Losartan as therapy for recessive dystrophic epidermolysis bullosa: Report of three cases
Author:
Affiliation:
1. Dermatology Department Coimbra University Hospital Centre Coimbra Portugal
Publisher
Hindawi Limited
Subject
Dermatology,General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/dth.15678
Reference9 articles.
1. Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility
2. Extracutaneous manifestations and complications of inherited epidermolysis bullosa
3. Losartan for treatment of epidermolysis bullosa: A new perspective
4. Losartan ameliorates dystrophic epidermolysis bullosa and uncovers new disease mechanisms
5. Medical Center – University of Freiburg.A dual‐center prospective phase I/II trial to establish safety tolerability and to obtain first data on efficacy of losartan in children with recessive dystrophic epidermolysis bullosa (RDEB). EudraCT Identifier: 2015‐003670‐32.
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1. Skin matrix meets immunomatrix—Implications for genetic and acquired diseases;JEADV Clinical Practice;2024-08-21
2. Treatment of Epidermolysis Bullosa and Future Directions: A Review;Dermatology and Therapy;2024-08
3. Epidermolysis Bullosa: A Review of Wound Care and Emerging Treatments;Current Dermatology Reports;2024-07-30
4. Innovations in the Treatment of Dystrophic Epidermolysis Bullosa (DEB): Current Landscape and Prospects;Therapeutics and Clinical Risk Management;2023-06
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