Oral and gastrointestinal manifestations of epidermolysis bullosa
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference12 articles.
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2. Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analyses;Coulombe;Cell,1991
3. Genetic linkage of type VII collagen (COL7A1) to dominant dystrophic epidermolysis bullosa in families with abnormal anchoring fibrils;Ryynanen;J Clin Invest,1992
4. Notes on unusual or rare forms of skin disease;Fox;Lancet,1879
5. Oropharyngeal lesions and their management in epidermolysis bullosa;Nowark;Arch Dermatol,1988
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1. New concept of intervention on the health of the stomatognathic system in patients with epidermolysis bullosa in combination with the topical application of Curefini® in the oral cavity;Gazzetta Medica Italiana Archivio per le Scienze Mediche;2024-09
2. Comprehensive orthodontic treatment using miniscrews and digital rehabilitation in a patient with severe recessive dystrophic epidermolysis bullosa;Special Care in Dentistry;2023-12-06
3. Management of acute sloughing of the esophageal lining in patients with dystrophic epidermolysis bullosa—A series of six pediatric patients;Pediatric Dermatology;2023-07-26
4. Our experience of using Losartan for esophageal stenosis in children with dystrophic form of congenital epidermolysis bullosa;Journal of Pediatric Surgery;2023-04
5. A global, cross-sectional survey of patient-reported outcomes, disease burden, and quality of life in epidermolysis bullosa simplex;Orphanet Journal of Rare Diseases;2022-07-15
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