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Hamoud Al-Mousa

Showing results (41-50 of 66) with videos related to

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Journal of Clinical Immunology|September 13, 2012
Clinical, immunological and molecular characterization of DOCK8 and DOCK8-like deficient patients: single center experience of twenty-five patientsZobaida Alsum, Abbas Hawwari, Osama Alsmadi, et al.
Clinical Immunology (Orlando, Fla.)|November 29, 2016
Novel mutation in DOCK8-HIES with severe phenotype and successful transplantationLatifa Al Shekaili, Farrukh Sheikh, Sulaiman Al Gazlan, et al.
Journal of Clinical Immunology|January 6, 2025
Outcomes of Hematopoietic Stem Cell Transplantation in 5 Patients with Autosomal Recessive RIPK1-DeficiencyRebecca B Walsh, Peter McNaughton, Zohreh Nademi, et al.
Human Mutation|June 7, 2017
A RAB27A duplication in several cases of Griscelli syndrome type 2: An explanation for cases lacking a genetic diagnosisVirginie Grandin, Fernando E Sepulveda, Nathalie Lambert, et al.
Journal of Clinical Immunology|November 8, 2022
Phenotypic and Genotypic Characterization of Hereditary Angioedema in Saudi ArabiaFarrukh Sheikh, Huda Alajlan, Maram Albanyan, et al.
Pediatric Rheumatology Online Journal|May 14, 2025
International multidisciplinary consensus on the definition and clinical approach for monogenic inflammatory immune dysregulation disordersHend M Alkwai, Ibrahim A Almaghlouth, Leonardo Oliveira Mendonça, et al.
La Tunisie Medicale|February 13, 2019
Primary Immunodeficiencies: Epidemiology in the MaghrebAhmed Aziz Bousfiha, Abderrrahmane Errami, Leila Jeddane, et al.
Clinical Genetics|January 28, 2021
Hematological findings associated with tubulin-folding cofactors D-related encephalopathy: Expanding the phenotypeAlbandary Al-Bakheet, Mohamed Tohary, Sameena Khan, et al.
Biomedicines|July 29, 2023
Outcome of BCG Vaccination in ADA-SCID Patients: A 12-Patient SeriesDaniele Canarutto, Chiara Oltolini, Federica Barzaghi, et al.
Journal of Clinical Immunology|March 29, 2018
Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi ArabiaAbdulrahman N Alodayani, Abdulnasir M Al-Otaibi, Caroline Deswarte, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
Journal of Clinical Immunology|September 13, 2012
Clinical, immunological and molecular characterization of DOCK8 and DOCK8-like deficient patients: single center experience of twenty-five patientsZobaida Alsum, Abbas Hawwari, Osama Alsmadi, et al.
Clinical Immunology (Orlando, Fla.)|November 29, 2016
Novel mutation in DOCK8-HIES with severe phenotype and successful transplantationLatifa Al Shekaili, Farrukh Sheikh, Sulaiman Al Gazlan, et al.
Journal of Clinical Immunology|January 6, 2025
Outcomes of Hematopoietic Stem Cell Transplantation in 5 Patients with Autosomal Recessive RIPK1-DeficiencyRebecca B Walsh, Peter McNaughton, Zohreh Nademi, et al.
Human Mutation|June 7, 2017
A RAB27A duplication in several cases of Griscelli syndrome type 2: An explanation for cases lacking a genetic diagnosisVirginie Grandin, Fernando E Sepulveda, Nathalie Lambert, et al.
Journal of Clinical Immunology|November 8, 2022
Phenotypic and Genotypic Characterization of Hereditary Angioedema in Saudi ArabiaFarrukh Sheikh, Huda Alajlan, Maram Albanyan, et al.
Pediatric Rheumatology Online Journal|May 14, 2025
International multidisciplinary consensus on the definition and clinical approach for monogenic inflammatory immune dysregulation disordersHend M Alkwai, Ibrahim A Almaghlouth, Leonardo Oliveira Mendonça, et al.
La Tunisie Medicale|February 13, 2019
Primary Immunodeficiencies: Epidemiology in the MaghrebAhmed Aziz Bousfiha, Abderrrahmane Errami, Leila Jeddane, et al.
Clinical Genetics|January 28, 2021
Hematological findings associated with tubulin-folding cofactors D-related encephalopathy: Expanding the phenotypeAlbandary Al-Bakheet, Mohamed Tohary, Sameena Khan, et al.
Biomedicines|July 29, 2023
Outcome of BCG Vaccination in ADA-SCID Patients: A 12-Patient SeriesDaniele Canarutto, Chiara Oltolini, Federica Barzaghi, et al.
Journal of Clinical Immunology|March 29, 2018
Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi ArabiaAbdulrahman N Alodayani, Abdulnasir M Al-Otaibi, Caroline Deswarte, et al.
Pageof 7