Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Daniele Tessaris"'
Autor:
Luisa De Sanctis, Daniele Tessaris
Publikováno v:
L'Endocrinologo. 22:48-51
Publikováno v:
European Journal of Pediatrics
In recent years, a more stable AVP surrogate, called copeptin, has been used as an adjuvant diagnostic tool for dysnatremia in adults and appears to be promising even in the pediatric age. The aim of this study is to present the distribution of plasm
Autor:
P Matarazzo, Raffaele Buganza, Gerdi Tuli, Daniele Tessaris, Silvia Einaudi, Luisa de Sanctis
Publikováno v:
Endocrine. 67:457-465
Hypoparathyroidism is characterized by the absence or inadequately low circulating concentrations of the parathyroid hormone, resulting in hypocalcemia, hyperphosphatemia, and elevated fractional excretion of calcium in the urine. The use of activate
Multidisciplinary Approach for Hypothalamic Obesity in Children and Adolescents: A Preliminary Study
Autor:
P Matarazzo, Alessandra Spinardi, Raffaele Buganza, Giorgia Fenocchio, Antonella Lezo, Ivana Rabbone, Gerdi Tuli, Luisa de Sanctis, Daniele Tessaris, Antonella Tuscano
Publikováno v:
Children
Children, Vol 8, Iss 531, p 531 (2021)
Volume 8
Issue 7
Children, Vol 8, Iss 531, p 531 (2021)
Volume 8
Issue 7
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
Autor:
Raffaele Buganza, Jessica Munarin, Daniele Tessaris, P Matarazzo, Luisa de Sanctis, Gerdi Tuli
Publikováno v:
Case Reports in Endocrinology
Case Reports in Endocrinology, Vol 2021 (2021)
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
Autor:
Marco Pitea, Giuseppe Scirè, Danilo Fintini, Malgorzata Wasniewska, M. Caruso-Nicoletti, Luisa de Sanctis, Daniele Tessaris, Giovanna Weber, Domenico Corica, Elisa Bonino
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-8 (2021)
Italian Journal of Pediatrics
Italian Journal of Pediatrics
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 clinical f
Autor:
Franco Bagnoli, Rosario Magaldi, Luisa de Sanctis, Annalisa Mori, Matteo Rinaldi, Paolo Ghirri, Gerdi Tuli, Daniele Tessaris
Publikováno v:
Journal of Perinatology. 39:934-940
The aim of this study is to establish the serum level distribution of cortisol and ACTH in VLBW preterm newborns and determine which neonates are ideal candidates for the stimulation test for adrenal insufficiency. Plasma cortisol and ACTH levels wer
Autor:
Gianpaolo Di Rosa, Francesca Verna, Raffaele Buganza, Luisa de Sanctis, Silvia Vannelli, Daniele Tessaris, Alberto Borraccino, Maria Baffico, Giulia Vinci
Publikováno v:
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-6 (2020)
Italian Journal of Pediatrics
Italian Journal of Pediatrics
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 predictiv
Publikováno v:
Endocrine. 71(1)
The incidence of primary congenital hypothyroidism (CH) has grown progressively and literature data indicate an association between CH and congenital malformations. The purpose of this study is to establish the current incidence of CH in the Italian
Autor:
Giorgia Pepe, Domenico Corica, Luisa De Sanctis, Mariacarolina Salerno, Maria Felicia Faienza, Daniele Tessaris, Gerdi Tuli, Iris Scala, Laura Penta, Angela Alibrandi, Giovanni Battista Pajno, Tommaso Aversa, Malgorzata Wasniewska
Objective To evaluate the prevalence and natural course of autoimmune and non-autoimmune subclinical hypothyroidism (SH) in Down syndrome (DS) children and adolescents. Design Prospective multicenter study. Methods For the study, 101 DS patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c17544956b83f94aabd729a77b6ee621
http://hdl.handle.net/2318/1798038
http://hdl.handle.net/2318/1798038