PENSIERO, STEFANO

PENSIERO, STEFANO  

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Titolo Data di pubblicazione Autori File
A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family 1-gen-2014 DI STAZIO, MARIATERESAMAGLIONE, MICHELEPENSIERO, STEFANO +
Essential Infantile Esotropia: A Course of Treatment From Our Experience 1-gen-2021 Pensiero, StefanoPresotto, MariannaRonfani, LucaBarbi, Egidio +
Horizontal gaze palsy and progressive scoliosis without ROBO3 mutations 1-gen-2011 Faletra, FlavioGasparini, PaoloPensiero, Stefano +
Ipertensione endocranica idiopatica (pseudotumor cerebri) in una bambina in terapia con ormone della crescita 1-gen-2007 Tornese, GianlucaPatarino, FedericaPensiero, Stefano +
Minimally-Invasive Surgical Approach to Congenital Dacryostenosis: Proposal for a New Protocol 1-gen-2021 Pensiero S.Visalli G.Barbi E. +
Optic Nerve Sheath Diameter Ultrasound: Optic Nerve Growth Curve and its Application to Detect Intracranial Hypertension in Children 1-gen-2019 Pensiero S.Ronfani L.Rosolen V.Barbi E. +
Optic Nerve Sheath Diameter Ultrasound: Optic Nerve Growth Curve and Its Application to Detect Intracranial Hypertension in Children 1-gen-2019 Pensiero S.Ronfani L.Rosolen V.Barbi E. +
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 1-gen-2015 GIROTTO, GIORGIAMORGAN, ANNAVOZZI, DiegoRUBINATO, ELISADI STAZIO, MARIATERESAPENSIERO, STEFANOGASPARINI, PAOLO +
Successful treatment of cortical visual impairment in children using anti-amblyopia treatment despite the absence of amblyopia: a case report 1-gen-2024 Sica, AttilioPensiero, StefanoBarbi, Egidio +
Two cases of unilateral limbal Vernal keratoconjunctivitis in the same family: first case report 1-gen-2023 Sica, AttilioBarbi, EgidioPensiero, Stefano +