• (New) antenatal ultrasound signs of fetal junctional epidermolysis bullosa: A case report and systematic review of literature
• <em>COL17A1</em> editing <em>via</em> homology-directed repair in junctional epidermolysis bullosa
• "Quality of Life in Epidermolysis Bullosa" and "Epidermolysis Bullosa Burden of Disease": Italian translation, cultural adaptation, and pilot testing of two disease-specific questionnaires
• A case of junctional epidermolysis bullosa intermediate with collagen XVII deficiency treated with dupilumab
• A heterozygous mutation in ITGB4 causing a mild phenotype of junctional epidermolysis bullosa
• A Novel Fluorescence-Based Screen of Gene Editing Molecules for Junctional Epidermolysis Bullosa
• A novel splice-site variant of the LAMB3 gene is associated with junctional epidermolysis bullosa
• A Retrospective Study on the Clinical, Laboratory, and Nutritional Status of Pediatric Epidermolysis Bullosa in a Tertiary Referral Hospital in West Java, Indonesia
• A single-centre study on predictors and determinants of pubertal delay and growth impairment in Epidermolysis Bullosa
• Acantholytic squamous cell carcinoma in a patient with junctional epidermolysis bullosa
• Advantages of whole-exome sequencing over immunomapping in 67 Brazilian patients with epidermolysis bullosa
• Amino Acid Substitution in the Cysteine-Rich Region of the Integrin beta4 Subunit Causes Late-Onset Mild Junctional Epidermolysis Bullosa without Extracutaneous Involvement
• Amino Acid Substitution in the Cysteine-Rich Region of the Integrin β4 Subunit Causes Late-Onset Mild Junctional Epidermolysis Bullosa without Extracutaneous Involvement
• Application of Amniotic Membrane in Skin Regeneration
• Autoimmunity against laminin 332
• Birch Bark Extract: A Review in Epidermolysis Bullosa
• Bloodstream Infection in Children With Epidermolysis Bullosa
• Case report: A case of epidermolysis bullosa complicated with pyloric atresia and a literature review
• Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
• Coexistence of junctional epidermolysis bullosa, autosomal recessive deafness type 57, and Angelman syndrome: A case report
• COL17A1 editing via homology-directed repair in junctional epidermolysis bullosa
• Congenital pyloric atresia associated with epidermolysis bullosa junctionalis: a novel lethal variant
• Cutaneous squamous cell carcinomas in EBDR: how can they be detected?
• Descriptive Study of the Clinical and Molecular Features of Epidermolysis Bullosa Patients in a Romanian European Reference Network-Skin Affiliated Reference Center
• Dystonin modifiers of junctional epidermolysis bullosa and models of epidermolysis bullosa simplex without dystonia musculorum
• Efficacy and safety of Oleogel-S10 (birch triterpenes) for epidermolysis bullosa: results from the phase III randomized double-blind phase of the EASE study
• En Route to Targeted Ribosome Editing to Replenish Skin Anchor Protein LAMB3 in Junctional Epidermolysis Bullosa
• Epidemiological Characteristics of Inherited Epidermolysis Bullosa in an Eastern European Population
• Epidemiology of inherited epidermolysis bullosa in Germany
• Epidermolysis Bullosa
• Epidermolysis bullosa in oral health: clinical manifestations and salivary alterations
• Epidermolysis Bullosa With Pyloric Stenosis: A Novel Lethal Variant
• Epidermolysis Bullosa-A Different Genetic Approach in Correlation with Genetic Heterogeneity
• Epidermolysis Bullosa-A Kindler Syndrome Case Report and Short Literature Review
• Epidermolysis Bullosa: Practical Clinical Tips From the Field
• Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
• Exploring the Impact of Epidermolysis Bullosa on Parents and Caregivers: A Cross-Cultural Validation of the Epidermolysis Bullosa Burden of Disease Questionnaire
• Eye Involvement and Management in Inherited Epidermolysis Bullosa
• First case report of complete paternal isodisomy of chromosome 10 harbouring a novel variant in COL17A1 that causes junctional epidermolysis bullosa intermediate
• Functional analysis of Collagen 17a1: A genetic modifier of junctional epidermolysis bullosa in mice
• Gastrostomy tube feeding in epidermolysis bullosa: A multi-center assessment of caregiver satisfaction
• Genotype and phenotype correlations in 441 patients with epidermolysis bullosa from China
• Genotype-Phenotype Correlation in Junctional Epidermolysis Bullosa: Signposts to Severity
• Gross motor development in children with epidermolysis bullosa
• Hereditary epidermolysis bullosa: clinical-epidemiological profile of 278 patients at a tertiary hospital in Sao Paulo, Brazil
• Heterozygous <em>COL17A1</em> variants are a frequent cause of amelogenesis imperfecta
• Identification of a novel homozygous <em>LAMB3</em> mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
• Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
• IgA nephropathy in adults with epidermolysis bullosa
• IL-6 levels dominate the serum cytokine signature of severe epidermolysis bullosa: A prospective cohort study
• Independent <em>COL17A1</em> Variants in Cats with Junctional Epidermolysis Bullosa
• Independent COL17A1 Variants in Cats with Junctional Epidermolysis Bullosa
• Inheritance of Monogenic Hereditary Skin Disease and Related Canine Breeds
• Integrin alpha 6 homozygous splice-site mutation causes a new form of junctional epidermolysis bullosa in Charolais cattle
• Integrin alpha3 mutation junctional epidermolysis bullosa presenting with hypotrichosis and lacrimal obstruction
• Integrin α3 mutation junctional epidermolysis bullosa presenting with hypotrichosis and lacrimal obstruction
• Interleukin-17A immune pattern across genetic acantholytic and blistering disorders
• Junctional Epidermolysis Bullosa Linked to Homozygous Mutation in LAMC2 Gene: A Case Report With Eosinophil-Rich Inflammatory Infiltrate
• Kidney-Urinary Tract Involvement in Intermediate Junctional Epidermolysis Bullosa
• Laryngo-Onycho-Cutaneous Syndrome (LOCS)
• Lessons to Learn About the Misdiagnosis of a Rare Case in China: Bart Syndrome or Carmi Syndrome?
• Lethal Carmi syndrome (junctional epidermolysis bullosa-pyloric atresia) with a novel and recurrent compound integrin beta 4 heterozygous mutation: A case report
• Longitudinal study of wound healing status and bacterial colonisation of Staphylococcus aureus and Corynebacterium diphtheriae in epidermolysis bullosa patients
• Mapping the burden of severe forms of epidermolysis bullosa - Implications for patient management
• Measuring the impact of pruritus in patients with epidermolysis bullosa: evaluation with an itch-specific instrument
• METTL14-mediated N6-methyladenosine modification of Col17a1/Itgα6/Itgβ4 governs epidermal homeostasis
• Mini-implant assisted palate expansion and digital design in junctional epidermolysis bullosa and amelogenesis imperfecta: Case report
• Modified Non-Cultured Cell Spray Induced Epithelization in LAMB3 Mutation Epidermolysis Bullosa
• Molecular genetic basis of epidermolysis bullosa
• Molecular profiling of an Indian EB cohort - a single centre experience
• Mutational analysis of epidermolysis bullosa in Taiwan by whole-exome sequencing complemented by RNA sequencing: a series of 77 patients
• Nail involvement in patients with epidermolysis bullosa: A systematic review
• Novel LAMB3 variants in two Asian patients and an overview of LAMB3 variants associated with generalized intermediate junctional epidermolysis bullosa
• Occam's Razor Versus Hickam's Dictum: A Case Report of Junctional Epidermolysis Bullosa and Lower Urinary Tract Infection
• Oral Alterations in Heritable Epidermolysis Bullosa: A Clinical Study and Literature Review
• Oral health status in patients with inherited epidermolysis bullosa: a comparative multicenter study
• Oral prosthetic rehabilitation in patients with Epidermolysis Bullosa Hereditaria: a systematic review
• Patients suffering from dystrophic epidermolysis bullosa are prone to developing autoantibodies against skin proteins: A longitudinal confirmational study
• Phenotype and genotype correlation of inherited epidermolysis bullosa in Indonesia
• Phenotypic differences in intermediate generalized junctional epidermolysis bullosa with homozygous LAMC2 mutation and a potential genetic modifier
• Phenotypic variability in LAMA3-associated amelogenesis imperfecta
• Practical Tips on Epidermolysis Bullosa for Caregivers: Part 2
• Pregnancy-associated blistering in a patient with junctional epidermolysis bullosa
• PRIMA-1(MET)/APR-246 Can Partially Rescue In Vitro Cell Adhesion of Patient-Derived Junctional Epidermolysis Bullosa Epidermal Cells
• PRIMA-1^MET/APR-246 Can Partially Rescue In Vitro Cell Adhesion of Patient-Derived Junctional Epidermolysis Bullosa Epidermal Cells
• Rare compound heterozygous variants of <em>LAMB3</em> and histological features of enamel and oral mucosa
• Revertant Mosaicism in Genodermatoses: Natural Gene Therapy Right before Your Eyes
• Seven naturally variant loci serve as genetic modifiers of Lamc2jeb induced non-Herlitz junctional Epidermolysis Bullosa in mice
• Severe tracheal involvement in type XVII collagen junctional epidermolysis bullosa
• Skin-Derived ABCB5⁺ Mesenchymal Stem Cells for High-Medical-Need Inflammatory Diseases: From Discovery to Entering Clinical Routine
• Spontaneous autoimmune subepidermal blistering diseases in animals: a comprehensive review
• Stem Cell Therapies for Epidermolysis Bullosa Treatment
• Strategy for the Optimization of Read-Through Therapy for Junctional Epidermolysis Bullosa with COL17A1 Nonsense Mutation
• Sucralfate-based cream as a novel and cost-effective topical agent in poorly healing ulcers in junctional epidermolysis bullosa
• The aggressive behaviour of squamous cell carcinoma in epidermolysis bullosa: analysis of clinical outcomes and tumour characteristics in the Dutch EB Registry
• Totally endoscopic concomitant aortic and mitral valve surgery in junctional epidermolysis bullosa: a case report
• Trametinib-Induced Epidermal Thinning Accelerates a Mouse Model of Junctional Epidermolysis Bullosa
• Treatment of Epidermolysis Bullosa and Future Directions: A Review
• Treatment With Ataluren for Wound Healing and Health Complications in a Patient With Junctional Epidermolysis Bullosa
• Whole exome sequencing in a sample of Peruvian patients diagnosed with epidermolysis bullosa