Michela Brena

Milan, Italy

Last Updated: 09/26/2026

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Found 44 publications

Correction to: Quality of life in children and adults with epidermolysis bullosa: the QoL-REB explorative study.

Correction to: Quality of life in children and adults with epidermolysis bullosa: the QoL-REB explorative study.

Journal: Orphanet journal of rare diseases

Published: August 07, 2026

Molecular epidemiology of non-syndromic epidermal differentiation disorders: geographic variability and implications for precision medicine.

Molecular epidemiology of non-syndromic epidermal differentiation disorders: geographic variability and implications for precision medicine.

Journal: Italian journal of dermatology and venereology

Published: June 04, 2026

Complicated Spastic Paraparesis: Study of a Patient With a De Novo Pathogenic Variant in ELOVL1.

Complicated Spastic Paraparesis: Study of a Patient With a De Novo Pathogenic Variant in ELOVL1.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

Published: March 16, 2026

Topical gene therapy for severe recessive dystrophic epidermolysis bullosa: clinical outcomes and multidisciplinary management in three patients treated with beremagene geperpavec (B-VEC) in Italy - a case series.

Topical gene therapy for severe recessive dystrophic epidermolysis bullosa: clinical outcomes and multidisciplinary management in three patients treated with beremagene geperpavec (B-VEC) in Italy - a case series.

Journal: Drugs in context

Published: February 17, 2026

Quality of life in children and adults with epidermolysis bullosa: the QoL-REB explorative study.

Quality of life in children and adults with epidermolysis bullosa: the QoL-REB explorative study.

Journal: Orphanet journal of rare diseases

Published: October 16, 2025

Quality of life in children and adults with epidermolysis bullosa: the QoL-REB explorative study.

Quality of life in children and adults with epidermolysis bullosa: the QoL-REB explorative study.

Journal: Orphanet journal of rare diseases

Published: October 16, 2025

Linear Subepidermal Calcified Nodule With Somatic FGFR3 Mutation.

Linear Subepidermal Calcified Nodule With Somatic FGFR3 Mutation.

Journal: The Australasian journal of dermatology

Published: September 10, 2025

Genotypes and Phenotypes of Patients With TSPEAR-Related Disorder: Evidence of a Predominant Dental Phenotype.

Genotypes and Phenotypes of Patients With TSPEAR-Related Disorder: Evidence of a Predominant Dental Phenotype.

Journal: American journal of medical genetics. Part A

Published: August 05, 2025

Taking care of patients with recessive dystrophic epidermolysis bullosa from birth to adulthood: a multidisciplinary Italian Delphi consensus.

Taking care of patients with recessive dystrophic epidermolysis bullosa from birth to adulthood: a multidisciplinary Italian Delphi consensus.

Journal: Orphanet journal of rare diseases

Published: November 25, 2024

A Rapidly Growing Nodule on the Eyebrow of a Pediatric Patient.

A Rapidly Growing Nodule on the Eyebrow of a Pediatric Patient.

Journal: Dermatopathology (Basel, Switzerland)

Published: July 31, 2024

Netherton Syndrome Caused by Heterozygous Frameshift Mutation Combined with Homozygous c.1258A>G Polymorphism in SPINK5 Gene.

Netherton Syndrome Caused by Heterozygous Frameshift Mutation Combined with Homozygous c.1258A>G Polymorphism in SPINK5 Gene.

Journal: Genes

Published: April 17, 2023

Multiple melanomas in ichthyosis with confetti: One more piece of evidence.

Multiple melanomas in ichthyosis with confetti: One more piece of evidence.

Journal: The Australasian journal of dermatology

Published: April 02, 2023

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Last Updated: 09/26/2026