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Last Updated: 10/31/2025
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Found 664 publications
Laryngo-Onycho-Cutaneous Syndrome Managed With Thalidomide.
Journal: Pediatric dermatology
Published: July 12, 2025
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
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.
Journal: International journal of dermatology
Published: February 09, 2025
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.
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.
Journal: Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
Published: November 11, 2024
Multiple Acantholytic Acanthomas in Junctional Epidermolysis Bullosa.
Journal: Acta dermato-venereologica
Published: October 14, 2024
Genotype-Phenotype Correlation in Junctional Epidermolysis Bullosa-Signposts to Severity: Enamel Phenotype.
Journal: The Journal of investigative dermatology
Published: September 20, 2024
Efficient Dual Cas9 Nickase Correction of a Prevalent Pathogenic LAMB 3 Variant for Junctional Epidermolysis Bullosa.
Journal: JID innovations : skin science from molecules to population health
Published: September 17, 2024
Last Updated: 10/31/2025