1. Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations. Issue 1 (December 2015) Authors: Mercier, Sandra; Küry, Sébastien; Salort-Campana, Emmanuelle; Magot, Armelle; Agbim, Uchenna; Besnard, Thomas; Bodak, Nathalie; Bou-Hanna, Chantal; Bréhéret, Flora; Brunelle, Perrine; Caillon, Florence; Chabrol, Brigitte; Cormier-Daire, Valérie; David, Albert; Eymard, Bruno; Faivre, Laurence; Fig... Journal: Orphanet journal of rare diseases Issue: Volume 9:Issue 1(2014) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Mechanistic insights into antiretroviral drug‐induced liver injury. Issue 4 (8th July 2020) Authors: Pillaye, Jamie N.; Marakalala, Mohlopheni J.; Khumalo, Nonhlanhla; Spearman, Wendy; Ndlovu, Hlumani Journal: Pharmacology research & perspectives Issue: Volume 8:Issue 4(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Mutations within the putative protease domain of the human FAM111B gene may predict disease severity and poor prognosis: A review of POIKTMP cases. Issue 5 (13th February 2022) Authors: Arowolo, Afolake; Rhoda, Cenza; Khumalo, Nonhlanhla Journal: Experimental dermatology Issue: Volume 31:Issue 5(2022) Page Start: 648 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. National suicide management guidelines with family as an interv'ention and suicide mortality rates: a systematic review protocol. Issue 7 (20th July 2020) Authors: Panesar, Balpreet; Soni, Divya; Khan, Mohammed I; Bdair, Faris; Holek, Matthew; Tahir, Talha; Woo, Julia; Khumalo, Nonhlanhla; Thabane, Lehana; Samaan, Zainab Journal: BMJ open Issue: Volume 10:Issue 7(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗