1. Bi‐allelic pathogenic variants in NDUFC2 cause early‐onset Leigh syndrome and stalled biogenesis of complex I. Issue 11 (24th September 2020) Authors: Alahmad, Ahmad; Nasca, Alessia; Heidler, Juliana; Thompson, Kyle; Oláhová, Monika; Legati, Andrea; Lamantea, Eleonora; Meisterknecht, Jana; Spagnolo, Manuela; He, Langping; Alameer, Seham; Hakami, Fahad; Almehdar, Abeer; Ardissone, Anna; Alston, Charlotte L; McFarland, Robert; Wittig, Ilka; Ghezz... Journal: EMBO molecular medicine Issue: Volume 12:Issue 11(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Diagnostic comparison between cord blood and filter paper for the screening of congenital hypothyroidism. Issue 1 (3rd December 2021) Authors: Alameer, Seham; Althobaiti, Eman; Alshaikh, Saud; Turjoman, Meshari; Badriq, Feras; AlSofyani, Abeer; Mujalled, Mohammed; Borai, Anwar Journal: Journal of clinical laboratory analysis Issue: Volume 36:Issue 1(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Urea cycle disorder misdiagnosed as multiple sclerosis: a case report and review of the literature. Issue 2 (April 2018) Authors: Algahtani, Hussein; Alameer, Seham; Marzouk, Yousef; Shirah, Bader Journal: Neuroradiology journal Issue: Volume 31:Issue 2(2018:Apr.) Page Start: 213 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗