1. A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C‐methyltransferase deficiency. Issue 1 (8th November 2017) Authors: Malicdan, May Christine V.; Vilboux, Thierry; Ben‐Zeev, Bruria; Guo, Jennifer; Eliyahu, Aviva; Pode‐Shakked, Ben; Dori, Amir; Kakani, Sravan; Chandrasekharappa, Settara C.; Ferreira, Carlos R.; Shelestovich, Natalia; Marek‐Yagel, Dina; Pri‐Chen, Hadass; Blatt, Ilan; Niederhuber, John E.; He, Lang... Journal: Human mutation Issue: Volume 39:Issue 1(2018) Page Start: 69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. An evaluation of pharmacist knowledge on treatment with antiepileptic drugs. (January 2016) Authors: Roth, Yifat; Neufeld, Miri Y.; Blatt, Ilan; Guy-Alfandary, Shiri; Rasaby, Sivan; Ekstein, Dana; Eyal, Sara Journal: Seizure Issue: Volume 34(2016) Page Start: 60 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Causative Drugs of Stevens‐Johnson Syndrome and Toxic Epidermal Necrolysis in Israel. (9th February 2017) Authors: Maggio, Nicola; Firer, Maria; Zaid, Huda; Bederovsky, Yana; Aboukaoud, Mohammed; Gandelman‐Marton, Revital; Noyman, Iris; Ekstein, Dana; Blatt, Ilan; Marom, Eli; Schwartzberg, Eyal; Israel, Shoshana; Ingber, Arieh; Brautbar, Chaim; Eyal, Sara Journal: Journal of clinical pharmacology Issue: Volume 57:Number 7(2017) Page Start: 823 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Early pathology in sleep studies of patients with familial Creutzfeldt–Jakob disease. (2nd June 2016) Authors: Givaty, Gili; Maggio, Nicola; Cohen, Oren S.; Blatt, Ilan; Chapman, Joab Journal: Journal of sleep research Issue: Volume 25:Number 5(2016:Oct.) Page Start: 571 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Excessive phase synchronization in cortical activation during locomotion in persons with Parkinson's disease. (August 2019) Authors: Miron-Shahar, Yael; Kantelhardt, Jan W.; Grinberg, Adam; Hassin-Baer, Sharon; Blatt, Ilan; Inzelberg, Rivka; Plotnik, Meir Journal: Parkinsonism & related disorders Issue: Volume 65(2019) Page Start: 210 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic risk factors for antiepileptic drug–induced hypersensitivity reactions in Israeli populations. (16th August 2016) Authors: Israel, Shoshana; Maggio, Nicola; Ekstein, Dana; Zaid, Huda; Firer, Maria; Bederovsky, Yana; Noyman, Iris; Gandelman‐Marton, Revital; Blatt, Ilan; Brautbar, Chaim; Marom, Eli; Nahlieli Dil, Dorit; Berman, Erez; Sabag, David; Ingber, Arieh; Eyal, Sara Journal: Epilepsia Issue: Volume 57:issue 10(2016) Page Start: e205 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Multiplex families with epilepsy: Success of clinical and molecular genetic characterization. (23rd February 2016) Authors: Afawi, Zaid; Oliver, Karen L.; Kivity, Sara; Mazarib, Aziz; Blatt, Ilan; Neufeld, Miriam Y.; Helbig, Katherine L.; Goldberg-Stern, Hadassa; Misk, Adel J.; Straussberg, Rachel; Walid, Simri; Mahajnah, Muhammad; Lerman-Sagie, Tally; Ben-Zeev, Bruria; Kahana, Esther; Masalha, Rafik; Kramer, Uri; Eks... Journal: Neurology Issue: Volume 86:Number 8(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Once‐daily USL255 as adjunctive treatment of partial‐onset seizures: Randomized phase III study. Issue 7 (5th June 2014) Authors: Chung, Steve S.; Fakhoury, Toufic A.; Hogan, R. Edward; Nagaraddi, Venkatesh N.; Blatt, Ilan; Lawson, Balduin; Arnold, Stephan; Anders, Bob; Clark, Annie M.; Laine, Dawn; Meadows, R. Shawn; Halvorsen, Mark B.; the PREVAIL Study Group Journal: Epilepsia Issue: Volume 55:Issue 7(2014:Jul.) Page Start: 1077 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. PRRT2 mutations: exploring the phenotypical boundaries. Issue 4 (7th October 2013) Authors: Djémié, Tania; Weckhuysen, Sarah; Holmgren, Philip; Hardies, Katia; Van Dyck, Tine; Hendrickx, Rik; Schoonjans, An-Sofie; Van Paesschen, Wim; Jansen, Anna C; De Meirleir, Linda; Selim, Laila Abdel Moteleb; Girgis, Marian Y; Buyse, Gunnar; Lagae, Lieven; Smets, Katrien; Smouts, Iris; Claeys, Krist... Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 85:Issue 4(2014) Page Start: 462 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Seizures as presenting and prominent symptom in chorea‐acanthocytosis with c.2343del VPS13A gene mutation. (27th January 2016) Authors: Benninger, Felix; Afawi, Zaid; Korczyn, Amos D.; Oliver, Karen L.; Pendziwiat, Manuela; Nakamura, Masayuki; Sano, Akira; Helbig, Ingo; Berkovic, Samuel F.; Blatt, Ilan Journal: Epilepsia Issue: Volume 57:issue 4(2016) Page Start: 549 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗