Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Daniele Tessaris"'
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:
Nicola Improda, Donatella Capalbo, Antonella Poloniato, Gisella Garbetta, Francesco Dituri, Laura Penta, Tommaso Aversa, Linda Sessa, Francesco Vierucci, Mariarosaria Cozzolino, Maria Cristina Vigone, Giulia Maria Tronconi, Marta del Pistoia, Laura Lucaccioni, Gerdi Tuli, Jessica Munarin, Daniele Tessaris, Luisa de Sanctis, Mariacarolina Salerno
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionPerinatal asphyxia is one of the three most important causes of neonatal mortality and morbidity. Therapeutic hypothermia represents the standard treatment for infants with moderate-severe perinatal asphyxia, resulting in reduction in the
Externí odkaz:
https://doaj.org/article/71b6119c39814392a957ec30baac2123
Autor:
Daniele Tessaris, Elisa Bonino, Giovanna Weber, Malgorzata Wasniewska, Domenico Corica, Marco Pitea, Giuseppe Scirè, Manuela Caruso-Nicoletti, Danilo Fintini, Luisa de Sanctis
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-8 (2021)
Abstract Background Pseudohypoparathyroidism (PHP) represents a heterogeneous group of rare endocrine disorders caused by (epi) genetic abnormalities affecting the GNAS locus. It is mainly characterized by resistance to PTH and TSH, and by peculiar c
Externí odkaz:
https://doaj.org/article/f98a88457a1d43e793f38a10305734c6
Autor:
Silvia Vannelli, Maria Baffico, Raffaele Buganza, Francesca Verna, Giulia Vinci, Daniele Tessaris, Gianpaolo Di Rosa, Alberto Borraccino, Luisa de Sanctis
Publikováno v:
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-6 (2020)
Abstract Background The phenotypic features of SHOX deficiency (SHOX-D) are highly variable and can be very mild, especially in young children. The aim of this retrospective study was to evaluate auxological and radiological indicators that could be
Externí odkaz:
https://doaj.org/article/2c020abf9cf24ccaa3634053f081c907
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
Autor:
Stefania Moia, Daniele Tessaris, Silvia Einaudi, Luisa de Sanctis, Gianni Bona, Simonetta Bellone, Flavia Prodam
Publikováno v:
Italian Journal of Pediatrics, Vol 43, Iss 1, Pp 1-4 (2017)
Abstract Background Mutations localized in the Growth Hormone Receptor (GHR) gene are often associated with the pathogenesis of Laron Syndrome, an autosomal recessive hereditary disorder characterized by severe growth retardation. Biochemically, pati
Externí odkaz:
https://doaj.org/article/a22ef0f817ec4cdf99517fdf66c8817f
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:
Luisa De Sanctis, Daniele Tessaris
Publikováno v:
L'Endocrinologo. 22:48-51
Publikováno v:
Pediatric Endocrinology Diabetes and Metabolism. 28:88-90