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Qutayba Hamid

Researcher at University of Sharjah

Publications -  585
Citations -  60271

Qutayba Hamid is an academic researcher from University of Sharjah. The author has contributed to research in topics: Cytokine & Eosinophil. The author has an hindex of 112, co-authored 557 publications receiving 55922 citations. Previous affiliations of Qutayba Hamid include King Saud University & Boston Children's Hospital.

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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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Predominant TH2-like bronchoalveolar T-lymphocyte population in atopic asthma

Douglas S. Robinson, +8 more
- 30 Jan 1992 - 
TL;DR: Atopic asthma is associated with activation in the bronchi of the interleukin-3, 4, and 5 and GM-CSF gene cluster, a pattern compatible with predominant activation of the TH2-like T-cell population.
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International ERS/ATS guidelines on definition, evaluation and treatment of severe asthma

Kian Fan Chung, +22 more
- 01 Feb 2014 - 
TL;DR: Recommendations and guidelines on the evaluation and treatment of severe asthma in children and adults and coordinated research efforts for improved phenotyping will provide safe and effective biomarker-driven approaches to severe asthma therapy are provided.
Journal ArticleDOI

New insights into atopic dermatitis

Donald Y.M. Leung, +4 more
- 01 Mar 2004 - 
TL;DR: This review summarizes recent progress in the understanding of the pathophysiology of atopic dermatitis and the implications for new management strategies.
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Long-Term Clinical Efficacy of Grass-Pollen Immunotherapy

Stephen R. Durham, +8 more
- 12 Aug 1999 - 
TL;DR: Althoughthere was a tendency for immediate sensitivity to allergen to return late after discontinuation, there was a sustained reduction in the late skin response and associated CD3+ T-cell infiltration and interleukin-4 messenger RNA expression.