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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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Carmelo Schepis

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Orphanet Journal of Rare Diseases|October 21, 2021

A multicenter study on quality of life of the "greater patient" in congenital ichthyosesDamiano Abeni, Roberta Rotunno, Andrea Diociaiuti, et al.

Molecular Genetics & Genomic Medicine|July 5, 2022

Exome sequencing in a child with neurodevelopmental disorder and epilepsy: Variant analysis of the AHNAK2 geneMirella Vinci, Petri Kursula, Donatella Greco, et al.

Quantitative Imaging in Medicine and Surgery|December 13, 2016

<i>Cutis tricolor</i>: a literature review and report of five new casesMartino Ruggieri, Agata Polizzi, Carmelo Schepis, et al.

Quantitative Imaging in Medicine and Surgery|December 13, 2016

Mixed vascular nevus syndrome: a report of four new cases and a literature reviewMartino Ruggieri, Agata Polizzi, Serena Strano, et al.

Acta Dermato-Venereologica|May 6, 2021

The Burden of Autosomal Recessive Congenital Ichthyoses on Patients and their Families: An Italian Multicentre StudyDamiano Abeni, Roberta Rotunno, Andrea Diociaiuti, et al.

European Journal of Medical Genetics|November 14, 2016

Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platformFrancesco Calì, Valeria Chiavetta, Giuseppa Ruggeri, et al.

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Search research articles

Showing results (11-20 of 16) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 16 results.

Orphanet Journal of Rare Diseases|October 21, 2021

A multicenter study on quality of life of the "greater patient" in congenital ichthyosesDamiano Abeni, Roberta Rotunno, Andrea Diociaiuti, et al.

Molecular Genetics & Genomic Medicine|July 5, 2022

Exome sequencing in a child with neurodevelopmental disorder and epilepsy: Variant analysis of the AHNAK2 geneMirella Vinci, Petri Kursula, Donatella Greco, et al.

Quantitative Imaging in Medicine and Surgery|December 13, 2016

<i>Cutis tricolor</i>: a literature review and report of five new casesMartino Ruggieri, Agata Polizzi, Carmelo Schepis, et al.

Quantitative Imaging in Medicine and Surgery|December 13, 2016

Mixed vascular nevus syndrome: a report of four new cases and a literature reviewMartino Ruggieri, Agata Polizzi, Serena Strano, et al.

Acta Dermato-Venereologica|May 6, 2021

The Burden of Autosomal Recessive Congenital Ichthyoses on Patients and their Families: An Italian Multicentre StudyDamiano Abeni, Roberta Rotunno, Andrea Diociaiuti, et al.

European Journal of Medical Genetics|November 14, 2016

Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platformFrancesco Calì, Valeria Chiavetta, Giuseppa Ruggeri, et al.

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