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The Journal of Allergy and Clinical Immunology. in Practice|February 26, 2014
Escalating doses of C1 esterase inhibitor (CINRYZE) for prophylaxis in patients with hereditary angioedemaJonathan A Bernstein, Michael E Manning, Henry Li, et al.The Lancet. Respiratory Medicine|February 19, 2020
Effect of fixed-dose subcutaneous reslizumab on asthma exacerbations in patients with severe uncontrolled asthma and corticosteroid sparing in patients with oral corticosteroid-dependent asthma: results from two phase 3, randomised, double-blind, placebo-controlled trialsJonathan A Bernstein, J Christian Virchow, Kevin Murphy, et al.Human Mutation|July 26, 2012
ALX4 gain-of-function mutations in nonsyndromic craniosynostosisGarima Yagnik, Apar Ghuman, Sundon Kim, et al.Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|May 11, 2016
Prenatally Diagnosed Cases of Binder Phenotype Complicated by Respiratory Distress in the Immediate Postnatal PeriodYair J Blumenfeld, Alexis S Davis, Susan R Hintz, et al.The Journal of Allergy and Clinical Immunology|August 13, 2021
Developing a standardized approach for assessing mast cells and eosinophils on tissue biopsies: A Work Group Report of the AAAAI Allergic Skin Diseases CommitteeNives Zimmermann, J Pablo Abonia, Stephen C Dreskin, et al.The British Journal of Dermatology|February 17, 2024
Benralizumab does not elicit therapeutic effect in patients with chronic spontaneous urticaria: results from the phase IIb multinational randomized double-blind placebo-controlled ARROYO trialSabine Altrichter, Ana Maria Giménez-Arnau, Jonathan A Bernstein, et al.The Journal of Allergy and Clinical Immunology|July 22, 2015
Defects of B-cell terminal differentiation in patients with type-1 Kabuki syndromeAndrew W Lindsley, Howard M Saal, Thomas A Burrow, et al.Nature Communications|December 10, 2015
Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutantEnrico Leipold, Andrea Hanson-Kahn, Miya Frick, et al.American Journal of Medical Genetics. Part A|August 18, 2017
Clinical and molecular characterization of de novo loss of function variants in HNRNPUMagalie S Leduc, Hsiao-Tuan Chao, Chunjing Qu, et al.Human Mutation|September 24, 2017
Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotypeLi Chen, Philip J Jensik, Joseph T Alaimo, et al.Pageof 61