1. Autoantibodies to neuronal antigens in children with new‐onset seizures classified according to the revised ILAE organization of seizures and epilepsies. Issue 12 (23rd October 2013) Authors: Suleiman, Jehan; Wright, Sukhvir; Gill, Deepak; Brilot, Fabienne; Waters, Patrick; Peacock, Ken; Procopis, Peter; Nibber, Anjan; Vincent, Angela; Dale, Russell C.; Lang, Bethan Journal: Epilepsia Issue: Volume 54:Issue 12(2013:Dec.) Page Start: 2091 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Autoimmune epilepsy in children: Case series and proposed guidelines for identification. (28th March 2013) Authors: Suleiman, Jehan; Brilot, Fabienne; Lang, Bethan; Vincent, Angela; Dale, Russell C. Journal: Epilepsia Issue: Volume 54:issue 6(2013:Jun.) Page Start: 1036 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical and molecular delineation of dysequilibrium syndrome type 2 and profound sensorineural hearing loss in an inbred Arab family. Issue 2 (5th October 2015) Authors: Komara, Makanko; John, Anne; Suleiman, Jehan; Ali, Bassam R.; Al‐Gazali, Lihadh Journal: American journal of medical genetics Issue: Volume 170:Issue 2(2016) Page Start: 540 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Expansion of the clinical and molecular spectrum of WWOX‐related epileptic encephalopathy. Issue 3 (19th December 2022) Authors: Chong, Shuk Ching; Cao, Ye; Fung, Eva L. W.; Kleppe, Soledad; Gripp, Karen W.; Hertecant, Jozef; El‐Hattab, Ayman W.; Suleiman, Jehan; Clark, Gary; von Allmen, Gretchen; Rodziyevska, Olga; Lewis, Richard A.; Rosenfeld, Jill A.; Dong, Jie; Wang, Xia; Miller, Marcus J.; Bi, Weimin; Liu, Pengfei; Sc... Journal: American journal of medical genetics Issue: Volume 191:Issue 3(2023) Page Start: 776 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Homozygous loss‐of‐function variants of TASP1, a gene encoding an activator of the histone methyltransferases KMT2A and KMT2D, cause a syndrome of developmental delay, happy demeanor, distinctive facial features, and congenital anomalies. Issue 11 (22nd July 2019) Authors: Suleiman, Jehan; Riedhammer, Korbinian M.; Jicinsky, Timothy; Mundt, Melinda; Werner, Laurie; Gusic, Mirjana; Burgemeister, Anna L.; Alsaif, Hessa S.; Abdulrahim, Maha; Moghrabi, Nabil N; Nicolas‐Jilwan, Manal; AlSayed, Moeenaldeen; Bi, Weimin; Sampath, Srirangan; Alkuraya, Fowzan S.; El‐Hattab, ... Journal: Human mutation Issue: Volume 40:Issue 11(2019) Page Start: 1985 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Pediatric Multiple Sclerosis in the United Arab Emirates: Characteristics From a Multicenter Study and Global Comparison. (May 2018) Authors: Ismail, Fatima Y.; Gordon-Lipkin, Eliza; Huether, Katherine; Blair, Iain; Szólics, Miklós; Alsaadi, Taoufik; Aziz, Faisal; Suleiman, Jehan; Schiess, Nicoline Journal: Journal of child neurology Issue: Volume 33:Number 6(2018:Jun.) Page Start: 422 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency. Issue 18 (5th May 2022) Authors: Riedhammer, Korbinian M; Burgemeister, Anna L; Cantagrel, Vincent; Amiel, Jeanne; Siquier-Pernet, Karine; Boddaert, Nathalie; Hertecant, Jozef; Kannouche, Patricia L; Pouvelle, Caroline; Htun, Stephanie; Slavotinek, Anne M; Beetz, Christian; Diego-Alvarez, Dan; Kampe, Kapil; Fleischer, Nicole; Aw... Journal: Human molecular genetics Issue: Volume 31:Issue 18(2022) Page Start: 3083 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The recognition and treatment of autoimmune epilepsy in children. (8th December 2014) Authors: Suleiman, Jehan; Dale, Russell C Journal: Developmental medicine & child neurology Issue: Volume 57:Number 5(2015:May) Page Start: 431 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. VPS26C homozygous nonsense variant in two cousins with neurodevelopmental deficits, growth failure, skeletal abnormalities, and distinctive facial features. Issue 4 (26th December 2019) Authors: Beetz, Christian; Ameziane, Najim; Kdissa, Ameni; Karageorgou, Vasiliki; Bauer, Peter; Suleiman, Jehan; Sutton, V. Reid; El‐Hattab, Ayman W. Journal: Clinical genetics Issue: Volume 97:Issue 4(2020) Page Start: 644 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. West syndrome, developmental and epileptic encephalopathy, and severe CNS disorder associated with WWOX mutations. Issue 5 (21st November 2018) Authors: Shaukat, Qudsia; Hertecant, Jozef; El‐Hattab, Ayman W.; Ali, Bassam R.; Suleiman, Jehan Journal: Epileptic disorders Issue: Volume 20:Issue 5(2018) Page Start: 401 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗