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Headache|November 9, 2010
Allergy and immunotherapy: are they related to migraine headache?Vincent T Martin, Fred Taylor, Bruce Gebhardt, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|April 4, 2013
Analysis of hereditary angioedema attacks requiring a second dose of ecallantideH Henry Li, Marilyn Campion, Timothy J Craig, et al.
Nature|October 18, 2013
SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patientsAleksandr Shcheglovitov, Olesya Shcheglovitova, Masayuki Yazawa, et al.
The Journal of Allergy and Clinical Immunology|December 26, 2024
Interplay between on-demand treatment trials for hereditary angioedema and treatment guidelinesDanny M Cohn, Daniel F Soteres, Timothy J Craig, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|February 20, 2007
Aspirin challenge and desensitization for aspirin-exacerbated respiratory disease: a practice paperEric Macy, Jonathan A Bernstein, Mariana C Castells, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|May 13, 2022
Insights into urticaria in pediatric and adult populations and its management with fexofenadine hydrochlorideIgnacio J Ansotegui, Jonathan A Bernstein, Giorgio W Canonica, et al.
The World Allergy Organization Journal|November 16, 2013
Consensus Definition of Nonallergic Rhinopathy, Previously Referred to as Vasomotor Rhinitis, Nonallergic Rhinitis, and/or Idiopathic RhinitisMichael A Kaliner, James N Baraniuk, Michael Benninger, et al.
American Journal of Medical Genetics. Part A|September 21, 2011
Ectopia lentis as the presenting and primary feature in Marfan syndromeNeda Zadeh, Jonathan A Bernstein, Anna Kaisa Niemi, et al.
Medrxiv : the Preprint Server for Health Sciences|June 22, 2026
Population-scale detection of methylation outliers from long-read genome sequencingTanner D Jensen, Rhina Kaur, Devon E Bonner, et al.
American Journal of Medical Genetics. Part A|March 13, 2016
RASA1 somatic mutation and variable expressivity in capillary malformation/arteriovenous malformation (CM/AVM) syndromeColleen F Macmurdo, Whitney Wooderchak-Donahue, Pinar Bayrak-Toydemir, et al.
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