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Michela Brena

Showing results (21-30 of 35) with videos related to

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Dermatopathology (Basel, Switzerland)|March 27, 2025
A Rapidly Growing Nodule on the Eyebrow of a Pediatric PatientItalo Francesco Aromolo, Michela Brena, Nicola Adriano Monzani, et al.
The Australasian Journal of Dermatology|August 14, 2023
Multiple melanomas in ichthyosis with confetti: One more piece of evidenceItalo Francesco Aromolo, Chiara Moltrasio, Luca Cozzaglio, et al.
JAMA Dermatology|September 12, 2014
The phenotypic and genotypic spectra of ichthyosis with confetti plus novel genetic variation in the 3' end of KRT10: from disease to a syndromeIris Spoerri, Michela Brena, Julie De Mesmaeker, et al.
Genes|May 27, 2023
Netherton Syndrome Caused by Heterozygous Frameshift Mutation Combined with Homozygous c.1258A>G Polymorphism in <i>SPINK5</i> GeneChiara Moltrasio, Maurizio Romagnuolo, Davide Riva, et al.
Italian Journal of Dermatology and Venereology|October 9, 2020
Family burden of children suffering from epidermolysis bullosaSanta DE Stefano, Francesca S Grassi, Faustina Lalatta, et al.
Pediatric Rheumatology Online Journal|July 24, 2021
Correction to: Juvenile idiopathic arthritis in Harlequin ichthyosis, a rare combination or the clinical spectrum of the disease? Report of a child treated with etanercept and review of the literatureFrancesco Baldo, Michela Brena, Simone Carbogno, et al.
Pediatric Rheumatology Online Journal|June 4, 2021
Juvenile idiopathic arthritis in Harlequin ichthyosis, a rare combination or the clinical spectrum of the disease? Report of a child treated with etanercept and review of the literatureFrancesco Baldo, Michela Brena, Simone Carbogno, et al.
Plos One|September 6, 2022
A single-centre study on predictors and determinants of pubertal delay and growth impairment in Epidermolysis BullosaGiulia Rodari, Sophie Guez, Simona Salera, et al.
Orphanet Journal of Rare Diseases|March 17, 2025
Taking care of patients with recessive dystrophic epidermolysis bullosa from birth to adulthood: a multidisciplinary Italian Delphi consensusMay El Hachem, Andrea Diociaiuti, Domenico Bonamonte, et al.
Skin Research and Technology : Official Journal of International Society for Bioengineering and the Skin (ISBS) [And] International Society for Digital Imaging of Skin (ISDIS) [And] International Society for Skin Imaging (ISSI)|February 27, 2021
Clinical, genetic, and ultrasonographic features of Periumbilical Perforating Pseudoxanthoma ElasticumCarlo Alberto Maronese, Cristina Beatrice Spigariolo, Francesca Laura Boggio, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Dermatopathology (Basel, Switzerland)|March 27, 2025
A Rapidly Growing Nodule on the Eyebrow of a Pediatric PatientItalo Francesco Aromolo, Michela Brena, Nicola Adriano Monzani, et al.
The Australasian Journal of Dermatology|August 14, 2023
Multiple melanomas in ichthyosis with confetti: One more piece of evidenceItalo Francesco Aromolo, Chiara Moltrasio, Luca Cozzaglio, et al.
JAMA Dermatology|September 12, 2014
The phenotypic and genotypic spectra of ichthyosis with confetti plus novel genetic variation in the 3' end of KRT10: from disease to a syndromeIris Spoerri, Michela Brena, Julie De Mesmaeker, et al.
Genes|May 27, 2023
Netherton Syndrome Caused by Heterozygous Frameshift Mutation Combined with Homozygous c.1258A>G Polymorphism in <i>SPINK5</i> GeneChiara Moltrasio, Maurizio Romagnuolo, Davide Riva, et al.
Italian Journal of Dermatology and Venereology|October 9, 2020
Family burden of children suffering from epidermolysis bullosaSanta DE Stefano, Francesca S Grassi, Faustina Lalatta, et al.
Pediatric Rheumatology Online Journal|July 24, 2021
Correction to: Juvenile idiopathic arthritis in Harlequin ichthyosis, a rare combination or the clinical spectrum of the disease? Report of a child treated with etanercept and review of the literatureFrancesco Baldo, Michela Brena, Simone Carbogno, et al.
Pediatric Rheumatology Online Journal|June 4, 2021
Juvenile idiopathic arthritis in Harlequin ichthyosis, a rare combination or the clinical spectrum of the disease? Report of a child treated with etanercept and review of the literatureFrancesco Baldo, Michela Brena, Simone Carbogno, et al.
Plos One|September 6, 2022
A single-centre study on predictors and determinants of pubertal delay and growth impairment in Epidermolysis BullosaGiulia Rodari, Sophie Guez, Simona Salera, et al.
Orphanet Journal of Rare Diseases|March 17, 2025
Taking care of patients with recessive dystrophic epidermolysis bullosa from birth to adulthood: a multidisciplinary Italian Delphi consensusMay El Hachem, Andrea Diociaiuti, Domenico Bonamonte, et al.
Skin Research and Technology : Official Journal of International Society for Bioengineering and the Skin (ISBS) [And] International Society for Digital Imaging of Skin (ISDIS) [And] International Society for Skin Imaging (ISSI)|February 27, 2021
Clinical, genetic, and ultrasonographic features of Periumbilical Perforating Pseudoxanthoma ElasticumCarlo Alberto Maronese, Cristina Beatrice Spigariolo, Francesca Laura Boggio, et al.
Pageof 4