Results 281 to 290 of about 196,344 (323)
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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 ...
Edward Wasserman, William I. Glass
openaire +3 more sources
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 ...
Edward Wasserman, William I. Glass
openaire +3 more sources
Erythema multiforme, Stevens‐Johnson syndrome/toxic epidermal necrolysis – diagnosis and treatment
Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2020Prior 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
Journal of dermatological treatment (Print), 2020
Background: Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS-TEN) is one of severe cutaneous adverse reactions with low morbidity but high mortality.
Shan Zhang+4 more
semanticscholar +1 more source
Background: Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS-TEN) is one of severe cutaneous adverse reactions with low morbidity but high mortality.
Shan Zhang+4 more
semanticscholar +1 more source
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.
B G Bryant, B L Mathews
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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.
B G Bryant, B L Mathews
openaire +3 more sources
Journal of the European Academy of Dermatology and Venereology, 2020
The SCORTEN score is a specific predictor of mortality for patients with Stevens–Johnson syndrome (SJS)/toxic epidermal necrolysis (TEN). There is little evidence in support of the common immunomodulating therapies for SJS/TEN.
I. Torres-Navarro+3 more
semanticscholar +1 more source
The SCORTEN score is a specific predictor of mortality for patients with Stevens–Johnson syndrome (SJS)/toxic epidermal necrolysis (TEN). There is little evidence in support of the common immunomodulating therapies for SJS/TEN.
I. Torres-Navarro+3 more
semanticscholar +1 more source
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.
Jeffrey P. Callen, Joseph J. Chanda
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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.
Jeffrey P. Callen, Joseph J. Chanda
openaire +3 more sources
British Journal of Dermatology, 2020
Because of its rarity, the exact incidence of and mortality from epidermal necrolysis (Stevens–Johnson syndrome/toxic epidermal necrolysis) is difficult to establish and closely depends on the size and type of the data source.
G. Chaby+11 more
semanticscholar +1 more source
Because of its rarity, the exact incidence of and mortality from epidermal necrolysis (Stevens–Johnson syndrome/toxic epidermal necrolysis) is difficult to establish and closely depends on the size and type of the data source.
G. Chaby+11 more
semanticscholar +1 more source
International Journal of Dermatology, 2020
The use of checkpoint inhibitors for treatment of advanced malignancies is increasing. Rashes, pruritus, and more rarely, reactions resembling Stevens‐Johnsons syndrome (SJS) or toxic epidermal necrolysis (TEN) may occur secondary to checkpoint ...
N. Maloney+4 more
semanticscholar +1 more source
The use of checkpoint inhibitors for treatment of advanced malignancies is increasing. Rashes, pruritus, and more rarely, reactions resembling Stevens‐Johnsons syndrome (SJS) or toxic epidermal necrolysis (TEN) may occur secondary to checkpoint ...
N. Maloney+4 more
semanticscholar +1 more source
Pediatric dermatology, 2021
Stevens‐Johnson syndrome (SJS) and toxic epidermal necrolysis Syndrome (TEN) are rare immune‐mediated diseases. Extensive research on adult triggers of SJS and TEN is available; however, research in children is more limited.
Kristyna L Gleghorn+2 more
semanticscholar +1 more source
Stevens‐Johnson syndrome (SJS) and toxic epidermal necrolysis Syndrome (TEN) are rare immune‐mediated diseases. Extensive research on adult triggers of SJS and TEN is available; however, research in children is more limited.
Kristyna L Gleghorn+2 more
semanticscholar +1 more source