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Magazine 1,927

Human orf complicated with erythema multiforme. A neglected disease in Italian women

Authors: Uccella I, Fabrizi P, Dell 'uomo V, Casinelli K, Lunghi F

Date: 2019

Scope of interest: infectious dermatology




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Magazine 2.07

Extracorporeal photochemotherapy in steroid refractory graft-versus-host disease: experience of Policlinico Tor Vergata”

Authors: Fiorelli E., Lanti A., Ferraro A.S., Basso L., Del Proposto G., Docimo F., Bonchi C., Guiducci G., Massarelli R., Pattofatto F., Ippolito M., Insalaco D., De Masi A., Messina F., Adorno G.

Date: 2014

Scope of interest: Clinical pathology


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Magazine 15.26

ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.

Authors: Montecchiani C, Pedace L, Lo Giudice T, Casella A, Mearini M, Gaudiello F, Pedroso JL, Terracciano C, Caltagirone C, et al

Date: 2016

Scope of interest: Neurogenetics


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Magazine 8.33

Structural Cerebellar Abnormalities and Parkinsonism in Patients with 22q11.2 Deletion Syndrome

Authors: Piervincenzi C, Fanella M, Petsas N, Frascarelli M, Morano A, Accinni T, Di Fabio F, Di Bonaventura C, Berardelli A, Pantano P.

Date: 2022

Scope of interest: Neuroimaging/rare diseases


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