Journal of Cellular and Molecular Medicine, Volume 29, Issue 14, July 2025.ABSTRACT Skin fibrosis in scleroderma is a chronic and debilitating condition that affects the quality of life of patients. In this study, we fabricated a niosomal hydrogel containing bromelain to reduce skin collagen and improve skin softness in scleroderma patients.
Hanieh Ardeshiri +5 more
wiley +1 more source
Dystrophic Calcinosis in a Patient with Scleroderma: Imaging Findings and Literature Review
Journal of Mazandaran University of Medical Sciences, 2020 Subcutaneous calcinosis consists of abnormal calcium deposition in soft tissues and is one of the complications of scleroderma, especially in limited systemic sclerosis.
Maryam Mobini +2 more
doaj
A Unique Presentation of Anti-RNA Polymerase III Positive Systemic Sclerosis Sine Scleroderma
Case Reports in Rheumatology, 2016 Systemic sclerosis is a rare autoimmune disorder with a wide spectrum of clinical manifestations and a multitude of autoantibodies that are associated with it.
Cody M. Lee +4 more
doaj +1 more source
Third Brazilian consensus for autoantibodies screening in HEp-2 cells (ANA) : recommendations for standardization of autoantibodies screening trial in HEp-2 cells, quality control and clinical associations [PDF]
, 2009 Objetivo: O 3º Consenso Brasileiro para pesquisa de autoanticorpos em Células HEp-2 (FAN) teve como propósito avaliar as dificuldades de implantação do 2º Consenso ocorrido no ano de 2002, discutir estratégias para controlar a qualidade do ensaio e ...
Andrade, Luis Eduardo Coelho +33 more
core +3 more sources
Arthritis &Rheumatology, Volume 77, Issue 6, Page 740-749, June 2025.Objective Little is known on the mechanisms necessary to maintain the physiologic adult human skin integrity. This study aims to quantitatively describe anatomic changes in systemic sclerosis (SSc)–skin compared with controls and investigate the underlying mechanisms.
Sara Chenguiti Fakhouri +18 more
wiley +1 more source
Paraneoplastic sclerodermiform syndrome--case report. [PDF]
, 2014 Occasionally, auto-immune diseases may emerge as paraneoplastic syndromes. This is especially recognized in the case of polymyositis/dermatomyostis, but it is an extremely rare event in systemic sclerosis (SSc).
Abreu, P +6 more
core
Peripheral blood natural killer cell percentages in granulomatosis with polyangiitis correlate with disease inactivity and stage [PDF]
, 2015 Introduction: The role of CD3−CD56+ natural killer (NK) cells in granulomatosis with polyangiitis (GPA) is poorly understood. Recently, it has been shown that peripheral blood NK cells can kill renal microvascular endothelial cells, suggesting a ...
Blank, Norbert +10 more
core +1 more source
Arthritis &Rheumatology, Volume 77, Issue 5, Page 506-520, May 2025.Clinical tools that can aid in the diagnostic differentiation of juvenile dermatomyositis from muscular dystrophy.
Jacqueline A. Madison +9 more
wiley +1 more source
Huriez syndrome with superadded dermatophyte infection
Indian Dermatology Online Journal, 2016 Palmoplantarkeratodermas (PPKs) are a heterogeneous group of hereditary and acquired disorders with underlying gene defects, and characterized by hyperkeratosis of palms and soles with or without other ectodermal and systemic abnormalities.
Trupti Surana +3 more
doaj +1 more source
Demographic associations for autoantibodies in disease-free individuals of a European population [PDF]
, 2016 The presence of autoantibodies usually precedes autoimmune disease, but is sometimes considered an incidental finding with no clinical relevance. The prevalence of immune-mediated diseases was studied in a group of individuals from the Estonian Genome ...
Alnek, Kristi +8 more
core +2 more sources