Journal of the American Academy of Dermatology
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- Gale, Sciencedirect from 1979, Ovid from 2000, and Mdconsult from 1995
Cutaneous delayed-type hypersensitivity in patients with atopic dermatitis: Reactivity to surfactants.
We sought to assess whether atopic patients in our database were more likely than nonatopic patients to patch test positive to the surfactants cocamidopropyl betaine (CAPB) and cocamide diethanolamide (DEA), or to the surfactant precursor amidoamine. Between January 1, 2001, and the present, a total...
Unusual palatal ulceration associated with chronic vomiting.
Improvement of Darier disease with diclofenac sodium 3% gel.
Specific targeting of interleukin-23p19 as effective treatment for psoriasis.
Interleukin (IL)-23 is a heterodimeric cytokine composed of a distinct p19 subunit and a p40 subunit, which it shares with IL-12. The dermatology and rheumatology communities have long surmised that anti-IL-12/23p40 antibodies suppress autoinflammatory disease owing to their effect on IL-12. The aim...
Management of psoriasis vulgaris and multiple sclerosis with fumaric acid.
Primary cutaneous T-cell lymphoma (mycosis fungoides and Sézary syndrome): part II. Prognosis, management, and future directions.
Both mycosis fungoides (MF) and Sézary syndrome (SS) have a chronic, relapsing course, with patients frequently undergoing multiple, consecutive therapies. Treatment is aimed at the clearance of skin disease, the minimization of recurrence, the prevention of disease progression, and the preservation...
Primary cutaneous T-cell lymphoma (mycosis fungoides and Sézary syndrome): part I. Diagnosis: clinical and histopathologic features and new ...
Mycosis fungoides (MF) and Sézary syndrome (SS) comprise approximately 53% of cutaneous lymphomas. Both MF and SS may clinically and histologically mimic benign skin conditions, posing a diagnostic challenge to the dermatologist. Precise clinicopathologic correlation is necessary to support a diagno...
Successful therapeutic transplantation of revertant skin in epidermolysis bullosa.
We sought to locally treat EB by transplantation of revertant skin. Persistent ulcers in a patient with non-Herlitz junctional EB caused by mutations in the LAMB3 gene were treated by transplantation of split-thickness biopsy specimens from one of his revertant patches. All transplanted biopsy speci...
Extended eosinophilic pustular folliculitis with reactive bone marrow hypereosinophilia responsive to combined treatment with indomethacin, ...
Update on necrobiosis lipoidica: a review of etiology, diagnosis, and treatment options.
Necrobiosis lipoidica (NL) is a rare chronic granulomatous disease that has historically been associated with diabetes mellitus. Debate exists regarding the etiology and pathogenesis of NL with a widely accepted theory that microangiopathy plays a significant role. NL typically presents clinically a...