Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Patrizia Matarazzo"'
Autor:
Enrica Abrigo, Jessica Munarin, Claudia Bondone, Gerdi Tuli, Emanuele Castagno, Luisa de Sanctis, Patrizia Matarazzo
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-6 (2023)
Abstract Background In patients with adrenal insufficiency (AI), adrenal crisis (AC) represents a clinical emergency. Early recognition and prompt management of AC or AC-risk conditions in the Emergency Department (ED) can reduce critical episodes an
Externí odkaz:
https://doaj.org/article/891ab6c6ee214cdf8f9921a7f5296743
Autor:
Francesco Quaglino, Alex Bruno Bellocchia, Gerdi Tuli, Jessica Munarin, Patrizia Matarazzo, Luca Cestino, Federico Festa, Giulia Carbonaro, Salvatore Oleandri, Claudia Manini, Riccardo Vergano, Luisa De Sanctis
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionPediatric thyroid carcinoma represents about 4-5% of all pediatric carcinoma with an incidence of 0.5 cases/100,000, compared to 2-10/100000 cases in the adult population. The aim of this study is to present the experience of a reference
Externí odkaz:
https://doaj.org/article/68d93a62ec8d46cfab5c4f856edd1a75
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:
Roberta Rossi, Emanuele Castagno, Patrizia Matarazzo, Gerdi Tuli, Paola Saracco, Antonio F. Urbino, Claudia Bondone
Publikováno v:
Emergency Care Journal, Vol 18, Iss 2 (2022)
Water intoxication is a potentially fatal hypo-osmolar syndrome with brain function impairment. Isolated symptomatic excessive ingestion of free water is very rare in childhood. We report a case of acute hyponatremia due to water intoxication without
Externí odkaz:
https://doaj.org/article/9c151201eb674fb2a90ab6a39be97398
Autor:
Elisa Bonino, Patrizia Matarazzo, Raffaele Buganza, Gerdi Tuli, Jessica Munarin, Claudia Bondone, Luisa de Sanctis
Publikováno v:
Children, Vol 10, Iss 4, p 614 (2023)
In children, hypothyroidism usually presents non-specific symptoms; symptoms can emerge gradually, compromising a timely diagnosis. We report the case of a 13-year-old male, who was admitted to the hospital due to swelling of the torso and neck. Besi
Externí odkaz:
https://doaj.org/article/0421770f0f3f450fb138b7171af58e29
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 19, p 5767 (2022)
3beta-hydroxysteroid dehydrogenase type II deficiency (HSD3B2 deficiency), a rare form of congenital adrenal hyperplasia (CAH), is characterized by varying degrees of salt loss and incomplete masculinization in males and mild virilization or normal e
Externí odkaz:
https://doaj.org/article/269a5dfe347a4b37b0599fd74d175823
Autor:
Gerdi Tuli, Jessica Munarin, Daniele Tessaris, Raffaele Buganza, Patrizia Matarazzo, Luisa De Sanctis
Publikováno v:
Case Reports in Endocrinology, Vol 2021 (2021)
Primary hyperparathyroidism (PHPT) is a rare disorder in children and adolescents. Typical biochemical features are hypercalcemia and hypophosphatemia, but the clinical features can be heterogeneous, and in some cases, symptoms are vague and nonspeci
Externí odkaz:
https://doaj.org/article/22963409f2b34022860f96479439a4d0
Multidisciplinary Approach for Hypothalamic Obesity in Children and Adolescents: A Preliminary Study
Autor:
Daniele Tessaris, Patrizia Matarazzo, Gerdi Tuli, Antonella Tuscano, Ivana Rabbone, Alessandra Spinardi, Antonella Lezo, Giorgia Fenocchio, Raffaele Buganza, Luisa de Sanctis
Publikováno v:
Children, Vol 8, Iss 7, p 531 (2021)
Hypothalamic obesity (HO) is delineated by an inexorable weight gain in subjects with hypothalamic disorder (congenital or acquired). The aim of the present study was to evaluate the effect of a multidisciplinary approach on weight trend and metaboli
Externí odkaz:
https://doaj.org/article/1c4edde778474b25a6e69725def9b086
Autor:
Andrea Carpino, Raffaele Buganza, Patrizia Matarazzo, Gerdi Tuli, Michele Pinon, Pier Luigi Calvo, Davide Montin, Francesco Licciardi, Luisa De Sanctis
Publikováno v:
Genes, Vol 12, Iss 2, p 169 (2021)
Autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy (APECED), caused by mutations in the AIRE gene, is mainly characterized by the triad of hypoparathyroidism, primary adrenocortical insufficiency and chronic mucocutaneous candidiasis,
Externí odkaz:
https://doaj.org/article/cd950c65542c4730b9b08ad0e4c1947d
Autor:
Martina Tetti, Silvia Monticone, Jacopo Burrello, Patrizia Matarazzo, Franco Veglio, Barbara Pasini, Xavier Jeunemaitre, Paolo Mulatero
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 3, p 812 (2018)
Liddle syndrome is an inherited form of low-renin hypertension, transmitted with an autosomal dominant pattern. The molecular basis of Liddle syndrome resides in germline mutations of the SCNN1A, SCNN1B and SCNN1G genes, encoding the α, β, and γ-s
Externí odkaz:
https://doaj.org/article/1d2267d6dea3449891dbf5ff40b4e88f