Oral Health Considerations for the Management of Patients with Junctional Epidermolysis Bullosa
Author:
Publisher
Jaypee Brothers Medical Publishing
Subject
Management of Technology and Innovation
Link
https://www.jsaapd.com/doi/pdf/10.5005/jp-journals-10077-3246
Reference18 articles.
1. 1. Siañez-González C, Pezoa-Jares R, Salas-Alanis JC. Congenital epidermolysis bullosa: a review. Actas Dermosifiliogr 2009;100(10):842–856. DOI: 10.1016/S1578-2190(09)70554-2
2. 2. Lanschuetzer CM, Fine J-D, Laimer M, et al. General aspects. In: Fine J-D, Hintner H, eds. Life with Epidermolysis Bullosa (EB). Vienna: Springer Vienna; 2009:1–95.
3. 3. Has C, Bauer JW, Bodemer C, et al. Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility. Br J Dermatol 2020;183(4):614–627. DOI: 10.1111/bjd.18921
4. 4. Has C, Liu L, Bolling MC, et al. Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosa. Br J Dermatol 2020;182(3):574–592. DOI: 10.1111/bjd.18128
5. 5. Fine JD. Epidemiology of inherited epidermolysis bullosa based on incidence and prevalence estimates from the National Epidermolysis Bullosa Registry. JAMA Dermatol 2016;152(11):1231–1238. DOI: 10.1001/jamadermatol.2016.2473
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