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Jonathan A Bernstein

Showing results (571-580 of 606) with videos related to

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The World Allergy Organization Journal|December 22, 2021
WAO-ARIA consensus on chronic cough - Part 1: Role of TRP channels in neurogenic inflammation of cough neuronal pathwaysPhilip W Rouadi, Samar A Idriss, Jean Bousquet, et al.
The World Allergy Organization Journal|March 17, 2025
WAO - ARIA consensus on chronic cough: Executive summaryPhilip W Rouadi, Samar A Idriss, Jean Bousquet, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 2, 2020
Automated syndrome diagnosis by three-dimensional facial imagingBenedikt Hallgrímsson, J David Aponte, David C Katz, et al.
Human Mutation|April 26, 2019
Mutation update for the SATB2 geneYuri A Zarate, Katherine A Bosanko, Aisling R Caffrey, et al.
Allergy|October 24, 2024
Validity, reliability and responsiveness of digital visual analogue scales for chronic spontaneous urticaria monitoring: A CRUSE® mobile health studyBernardo Sousa-Pinto, Aiste Ramanauskaite, Sophia Neisinger, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2026
Building an Interoperable Rare Disease Multi-omic Resource: The GREGoR Data Model and DatasetBenjamin D Heavner, Marsha M Wheeler, Jesse D Bengtsson, et al.
Human Mutation|November 19, 2011
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesisOlivier Gribouval, Vincent Morinière, Audrey Pawtowski, et al.
Allergy|September 13, 2025
The Prevalence of Symptomatic Dermographism: Results of the International UCARE PREVALENCE-D StudyKanokvalai Kulthanan, Jonathan A Bernstein, Michael Rudenko, et al.
The New England Journal of Medicine|September 8, 2010
Icatibant, a new bradykinin-receptor antagonist, in hereditary angioedemaMarco Cicardi, Aleena Banerji, Francisco Bracho, et al.
Journal of Inherited Metabolic Disease|July 19, 2020
Predominant and novel de novo variants in 29 individuals with ALG13 deficiency: Clinical description, biomarker status, biochemical analysis, and treatment suggestionsBobby G Ng, Erik A Eklund, Sergey A Shiryaev, et al.
Pageof 61

Showing results (571-580 of 606) with videos related to

Sort By:
Pageof 61
The World Allergy Organization Journal|December 22, 2021
WAO-ARIA consensus on chronic cough - Part 1: Role of TRP channels in neurogenic inflammation of cough neuronal pathwaysPhilip W Rouadi, Samar A Idriss, Jean Bousquet, et al.
The World Allergy Organization Journal|March 17, 2025
WAO - ARIA consensus on chronic cough: Executive summaryPhilip W Rouadi, Samar A Idriss, Jean Bousquet, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 2, 2020
Automated syndrome diagnosis by three-dimensional facial imagingBenedikt Hallgrímsson, J David Aponte, David C Katz, et al.
Human Mutation|April 26, 2019
Mutation update for the SATB2 geneYuri A Zarate, Katherine A Bosanko, Aisling R Caffrey, et al.
Allergy|October 24, 2024
Validity, reliability and responsiveness of digital visual analogue scales for chronic spontaneous urticaria monitoring: A CRUSE® mobile health studyBernardo Sousa-Pinto, Aiste Ramanauskaite, Sophia Neisinger, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2026
Building an Interoperable Rare Disease Multi-omic Resource: The GREGoR Data Model and DatasetBenjamin D Heavner, Marsha M Wheeler, Jesse D Bengtsson, et al.
Human Mutation|November 19, 2011
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesisOlivier Gribouval, Vincent Morinière, Audrey Pawtowski, et al.
Allergy|September 13, 2025
The Prevalence of Symptomatic Dermographism: Results of the International UCARE PREVALENCE-D StudyKanokvalai Kulthanan, Jonathan A Bernstein, Michael Rudenko, et al.
The New England Journal of Medicine|September 8, 2010
Icatibant, a new bradykinin-receptor antagonist, in hereditary angioedemaMarco Cicardi, Aleena Banerji, Francisco Bracho, et al.
Journal of Inherited Metabolic Disease|July 19, 2020
Predominant and novel de novo variants in 29 individuals with ALG13 deficiency: Clinical description, biomarker status, biochemical analysis, and treatment suggestionsBobby G Ng, Erik A Eklund, Sergey A Shiryaev, et al.
Pageof 61