Results 91 to 100 of about 1,428,643 (254)
Rheumatology, 2020 OBJECTIVE SSc and localized sclerosis (LoS) are considered clinically distinct entities. We describe herein the coexistence of SSc and LoS by both a systematic literature review and an observational cohort study of unselected SSc patients.
A. Vanhaecke +8 more
semanticscholar +1 more source
Capillaroscopy in 2016 : new perspectives in systemic sclerosis [PDF]
, 2016 Systemic sclerosis (SSc) is an autoimmune disorder of unknown etiology characterized by early impairment of the microvascular system. Nailfold microangiopathy and decreased peripheral blood perfusion are typical clinical aspects of SSc.
Cutolo, M +6 more
core +1 more source
Acquired Strabismus in Linear Scleroderma of the Face
Acta Dermato-Venereologica, 2019 is missing (Short communication)
Giorgia Martini +4 more
doaj +1 more source
Pansclerotic Morphea with Features of Eosinophilic Fasciitis: Distinct Entities or Part of a Continuum? [PDF]
, 2014 Scleroderma is a highly complex disorder in its clinical manifestations and pathogenesis. It has a wide range of clinical manifestations due to varying degrees of vasculopathy, autoimmunity, altered endothelium function, and abnormal fibrosis.
Canty, Kristi +2 more
core +1 more source
Transplant Infectious Disease, EarlyView.A novel regimen of sulfamethoxazole/trimethoprim single strength one tablet twice weekly for Pneumocystis jiroveci Pneumonia (PJP) prophylaxis in lung transplant patients found no cases of PJP over an 8‐year period and may reduce the incidence of medication discontinuation due to adverse effects. ABSTRACT Background Pneumocystis jiroveci pneumonia (PJP)
Chloe Munroe +8 more
wiley +1 more source
Experimental Dermatology, 2020 Ultraviolet A1 (UVA1) phototherapy (spectral range 340‐400 nm) is a well‐established treatment option for various skin diseases such as localized scleroderma. Recent improvements of conventional UVA1 light sources (metal‐halide or fluorescent lamps) have
S. Arndt +5 more
semanticscholar +1 more source
Parry Romberg Syndrome with localized scleroderma: a case report [PDF]
, 2014 Parry Romberg syndrome(PRS) is a rare acquired poorly understood neurocutaneous syndrome of unknown etiology characterized by slow progressive atrophic changes commonly affecting one half of the face. The exact incidence and etiology towards the syndrome
Gupta, Nikita +3 more
core +1 more source
DEN Open, Volume 6, Issue 1, April 2026.ABSTRACT Barium sulfate is widely used as a radiographic contrast medium in upper gastrointestinal barium X‐ray radiography for cancer screening in Japan. Although generally considered safe, rare complications such as bowel obstruction due to impacted barium stools can occur.
Takaaki Kishino +2 more
wiley +1 more source
Recent Advances in Systemic Scleroderma in Childhood [PDF]
, 2015 Ann Paediatr Rheumatol Annals of paediatric rheumatolog http://www.aprjournal.org/ 2146-2909 ...
Constantin, Tamás +4 more
core +1 more source
Apoptotic Bodies Restore NAD and Mitochondrial Homeostasis in Fibroblasts
Advanced Science, Volume 12, Issue 29, August 7, 2025.Mesenchymal stem cell‐derived apoptotic bodies (MSC‐ABs) target keloid fibroblasts (KFs), restoring nicotinamide adenine dinucleotide (NAD) metabolism and mitochondrial function, suppressing collagen overproduction, and rebalancing tissue homeostasis, offering a novel therapy for keloid.
Shutong Qian +10 more
wiley +1 more source