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Hamoud Al-Mousa

Showing results (11-20 of 66) with videos related to

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Metabolites|November 14, 2019
Metabolomics Distinguishes DOCK8 Deficiency from Atopic Dermatitis: Towards a Biomarker DiscoveryMinnie Jacob, Xinyun Gu, Xian Luo, et al.
Journal of Clinical Immunology|February 2, 2013
C5 complement deficiency in a Saudi family, molecular characterization of mutation and literature reviewRand Arnaout, Sahar Al Shorbaghi, Hasan Al Dhekri, et al.
BMC Medical Genetics|November 17, 2009
Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi ArabiaOsama Alsmadi, Abdulaziz Al-Ghonaium, Saleh Al-Muhsen, et al.
Frontiers in Allergy|April 7, 2022
Proteomics Profiling to Distinguish DOCK8 Deficiency From Atopic DermatitisMinnie Jacob, Afshan Masood, Zakiya Shinwari, et al.
Modern Rheumatology|February 10, 2021
Lupus manifestations in children with primary immunodeficiency diseases: Comprehensive phenotypic and genetic features and outcomeSulaiman M Al-Mayouf, Hajar A Alreefi, Tuqa A Alsinan, et al.
The Pediatric Infectious Disease Journal|December 6, 2011
Disseminated cryptococcal infection in patient with novel JAK3 mutation severe combined immunodeficiency, with resolution after stem cell transplantationZobaida Alsum, Bandar Al-Saud, Abdulaziz Al-Ghonaium, et al.
Allergy|September 26, 2018
Quantitative profiling of cytokines and chemokines in DOCK8-deficient and atopic dermatitis patientsMinnie Jacob, Duaa Bin Khalaf, Safa Alhissi, et al.
Journal of Clinical Immunology|September 30, 2025
Homozygous Loss of Function PIK3CD Mutation in Multiple Siblings Leading To B Cell Dysregulation and AutoimmunityHuda Alajlan, Amer Al-Mazrou, Hibah Alruwaili, et al.
Immunological Reviews|January 22, 2005
Inherited disorders of human Toll-like receptor signaling: immunological implicationsCheng-Lung Ku, Kun Yang, Jacinta Bustamante, et al.
Journal of Endotoxin Research|September 24, 2005
Heritable defects of the human TLR signalling pathwaysAnne Puel, Kun Yang, Cheng-Lung Ku, et al.
Pageof 7

Showing results (11-20 of 66) with videos related to

Sort By:
Pageof 7
Metabolites|November 14, 2019
Metabolomics Distinguishes DOCK8 Deficiency from Atopic Dermatitis: Towards a Biomarker DiscoveryMinnie Jacob, Xinyun Gu, Xian Luo, et al.
Journal of Clinical Immunology|February 2, 2013
C5 complement deficiency in a Saudi family, molecular characterization of mutation and literature reviewRand Arnaout, Sahar Al Shorbaghi, Hasan Al Dhekri, et al.
BMC Medical Genetics|November 17, 2009
Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi ArabiaOsama Alsmadi, Abdulaziz Al-Ghonaium, Saleh Al-Muhsen, et al.
Frontiers in Allergy|April 7, 2022
Proteomics Profiling to Distinguish DOCK8 Deficiency From Atopic DermatitisMinnie Jacob, Afshan Masood, Zakiya Shinwari, et al.
Modern Rheumatology|February 10, 2021
Lupus manifestations in children with primary immunodeficiency diseases: Comprehensive phenotypic and genetic features and outcomeSulaiman M Al-Mayouf, Hajar A Alreefi, Tuqa A Alsinan, et al.
The Pediatric Infectious Disease Journal|December 6, 2011
Disseminated cryptococcal infection in patient with novel JAK3 mutation severe combined immunodeficiency, with resolution after stem cell transplantationZobaida Alsum, Bandar Al-Saud, Abdulaziz Al-Ghonaium, et al.
Allergy|September 26, 2018
Quantitative profiling of cytokines and chemokines in DOCK8-deficient and atopic dermatitis patientsMinnie Jacob, Duaa Bin Khalaf, Safa Alhissi, et al.
Journal of Clinical Immunology|September 30, 2025
Homozygous Loss of Function PIK3CD Mutation in Multiple Siblings Leading To B Cell Dysregulation and AutoimmunityHuda Alajlan, Amer Al-Mazrou, Hibah Alruwaili, et al.
Immunological Reviews|January 22, 2005
Inherited disorders of human Toll-like receptor signaling: immunological implicationsCheng-Lung Ku, Kun Yang, Jacinta Bustamante, et al.
Journal of Endotoxin Research|September 24, 2005
Heritable defects of the human TLR signalling pathwaysAnne Puel, Kun Yang, Cheng-Lung Ku, et al.
Pageof 7