Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Hamoud Al-Mousa

Showing results (1-10 of 66) with videos related to

Pageof 7
Sort By:
The Journal of Allergy and Clinical Immunology|January 17, 2013
Combined immunodeficiency: the Middle East experienceWaleed Al-Herz, Hamoud Al-Mousa
Frontiers in Immunology|July 12, 2017
Primary Immunodeficiency Diseases in Highly Consanguineous Populations from Middle East and North Africa: Epidemiology, Diagnosis, and CareHamoud Al-Mousa, Bandar Al-Saud
Seminars in Immunology|April 19, 2023
Genetics of Inborn Errors of Immunity in highly consanguineous Middle Eastern and North African populationsHamoud Al-Mousa, Mohamed-Ridha Barbouche
Frontiers in Immunology|February 9, 2026
Expanding the clinical spectrum of interleukin-2 receptor alpha chain deficiency: two novel cases with long-term hematopoietic stem cell transplantation outcome and literature reviewMaha Alzubedy, Ahmed Sayed Osman, Huda Alajlan, et al.
Clinical and Experimental Rheumatology|January 31, 2017
Evolving spectrum of LRBA deficiency-associated chronic arthritis: is there a causative role in juvenile idiopathic arthritis?Sulaiman M Al-Mayouf, Hamzah Naji, Khalid Alismail, et al.
International Journal of Rheumatic Diseases|November 9, 2017
Monogenic interferonopathies: Phenotypic and genotypic findings of CANDLE syndrome and its overlap with C1q deficient SLESulaiman M Al-Mayouf, Alhanouf AlSaleem, Nora AlMutairi, et al.
Biosensors & Bioelectronics|July 14, 2018
Multiplexed detection of DOCK8, PGM3 and STAT3 proteins for the diagnosis of Hyper-Immunoglobulin E syndrome using gold nanoparticles-based immunosensor array platformShimaa Eissa, Haya Abdulkarim, Majed Dasouki, et al.
Modern Rheumatology|February 13, 2014
Grave aortic aneurysmal dilatation in DOCK8 deficiencyMuna Al Mutairi, Hamoud Al-Mousa, Bander AlSaud, et al.
Frontiers in Immunology|May 2, 2018
High Incidence of Severe Combined Immunodeficiency Disease in Saudi Arabia Detected Through Combined T Cell Receptor Excision Circle and Next Generation Sequencing of Newborn Dried Blood SpotsHamoud Al-Mousa, Ghadah Al-Dakheel, Amal Jabr, et al.
Frontiers in Pediatrics|March 3, 2020
Multiple Family Members With Delayed Cord Separtion and Combined Immunodeficiency With Novel Mutation in <i>IKBKB</i>Zobaida Alsum, Mofareh S AlZahrani, Hamoud Al-Mousa, et al.
Pageof 7

Showing results (1-10 of 66) with videos related to

Sort By:
Pageof 7
The Journal of Allergy and Clinical Immunology|January 17, 2013
Combined immunodeficiency: the Middle East experienceWaleed Al-Herz, Hamoud Al-Mousa
Frontiers in Immunology|July 12, 2017
Primary Immunodeficiency Diseases in Highly Consanguineous Populations from Middle East and North Africa: Epidemiology, Diagnosis, and CareHamoud Al-Mousa, Bandar Al-Saud
Seminars in Immunology|April 19, 2023
Genetics of Inborn Errors of Immunity in highly consanguineous Middle Eastern and North African populationsHamoud Al-Mousa, Mohamed-Ridha Barbouche
Frontiers in Immunology|February 9, 2026
Expanding the clinical spectrum of interleukin-2 receptor alpha chain deficiency: two novel cases with long-term hematopoietic stem cell transplantation outcome and literature reviewMaha Alzubedy, Ahmed Sayed Osman, Huda Alajlan, et al.
Clinical and Experimental Rheumatology|January 31, 2017
Evolving spectrum of LRBA deficiency-associated chronic arthritis: is there a causative role in juvenile idiopathic arthritis?Sulaiman M Al-Mayouf, Hamzah Naji, Khalid Alismail, et al.
International Journal of Rheumatic Diseases|November 9, 2017
Monogenic interferonopathies: Phenotypic and genotypic findings of CANDLE syndrome and its overlap with C1q deficient SLESulaiman M Al-Mayouf, Alhanouf AlSaleem, Nora AlMutairi, et al.
Biosensors & Bioelectronics|July 14, 2018
Multiplexed detection of DOCK8, PGM3 and STAT3 proteins for the diagnosis of Hyper-Immunoglobulin E syndrome using gold nanoparticles-based immunosensor array platformShimaa Eissa, Haya Abdulkarim, Majed Dasouki, et al.
Modern Rheumatology|February 13, 2014
Grave aortic aneurysmal dilatation in DOCK8 deficiencyMuna Al Mutairi, Hamoud Al-Mousa, Bander AlSaud, et al.
Frontiers in Immunology|May 2, 2018
High Incidence of Severe Combined Immunodeficiency Disease in Saudi Arabia Detected Through Combined T Cell Receptor Excision Circle and Next Generation Sequencing of Newborn Dried Blood SpotsHamoud Al-Mousa, Ghadah Al-Dakheel, Amal Jabr, et al.
Frontiers in Pediatrics|March 3, 2020
Multiple Family Members With Delayed Cord Separtion and Combined Immunodeficiency With Novel Mutation in <i>IKBKB</i>Zobaida Alsum, Mofareh S AlZahrani, Hamoud Al-Mousa, et al.
Pageof 7