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Peter D Arkwright

Showing results (161-170 of 170) with videos related to

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Blood|April 5, 2024
Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survivalTanja C Vallée, Jannik S Glasmacher, Hannes Buchner, 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.
Medicine|November 9, 2010
Clinical features and outcome of patients with IRAK-4 and MyD88 deficiencyCapucine Picard, Horst von Bernuth, Pegah Ghandil, 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.
The Journal of Allergy and Clinical Immunology. in Practice|February 16, 2025
Efficacy and Safety of Epicutaneous Immunotherapy in Peanut-Allergic Toddlers: Open-Label Extension to EPITOPEMatthew Greenhawt, Deborah Albright, Sara Anvari, et al.
The Journal of Clinical Investigation|July 4, 2018
Inherited p40phox deficiency differs from classic chronic granulomatous diseaseAnnemarie van de Geer, Alejandro Nieto-Patlán, Douglas B Kuhns, et al.
The New England Journal of Medicine|May 10, 2023
Phase 3 Trial of Epicutaneous Immunotherapy in Toddlers with Peanut AllergyMatthew Greenhawt, Sayantani B Sindher, Julie Wang, et al.
The Journal of Allergy and Clinical Immunology|May 7, 2018
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjectsCharlotte Schwab, Annemarie Gabrysch, Peter Olbrich, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2026
Recessive Loss of DIAPH1 Function Causes a Progressive Neurodevelopmental Syndrome with Variable Immunological InvolvementValentina Galassi Deforie, Reza Maroofian, Irem Karagoz, et al.
Pageof 17

Showing results (161-170 of 170) with videos related to

Sort By:
Pageof 17
You have reached the last page of results.This site can display upto 170 results.
Blood|April 5, 2024
Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survivalTanja C Vallée, Jannik S Glasmacher, Hannes Buchner, 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.
Medicine|November 9, 2010
Clinical features and outcome of patients with IRAK-4 and MyD88 deficiencyCapucine Picard, Horst von Bernuth, Pegah Ghandil, 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.
The Journal of Allergy and Clinical Immunology. in Practice|February 16, 2025
Efficacy and Safety of Epicutaneous Immunotherapy in Peanut-Allergic Toddlers: Open-Label Extension to EPITOPEMatthew Greenhawt, Deborah Albright, Sara Anvari, et al.
The Journal of Clinical Investigation|July 4, 2018
Inherited p40phox deficiency differs from classic chronic granulomatous diseaseAnnemarie van de Geer, Alejandro Nieto-Patlán, Douglas B Kuhns, et al.
The New England Journal of Medicine|May 10, 2023
Phase 3 Trial of Epicutaneous Immunotherapy in Toddlers with Peanut AllergyMatthew Greenhawt, Sayantani B Sindher, Julie Wang, et al.
The Journal of Allergy and Clinical Immunology|May 7, 2018
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjectsCharlotte Schwab, Annemarie Gabrysch, Peter Olbrich, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2026
Recessive Loss of DIAPH1 Function Causes a Progressive Neurodevelopmental Syndrome with Variable Immunological InvolvementValentina Galassi Deforie, Reza Maroofian, Irem Karagoz, et al.
Pageof 17