Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Kelli W. Williams"'
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Externí odkaz:
https://doaj.org/article/eaf251be9cdc49f2a8e14240e86d9322
Autor:
Inka Sastalla, Kelli W. Williams, Erik D. Anderson, Ian A. Myles, Jensen D. Reckhow, Marlene Espinoza-Moraga, Alexandra F. Freeman, Sandip K. Datta
Publikováno v:
Pathogens, Vol 6, Iss 2, p 23 (2017)
Autosomal dominant hyper IgE syndrome (AD-HIES) is a primary immunodeficiency caused by a loss-of-function mutation in the Signal Transducer and Activator of Transcription 3 (STAT3). This immune disorder is clinically characterized by increased susce
Externí odkaz:
https://doaj.org/article/136d372d7d474ddba9b2d838f429b145
Publikováno v:
Journal of Food Allergy. 4:163-171
Background: Approximately 6 million children in the United States have a diagnosed food allergy, and 32% of caregivers experience significant psychological distress due to the diagnosis. Despite substantial impacts on psychosocial health and quality
Publikováno v:
The Journal of Allergy and Clinical Immunology: In Practice. 10:1131-1138
Hypereosinophilic syndrome (HES) is a diverse group of disorders characterized by peripheral blood eosinophilia of 1.5 × 10
Autor:
Laurel G. Wolf, Kelli W. Williams
Publikováno v:
Pediatrics. 150:S57-S58
Autor:
Kelli W. Williams
Publikováno v:
Pediatrics. 150:S56-S57
Autor:
Adam Bartholomeo, Kelli W. Williams
Publikováno v:
Pediatrics. 150:S68-S69
Autor:
Adam Bartholomeo, Kelli W. Williams
Publikováno v:
Pediatrics. 150:S69-S70
Autor:
Yasmin W. Khan, Kelli W. Williams
Publikováno v:
Annals of allergy, asthmaimmunology : official publication of the American College of Allergy, Asthma,Immunology. 129(5)
To review the characteristic clinical and laboratory features of inborn errors of immunity (IEI) that are associated with elevated immunoglobulin (Ig)E levels.Primary peer-reviewed literature.Original research articles reviewed include interventional
Autor:
Hey J Chong, Benjamin T Prince, Danielle E. Arnold, Kelli W. Williams, Wilfredo Cosme-Blanco, Margaret Redmond, Nicholas L. Hartog, Steven M. Holland, Beth K Thielen, Erinn S. Kellner
Publikováno v:
Pediatric Health, Medicine and Therapeutics. 11:257-268
Chronic granulomatous disease (CGD) is a rare but serious primary immunodeficiency with varying prevalence and rates of X-linked and autosomal recessive disease worldwide. Functional defects in the phagocyte nicotinamide adenine dinucleotide phosphat