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The Journal of Allergy and Clinical Immunology
|
December 1, 2022
The diagnosis of severe combined immunodeficiency (SCID): The Primary Immune Deficiency Treatment Consortium (PIDTC) 2022 Definitions
Christopher C Dvorak, Elie Haddad, Jennifer Heimall, et al.
Gene Therapy
|
June 29, 2007
Sendai virus-mediated CFTR gene transfer to the airway epithelium
S Ferrari, U Griesenbach, A Iida, et al.
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 infections
Dana 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 Immunity
Luana L T N Porto, Dina Yazji, Dana Unninayar, et al.
Blood Advances
|
December 10, 2025
Clinical Characteristics, Management, and Hematopoietic Cell Transplantation of Patients with TLR8 Gain-of-Function
Danielle E Arnold, Saara Kaviany, Jahnavi Aluri, et al.
NPJ Genomic Medicine
|
November 18, 2025
RareLink: scalable REDCap-based framework for rare disease interoperability linking international registries to FHIR and Phenopackets
Adam S L Graefe, Filip Rehburg, Samer Alkarkoukly, 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 interoperability
Adam 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 colitis
Samuel C C Chiang, Li Yang, Erika Owsley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 16, 2023
Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy
Vandana Shashi, Kelly Schoch, Rebecca Ganetzky, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
June 4, 2026
IMPACT (Immune Monitoring and Phenotype Assessment of Clinical Trajectory) for Patients with Inborn Errors of Immunity from the Primary Immune Deficiency Treatment Consortium (PIDTC)
Danielle E Arnold, Hesham Eissa, Elizabeth Dunn, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 73) with videos related to
Sort By:
Page
of 8
The Journal of Allergy and Clinical Immunology
|
December 1, 2022
The diagnosis of severe combined immunodeficiency (SCID): The Primary Immune Deficiency Treatment Consortium (PIDTC) 2022 Definitions
Christopher C Dvorak, Elie Haddad, Jennifer Heimall, et al.
Gene Therapy
|
June 29, 2007
Sendai virus-mediated CFTR gene transfer to the airway epithelium
S Ferrari, U Griesenbach, A Iida, et al.
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 infections
Dana 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 Immunity
Luana L T N Porto, Dina Yazji, Dana Unninayar, et al.
Blood Advances
|
December 10, 2025
Clinical Characteristics, Management, and Hematopoietic Cell Transplantation of Patients with TLR8 Gain-of-Function
Danielle E Arnold, Saara Kaviany, Jahnavi Aluri, et al.
NPJ Genomic Medicine
|
November 18, 2025
RareLink: scalable REDCap-based framework for rare disease interoperability linking international registries to FHIR and Phenopackets
Adam S L Graefe, Filip Rehburg, Samer Alkarkoukly, 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 interoperability
Adam 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 colitis
Samuel C C Chiang, Li Yang, Erika Owsley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 16, 2023
Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy
Vandana Shashi, Kelly Schoch, Rebecca Ganetzky, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
June 4, 2026
IMPACT (Immune Monitoring and Phenotype Assessment of Clinical Trajectory) for Patients with Inborn Errors of Immunity from the Primary Immune Deficiency Treatment Consortium (PIDTC)
Danielle E Arnold, Hesham Eissa, Elizabeth Dunn, et al.
Page
of 8