The molecular pathogenesis of morphoea: from genetics to future treatment targets

Author:

Saracino A.M.12,Denton C.P.23,Orteu C.H.1

Affiliation:

1. The Royal Free London NHS Foundation Trust; Department of Dermatology; London U.K

2. University College London; Centre for Rheumatology and Connective Tissue Diseases; Division of Medicine; London U.K

3. The Royal Free London NHS Foundation Trust; Department of Rheumatology; London U.K

Publisher

Wiley

Subject

Dermatology

Reference196 articles.

1. Major histocompatibility complex class I and class II alleles may confer susceptibility to or protection against morphea: findings from the Morphea in Adults and Children cohort;Jacobe;Arthritis Rheumatol,2014

2. Distinct autoimmune syndromes in morphea: a review of 245 adult and pediatric cases;Leitenberger;Arch Dermatol,2009

3. Familial linear scleroderma (en coup de sabre) responsive to antimalarials and narrowband ultraviolet B therapy;Brownell;Dermatol Online J,2007

4. Familial Parry-Romberg disease;Anderson;Int J Pediatr Otorhinolaryngol,2005

5. Juvenile localized scleroderma: clinical and epidemiological features in 750 children. An international study;Zulian;Rheumatology,2006

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