Zobrazeno 1 - 10
of 507
pro vyhledávání: '"Krishnaswamy Guha"'
Publikováno v:
In Annals of Allergy, Asthma & Immunology October 2024
Publikováno v:
Clinical and Molecular Allergy, Vol 10, Iss 1, p 5 (2012)
Abstract Objective While most allergic responses to food are directed against protein epitopes and occur within 30 minutes of ingesting the allergen, recent studies suggest that delayed reactions may occur, sometimes mediated by IgE antibodies direct
Externí odkaz:
https://doaj.org/article/69ef2fd74f1d4ee69bbe73c218f50de5
Autor:
Chi David S, Lin Ta-Chang, Hall Kenton, Ha Tuanzhu, Li Chuanfu, Wu Zong, Soike Thomas, Krishnaswamy Guha
Publikováno v:
Clinical and Molecular Allergy, Vol 10, Iss 1, p 3 (2012)
Abstract Background Human mast cells are capable of a wide variety of inflammatory responses and play a vital role in the pathogenesis of inflammatory diseases such as allergy, asthma, and atherosclerosis. We have reported that cigarette smoke extrac
Externí odkaz:
https://doaj.org/article/b49c6709f6a24ec9afffaf25bd4d334d
Autor:
Watkins Casey E, Litchfield John, Song Eunkyung, Jaishankar Gayatri B, Misra Niva, Holla Nikhil, Duffourc Michelle, Krishnaswamy Guha
Publikováno v:
Clinical and Molecular Allergy, Vol 9, Iss 1, p 13 (2011)
Abstract Chronic Granulomatous Disease (CGD), a disorder of the NADPH oxidase system, results in phagocyte functional defects and subsequent infections with bacterial and fungal pathogens (such as Aspergillus species and Candida albicans). Deletions
Externí odkaz:
https://doaj.org/article/999abda06da8411cb6be03452e42754c
Autor:
Sahni Ryan, Jithpratuck Warit, Saleh Hana, Jaishankar Gayatri, Song EunKyung, Krishnaswamy Guha
Publikováno v:
Clinical and Molecular Allergy, Vol 9, Iss 1, p 10 (2011)
Abstract Chronic Granulomatous Disease is the most commonly encountered immunodeficiency involving the phagocyte, and is characterized by repeated infections with bacterial and fungal pathogens, as well as the formation of granulomas in tissue. The d
Externí odkaz:
https://doaj.org/article/a5711dc0d49f4c33b2e26a68be70dc98
Autor:
Chi David S, Youngberg George, Saleh Hana, Elshenawy Yasmin, Jithpratuck Warit, Krishnaswamy Guha
Publikováno v:
Clinical and Molecular Allergy, Vol 9, Iss 1, p 9 (2011)
Abstract Henoch-Schonlein Purpura (HSP) is a small vessel vasculitis mediated by IgA-immune complex deposition. It is characterized by the clinical tetrad of non-thrombocytopenic palpable purpura, abdominal pain, arthritis and renal involvement. Path
Externí odkaz:
https://doaj.org/article/2eb91ce320144e8082e6c46ee96d0f1d
Autor:
Youngberg George, Chi David S, Michaels Mini, Wilgenbusch Sara, Miller Christopher, Krishnaswamy Guha
Publikováno v:
Clinical and Molecular Allergy, Vol 8, Iss 1, p 6 (2010)
Abstract Mannose-binding lectin (MBL) and the Mannose-binding lectin-associated serine proteases (MASPs) are an essential aspect of innate immune responses that probably play an important but understudied role in cutaneous function. The MBL-MASP path
Externí odkaz:
https://doaj.org/article/384088efb65540b08e045da94c74964d
Publikováno v:
Clinical and Molecular Allergy, Vol 8, Iss 1, p 3 (2010)
Abstract Background Altered levels of Immunoglobulin E (IgE) represent a dysregulation of IgE synthesis and may be seen in a variety of immunological disorders. The object of this review is to summarize the historical and molecular aspects of IgE syn
Externí odkaz:
https://doaj.org/article/823e628d426f4e9cb765880caa0afc7a
Publikováno v:
Clinical and Molecular Allergy, Vol 6, Iss 1, p 8 (2008)
Abstract In the 1920's, Hoover described a sign that could be considered a marker of severe airway obstruction. While readily recognizable at the bedside, it may easily be missed on a cursory physical examination. Hoover's sign refers to the inspirat
Externí odkaz:
https://doaj.org/article/a2e6f29fab484ad39fdc1fc30aa95384
Publikováno v:
Clinical and Molecular Allergy, Vol 6, Iss 1, p 5 (2008)
Abstract Background Common variable immune deficiency (CVID), one of the most common primary immunodeficiency diseases presents in adults, whereas X-linked agammaglobulinemia (XLA), an inherited humoral immunodeficiency, is usually diagnosed early in
Externí odkaz:
https://doaj.org/article/dd2fbc9ae8aa49eea11b9cee97297407