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European Journal of Pediatrics|May 22, 2026
Application of machine learning to predict bronchiolitis severity in children: a single-centre retrospective cohort studySara Manti, Antonella Gambadauro, Matteo Stocchero, et al.
Frontiers in Endocrinology|July 11, 2018
Peculiarities of Precocious Puberty in Boys and Girls With McCune-Albright SyndromeDomenico Corica, Tommaso Aversa, Giorgia Pepe, et al.
Italian Journal of Pediatrics|March 9, 2010
At the end of a two-year follow-up elevated TSH levels normalize or remain unchanged in most the children with subclinical hypothyroidismFilippo De Luca, Malgorzata Wasniewska, Giuseppina Zirilli, et al.
Italian Journal of Pediatrics|November 21, 2018
Phenotypic testicular abnormalities and pubertal development in boys with McCune-Albright syndromeTommaso Aversa, Giuseppina Zirilli, Domenico Corica, et al.
Vaccine|August 31, 2014
Post vaccine acute disseminated encephalomyelitis as the first manifestation of chromosome 22q11.2 deletion syndrome in a 15-month old baby: a case reportMariella Valenzise, Antonio Cascio, Malgorzata Wasniewska, et al.
Hormone Research in Paediatrics|November 4, 2015
Central Precocious Puberty: Adult Height in Girls Treated with Quarterly or Monthly Gonadotropin-Releasing Hormone Analog TriptorelinSilvano Bertelloni, Francesco Massart, Silvia Einaudi, et al.
Thyroid : Official Journal of the American Thyroid Association|December 12, 2013
In young patients with Turner or Down syndrome, Graves' disease presentation is often preceded by Hashimoto's thyroiditisTommaso Aversa, Fortunato Lombardo, Andrea Corrias, et al.
Minerva Pediatrica|May 15, 2014
Key-role of thyrotropin deficiency in disclosing craniopharyngioma diagnosis in a short girl with Hashimoto's thyroiditisTommaso Aversa, Mariella Valenzise, Giuseppina Zirilli, et al.
Frontiers in Pediatrics|October 5, 2020
Nutrition and Avoidance Diets in Children With Food AllergyDomenico Corica, Tommaso Aversa, Lucia Caminiti, et al.
Gene|March 28, 2012
Identification of two novel mutations in the first Sicilian APECED patient with no R203X mutation in AIRE gene and review of Italian APECED genotypesMariella Valenzise, Malgorzata Wasniewska, Silvestro Mirabelli, et al.
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