1. A novel biallelic loss‐of‐function mutation in TMCO1 gene confirming and expanding the phenotype spectrum of cerebro‐facio‐thoracic dysplasia. Issue 7 (18th May 2019) Authors: Sharkia, Rajech; Zalan, Abdelnaser; Jabareen‐Masri, Azhar; Hengel, Holger; Schöls, Ludger; Kessel, Amit; Azem, Abdussalam; Mahajnah, Muhammad Journal: American journal of medical genetics Issue: Volume 179:Issue 7(2019) Page Start: 1338 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Absence seizure provocation during routine EEG: Does position of the child during hyperventilation affect the diagnostic yield?. (July 2020) Authors: Rozenblat, Tal; Kraus, Dror; Mahajnah, Muhammad; Goldberg-Stern, Hadassah; Watemberg, Nathan Journal: Seizure Issue: Volume 79(2020) Page Start: 86 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. CHANGES IN MARRIAGE PATTERNS AMONG THE ARAB COMMUNITY IN ISRAEL OVER A 60-YEAR PERIOD. Issue 2 (22nd May 2015) Authors: Sharkia, Rajech; Mahajnah, Muhammad; Athamny, Esmael; Khatib, Mohammad; Sheikh-Muhammad, Ahmad; Zalan, Abdelnaser Journal: Journal of biosocial science Issue: Volume 48:Issue 2(2016) Page Start: 283 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Clinical Characteristics of Autism Spectrum Disorder in Israel: Impact of Ethnic and Social Diversities. (23rd April 2015) Authors: Mahajnah, Muhammad; Sharkia, Rajech; Shalabe, Haitham; Terkel-Dawer, Ruth; Akawi, Ashraf; Zelnik, Nathanel Other Names: Mehta Jyutika Academic Editor. Journal: BioMed research international Issue: Volume 2015(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Clinical, radiological, and genetic characteristics of 16 patients with ACO2 gene defects: Delineation of an emerging neurometabolic syndrome. Issue 2 (28th January 2019) Authors: Sharkia, Rajech; Wierenga, Klaas J.; Kessel, Amit; Azem, Abdussalam; Bertini, Enrico; Carrozzo, Rosalba; Torraco, Alessandra; Goffrini, Paola; Ceccatelli Berti, Camilla; McCormick, M. Eileen; Plecko, Barbara; Klein, Andrea; Abela, Lucia; Hengel, Holger; Schöls, Ludger; Shalev, Stavit; Khayat, Mor... Journal: Journal of inherited metabolic disease Issue: Volume 42:Issue 2(2019) Page Start: 264 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Corrigendum to "Absence seizure provocation during routine EEG: Does position of the child during hyperventilation affect diagnostic yield?" [Seizure 79 (2020) 86–89]. (January 2021) Authors: Rozenblat, Tal; Kraus, Dror; Mahajnah, Muhammad; Goldberg-Stern, Hadassah; Watemberg, Nathan Journal: Seizure Issue: Volume 84(2021) Page Start: 132 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Exploration of Risk Factors for Type 2 Diabetes among Arabs in Israel. Issue 1 (10th May 2019) Authors: Sharkia, Rajech; Sheikh-Muhammad, Ahmad; Mahajnah, Muhammad; Khatib, Mohammad; Zalan, Abdelnaser Journal: Annals of global health Issue: Volume 85:Issue 1(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Homozygous mutation in PTRH2 gene causes progressive sensorineural deafness and peripheral neuropathy. Issue 4 (22nd March 2017) Authors: Sharkia, Rajech; Shalev, Stavit A.; Zalan, Abdelnaser; Marom‐David, Milit; Watemberg, Nathan; Urquhart, Jill E.; Daly, Sarah B.; Bhaskar, Sanjeev S.; Williams, Simon G.; Newman, William G.; Spiegel, Ronen; Azem, Abdussalam; Elpeleg, Orly; Mahajnah, Muhammad Journal: American journal of medical genetics Issue: Volume 173:Issue 4(2017) Page Start: 1051 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Modeling genetic epileptic encephalopathies using brain organoids. Issue 8 (15th July 2021) Authors: Steinberg, Daniel J; Repudi, Srinivasarao; Saleem, Afifa; Kustanovich, Irina; Viukov, Sergey; Abudiab, Baraa; Banne, Ehud; Mahajnah, Muhammad; Hanna, Jacob H; Stern, Shani; Carlen, Peter L; Aqeilan, Rami I Journal: EMBO molecular medicine Issue: Volume 13:Issue 8(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Multidomain Cognitive Impairment in Children With Pseudotumor Cerebri Syndrome. Issue 1 (4th March 2022) Authors: Mahajnah, Muhammad; Suchi, Ariel T.; Zahakah, Hazar; Sharkia, Rajech; Shuhaiber, Shaden R.; Srugo, Isaac; Genizi, Jacob Editors: Fraser, Clare; Mollan, Susan Journal: Journal of neuro-ophthalmology Issue: Volume 42:Issue 1(2022) Page Start: e93 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗