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Latin American guidelines for the diagnosis and treatment of Stevens-Johnson syndrome and toxic epidermal necrolysis. [PDF]

open access: yesWorld Allergy Organ J
Murillo-Casas AD   +12 more
europepmc   +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
  +7 more sources

Stevens-Johnson syndrome

European Journal of Pediatrics, 2007
A 13-year-old boy was brought to the emergency department (ED) with a generalized itchy rash of 2 days' duration. For the past 3 days, he had dry, itchy eyes with a purulent discharge (Figure 1) and nonbilious emesis 2 or 3 times per day, with some blood streaks in the vomitus on the third day of illness.
M H, de Ru, R N, Sukhai
openaire   +2 more sources

Stevens–Johnson syndrome

Internal and Emergency Medicine, 2018
Stevens–Johnson syndrome is a rare, yet life-threatening, delayed-type hypersensitivity reaction characterized by mucocutaneous epidermal necrolysis. Toxic epidermal necrolysis is a severe manifestation of Stevens–Johnson syndrome, defined as greater than 30% skin detachment.
Wesley D, Davis, Phillip A, Schafer
openaire   +4 more sources

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