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Exome sequencing unravels genetic variants associated with chronic kidney disease in Saudi Arabian patients.
Al-Hamed MH, Hussein MH, Shah Y, Al-Mojalli H, Alsabban E, Alshareef T, Altayyar A, Elshouny S, Ali W, Abduljabbar M, AlOtaibi A, AlShammasi A, Akili R, Abouelhoda M, Sayer JA, Dasouki MJ, Imtiaz F. Al-Hamed MH, et al. Among authors: abduljabbar m. Hum Mutat. 2022 Dec;43(12):e24-e37. doi: 10.1002/humu.24480. Epub 2022 Oct 8. Hum Mutat. 2022. PMID: 36177613
Carbon nanofiber-based multiplexed immunosensor for the detection of survival motor neuron 1, cystic fibrosis transmembrane conductance regulator and Duchenne Muscular Dystrophy proteins.
Eissa S, Alshehri N, Abduljabbar M, Rahman AMA, Dasouki M, Nizami IY, Al-Muhaizea MA, Zourob M. Eissa S, et al. Among authors: abduljabbar m. Biosens Bioelectron. 2018 Oct 15;117:84-90. doi: 10.1016/j.bios.2018.05.048. Epub 2018 May 28. Biosens Bioelectron. 2018. PMID: 29890394
Centro-temporal benign epilepsy in Saudi children.
Kabiraj MM, al Rajeh S, Awada A, Abduljabbar M, Daif A, al Tahan A, al Bunyan M. Kabiraj MM, et al. Among authors: abduljabbar m. Seizure. 1997 Apr;6(2):139-44. doi: 10.1016/s1059-1311(97)80068-4. Seizure. 1997. PMID: 9153727 Free article.
Dementia in Saudi Arabia: experience from a university hospital.
Ogunniyi A, Daif AK, Al-Rajeh S, AbdulJabbar M, Al-Tahan AR, Al-Bunyan M, Shamina AR. Ogunniyi A, et al. Among authors: abduljabbar m. Acta Neurol Scand. 1998 Aug;98(2):116-20. doi: 10.1111/j.1600-0404.1998.tb01729.x. Acta Neurol Scand. 1998. PMID: 9724009
81 results