Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Daniele Tessaris"'
Publikováno v:
Pediatric Endocrinology Diabetes and Metabolism. 28:88-90
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
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:
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:
Luisa De Sanctis, Patrizia Matarazzo, Daniele Tessaris, Massimiliano Bergallo, Ilaria Galliano, Paola Montanari
Publikováno v:
Hormone Research in Paediatrics. 87:342-349
Background/Aim: The McCune-Albright syndrome (MAS) is a potentially severe disorder hallmarked by fibrous bone dysplasia, café-au-lait skin spots, and endocrine hyperfunction. It is caused by postzygotic activating mutations at the R201 codon of the
Autor:
Stefania Moia, Luisa De Sanctis, S. Bellone, Gianni Bona, Daniele Tessaris, Silvia Einaudi, Flavia Prodam
Publikováno v:
Italian Journal of Pediatrics
Italian Journal of Pediatrics, Vol 43, Iss 1, Pp 1-4 (2017)
Italian Journal of Pediatrics, Vol 43, Iss 1, Pp 1-4 (2017)
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, patients pres
Autor:
Daniele Tessaris, Donatella Capalbo, Mariella Valenzise, Filippo De Luca, Mariacarolina Salerno, Lorenzo Iughetti, Barbara Predieri, Tommaso Aversa, Andrea Corrias, Malgorzata Wasniewska
BACKGROUND It is known that the association with Down syndrome (DS) can affect the phenotypic expression of autoimmune thyroid diseases (AITDs), whilst is unknown whether the clustering of extra-thyroidal autoimmune diseases (ETADs) may also be atypi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79c3b004424c856050670878303eff44
http://hdl.handle.net/11588/647815
http://hdl.handle.net/11588/647815
McCune-Albright syndrome (MAS) is characterized by the triad of polyostotic bone fibrous dysplasia (PFD), endocrine disorders, and café-au-lait skin pigmentation. Ninety percent of MAS patients have fibrous dysplasia (FD) craniofacial lesions. Osteo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9465729ada82c97e244819440187310f
http://hdl.handle.net/2318/1556588
http://hdl.handle.net/2318/1556588
Autor:
Daniele Tessaris, Patrizia Matarazzo, L. de Sanctis, Malgorzata Wasniewska, Andrea Corrias, Roberto Lala, M. F. Messina, Maria Cristina Vigone
Publikováno v:
Hormone Research in Paediatrics. 78:151-157
Background: To date, there is no agreement about the frequency or the features of thyroid abnormalities in McCune-Albright syndrome (MAS). The aim of our study was to detect thyroid abnormalities in a cohort of MAS children and adolescents and to giv
Management of sodium metabolism derangements in children treated for hypothalamic-hypophyseal tumors
Autor:
Roberto Lala, Marialia Repici, Alessandro Mussa, Ludovica Fiore, Daniele Tessaris, Francesca Verna, Gerdi Tuli, Patrizia Matarazzo
Publikováno v:
Journal of Pediatric Biochemistry. :289-296
Hyponatremia and hypernatremia, common electrolyte abnormalities in children hospitalized for intracranial diseases, are life-threatening events. Diagnosis and adequate treatment of hypo- and hypernatremia are mandatory to prevent neurological sequel