1. Exome sequencing unravels genetic variants associated with chronic kidney disease in Saudi Arabian patients. Issue 12 (8th October 2022) Authors: Al‐Hamed, Mohamed H.; Hussein, Maged H.; Shah, Yaser; Al‐Mojalli, Hamad; Alsabban, Essam; Alshareef, Turki; Altayyar, Ali; Elshouny, Samir; Ali, Wafaa; Abduljabbar, Mai; AlOtaibi, Afaf; AlShammasi, Amal; Akili, Rana; Abouelhoda, Mohamed; Sayer, John A.; Dasouki, Majed J.; Imtiaz, Faiqa Journal: Human mutation Issue: Volume 43:Issue 12(2022) Page Start: e24 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. FP823ECULIZUMAB FOR THE TREATMENT OF ATYPICAL HEMOLYTIC UREMIC SYNDROME IN PEDIATRIC PATIENTS, A TERTIARY CARE HOSPITAL EXPERIENCE. (13th June 2019) Authors: Alsakran, Aljohara; Ibrahim, Alhassoun; Alshareef, Turki; Saadeh, Sermin; Alsabban, Essam Journal: Nephrology dialysis transplantation Issue: Volume 34(2019)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗