1. A Possible Genotype-Phenotype Correlation in Ashkenazi-Jewish Individuals With Aicardi-Goutières Syndrome Associated With SAMHD1 Mutation. (March 2015) Authors: Straussberg, Rachel; Marom, Daphna; Sanado-Inbar, Esther; Lakovsky, Yaniv; Horev, Gadi; Shalev, Stavit A.; Lev, Dorit; Lerman-Sagie, Tally; Leshinsky-Silver, Esther Journal: Journal of child neurology Issue: Volume 30:Number 4(2015:Mar.) Page Start: 490 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A practical approach to prenatal diagnosis of malformations of cortical development. (September 2021) Authors: Lerman-Sagie, Tally; Pogledic, Ivana; Leibovitz, Zvi; Malinger, Gustavo Journal: European journal of paediatric neurology Issue: Volume 34(2021) Page Start: 50 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Atypical presentation of Costeff syndrome-severe psychomotor involvement and electrical status epilepticus during slow wave sleep. (November 2015) Authors: Carmi, Nirit; Lev, Dorit; Leshinsky-Silver, Esther; Anikster, Yair; Blumkin, Lubov; Kivity, Sara; Lerman-Sagie, Tally; Zerem, Ayelet Journal: European journal of paediatric neurology Issue: Volume 19:Number 6(2015:Nov.) Page Start: 733 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Autoimmune Epilepsy: Some Epilepsy Patients Harbor Autoantibodies to Glutamate Receptors and dsDNA on both Sides of the Blood-brain Barrier, which may Kill Neurons and Decrease in Brain Fluids after Hemispherotomy. Issue 3 (2004) Authors: Ganor, Yonatan; Goldberg-Stern, Hadassa; Amrom, Dina; Lerman-Sagie, Tally; Teichberg, Vivian I.; Pelled, Dori; Futerman, Anthony H.; Ben Zeev, Bruria; Freilinger, Michael; Verheulpen, Denis; Van Bogaert, Patrick; Levite, Mia Journal: Clinical & developmental immunology Issue: Volume 11:Issue 3/4(2004) Page Start: 241 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological features. (May 2020) Authors: Blumkin, Lubov; Leibovitz, Zvi; Krajden-Haratz, Karina; Arad, Ayala; Yosovich, Keren; Gindes, Liat; Zerem, Ayelet; Ben-Sira, Liat; Lev, Dorit; Nissenkorn, Andrea; Kidron, Dvora; Dobyns, William B.; Malinger, Gustavo; Bahi-Buisson, Nadia; Leventer, Richard J.; Lerman-Sagie, Tally Journal: European journal of paediatric neurology Issue: Volume 26(2020) Page Start: 46 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Clinical phenotypes of infantile onset CACNA1A-related disorder. (January 2021) Authors: Gur-Hartman, Tamar; Berkowitz, Oren; Yosovich, Keren; Roubertie, Agathe; Zanni, Ginevra; Macaya, Alfons; Heimer, Gali; Dueñas, Belén Pérez; Sival, Deborah A.; Pode-Shakked, Ben; López-Laso, Eduardo; Humbertclaude, Véronique; Riant, Florence; Bosco, Luca; Cayron, Lital Bachar; Nissenkorn, Andreea;... Journal: European journal of paediatric neurology Issue: Volume 30(2021) Page Start: 144 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Cone and rod dysfunction in the NARP syndrome. Issue 2 (1st February 1999) Authors: Chowers, Itay; Lerman-Sagie, Tally; Elpeleg, Orly N; Shaag, Avraham; Merin, Saul Journal: British journal of ophthalmology Issue: Volume 83:Issue 2(1999) Page Start: 190 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Congenital Mirror Movements Associated With Brain Malformations. (June 2021) Authors: Nissenkorn, Andreea; Yosovich, Keren; Leibovitz, Zvi; Hartman, Tamar Gur; Zelcer, Itay; Hugirat, Mohammad; Lev, Dorit; Lerman-Sagie, Tally; Blumkin, Lubov Journal: Journal of child neurology Issue: Volume 36:Number 7(2021) Page Start: 545 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Delineation of the phenotype of MED17-related disease in Caucasus-Jewish families. (May 2021) Authors: Fattal-Valevski, Aviva; Ben Sira, Liat; Lerman-Sagie, Tally; Strausberg, Rachel; Bloch-Mimouni, Aviva; Edvardson, Simon; Kaufman, Rami; Chernuha, Veronika; Schneebaum Sender, Nira; Heimer, Gali; Ben Zeev, Bruria Journal: European journal of paediatric neurology Issue: Volume 32(2021) Page Start: 40 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Diagnostic approach to fetal microcephaly. (November 2018) Authors: Leibovitz, Zvi; Lerman-Sagie, Tally Journal: European journal of paediatric neurology Issue: Volume 22:Number 6(2018:Nov.) Page Start: 935 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗