1. A Rare Case of Lemierre-Like Syndrome: A Case Report and Literature Review. (1st April 2018) Authors: Ibrahim, Judy; Noureddin, Muhammad Bassel; Lootah, Ali; Al Khalidi, Aisha; Ghatasheh, Ghassan; Al Tatari, Hossam Other Names: Schiavetti Amalia Academic Editor. Journal: Case reports in pediatrics Issue: Volume 2018(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A recessive truncating variant in thrombospondin‐1 domain containing protein 1 gene THSD1 is the underlying cause of nonimmune hydrops fetalis, congenital cardiac defects, and haemangiomas in four patients from a consanguineous family. Issue 9 (28th July 2018) Authors: Abdelrahman, Hanadi A.; Al‐Shamsi, Aisha; John, Anne; Hertecant, Jozef; Lootah, Ali; Ali, Bassam R.; Al‐Gazali, Lihadh Journal: American journal of medical genetics Issue: Volume 176:Issue 9(2018) Page Start: 1996 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗