MAGNOLATO, ANDREA

MAGNOLATO, ANDREA  

Dipartimento Universitario Clinico di Scienze mediche, chirurgiche e della salute  

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Titolo Data di pubblicazione Autori File
A Child With Self-Improving Hypotonia: Look at the Skin! 1-gen-2020 Conversano, EsterAgrusti, AnnaConti, RosauraMagnolato, AndreaBruno, IreneBarbi, EgidioFaletra, Flavio +
Administration of bicarbonates through percutaneous gastrostomy with continuous nocturnal infusion in a patient with Kearns-Sayre disease: a life changing therapeutical paradigm 1-gen-2024 Traunero, AriannaBaldo, FrancescoMagnolato, AndreaDi Leo, GraziaBarbi, Egidio +
Beneficial effect of gabapentin in two children with Noonan syndrome and early-onset neuropathic pain 1-gen-2020 Cortellazzo Wiel L.De Nardi L.Magnolato A.Barbi E. +
Characterization of Cardiac Function by Echocardiographic Global Longitudinal Strain in a Cohort of Children with Neurofibromatosis Type 1 Treated with Selumetinib 1-gen-2023 Caiffa, ThomasTessitore, AntimoMagnolato, AndreaBobbo, MarcoChicco, DanielaD'Agata Mottolese, BiancamariaPorcari, AldostefanoBarbi, EgidioSinagra, GianfrancoBruno, Irene +
Child with a non-painful red scrotum 1-gen-2021 Pascolo P.Magnolato A.Barbi E.Cozzi G. +
Clinical and Cytometric Study of Immune Involvement in a Heterogeneous Cohort of Subjects With RASopathies and mTORopathies 1-gen-2021 Valencic, EricaDa Lozzo, PriscaTornese, GianlucaGhirigato, ElenaPiscianz, ElisaFaletra, FlavioTaddio, AndreaTommasini, AlbertoMagnolato, Andrea +
Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: A case report 1-gen-2020 Nistico D.Bobbo M.Magnolato A.D'Adamo A. P.Barbi E.Gasparini P.Cadenaro M. +
Elevated creatine kinase is mainly harmless in children but persistent and severe hyperCKaemia should raise suspicions of serious muscle damage 1-gen-2023 Burlo, FrancescaGrigoletto, VeronicaPastore, SerenaVaivoda, AnnaTrombetta, AndreaTamaro, GianlucaMagnolato, AndreaTommasini, AlbertoTaddio, Andrea
Epiphyseal Cleft: A Misleading Radiologic Finding 1-gen-2020 Trevisan M.Elefante P.Rozzo M.Barbi E.Magnolato A. +
Juvenile xanthogranuloma: A possible diagnostic criterion for Neurofibromatosis type 1 in young children 1-gen-2021 Calligaris, LorenzoCortellazzo Wiel, LuisaBruno, IreneBarbi, EgidioMagnolato, Andrea +
Malattie rare a cavallo dell’innovazione: una sfida etica e scientifica 1-gen-2018 Tommasini A.Magnolato A.Pastore S.Bruno I.
Medicina di precisione nelle malattie rare: il caso della Neurofibromatosi di tipo 1. Analisi di dati clinici e trascrittomica 21-mar-2024 MAGNOLATO, ANDREA
Selumetinib in the Treatment of Symptomatic Intractable Plexiform Neurofibromas in Neurofibromatosis Type 1: A Prospective Case Series with Emphasis on Side Effects 1-gen-2020 Baldo F.Cortellazzo Wiel L.Maestro A.Magnolato A.Bruno I.Barbi E. +
Selumetinib side effects in children treated for plexiform neurofibromas: first case reports of peripheral edema and hair color change 1-gen-2021 Baldo F.Magnolato A.Barbi E. +
Teaching pain recognition through art: The Ramsay-Caravaggio sedation scale 1-gen-2018 Poropat, FedericoCozzi, GiorgioMAGNOLATO, ANDREAVentura, AlessandroBarbi, Egidio +
TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition 1-gen-2022 Faletra, FlavioZanus, CaterinaMagnolato, AndreaLa Bianca, MartinaFeresin, AgneseGirotto, GiorgiaGasparini, PaoloCosta, PaolaCarrozzi, Marco +
Twin girls with hypophosphataemic rickets and papilloedema 1-gen-2020 Migliarino V.Magnolato A.Barbi E.
Ulnar Pseudarthrosis in a Child with Type 1 Neurofibromatosis 1-gen-2021 Occhipinti, Alessandro AgostinoDa Lozzo, PriscaFavaretto, ElenaMagnolato, AndreaBruno, IreneBarbi, Egidio
When Long-Lasting Food Selectivity Leads to an Unusual Genetic Diagnosis: A Case Report 1-gen-2019 Da Lozzo, PriscaMagnolato, AndreaDel Rizzo, IreneBarbi, Egidio +