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المؤلفAl Chalabi, Radi
المؤلفSherbash, Mohamed
المؤلفAl-Marri, Fahad
المؤلفIqneibi, Mariam
المؤلفJoy, Febu Elizabeth
المؤلفJochebeth, Anh
المؤلفAl-Khawaga, Sara
المؤلفBuddenkotte, Joerg
المؤلفSteinhoff, Martin
تاريخ الإتاحة2024-12-24T10:20:42Z
تاريخ النشر2024-04-23
اسم المنشورJournal of the European Academy of Dermatology and Venereology
المعرّفhttp://dx.doi.org/10.1111/jdv.20037
الاقتباسAl Chalabi, R., Sherbash, M., Al-Marri, F., Iqneibi, M., Joy, F. E., Jochebeth, A., ... & Steinhoff, M. (2024). Severe atopic dermatitis in an Asian-Arabic population treated with dupilumab: A retrospective observational study. Journal of the European Academy of Dermatology and Venereology: JEADV.
الرقم المعياري الدولي للكتاب0926-9959
معرّف المصادر الموحدhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85191192738&origin=inward
معرّف المصادر الموحدhttp://hdl.handle.net/10576/61993
الملخصAtopic dermatitis (AD) is a common, inflammatory skin disease characterized by a TH2-deviated immune response in the acute phase and a TH2/TH1/TH17/TH22-skewed immune response in the chronic phase1 associated with pruritus. Dupilumab, a therapeutic targeting IL-4, IL-13 signalling pathways2, 3 and the first biologic approved for the treatment of moderate-to-severe AD4 demonstrated substantial efficacy, minor side effects and good tolerability.2 Long term real-world studies investigating the efficacy, safety and tolerability of dupilumab in AD patients have been conducted mainly in Caucasians, Hispanic and southeast Asian populations but not Asian-Arabic descent population. To fill this gap, we investigated dupilumab in AD patients among Asian-Arabic population of Qatari descent.
راعي المشروعSupported by Internal Research Grand Competition (IRGC-04-SI-17-151) of the MRC fund, Hamad Medical Corporation, Qatar (to M.S. and J.B.).
اللغةen
الناشرJohn Wiley and Sons
الموضوعdupilumab
Atopic dermatitis
العنوانSevere atopic dermatitis in an Asian-Arabic population treated with dupilumab: A retrospective observational study
النوعOther
رقم العدد11
رقم المجلد38
ESSN1468-3083
dc.accessType Full Text


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