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Stevens-Johnson-Syndrom

Klinische Wochenschrift, 1947
Es wird uber einen Fall vonStevens-Johnson-Syndrom mit wochenlangem hohen Fieber, typischem vesicularen Exanthem, blaschenformiger Conjunctivitis und leichter Stomatitis berichtet, der sekundar durch ein Erythema nodosum mit spezifischen Lungen- und Pleuraveranderungen kompliziert wurde.
openaire   +2 more sources

Clinical features, outcomes and treatment in children with drug induced Stevens-Johnson syndrome and toxic epidermal necrolysis

Acta bio-medica : Atenei Parmensis, 2019
Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN), which can be considered a late-onset allergic reaction, can cause serious long-term sequelae. SJS/TEN are considered a spectrum of life-threatening adverse drug reactions. They have the
Liotti Lucia   +9 more
semanticscholar   +1 more source

Incidence of and mortality from epidermal necrolysis (Stevens–Johnson syndrome/toxic epidermal necrolysis) in France during 2003–16: a four‐source capture–recapture estimate

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

Stevens‐Johnson syndrome and toxic epidermal necrolysis‐like reactions to checkpoint inhibitors: a systematic review

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

Retrospective review of drug‐induced Stevens‐Johnson syndrome and toxic epidermal necrolysis cases at a pediatric tertiary care institution

Pediatric dermatology, 2020
Stevens‐Johnson syndrome and toxic epidermal necrolysis represent important sources of potential mortality and morbidity in children. There is a need for more clinical data in this population to determine whether specific treatments preferentially ...
C. Sibbald   +4 more
semanticscholar   +1 more source

Stevens-Johnson Syndrome

JAMA, 1967
THE CLINICAL manifestations of Stevens-Johnson syndrome (erythema multiforme exudativum) were frequently observed in the dermatology and dental services at the US Naval Hospital, Great Lakes, Ill, during the late summer and fall of 1965. The apparently increased incidence of this syndrome prompted clinical as well as laboratory investigations.
openaire   +1 more source

[Stevens-Johnson syndrome].

Algerie medicale, 2002
Stevens-Johnson Syndrome (SJS), or erythema multiforme, is a severe, acute, adverse, cutaneous reaction to certain medications, such as phenytoin and topical nitrogen mustard. The risk of developing SJS is high when phenytoin and steroids are administered during cranial irradiation.
A, Fourrier   +5 more
openaire   +3 more sources

Late-onset Stevens–Johnson syndrome due to nivolumab use for hepatocellular carcinoma

Journal of Oncology Pharmacy Practice, 2019
Nivolumab is a fully human immunoglobulin G4 immune checkpoint inhibitor antibody approved for use in the treatment of several malignancies. Severe side effects such as Stevens–Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) have only extremely ...
C. Dasanu
semanticscholar   +1 more source

Clinical classification of cases of toxic epidermal necrolysis, Stevens-Johnson syndrome, and erythema multiforme.

Archives of Dermatology, 1993
S. Bastuji‐Garin   +5 more
semanticscholar   +1 more source

Current Perspectives on Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis

Clinical reviews in allergy and immunology, 2018
M. Lerch   +3 more
semanticscholar   +1 more source

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