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Frontiers in Immunology
|
May 3, 2021
Wiskott Aldrich Syndrome: A Multi-Institutional Experience From India
Deepti Suri, Rashmi Rikhi, Ankur K Jindal, et al.
Frontiers in Immunology
|
September 28, 2017
Patients with Primary Immunodeficiencies Are a Reservoir of Poliovirus and a Risk to Polio Eradication
Asghar Aghamohammadi, Hassan Abolhassani, Necil Kutukculer, et al.
Frontiers in Immunology
|
February 15, 2021
Clinical and Genetic Profile of X-Linked Agammaglobulinemia: A Multicenter Experience From India
Amit Rawat, Ankur Kumar Jindal, Deepti Suri, et al.
The World Allergy Organization Journal
|
July 5, 2022
Allergic manifestations of inborn errors of immunity and their impact on the diagnosis: A worldwide study
Zeinab A El-Sayed, Dalia H El-Ghoneimy, José A Ortega-Martell, et al.
Frontiers in Immunology
|
March 15, 2021
Clinical, Immunological, and Molecular Profile of Chronic Granulomatous Disease: A Multi-Centric Study of 236 Patients From India
Amit Rawat, Pandiarajan Vignesh, Murugan Sudhakar, et al.
Frontiers in Immunology
|
February 10, 2022
Phenomic Analysis of Chronic Granulomatous Disease Reveals More Severe Integumentary Infections in X-Linked Compared With Autosomal Recessive Chronic Granulomatous Disease
Timothy Lok-Hin Chiu, Daniel Leung, Koon-Wing Chan, et al.
Frontiers in Immunology
|
February 25, 2021
Clinical, Immunological, and Molecular Features of Severe Combined Immune Deficiency: A Multi-Institutional Experience From India
Pandiarajan Vignesh, Amit Rawat, Rajni Kumrah, et al.
Paediatrics & Child Health
|
December 1, 2025
The landscape of inter-institutional and multinational collaborations in Kawasaki disease
Rocio Gutierrez Rojas, Fabiola Breault, Raed Alzyoud, et al.
The World Allergy Organization Journal
|
April 3, 2019
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world
Zeinab A El-Sayed, Irina Abramova, Juan Carlos Aldave, et al.
Frontiers in Immunology
|
July 28, 2017
Family History of Early Infant Death Correlates with Earlier Age at Diagnosis But Not Shorter Time to Diagnosis for Severe Combined Immunodeficiency
Anderson Dik Wai Luk, Pamela P Lee, Huawei Mao, et al.
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of 52
Search research articles
Search
Showing results (501-510 of 513) with videos related to
Sort By:
Page
of 52
Frontiers in Immunology
|
May 3, 2021
Wiskott Aldrich Syndrome: A Multi-Institutional Experience From India
Deepti Suri, Rashmi Rikhi, Ankur K Jindal, et al.
Frontiers in Immunology
|
September 28, 2017
Patients with Primary Immunodeficiencies Are a Reservoir of Poliovirus and a Risk to Polio Eradication
Asghar Aghamohammadi, Hassan Abolhassani, Necil Kutukculer, et al.
Frontiers in Immunology
|
February 15, 2021
Clinical and Genetic Profile of X-Linked Agammaglobulinemia: A Multicenter Experience From India
Amit Rawat, Ankur Kumar Jindal, Deepti Suri, et al.
The World Allergy Organization Journal
|
July 5, 2022
Allergic manifestations of inborn errors of immunity and their impact on the diagnosis: A worldwide study
Zeinab A El-Sayed, Dalia H El-Ghoneimy, José A Ortega-Martell, et al.
Frontiers in Immunology
|
March 15, 2021
Clinical, Immunological, and Molecular Profile of Chronic Granulomatous Disease: A Multi-Centric Study of 236 Patients From India
Amit Rawat, Pandiarajan Vignesh, Murugan Sudhakar, et al.
Frontiers in Immunology
|
February 10, 2022
Phenomic Analysis of Chronic Granulomatous Disease Reveals More Severe Integumentary Infections in X-Linked Compared With Autosomal Recessive Chronic Granulomatous Disease
Timothy Lok-Hin Chiu, Daniel Leung, Koon-Wing Chan, et al.
Frontiers in Immunology
|
February 25, 2021
Clinical, Immunological, and Molecular Features of Severe Combined Immune Deficiency: A Multi-Institutional Experience From India
Pandiarajan Vignesh, Amit Rawat, Rajni Kumrah, et al.
Paediatrics & Child Health
|
December 1, 2025
The landscape of inter-institutional and multinational collaborations in Kawasaki disease
Rocio Gutierrez Rojas, Fabiola Breault, Raed Alzyoud, et al.
The World Allergy Organization Journal
|
April 3, 2019
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world
Zeinab A El-Sayed, Irina Abramova, Juan Carlos Aldave, et al.
Frontiers in Immunology
|
July 28, 2017
Family History of Early Infant Death Correlates with Earlier Age at Diagnosis But Not Shorter Time to Diagnosis for Severe Combined Immunodeficiency
Anderson Dik Wai Luk, Pamela P Lee, Huawei Mao, et al.
Page
of 52