1. A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories. Issue 6 (4th April 2014) Authors: Akimoto, Chizuru; Volk, Alexander E; van Blitterswijk, Marka; Van den Broeck, Marleen; Leblond, Claire S; Lumbroso, Serge; Camu, William; Neitzel, Birgit; Onodera, Osamu; van Rheenen, Wouter; Pinto, Susana; Weber, Markus; Smith, Bradley; Proven, Melanie; Talbot, Kevin; Keagle, Pamela; Chesi, Ales... Journal: Journal of medical genetics Issue: Volume 51:Issue 6(2014) Page Start: 419 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population. Issue 7 (27th November 2015) Authors: Amy, Maïté; Staehlin, Oliver; René, Frédérique; Blasco, Hélène; Marouillat, Sylviane; Daoud, Hussein; Vourc'h, Patrick; Gordon, Paul H.; Camu, William; Corcia, Philippe; Loeffler, Jean-Philippe; Palkovits, Miklós; Sommer, Wolfgang H.; Andres, Christian R. Journal: Amyotrophic lateral sclerosis and frontotemporal degeneration Issue: Volume 16:Issue 7/8(2015) Page Start: 490 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Acute Coronary Syndrome (ACS) due to Coronary Artery Embolism in a Patient with Atrial Fibrillation. (10th October 2019) Authors: Daoud, Hussein; Abugroun, Ashraf; Erramilli, Shruti; Kumar, Surender Other Names: Abidov Aiden Academic Editor. Journal: Case reports in cardiology Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature. Issue 1 (December 2016) Authors: Luco, Stephanie; Pohl, Daniela; Sell, Erick; Wagner, Justin; Dyment, David; Daoud, Hussein Journal: BMC medical genetics Issue: Volume 17:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Chronic Type A Aortic Dissection: Rare Presentation of Incidental Pericardial Effusion. (2nd May 2019) Authors: Abugroun, Ashraf; Subahi, Ahmed; Gaznabi, Safwan; Daoud, Hussein Other Names: Jim Man-Hong Academic Editor. Journal: Case reports in cardiology Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. De Novo Balanced Translocation t (7;16) (p22.1; p11.2) Associated with Autistic Disorder. (23rd April 2008) Authors: Bayou, Nadia; M'rad, Ridha; Belhaj, Ahlem; Daoud, Hussein; Ben Jemaa, Lamia; Zemni, Ramzi; Briault, Sylvain; Helayem, M. Bechir; Chaabouni, Habiba Other Names: Fellous Marc Academic Editor. Journal: Journal of biomedicine and biotechnology Issue: Volume 2008(2008) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Exploring the 7p22.1 Chromosome as a Candidate Region for Autism. (18th April 2010) Authors: Bayou, Nadia; Belhadj, Ahlem; Daoud, Hussein; Briault, Sylvain; Helayem, M. Bechir; Chaabouni, Habiba; M'rad, Ridha Journal: Journal of biomedicine and biotechnology Issue: Volume 2010(2010) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Giant right atrium: a long-term complication of rheumatic heart disease. Issue 2 (28th February 2020) Authors: Abugroun, Ashraf; Taha, Mohamed; Daoud, Hussein; Ibrahim, Walid Journal: Oxford medical case reports Issue: Volume 2020:Issue 2(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Identification of a pathogenic FTO mutation by next-generation sequencing in a newborn with growth retardation and developmental delay. Issue 3 (16th September 2015) Authors: Daoud, Hussein; Zhang, Dong; McMurray, Fiona; Yu, Andrea; Luco, Stephanie M; Vanstone, Jason; Jarinova, Olga; Carson, Nancy; Wickens, James; Shishodia, Shifali; Choi, Hwanho; McDonough, Michael A; Schofield, Christopher J; Harper, Mary-Ellen; Dyment, David A; Armour, Christine M Journal: Journal of medical genetics Issue: Volume 53:Issue 3(2016) Page Start: 200 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Infective endocarditis and brain abscess secondary to Aggregatibacter aphrophilus. (2019) Authors: Daoud, Hussein; Abugroun, Ashraf; Olanipekun, Olalekan; Garrison, Daniel Journal: IDCases Issue: Volume 17(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗