Results 131 to 140 of about 11,119 (206)
Radiology‐Dermatology Diagnostic Variation in Skin and Soft Tissue Infections: A Cohort Analysis
International Journal of Dermatology, EarlyView.
Varshita Chirumamilla +5 more
wiley +1 more source
Genomic and proteomic insights into hidradenitis suppurativa
A dual pathogenic model of HS involving both epithelial dysfunction and systemic inflammation is supported. The HLA‐DRA association hints at autoimmune overlap, but the proteomic signature which is dominated by innate immune mediators favours an autoinflammatory classification, which may guide future therapeutic strategies and patient stratification ...
Maria Argyropoulou +8 more
wiley +1 more source
Rodrigo Fedatto Beraldo,1 Mariana Barros Marcondes,1 Julio Pinheiro Baima,1 Jaqueline Ribeiro Barros,1 Madhoor Ramdeen,2 Rogerio Saad-Hossne,3 Ligia Yukie Sassaki1 1Department of Internal Medicine, São Paulo State University (Unesp), Medical ...
Beraldo RF +6 more
doaj
OX40/OX40L modulation: A target for regulating T cells in cutaneous inflammatory disorders
OX40 and OX40L are a co‐stimulatory immune checkpoint pair. Modulation of this pair impacts multiple immune phenotypes and is an attractive target for immunotherapy in dermatological disorders. Trials are underway with the majority in atopic dermatitis and currently in phase 3 trials.
Aditya K. Gupta +4 more
wiley +1 more source
Prescribing Patterns in Pediatric Hidradenitis Suppurativa
ABSTRACT Hidradenitis suppurativa (HS) is an inflammatory skin condition increasingly diagnosed in pediatric populations; however, data on treatment practices in this group remains limited. In this retrospective study of 163 patients diagnosed with HS ≤ 18 years of age, we found that treatment patterns varied significantly by disease severity.
Hannah Neimy +3 more
wiley +1 more source
A protocol for a randomized controlled trial for assessing the efficacy and safety of tratments in hidradenitis [PDF]
Δαλαμπούρα, Δέσποινα
core +1 more source
Familial Alzheimer's Disease Mutations in Presenilin Generate Amyloidogenic Ab Peptide Seeds [PDF]
Recently it was proposed that the familial Alzheimer’s disease (FAD) causing presenilin (PSEN) mutations PSEN1-L435F and PSEN1-C410Y do not support the generation of Aβ-peptides from the amyloid precursor protein (APP).
Chavez-Gutierrez, L +4 more
core
Racial Differences in Dermatologic Treatment for Adolescents With PCOS‐Related Acne Vulgaris
ABSTRACT Background/Objectives Polycystic ovary syndrome (PCOS) is a common endocrine disorder in women, with acne frequently appearing during adolescence. Racial and ethnic disparities in PCOS phenotype and adult acne treatment are well documented, yet differences in acne management among adolescents with PCOS remain unclear.
Samantha Garcia, Brandi Kenner‐Bell
wiley +1 more source
Setmelanotide in Bardet‐Biedl Syndrome: A Case Report
ABSTRACT Setmelanotide is a melanocortin‐4‐receptor agonist used for the treatment of hyperphagia in the genetic obesity syndrome Bardet‐Biedl. Presented is a case of diffuse hyperpigmentation in a patient treated with setmelanotide, which represents the most common side effect of this medication.
Shelby Smith +2 more
wiley +1 more source

