Epidermolysis bullosa
Author:
Affiliation:
1. King's College London, and Honorary Consultant Dermatologist, Guy's and St Thomas' NHS Foundation Trust and
2. Guy's and St Thomas' NHS Foundation Trust and Great Ormond Street Hospital for Children, London SE1 7EH
Publisher
Mark Allen Group
Subject
General Medicine
Link
http://www.magonlinelibrary.com/doi/pdf/10.12968/hmed.2006.67.4.20864
Reference19 articles.
1. Kindler syndrome
2. Prenatal Diagnosis for Recessive Dystrophic Epidermolysis Bullosa in 10 Families by Mutation and Haplotype Analysis in the Type VII Collagen Gene (COL7A1)
3. MUTATION-BASED PRENATAL DIAGNOSIS OF HERLITZ JUNCTIONAL EPIDERMOLYSIS BULLOSA
4. Epidermolysis Bullosa: Scientific Advances and Therapeutic Challenges
5. Revised classification system for inherited epidermolysis bullosa
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1. [Artículo traducido] Error diagnóstico en un caso de epidermólisis bullosa: una carga más para los pacientes y sus familiares;Actas Dermo-Sifiliográficas;2023-10
2. Epidermolysis bullosa;hautnah dermatologie;2023-02
3. Misdiagnosis in Epidermolysis Bullosa: Yet Another Burden on Patients and their Families;Actas Dermo-Sifiliográficas;2022-10
4. A Novel Heterozygous Missense Mutation in COL7A1 Gene in Dystrophic Epidermolysis Bullosa;INTERNATIONAL JOURNAL OF HUMAN GENETICS;2021-05-05
5. The Frequency of Signs of Meibomian Gland Dysfunction in Children with Epidermolysis Bullosa;Ophthalmology;2016-05
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