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Alexandra F Freeman

Showing results (251-260 of 268) with videos related to

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Research Square|March 30, 2023
Multiomics integration of 22 immune-mediated monogenic diseases reveals an emergent axis of human immune healthRachel Sparks, Nicholas Rachmaninoff, Dylan C Hirsch, et al.
The Journal of Allergy and Clinical Immunology|April 30, 2026
Clinical features, genetics, treatment, and long-term outcomes of STAT3 hyper-IgE syndrome: a single-center cohort analysisAlexandra F Freeman, Chen Wang, Amanda Urban, et al.
The Journal of Allergy and Clinical Immunology|September 27, 2020
Coronavirus disease 2019 in patients with inborn errors of immunity: An international studyIsabelle Meyts, Giorgia Bucciol, Isabella Quinti, et al.
The Journal of Allergy and Clinical Immunology|March 1, 2015
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiencyKarin R Engelhardt, Michael E Gertz, Sevgi Keles, et al.
The Journal of Experimental Medicine|May 2, 2025
Immunopathological and microbial signatures of inflammatory bowel disease in partial RAG deficiencyRiccardo Castagnoli, Francesca Pala, Poorani Subramanian, et al.
Transplantation|July 31, 2025
Further Personalizing Medicine in Immune Disorders: Genomic Findings and Hematopoietic Cell Transplantation SurvivalMorgan N Similuk, Sarah A Bannon, Jia Yan, et al.
The Journal of Allergy and Clinical Immunology|December 28, 2023
Perturbations of the T-cell receptor repertoire in response to SARS-CoV-2 in immunocompetent and immunocompromised individualsOttavia M Delmonte, Cihan Oguz, Kerry Dobbs, et al.
The Journal of Allergy and Clinical Immunology|September 1, 2018
Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic diseaseBatsukh Dorjbal, Jeffrey R Stinson, Chi A Ma, et al.
Journal of Clinical Immunology|January 29, 2015
DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patientsSusanne E Aydin, Sara Sebnem Kilic, Caner Aytekin, et al.
The Journal of Experimental Medicine|June 10, 2020
Correction: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndromeVivien Béziat, Simon J Tavernier, Yin-Huai Chen, et al.
Pageof 27

Showing results (251-260 of 268) with videos related to

Sort By:
Pageof 27
Research Square|March 30, 2023
Multiomics integration of 22 immune-mediated monogenic diseases reveals an emergent axis of human immune healthRachel Sparks, Nicholas Rachmaninoff, Dylan C Hirsch, et al.
The Journal of Allergy and Clinical Immunology|April 30, 2026
Clinical features, genetics, treatment, and long-term outcomes of STAT3 hyper-IgE syndrome: a single-center cohort analysisAlexandra F Freeman, Chen Wang, Amanda Urban, et al.
The Journal of Allergy and Clinical Immunology|September 27, 2020
Coronavirus disease 2019 in patients with inborn errors of immunity: An international studyIsabelle Meyts, Giorgia Bucciol, Isabella Quinti, et al.
The Journal of Allergy and Clinical Immunology|March 1, 2015
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiencyKarin R Engelhardt, Michael E Gertz, Sevgi Keles, et al.
The Journal of Experimental Medicine|May 2, 2025
Immunopathological and microbial signatures of inflammatory bowel disease in partial RAG deficiencyRiccardo Castagnoli, Francesca Pala, Poorani Subramanian, et al.
Transplantation|July 31, 2025
Further Personalizing Medicine in Immune Disorders: Genomic Findings and Hematopoietic Cell Transplantation SurvivalMorgan N Similuk, Sarah A Bannon, Jia Yan, et al.
The Journal of Allergy and Clinical Immunology|December 28, 2023
Perturbations of the T-cell receptor repertoire in response to SARS-CoV-2 in immunocompetent and immunocompromised individualsOttavia M Delmonte, Cihan Oguz, Kerry Dobbs, et al.
The Journal of Allergy and Clinical Immunology|September 1, 2018
Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic diseaseBatsukh Dorjbal, Jeffrey R Stinson, Chi A Ma, et al.
Journal of Clinical Immunology|January 29, 2015
DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patientsSusanne E Aydin, Sara Sebnem Kilic, Caner Aytekin, et al.
The Journal of Experimental Medicine|June 10, 2020
Correction: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndromeVivien Béziat, Simon J Tavernier, Yin-Huai Chen, et al.
Pageof 27