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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 survival
Tanja 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 deficiency
Karin R Engelhardt, Michael E Gertz, Sevgi Keles, et al.
Medicine
|
November 9, 2010
Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency
Capucine 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 disease
Batsukh 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 EPITOPE
Matthew Greenhawt, Deborah Albright, Sara Anvari, et al.
The Journal of Clinical Investigation
|
July 4, 2018
Inherited p40phox deficiency differs from classic chronic granulomatous disease
Annemarie 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 Allergy
Matthew 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 subjects
Charlotte Schwab, Annemarie Gabrysch, Peter Olbrich, et al.
The Journal of Allergy and Clinical Immunology
|
June 10, 2021
Therapeutic options for CTLA-4 insufficiency
David 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 Involvement
Valentina Galassi Deforie, Reza Maroofian, Irem Karagoz, et al.
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of 17
Search research articles
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Showing results (161-170 of 170) with videos related to
Sort By:
Page
of 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 survival
Tanja 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 deficiency
Karin R Engelhardt, Michael E Gertz, Sevgi Keles, et al.
Medicine
|
November 9, 2010
Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency
Capucine 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 disease
Batsukh 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 EPITOPE
Matthew Greenhawt, Deborah Albright, Sara Anvari, et al.
The Journal of Clinical Investigation
|
July 4, 2018
Inherited p40phox deficiency differs from classic chronic granulomatous disease
Annemarie 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 Allergy
Matthew 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 subjects
Charlotte Schwab, Annemarie Gabrysch, Peter Olbrich, et al.
The Journal of Allergy and Clinical Immunology
|
June 10, 2021
Therapeutic options for CTLA-4 insufficiency
David 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 Involvement
Valentina Galassi Deforie, Reza Maroofian, Irem Karagoz, et al.
Page
of 17