Results 131 to 140 of about 1,415,478 (254)
Ultrasonography, MRI and classic radiography of skin and MSK involvement in juvenile scleroderma
Journal of Ultrasonography, 2020 Scleroderma is a rare, autoimmune, chronic condition that affects the connective tissue by excessive collagen production. If diagnosed before the age of 16, it is referred to as juvenile scleroderma.
Idzior Marta +4 more
doaj +1 more source
Parry-Romberg Syndrome Associated with Localized Scleroderma
Case Reports in Neurology, 2010 Parry-Romberg syndrome is a rare neurocutaneous disorder of unknown origin. It is characterized by progressive facial hemiatrophy and frequently overlaps with a condition known as linear scleroderma ‘en coup de sabre’.
Jelena Maletic +4 more
doaj +1 more source
Journal of Rheumatology, 2019 Objective. To perform a comparative effectiveness feasibility study in juvenile localized scleroderma (LS), using standardized treatment regimens (consensus treatment plans; CTP). Methods.
Suzanne C. Li +14 more
semanticscholar +1 more source
Eosinophilic fasciitis: demographics, disease pattern and response to treatment: report of 12 cases and review of the literature [PDF]
, 2007 BACKGROUND: Eosinophilic fasciitis is a rare scleroderma-like illness. The clinical spectrum of the disease has evolved since its initial description. METHODS: We identified all patients diagnosed with eosinophilic fasciitis over the past 10 years at our
Bischoff, Lindsay, Derk, Chris T
core +2 more sources
A case of localized bullous scleroderma
Vestnik Dermatologii i Venerologii, 2017 Bullous scleroderma is a rare type of the focal form of the disease mainly affecting the skin and characterized by induration and sclerosis foci as well as subepidermal blisters containing a transparent matter.
A. L. Bakulev +3 more
doaj +1 more source
Successful Amplification of DNA Specific for Finnish Borrelia burgdorferi Isolates in Erythema Chronicum Migrans but Not in Circumscribed Scleroderma Lesions [PDF]
, 1994 Early diagnosis of Borrelia burgdorferi infection, hampered by the absence of detectable antibodies in most patients with erythema chronicum migrans is important to prevent late-stage neurologic, rheumatologic, and skin disorders.
Aavik, Einari +4 more
core +1 more source
Dermatology Review, 2019 Localized scleroderma (morphea) is a chronic autoimmune disease of the connective tissue. Its etiopathogenesis is unknown. Most often the disease affects the skin, but may also involve the subcutis, muscles, and the osteoarticular system.
D. Krasowska +10 more
semanticscholar +1 more source
Connective Tissue Growth Factor Causes Persistent Proα2(I) Collagen Gene Expression Induced by Transforming Growth Factor-β in a Mouse Fibrosis Model [PDF]
, 2004 Skin fibrotic disorders such as systemic sclerosis (SSc) are characterized by an excessive production of extracellular matrix (ECM) and understood to develop under the influence of certain growth factors.
Abreu +45 more
core +1 more source
How I explore ... the skin functional involvement in scleroderma [PDF]
, 2013 peer reviewedScleroderma refers to distinct clinical presentations sharing in common a sclerotic process most often clinically obvious on the skin. The involvement possibly affects the skin alone in morphea or in combination with internal lesions in ...
Andre, B. +6 more
core
Journal of Cosmetic Dermatology, Volume 24, Issue 5, May 2025.
Sofia Gomez‐Martinez +12 more
wiley +1 more source