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European Journal of Medicinal Chemistry|April 29, 2016
Locking PDK1 in DFG-out conformation through 2-oxo-indole containing molecules: Another tools to fight glioblastomaSimona Sestito, Simona Daniele, Giulia Nesi, et al.
The Journal of Pediatrics|February 10, 2015
Postinfectious functional gastrointestinal disorders in children: a multicenter prospective studyLicia Pensabene, Valentina Talarico, Daniela Concolino, et al.
Scientific Reports|April 22, 2015
Combined inhibition of AKT/mTOR and MDM2 enhances Glioblastoma Multiforme cell apoptosis and differentiation of cancer stem cellsSimona Daniele, Barbara Costa, Elisa Zappelli, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 6, 2016
Total and single species of uronic acid-bearing glycosaminoglycans in urine of newborns of 2-3days of age for early diagnosis applicationFrancesca Maccari, Fabio Galeotti, Lucia Zampini, et al.
Molecules (Basel, Switzerland)|March 1, 2020
Endogenous 3-Iodothyronamine (T1AM) and Synthetic Thyronamine-like Analog SG-2 Act as Novel Pleiotropic Neuroprotective Agents Through the Modulation of SIRT6Lorenza Bellusci, Massimiliano Runfola, Vittoria Carnicelli, et al.
Food Science & Nutrition|October 31, 2024
Anticancer potential of decursin, decursinol angelate, and decursinol from Angelica gigas Nakai: A comprehensive review and future therapeutic prospectsSimona Sestito, Roberta Ibba, Federico Riu, et al.
Journal of Inherited Metabolic Disease|January 15, 2015
The proteome of cblC defect: in vivo elucidation of altered cellular pathways in humansMarianna Caterino, Anna Pastore, Maria Grazia Strozziero, et al.
Molecules (Basel, Switzerland)|April 3, 2021
Delivery of Thyronamines (TAMs) to the Brain: A Preliminary StudyNicoletta di Leo, Stefania Moscato, Marco Borso', et al.
Jornal De Pediatria|April 28, 2019
Low FODMAPs diet for functional abdominal pain disorders in children: critical review of current knowledgeLicia Pensabene, Silvia Salvatore, Rossella Turco, et al.
Orphanet Journal of Rare Diseases|July 21, 2023
Screening for lysosomal diseases in a selected pediatric population: the case of Gaucher disease and acid sphingomyelinase deficiencyMaja Di Rocco, Carlo Dionisi Vici, Alberto Burlina, et al.
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