Results 51 to 60 of about 3,018 (196)

Эритодермическая форма красного волосяного лишая [PDF]

open access: yes, 2016
ПИТИРИАЗ КРАСНЫЙ ВОЛОСЯНОЙ /диагнлишай красный волосянойЭРИТЕМАКОЖНЫЕ БОЛЕЗНИ ПАПУЛЕЗНО-ЧЕШУЙЧАТЫЕ ...
Адаскевич, В. П.   +1 more
core   +2 more sources

Pityriasis rubra pilaris (Devergie's disease): clinical case [PDF]

open access: yesСаратовский научно-медицинский журнал, 2016
Pityriasis rubra pilaris (Devergie's disease) is a rare chronic papulosquamous skin disease, it is of unknown etiology, leading to palmoplantar keratoderma, erythroderma and ectropion. Due to its rarity and difficulty in differentiating it with psoriasis,
Galkina ЕМ   +3 more
doaj  

Dermatology 2.0: Precision medicine for inflammatory skin diseases

open access: yesJournal of the European Academy of Dermatology and Venereology, Volume 40, Issue 3, Page 440-445, March 2026.
Digital immune mapping of transcriptomics profiles from inflammatory skin disease biopsies enables precise molecular diagnosis, quantification of immune modules and personalized therapy selection by matching dominant immune signatures to targeted treatments.
Jeremy Di Domizio   +4 more
wiley   +1 more source

Eritrodermie: între limfom cutanat și pityriasis rubra pilaris [PDF]

open access: yes, 2022
Background. Erythroderma is defined as generalized erythema, which involves more than 90% of the skin surface. The most common causes are considered to be: psoriasis, post-drug allergic reactions, lymphoma/leukemia, atopic dermatitis, pityriasis rubra ...
Bețiu, Mircea   +5 more
core  

Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management

open access: yesDermatologic Therapy, Volume 2026, Issue 1, 2026.
Folliculotropic mycosis fungoides (FMF) is a rare subtype of MF, characterized by prominent folliculotropism in histopathology. Clinically, FMF exhibits polymorphic presentations, mainly including follicular papules, plaques, alopecia, and other nonspecific lesions, with a predilection for the head and neck region, leading to frequent misdiagnosis ...
Xingyu Li, Jie Liu, Nicola Pimpinelli
wiley   +1 more source

Review of Biological Agents in the Therapeutic Management of Monogenic Genodermatoses

open access: yesDermatologic Therapy, Volume 2026, Issue 1, 2026.
Monogenic genodermatoses encompass a diverse group of over 400 distinct disorders, presenting significant therapeutic challenges. Recent advancements in the clinical application of biological agents have heralded a new era in the management of these conditions.
Xueying Wang   +4 more
wiley   +1 more source

Body image and mental health in chronic skin conditions: A psychosomatic perspective from a systematic review

open access: yesApplied Psychology: Health and Well-Being, Volume 17, Issue 6, December 2025.
Abstract This systematic review aimed to consolidate evidence regarding the effect of skin diseases (SD) on body image (BI) and to examine the sociodemographic, clinical, and psychosocial correlates of BI in individuals with SD. A comprehensive search was conducted in December 2024 across nine databases, including MEDLINE, Web of Knowledge, PsycINFO ...
Tatiane Fidelis   +3 more
wiley   +1 more source

Histopathological spectrum of non-infectious erythematous, papulo-squamous lesions: at a teritary care institute [PDF]

open access: yes, 2018
Background: Dermatologic disorders are common in many countries, but the spectrum varies greatly. Papulosquamous lesions of the skin are encountered with considerable frequency. There is overlap of both clinical pattern and distribution of papulosquamous
Agrawal, Sonal   +2 more
core   +2 more sources

Classical Juvenile Pityriasis Rubra Pilaris Treated With Secukinumab: Case Report and a Review of Biological Treatments in the Pediatric Population

open access: yesPediatric Dermatology, Volume 42, Issue 6, Page 1214-1220, November/December 2025.
ABSTRACT Pityriasis rubra pilaris (PRP) is a rare, chronic papulosquamous disorder with limited treatment options in pediatric patients. We report the case of a 9‐year‐old boy with juvenile PRP (type III), who achieved complete disease remission after treatment with secukinumab, an IL‐17A inhibitor, following initial therapeutic resistance to topical ...
Zeno Fratton   +2 more
wiley   +1 more source

The phenotypic and genotypic spectra of ichthyosis with confetti plus novel genetic variation in the 3' end of KRT10: from disease to a syndrome [PDF]

open access: yes, 2015
Ichthyosis with confetti (IWC) is a genodermatosis caused by dominant negative mutations in the gene encoding keratin 10 (KRT10). We investigated clinical and genetic details of a substantial number of patients with IWC in order to define major and minor
Brena, Michela   +7 more
core   +1 more source

Home - About - Disclaimer - Privacy