Results 41 to 50 of about 13,415 (150)
International Journal of Dermatology, EarlyView.ABSTRACT Despite increasing attention regarding skin diseases in individuals with skin of color (SoC), there remains a significant gap in understanding and identifying inflammatory nail disorders in this population. This systematic review aims to synthesize the clinical and onychoscopic features of inflammatory nail disorders in patients with SoC ...
Lea Tordjman +3 more
wiley +1 more source
Cutaneous Side Effects of PD‐1 Inhibitors: A Single‐Center Retrospective Study
International Journal of Dermatology, EarlyView.ABSTRACT Background The introduction of immune checkpoint inhibitors (ICIs) opened a new era in cancer immunotherapy. In particular, PD‐1 inhibitors have shown remarkable efficacy in various cancers, most notably melanoma. However, the widespread use of immune checkpoint inhibitors comes with the challenge of immune‐related adverse events (irAEs), with
Melánia Pozsgai +5 more
wiley +1 more source
Type 2 Inflammation and Its Role in Dermatologic Diseases
International Journal of Dermatology, EarlyView.ABSTRACT Atopic dermatitis, prurigo nodularis, and chronic spontaneous urticaria are immune‐mediated, inflammatory skin conditions characterized by intense itch and disease‐specific skin lesions. Despite their different clinical presentations, the three diseases are unified by an aberrant type 2 immune response involving type 2 cytokines, immune cells,
Raj Chovatiya +5 more
wiley +1 more source
World Journal of Pediatrics, 2009 Vitiligo is an acquired depigmentary disorder affecting around 1% of the world's population. In 25% of cases it has its onset prior to the age of 14 years.Articles on vitiligo in children published after 1995 were retrieved from PubMed. The prevalence, etiology, clinical presentation, differential diagnosis, treatment and management of vitiligo in ...
openaire +4 more sources
Dermatologic manifestations of hereditary hemochromatosis: A systematic review
Journal of the European Academy of Dermatology and Venereology, EarlyView.Abstract Hereditary hemochromatosis (HH) is a genetic disorder leading to excessive iron absorption, impacting multiple organs, notably the skin, nails and mucosae. The objective of this study is to elucidate the dermatologic manifestations, associated symptoms, pathophysiology and management recommendations of HH.
Hossein Akbarialiabad +3 more
wiley +1 more source
THE AETIOLOGY OF ALOPECIA AREATA AND ITS RELATIONSHIP TO VITILIGO AND POSSIBLY SCLERODERMIA* [PDF]
, 1929 Wade H. Brown
openalex +1 more source
Upadacinib for the Treatment of Refractory Morphea
Australasian Journal of Dermatology, EarlyView.
Vincenzo Maione +5 more
wiley +1 more source
Journal of the European Academy of Dermatology and Venereology, EarlyView.Background, key points, current state of management in dermato‐oncology centres and algorithm for standardized monitoring and management of ICIPI; *routine radiographic imaging according to respective guidelines; **3 months after routine radiographic staging (6‐monthly); ***if not recently performed as part of the routine staging.
M. Brandlmaier +14 more
wiley +1 more source