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Page 1
Neurodevelopmental outcome of children born with an isolated atretic cephalocele.
Tokatly Latzer I, Roth J, Constantini S, Malinger G, Weissmann-Brenner A, Ben-Sira L, Fattal-Valevski A, Meirson H. Tokatly Latzer I, et al. Among authors: meirson h. Childs Nerv Syst. 2021 Apr;37(4):1295-1300. doi: 10.1007/s00381-020-04997-6. Epub 2021 Jan 6. Childs Nerv Syst. 2021. PMID: 33404719
The role of ICP monitoring in paediatric IIH.
Lalgudi Srinivasan H, Richetta C, Manoim N, Zipori AB, Shiran SI, Meirson H, Roth J, Constantini S. Lalgudi Srinivasan H, et al. Among authors: meirson h. Childs Nerv Syst. 2020 Dec;36(12):3027-3033. doi: 10.1007/s00381-020-04618-2. Epub 2020 Apr 22. Childs Nerv Syst. 2020. PMID: 32322974
Medical treatment of tuberous sclerosis-related epilepsy.
Uliel-Sibony S, Chernuha V, Meirson H, Fattal-Valevski A. Uliel-Sibony S, et al. Among authors: meirson h. Childs Nerv Syst. 2020 Oct;36(10):2511-2517. doi: 10.1007/s00381-020-04772-7. Epub 2020 Aug 22. Childs Nerv Syst. 2020. PMID: 32829444 Review.
Sleep Disturbances in Adolescents With Idiopathic Intracranial Hypertension.
Tokatly Latzer I, Tauman R, Senderowich N, Markovitz R, Bachar-Zipori A, Klein A, Meirson H, Fattal-Valevski A, Hausman-Kedem M. Tokatly Latzer I, et al. Among authors: meirson h. Pediatr Neurol. 2023 May;142:39-46. doi: 10.1016/j.pediatrneurol.2023.02.006. Epub 2023 Feb 15. Pediatr Neurol. 2023. PMID: 36905761
Utility of genetic testing in children with leukodystrophy.
Zerem A, Libzon S, Ben Sira L, Meirson H, Hausman-Kedem M, Haviv N, Yosovich K, Mory A, Baris Feldman H, Lev D, Lerman-Sagie T, Fattal-Valevski A, Hacohen Y, Marom D. Zerem A, et al. Among authors: meirson h. Eur J Paediatr Neurol. 2023 Jul;45:29-35. doi: 10.1016/j.ejpn.2023.05.008. Epub 2023 May 27. Eur J Paediatr Neurol. 2023. PMID: 37267771
Autoimmune encephalitis in Israeli children - A retrospective nationwide study.
Sachs N, Zohar-Dayan E, Ben Zeev B, Gilboa T, Kurd M, Latzer IT, Meirson H, Krause I, Dizitzer Y, Cohen EG. Sachs N, et al. Among authors: meirson h. Eur J Paediatr Neurol. 2024 May;50:1-5. doi: 10.1016/j.ejpn.2024.03.001. Epub 2024 Mar 15. Eur J Paediatr Neurol. 2024. PMID: 38518418
Novel WWOX deleterious variants cause early infantile epileptic encephalopathy, severe developmental delay and dysmorphism among Yemenite Jews.
Weisz-Hubshman M, Meirson H, Michaelson-Cohen R, Beeri R, Tzur S, Bormans C, Modai S, Shomron N, Shilon Y, Banne E, Orenstein N, Konen O, Marek-Yagel D, Veber A, Shalva N, Imagawa E, Matsumoto N, Lev D, Lerman Sagie T, Raas-Rothschild A, Ben-Zeev B, Basel-Salmon L, Behar DM, Heimer G. Weisz-Hubshman M, et al. Among authors: meirson h. Eur J Paediatr Neurol. 2019 May;23(3):418-426. doi: 10.1016/j.ejpn.2019.02.003. Epub 2019 Feb 19. Eur J Paediatr Neurol. 2019. PMID: 30853297
13 results