Épidermolyse bulleuse jonctionnelle
Author:
Publisher
Elsevier BV
Subject
Dermatology
Reference19 articles.
1. Epidermolysis bullosa: a spectrum of clinical phenotypes explained by molecular heterogeneity;Uitto;Mol Med Today,1997
2. Herlitz vs Laminin 5 mutations in junctional epidermolysis bullosa: molecular basis of non-Herlitz phenotypes;Nakano;Hum Genet,2002
3. Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa Registry;Fine;J Am Acad Dermatol,1991
4. Revised classification system for inherited epidermolysis bullosa. Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa;Fine;J Am Acad Dermatol,2000
5. Laminin 5 binds the NC-1 domain of type VII collagen;Rousselle;J Cell Biol,1997
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1. Genotype–Phenotype Correlation in Junctional Epidermolysis Bullosa: Signposts to Severity;Journal of Investigative Dermatology;2023-12
2. Challenges of the differential diagnosis between the subtypes of the junctional epidermolysis bullosa: presentation of two clinical cases;Almanac of Clinical Medicine;2019-02-26
3. Genotype, Clinical Course, and Therapeutic Decision Making in 76 Infants with Severe Generalized Junctional Epidermolysis Bullosa;Journal of Investigative Dermatology;2016-11
4. A Novel LAMA3 Mutation in a Newborn with Junctional Epidermolysis Bullosa Herlitz Type;Neonatology;2011
5. Genetic Disorders in Lebanon;Genetic Disorders Among Arab Populations;2010
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