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Jonathan A Bernstein

Showing results (521-530 of 606) with videos related to

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Allergy|January 30, 2026
International Guideline on the Diagnosis and Management of Pediatric Patients With Hereditary AngioedemaHenriette Farkas, Inmaculada Martinez-Saguer, Konrad Bork, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|June 20, 2024
Topical corticosteroids for hives and itch (urticaria): Systematic review and Bayesian meta-analysis of randomized trialsAlexandro W L Chu, Daniel G Rayner, Xiajing Chu, et al.
The New England Journal of Medicine|May 31, 2024
Oral Sebetralstat for On-Demand Treatment of Hereditary Angioedema AttacksMarc A Riedl, Henriette Farkas, Emel Aygören-Pürsün, et al.
The World Allergy Organization Journal|April 30, 2026
Clinical remission in allergy and clinical immunology practice: State of the art and World Allergy Organization (WAO) call to actionMário Morais-Almeida, Giorgio Walter Canonica, Pedro Giavina-Bianchi, et al.
American Journal on Intellectual and Developmental Disabilities|August 26, 2025
Characterizing Developmental and Behavioral Profiles in Developmental Synaptopathies to Inform Clinical Trial EndpointsLatha Valluripalli Soorya, Camille W Brune, Cristan A Farmer, et al.
American Journal of Human Genetics|March 21, 2020
De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic DecompensationDongxue Mao, Chloe M Reuter, Maura R Z Ruzhnikov, et al.
JAMA Dermatology|October 8, 2025
Patient Values and Preferences in Chronic Urticaria Treatment: A Systematic ReviewXiajing Chu, Javeria Mubasher, Lina Chen, et al.
European Journal of Human Genetics : EJHG|May 7, 2015
DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct faciesJianling Ji, Hane Lee, Bob Argiropoulos, et al.
The World Allergy Organization Journal|February 23, 2023
Latin American anaphylaxis registryEdgardo J Jares, Victoria Cardona, R Maximiliano Gómez, et al.
European Journal of Human Genetics : EJHG|January 28, 2026
De novo heterozygous variants of the RSF1 gene are responsible for a syndromic neurodevelopmental disorderCéline Jost, Tiffany Busa, Daniel Wegner, et al.
Pageof 61

Showing results (521-530 of 606) with videos related to

Sort By:
Pageof 61
Allergy|January 30, 2026
International Guideline on the Diagnosis and Management of Pediatric Patients With Hereditary AngioedemaHenriette Farkas, Inmaculada Martinez-Saguer, Konrad Bork, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|June 20, 2024
Topical corticosteroids for hives and itch (urticaria): Systematic review and Bayesian meta-analysis of randomized trialsAlexandro W L Chu, Daniel G Rayner, Xiajing Chu, et al.
The New England Journal of Medicine|May 31, 2024
Oral Sebetralstat for On-Demand Treatment of Hereditary Angioedema AttacksMarc A Riedl, Henriette Farkas, Emel Aygören-Pürsün, et al.
The World Allergy Organization Journal|April 30, 2026
Clinical remission in allergy and clinical immunology practice: State of the art and World Allergy Organization (WAO) call to actionMário Morais-Almeida, Giorgio Walter Canonica, Pedro Giavina-Bianchi, et al.
American Journal on Intellectual and Developmental Disabilities|August 26, 2025
Characterizing Developmental and Behavioral Profiles in Developmental Synaptopathies to Inform Clinical Trial EndpointsLatha Valluripalli Soorya, Camille W Brune, Cristan A Farmer, et al.
American Journal of Human Genetics|March 21, 2020
De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic DecompensationDongxue Mao, Chloe M Reuter, Maura R Z Ruzhnikov, et al.
JAMA Dermatology|October 8, 2025
Patient Values and Preferences in Chronic Urticaria Treatment: A Systematic ReviewXiajing Chu, Javeria Mubasher, Lina Chen, et al.
European Journal of Human Genetics : EJHG|May 7, 2015
DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct faciesJianling Ji, Hane Lee, Bob Argiropoulos, et al.
The World Allergy Organization Journal|February 23, 2023
Latin American anaphylaxis registryEdgardo J Jares, Victoria Cardona, R Maximiliano Gómez, et al.
European Journal of Human Genetics : EJHG|January 28, 2026
De novo heterozygous variants of the RSF1 gene are responsible for a syndromic neurodevelopmental disorderCéline Jost, Tiffany Busa, Daniel Wegner, et al.
Pageof 61