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1 was sporadically positive in a patient with Stevens-Johnson syndrome.
2 ocular cicatricial pemphigoid>chemical burns>Stevens-Johnson syndrome.
3 dication, should be screened for symptoms of Stevens-Johnson syndrome.
4 rane grafting due to intense inflammation in Stevens-Johnson syndrome.
5 aplasia on amniotic membrane associated with Stevens-Johnson syndrome.
6 ctival squamous metaplasia in a patient with Stevens-Johnson syndrome.
11 ty and HLA-B*57:01 and carbamazepine-induced Stevens-Johnson syndrome and HLA-B*15:02 have been imple
12 oat (ENT) lesions are frequently involved in Stevens-Johnson syndrome and toxic epidermal necrolysis
15 wn to be associated with allopurinol-induced Stevens-Johnson syndrome and toxic epidermal necrolysis
20 h an increased risk of carbamazepine-induced Stevens-Johnson syndrome and toxic epidermal necrolysis
22 ous adverse reactions (SCARs), which include Stevens-Johnson syndrome and toxic epidermal necrolysis,
23 erum levels and the outcome of patients with Stevens-Johnson syndrome and toxic epidermal necrolysis.
24 valuated for the life-threatening dermatoses Stevens-Johnson syndrome and toxic epidermal necrolysis.
25 ion between enfortumab vedotin treatment and Stevens-Johnson Syndrome and toxic epidermal necrolysis.
26 ne triage system for patients with suspected Stevens-Johnson syndrome and toxic epidermal necrolysis.
27 mmune mechanisms in the pathogenesis of both Stevens-Johnson syndrome and vanishing bile duct syndrom
28 oration, malignant neoplasm progression, and Stevens-Johnson syndrome) and two patients treated with
29 keratopathy, lattice and Avellino dystrophy, Stevens-Johnson syndrome, and chemical/thermal injury.
30 nditions such as toxic epidermal necrolysis, Stevens-Johnson syndrome, and hypersensitivity syndrome.
31 are bilaterally blind from diseases such as Stevens-Johnson syndrome, and ocular pemphigoid have lit
32 lated syndromes such as erythema multiforme, Stevens-Johnson syndrome, and toxic epidermal necrolysis
33 mediated, or type I, reactions, anaphylaxis, Stevens-Johnson syndrome, and toxic epidermal necrolysis
34 disorders such as graft-versus-host disease, Stevens-Johnson syndrome, and toxic epidermal necrolysis
35 approximately 1 month (erythema multiforme, Stevens-Johnson syndrome, and toxic epidermal necrolysis
37 iform, granulomatous, erythema multiforme or Stevens Johnson Syndrome, drug rash with eosinophilia an
38 iously to corneal diseases, astigmatism, and Stevens-Johnson syndrome fall within corneal epithelial
39 toxic epidermal necrolysis (IC(025) = 0.95), Stevens-Johnson syndrome (IC(025) = 0.41), drug eruption
40 The most common indications for surgery were Stevens-Johnson syndrome in 41.7% (20 of 48 eyes) and mu
42 though, it is not clear whether the cause of Stevens-Johnson syndrome in COVID-19 patients is the vir
44 e vanishing bile duct syndrome shortly after Stevens-Johnson syndrome is described; this was temporal
45 tric oxide in toxic epidermal necrolysis and Stevens-Johnson syndrome may cause the epidermal apoptos
46 with other preoperative diagnoses (excluding Stevens-Johnson syndrome, mucous membrane pemphigoid, an
47 cause, neutropenic sepsis, myocarditis, and Stevens-Johnson syndrome); myocarditis and Stevens-Johns
49 patients with bronchiolitis obliterans from Stevens-Johnson syndrome often have progressive disease
50 Better BCVA outcomes were observed in the Stevens-Johnson syndrome or toxic epidermal necrolysis (
51 rom seven patients with actively progressing Stevens-Johnson syndrome or toxic epidermal necrolysis.
52 ing the keywords toxic epidermal necrolysis, Stevens-Johnson syndrome, photo-distributed, photo-induc
56 utaneous adverse reactions (SCAR), including Stevens-Johnson syndrome (SJS) and toxic epidermal necro
57 notypes, including the blistering conditions Stevens-Johnson syndrome (SJS) and toxic epidermal necro
58 nce of a relationship between HLA-B*1502 and Stevens-Johnson syndrome (SJS) and toxic epidermal necro
60 severe to life-threatening reactions such as Stevens-Johnson syndrome (SJS) and toxic epidermal necro
65 ence of epidermal necrolysis (EN), including Stevens-Johnson syndrome (SJS) and toxic epidermal necro
67 ffective ophthalmologic treatments for acute Stevens-Johnson syndrome (SJS) as well as the emerging t
71 tion of drug-induced liver injury (DILI) and Stevens-Johnson syndrome (SJS) or toxic epidermal necros
73 vity reactions (DHR) induced by PPI, such as Stevens-Johnson syndrome (SJS), toxic epidermal necrolys
74 tively analyzed 74 cases of SCARs, including Stevens-Johnson syndrome (SJS), toxic epidermal necrolys
76 rane transplantation (AMT) for severe ocular Stevens-Johnson Syndrome (SJS), toxic epidermal necrolys
77 e the case of a 7-year-old male patient with Stevens-Johnson syndrome (SJS), which was suspected to b
79 redisposition to carbamazepine (CBZ)-induced Stevens-Johnson syndrome (SJS)/toxic epidermal necrolysi
80 nced a mucocutaneous reaction described as a Stevens-Johnson syndrome that was attributed to chemothe
81 cutaneous adverse reactions (SCARs) such as Stevens-Johnson syndrome, toxic epidermal necrolysis (SJ
82 a severe complicated adverse event of either Stevens-Johnson syndrome, toxic epidermal necrolysis, or
83 e cutaneous adverse reaction (SCAR), such as Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS
86 volved in the ocular complications following Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS
87 genesis of severe systemic forms of disease, Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS
89 nical ventilation is required in one of four Stevens-Johnson syndrome/toxic epidermal necrolysis pati
93 sinophilia and systemic symptoms, and 7 with Stevens-Johnson syndrome/toxic epidermal necrolysis).
94 R were included, including 236 patients with Stevens-Johnson syndrome/toxic epidermal necrolysis, 86
95 nophilia and systemic symptoms syndrome, and Stevens-Johnson syndrome/toxic epidermal necrolysis, can
96 dence of various nail changes as sequalae to Stevens-Johnson syndrome/toxic epidermal necrolysis.
98 d Stevens-Johnson syndrome); myocarditis and Stevens-Johnson syndrome were considered related to pemb