Results 121 to 130 of about 154,096 (287)

Multigene Next-Generation Sequencing Panel Identifies Pathogenic Variants in Patients with Unknown Subtype of Epidermolysis Bullosa: Subclassification with Prognostic Implications [PDF]

open access: yes, 2017
Purpose: Epidermolysis bullosa (EB), the prototype of heritable blistering diseases, is caused by mutations in as many as 19 distinct genes. In this study, we evaluated the molecular basis of EB in 93 families, many of them of unknown subtype. Methods:
Abiri, Maryam   +15 more
core   +1 more source

A Guide to Screening for Autoimmune Diseases in Patients With Vulvar Lichen Sclerosus

open access: yesAustralasian Journal of Dermatology, EarlyView.
ABSTRACTBackgroundThe aetiology of vulvar lichen sclerosus (VLS) remains unknown. However, there is evidence that in addition to a genetic predisposition, autoimmunity contributes to the pathogenesis.ObjectivesThe objective of this study was to determine the prevalence of autoimmune disease and positive autoantibody serology in patients with VLS ...
Annabel Guttentag   +5 more
wiley   +1 more source

Drug-induced anti-Ro positive subacute cutaneous lupus in a man treated with olmesartan [PDF]

open access: yes, 2019
A 66-year-old man presented to the outpatient dermatology clinic with a chief complaint of a pruritic rash on his upper trunk and proximal upper extremities, which had been present for three weeks.
Farsi, Maheera   +4 more
core  

Heterogeneous lupus‐specific lesions and treatment outcome, in a single patient, over a period of time [PDF]

open access: yes, 2019
The report highlights the importance of strict clinico-histological correlations when skin biopsies are performed in diagnostic doubt in systemic lupus erythematosus.
Agostini, Patrick   +5 more
core   +2 more sources

Erythematoviolaceous Papules and Plaques on Sun‐Exposed Areas

open access: yes
JEADV Clinical Practice, EarlyView.
Ana C. Martín‐Zamora   +3 more
wiley   +1 more source

Topical calcineurin inhibitors in systemic lupus erythematosus

open access: yesTherapeutics and Clinical Risk Management, 2010
Christos E Lampropoulos, David P D’CruzLupus Research Unit, Rayne Institute, St. Thomas’ Hospital, London, UKAbstract: Cutaneous lupus erythematosus (CLE) encompasses a variety of lesions that may be refractory to systemic or topical ...
Christos E Lampropoulos   +1 more
doaj  

Congenital and neonatal lupus erythematosus: two case reports Lúpus eritematoso congênito e neonatal: relato de dois casos

open access: yesAnais Brasileiros de Dermatologia, 2012
Neonatal lupus erythematosus is an autoimmune disease produced by the passage of maternal antinuclear antibodies and extractable nuclear antigen antibodies through the placenta. At the moment of the diagnosis, the mothers are asymptomatic in 40 to 60% of
Marcos Noronha Frey   +4 more
doaj   +1 more source

Visual Analytics of Group Differences in Tensor Fields: Application to Clinical DTI [PDF]

open access: yesarXiv, 2017
We present a visual analytics system for exploring group differences in tensor fields with respect to all six degrees of freedom that are inherent in symmetric second-order tensors. Our framework closely integrates quantitative analysis, based on multivariate hypothesis testing and spatial cluster enhancement, with suitable visualization tools that ...
arxiv  

Targeting the Galectin‐7/TRPM2/Zn2+/DRP‐1 Signaling Pathway: A Potential Therapeutic Intervention in the Pathogenesis of SJS/TEN

open access: yesAllergy, EarlyView.
This study investigates the role of mitochondrial fission in keratinocyte apoptosis in blister fluid‐derived exosomes from patients with SJS/TEN, erythema multiforme, and in healthy individuals. Galectin‐7 is upregulated in exosomes of patients with SJS/TEN and shows a correlation with disease severity.
Chen Zhang   +16 more
wiley   +1 more source

Rosacea in childhood and adolescence: A review

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Despite presenting with similar symptoms, triggers, and progression patterns as adults, rosacea in children and adolescents is frequently overlooked as a primary differential diagnosis. However, initial manifestations of classic clinical types can be observed from infancy onwards.
Sören Korsing   +4 more
wiley   +1 more source

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