Results 221 to 230 of about 128,263 (274)
Some of the next articles are maybe not open access.

Stevens-Johnson Syndrome

Drug Intelligence & Clinical Pharmacy, 1986
Stevens-Johnson syndrome (SJS) is an acute inflammatory eruption of the skin and mucous membranes. Presented here is a case of an 18-month-old child admitted to the hospital with raised erythematous rash with some vesicular formation. The rash and associated symptomatology developed in a manner consistent with SJS. The child was treated for 27 days and
B G, Bryant, B L, Mathews
openaire   +2 more sources

Lid margin keratinization in Stevens-Johnson syndrome: Review of pathophysiology and histopathology.

The ocular surface, 2021
Lid margin keratinization (LMK) is a chronic ocular sequela of Stevens-Johnson syndrome (SJS), which causes lid wiper epitheliopathy and progressive ocular surface damage. The exact etiopathogenesis of LMK, however, remains elusive.
Swati Singh   +5 more
semanticscholar   +1 more source

Stevens-Johnson Syndrome

Archives of Dermatology, 1978
To the Editor.— With regards to the brief report, "Permanent Anonychia After Stevens-Johnson Syndrome," in the JulyArchives(113:970, 1977), the authors state that nothing has been written about nail changes in the Stevens-Johnson syndrome. This is not the case.
J J, Chanda, J P, Callen
openaire   +2 more sources

Stevens-Johnson Syndrome

Archives of Internal Medicine, 1959
This syndrome is characterized by a variation in skin reaction, involvement of the mucous membranes, severe ophthalmia, and a marked general reaction. Stevens and Johnson, in 1922,1described two cases of dramatic onset with fever, conjunctivitis, and a cutaneous eruption, which thereafter has been known as Stevens-Johnson syndrome, or erythema ...
E, WASSERMAN, W I, GLASS
openaire   +2 more sources

Interleukin-15 Is Associated with Severity and Mortality in Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis

open access: yesJournal of Investigative Dermatology, 2017
Shih-Chi Su   +2 more
exaly   +2 more sources

Update on Stevens–Johnson Syndrome and Toxic Epidermal Necrolysis: Diagnosis and Management

American Journal of Clinical Dermatology
Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are the most severe cutaneous adverse reactions that are typically drug-induced in adults. Both SJS and TEN have high morbidity and mortality rates.
Hemali Shah   +4 more
semanticscholar   +1 more source

Stevens–Johnson syndrome in children

Current Opinion in Pediatrics, 2022
Purpose of review The concept of Stevens–Johnson syndrome (SJS) in children is evolving. This manuscript reviews recent advances with the lens of new terminology namely infection-triggered reactive infectious mucocutaneous eruption and drug-induced epidermal necrolysis, with the objective of integrating this novel terminology ...
openaire   +2 more sources

Lamotrigine and Stevens-Johnson Syndrome Prevention.

Psychopharmacology bulletin, 2021
Stevens-Johnson Syndrome (SJS) is a rare life-threatening condition characterized by severe mucocutaneous epidermal necrolysis and detachment of the epidermis.
Amber N. Edinoff   +13 more
semanticscholar   +1 more source

Erythema multiforme, Stevens‐Johnson syndrome/toxic epidermal necrolysis – diagnosis and treatment

Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2020
Prior to the first international consensus classification published in 1993, the clinical distinction between erythema multiforme (EM), Stevens‐Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) had been subject to uncertainty and controversy ...
P. Grünwald   +3 more
semanticscholar   +1 more source

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