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Last Updated: 01/07/2026

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Found 667 publications

Cutaneous Squamous Cell Carcinoma in Epidermolysis Bullosa: A Review of Pathogenesis, Diagnosis and Management.

Cutaneous Squamous Cell Carcinoma in Epidermolysis Bullosa: A Review of Pathogenesis, Diagnosis and Management.

Journal: Cancers
Published: August 09, 2025

Laryngo-Onycho-Cutaneous Syndrome Managed With Thalidomide.

Laryngo-Onycho-Cutaneous Syndrome Managed With Thalidomide.

Journal: Pediatric dermatology
Published: July 12, 2025

Real-world case series: Birch triterpenes gel efficacy in 2 patients with junctional epidermolysis bullosa.

Real-world case series: Birch triterpenes gel efficacy in 2 patients with junctional epidermolysis bullosa.

Journal: JAAD case reports
Published: July 03, 2025

Junctional Epidermolysis Bullosa Caused by a Hemiallelic Nonsense Mutation in LAMA3 Revealed by 18q11.2 Microdeletion.

Junctional Epidermolysis Bullosa Caused by a Hemiallelic Nonsense Mutation in LAMA3 Revealed by 18q11.2 Microdeletion.

Journal: International journal of molecular sciences
Published: June 30, 2025

Ayurvedic management for Epidermolysis bullosa - A case report.

Ayurvedic management for Epidermolysis bullosa - A case report.

Journal: Journal of Ayurveda and integrative medicine
Published: May 02, 2025

Prime editing as a promising therapeutic strategy for junctional epidermolysis bullosa.

Prime editing as a promising therapeutic strategy for junctional epidermolysis bullosa.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: April 25, 2025

Novel eRF3a degrader enhances gentamicin-induced premature termination codon readthrough in epidermolysis bullosa.

Novel eRF3a degrader enhances gentamicin-induced premature termination codon readthrough in epidermolysis bullosa.

Journal: Molecular therapy. Nucleic acids
Published: March 18, 2025

Compound Heterozygous Null Variants in ITGB4 Gene Causing Severe Phenotype of Junctional Epidermolysis Bullosa With Pyloric Atresia in Thai Newborn: Genotype-Phenotype Correlation From a Case Report and Review of the Literature.

Compound Heterozygous Null Variants in ITGB4 Gene Causing Severe Phenotype of Junctional Epidermolysis Bullosa With Pyloric Atresia in Thai Newborn: Genotype-Phenotype Correlation From a Case Report and Review of the Literature.

Journal: International journal of genomics
Published: February 21, 2025

The Spectrum of Epidermolysis Bullosa in KwaZulu-Natal, South Africa.

The Spectrum of Epidermolysis Bullosa in KwaZulu-Natal, South Africa.

Journal: International journal of dermatology
Published: February 09, 2025

A novel bladder phenotype in junctional epidermolysis bullosa: a case report.

A novel bladder phenotype in junctional epidermolysis bullosa: a case report.

Journal: Frontiers in pediatrics
Published: January 05, 2025

Enamel Phenotype in Junctional Epidermolysis Bullosa.

Enamel Phenotype in Junctional Epidermolysis Bullosa.

Journal: The Journal of investigative dermatology
Published: November 26, 2024

Skin microbiome analysis of a junctional epidermolysis bullosa patient treated with genetically modified stem cells.

Skin microbiome analysis of a junctional epidermolysis bullosa patient treated with genetically modified stem cells.

Journal: Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
Published: November 11, 2024
Showing 1-12 of 667

Last Updated: 01/07/2026