Results 101 to 110 of about 2,491,702 (230)

European S2k guidelines on management of autoimmune blistering diseases in children and adolescents

open access: yesJournal of the European Academy of Dermatology and Venereology, Volume 40, Issue 7, Page 1137-1161, July 2026.
Autoimmune blistering disorders (AIBDs) in children are rare, challenging to diagnose and treat and often require immunosuppressants. Until now, no paediatric care guidelines existed. The EADV Task Force for AIBDs has developed the consensus‐based recommendations, enabling physicians to adopt a uniform, tailored treatment strategy to improve outcomes ...
A. Nanda   +31 more
wiley   +1 more source

Liver Injury From Medications Used for Treating Inflammatory Bowel Disease: The Drug‐Induced Liver Injury Network Experience

open access: yesLiver International, Volume 46, Issue 7, July 2026.
ABSTRACT Background We aimed to investigate and characterise DILI due to approved therapies for inflammatory bowel disease (IBD). Methods Using the Drug‐Induced Liver Injury Network (DILIN) prospective study, we evaluated definite, highly likely, or probable DILI attributed to IBD therapies, including use for non‐IBD indications (but excluding ...
Harish Gopalakrishna   +9 more
wiley   +1 more source

Stevens-Johnson syndrome induced by phenytoin: a case report

open access: yes, 2016
Stevens-Johnson syndrome (SJS) and Toxic epidermal necrolysis (TEN) are rare (one to two per 10,00,00 population per year) but life threatening adverse drug reactions.
Bhanu, Lalkota Prakash   +4 more
core   +2 more sources

Toxic epidermal necrolysis and Stevens-Johnson syndrome

open access: yesOrphanet Journal of Rare Diseases, 2010
Toxic epidermal necrolysis (TEN) and Stevens Johnson Syndrome (SJS) are severe adverse cutaneous drug reactions that predominantly involve the skin and mucous membranes.
T. Harr, L. French
semanticscholar   +1 more source

Evaluation of conjunctival bacterial flora in patients with Stevens-Johnson Syndrome

open access: yesClinics, 2014
OBJECTIVE: To determine the conjunctival bacterial flora present in patients with Stevens-Johnson syndrome. METHODS: A prospective study of the conjunctival bacterial flora was performed in 41 eyes of 22 patients with Stevens-Johnson syndrome.
Luciana Frizon   +6 more
doaj   +1 more source

The Stevens-Johnson syndrome: a case report

open access: yes, 2012
Stevens-Johnson syndrome is a serious systemic disorder in which there are fever, vesicobullous lesions involving the skin and mucous membranes. It can result as an immune response to an antigen or as a drug reaction.
Kose, ŞÜKRAN   +2 more
core  

Chlordiazepoxide-induced Stevens-Johnson Syndrome

open access: yes, 2005
The causes of Stevens-Johnson syndrome (SJS) can be categorized as iatrogenic, infectious or idiopathic. Drug-induced SJS is associated with various antibiotics, anticonvulsants, and other drugs. However, no previous reports have mentioned an association
Huang, Po-Hsun, Tsai, Wei-Jen
core   +1 more source

Stevens Johnson Syndrome induced by a combination of lamotrigine and valproic acid in a patient with bipolar disorder: A case report

open access: yesPsychiatry and Clinical Psychopharmacology, 2021
Stevens Johnson syndrome is a severe and potentially lifethreatening cutaneous reaction associated with lamotrigine. The incidence of developing Steven- Johnson syndrome during lamotrigine therapy is low.
Uğur Öner, Julide Güler, Elif Yılmaz
doaj  

Stevens-Johnson syndrome with overlapping features of DRESS syndrome: A report of two cases

open access: yesSAGE Open Medical Case Reports
Stevens-Johnson syndrome and drug reaction with eosinophilia and systemic symptoms are severe cutaneous adverse reactions to drugs that are generally considered distinct entities.
Laura D Chin   +3 more
doaj   +2 more sources

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