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Page 1
Complex Inheritance of Rare Missense Variants in PAK2, TAP2, and PLCL1 Genes in a Consanguineous Arab Family With Multiple Autoimmune Diseases Including Celiac Disease.
Alharthi AM, Banaganapalli B, Hassan SM, Rashidi O, Al-Shehri BA, Alaifan MA, Alhussaini BH, Alsufyani HA, Alghamdi KS, Nasser KK, Bin-Taleb Y, Elango R, Shaik NA, Saadah OI. Alharthi AM, et al. Among authors: alaifan ma. Front Pediatr. 2022 Jun 15;10:895298. doi: 10.3389/fped.2022.895298. eCollection 2022. Front Pediatr. 2022. PMID: 35783297 Free PMC article.
Rare variant burden analysis from exomes of three consanguineous families reveals LILRB1 and PRSS3 as potential key proteins in inflammatory bowel disease pathogenesis.
Jan RM, Al-Numan HH, Al-Twaty NH, Alrayes N, Alsufyani HA, Alaifan MA, Alhussaini BH, Shaik NA, Awan Z, Qari Y, Saadah OI, Banaganapalli B, Mosli MH, Elango R. Jan RM, et al. Among authors: alaifan ma. Front Med (Lausanne). 2023 May 5;10:1164305. doi: 10.3389/fmed.2023.1164305. eCollection 2023. Front Med (Lausanne). 2023. PMID: 37215724 Free PMC article.
Effectiveness of phototherapy with and without probiotics for the treatment of indirect hyperbilirubinaemia in preterm neonates: a randomised controlled trial.
Nasief H, Alaifan MA, Tamur S, Khadawardi K, Bahauddin AA, Ahmed A, Ahmad S, Singh R, Alhussaini BH, Hassan A. Nasief H, et al. Among authors: alaifan ma. Paediatr Int Child Health. 2024 May;44(1):24-29. doi: 10.1080/20469047.2024.2328416. Epub 2024 Mar 14. Paediatr Int Child Health. 2024. PMID: 38482867 Clinical Trial.
13 results