Epidermolysis bullosa simplex generalized severe induces a T helper 17 response and is improved by apremilast treatment

Author:

Castela E.12,Tulic M.K.3,Rozières A.2,Bourrat E.4,Nicolas J.‐F.25,Kanitakis J.67,Vabres P.8,Bessis D.9ORCID,Mazereeuw J.10ORCID,Morice‐Picard F.11ORCID,Baty D.12,Berard F.5,Lacour J.‐P.113,Passeron T.13,Chiaverini C.113ORCID

Affiliation:

1. Department of Dermatology CHU de Nice Hôpital Archet 2, 151 Route de Saint Antoine de Ginestière, 06202 Nice CEDEX 2 France

2. INSERM U1111‐CIRI851, Université Lyon 1 Lyon France

3. INSERM U1065 Team 12 C3M Nice France

4. MAGEC, Saint‐Louis Hospital Paris France

5. Department of Allergology and Clinical Immunology Hospices Civils de Lyon LyonFrance

6. Department of Dermatology Hospices Civils de Lyon LyonFrance

7. Department of Pathology Hospices Civils de Lyon Lyon France

8. Department of Dermatology CHU de Dijon Dijon France

9. Department of Dermatology CHU de Montpellier Montpellier France

10. CRMRP CHU de Toulouse Toulouse France

11. CRMRP CHU de Bordeaux Bordeaux France

12. Scottish Molecular Genetics Consortium Ninewells Hospital Dundee U.K

13. CREBHN CHU de Nice Nice France

Funder

Dystrophic Epidermolysis Bullosa Research Association of America

Chung Hua University

Publisher

Wiley

Subject

Dermatology

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1. Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives;International Journal of Molecular Sciences;2024-08-31

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. Systematic review on antipruritic therapies for patients with Epidermolysis bullosa;Journal of Dermatological Treatment;2024-07-28

5. Paediatrics and genetics;Clinical and Experimental Dermatology;2024-04-04

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