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Beata Derfalvi

Showing results (21-30 of 31) with videos related to

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Frontiers in Immunology|February 5, 2025
Humoral and cell-mediated immune responses to COVID-19 vaccines up to 6 months post three-dose primary series in adults with inborn errors of immunity and their breakthrough infectionsDana Unninayar, Emilia L Falcone, Hugo Chapdelaine, et al.
Journal of Clinical Immunology|April 25, 2026
Three Doses and Six Months Later: Real-World SARS-CoV-2 Specific Humoral and Cell-Mediated Immunity in Children With Inborn Errors of ImmunityLuana L T N Porto, Dina Yazji, Dana Unninayar, et al.
NPJ Genomic Medicine|November 18, 2025
RareLink: scalable REDCap-based framework for rare disease interoperability linking international registries to FHIR and PhenopacketsAdam S L Graefe, Filip Rehburg, Samer Alkarkoukly, et al.
Nature Communications|June 22, 2023
Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signalingCristiane J Nunes-Santos, HyeSun Kuehn, Brigette Boast, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Linking international registries to FHIR and Phenopackets with RareLink: a scalable REDCap-based framework for rare disease data interoperabilityAdam S L Graefe, Filip Rehburg, Samer Alkarkoukly, et al.
The Journal of Allergy and Clinical Immunology|April 12, 2025
Lipopolysaccharide-responsive and beige-like anchor protein (LRBA) functional deficiency caused by biallelic LRBA missense variants characterized by Evans syndrome or colitisSamuel C C Chiang, Li Yang, Erika Owsley, et al.
The Journal of Allergy and Clinical Immunology|May 15, 2021
Curation and expansion of Human Phenotype Ontology for defined groups of inborn errors of immunityMatthias Haimel, Julia Pazmandi, Raúl Jiménez Heredia, et al.
Clinical Immunology (Orlando, Fla.)|October 6, 2024
Clinical exome sequencing data from patients with inborn errors of immunity: Cohort level diagnostic yield and the benefit of systematic reanalysisEmil E Vorsteveld, Caspar I Van der Made, Sanne P Smeekens, et al.
The World Allergy Organization Journal|April 3, 2019
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the worldZeinab A El-Sayed, Irina Abramova, Juan Carlos Aldave, et al.
The Journal of Allergy and Clinical Immunology|June 10, 2021
Therapeutic options for CTLA-4 insufficiencyDavid Egg, Ina Caroline Rump, Noriko Mitsuiki, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

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Pageof 4
Frontiers in Immunology|February 5, 2025
Humoral and cell-mediated immune responses to COVID-19 vaccines up to 6 months post three-dose primary series in adults with inborn errors of immunity and their breakthrough infectionsDana Unninayar, Emilia L Falcone, Hugo Chapdelaine, et al.
Journal of Clinical Immunology|April 25, 2026
Three Doses and Six Months Later: Real-World SARS-CoV-2 Specific Humoral and Cell-Mediated Immunity in Children With Inborn Errors of ImmunityLuana L T N Porto, Dina Yazji, Dana Unninayar, et al.
NPJ Genomic Medicine|November 18, 2025
RareLink: scalable REDCap-based framework for rare disease interoperability linking international registries to FHIR and PhenopacketsAdam S L Graefe, Filip Rehburg, Samer Alkarkoukly, et al.
Nature Communications|June 22, 2023
Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signalingCristiane J Nunes-Santos, HyeSun Kuehn, Brigette Boast, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Linking international registries to FHIR and Phenopackets with RareLink: a scalable REDCap-based framework for rare disease data interoperabilityAdam S L Graefe, Filip Rehburg, Samer Alkarkoukly, et al.
The Journal of Allergy and Clinical Immunology|April 12, 2025
Lipopolysaccharide-responsive and beige-like anchor protein (LRBA) functional deficiency caused by biallelic LRBA missense variants characterized by Evans syndrome or colitisSamuel C C Chiang, Li Yang, Erika Owsley, et al.
The Journal of Allergy and Clinical Immunology|May 15, 2021
Curation and expansion of Human Phenotype Ontology for defined groups of inborn errors of immunityMatthias Haimel, Julia Pazmandi, Raúl Jiménez Heredia, et al.
Clinical Immunology (Orlando, Fla.)|October 6, 2024
Clinical exome sequencing data from patients with inborn errors of immunity: Cohort level diagnostic yield and the benefit of systematic reanalysisEmil E Vorsteveld, Caspar I Van der Made, Sanne P Smeekens, et al.
The World Allergy Organization Journal|April 3, 2019
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the worldZeinab A El-Sayed, Irina Abramova, Juan Carlos Aldave, et al.
The Journal of Allergy and Clinical Immunology|June 10, 2021
Therapeutic options for CTLA-4 insufficiencyDavid Egg, Ina Caroline Rump, Noriko Mitsuiki, et al.
Pageof 4