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Saudi Medical Journal|November 28, 2023
Single nucleotide polymorphisms in cytokine genes and their association with primary Sjögren's syndrome in Saudi patients: A cross-sectional studyBashaer Alqahtani, Maha Daghestani, Mohammed A Omair, et al.
Open Access Rheumatology : Research and Reviews|December 9, 2020
Fatigue in Saudi Patients with Primary Sjögren's Syndrome and Its Correlation with Disease Characteristics and Outcome Measures: A Cross-Sectional StudyFahidah AlEnzi, Bashaer Alqahtani, Esam H Alhamad, et al.
Gene|October 16, 2012
Identification of a novel IVD mutation in a consanguineous family with isovaleric acidemiaNamik Kaya, Dilek Colak, Albandary Al-Bakheet, et al.
Medicine|August 16, 2021
National systemic lupus erythematosus prospective cohort in Saudi Arabia: A study protocolIbrahim A Almaghlouth, Lena M Hassen, Hana S Alahmari, et al.
American Journal of Medical Genetics. Part A|March 27, 2014
Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephalyEissa A Faqeih, Mohammed Al-Owain, Dilek Colak, 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.
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