappa, Ludovico D’Incerti, Maria Luisa Garrè, Armando Grossi, Lorenzo Iughetti, Patrizia Matarazzo, Maria Parpagnoli, Gabriella Pozzobon, Mariacarolina Salerno, Iacopo Sardi, Malgorzata Gabriela Wasniewska, Stefano Zucchini, Andrea Rossi, Mohamad Maghnie
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
BackgroundGrowth hormone deficiency (GHD) is the first and most common endocrine complication in pediatric brain tumor survivors (BTS). GHD can occur due to the presence of the tumor itself, surgery, or cranial radiotherapy (CRT).AimsThis study aimed
Externí odkaz:
https://doaj.org/article/f5343cda23ee4160b56c1db73ce8b717
Autor:
Ramona Cordani, Marco Veneruso, Flavia Napoli, Natascia Di Iorgi, Claudia Milanaccio, Alessandro Consales, Nicola Disma, Elisa De Grandis, Mohamad Maghnie, Lino Nobili
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Craniopharyngiomas are rare brain tumors of the sellar region and are the most common non-neuroepithelial intracerebral neoplasm in children. Despite a low-grade histologic classification, craniopharyngiomas can have a severe clinical course due to h
Externí odkaz:
https://doaj.org/article/d8ac363fc80f4c049b1c0d04a28ec565
Autor:
Giovanni Del Borrello, Maurizio Miano, Concetta Micalizzi, Michela Lupia, Isabella Ceccherini, Alice Grossi, Andrea Cavalli, Stefano Gustincich, Marta Rusmini, Maura Faraci, Gianluca Dell’Orso, Ugo Ramenghi, Alessio Mesini, Erica Ricci, Maurizio Schiavone, Natascia Di Iorgi, Carlo Dufour
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Cartilage-hair hypoplasia (CHH) is a syndromic immunodeficiency characterized by metaphyseal dysplasia, cancer predisposition, and varying degrees of anemia. It may present as severe combined immunodeficiency in infancy, or slowly progress until full
Externí odkaz:
https://doaj.org/article/8eef0c2569d74cd783e611f2be171661