Cohen R - Search Results

1

Prospective, Cross-Sectional Study Finds No Common Viruses in Cerebrospinal Fluid of Children with Pseudotumor Cerebri.

Cohen R, Mahajnah M, Shlonsky Y, Golan-Shany O, Romem A, Halevy A, Natan K, Genizi J. Cohen R, et al. Brain Sci. 2023 Feb 19;13(2):361. doi: 10.3390/brainsci13020361. Brain Sci. 2023. PMID: 36831904 Free PMC article.

2

Children's sleep disturbance scale in differentiating neurological disorders.

Cohen R, Halevy A, Shuper A. Cohen R, et al. Pediatr Neurol. 2013 Dec;49(6):465-8. doi: 10.1016/j.pediatrneurol.2013.06.010. Epub 2013 Sep 27. Pediatr Neurol. 2013. PMID: 24080271

3

Brain imaging findings and social/emotional problems in Israeli children with neurofibromatosis type 1.

Cohen R, Steinberg T, Kornreich L, Aharoni S, Halevy A, Shuper A. Cohen R, et al. Eur J Pediatr. 2015 Feb;174(2):199-203. doi: 10.1007/s00431-014-2366-7. Epub 2014 Jul 16. Eur J Pediatr. 2015. PMID: 25027832

4

Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22.

Cohen R, Basel-Vanagaite L, Goldberg-Stern H, Halevy A, Shuper A, Feingold-Zadok M, Behar DM, Straussberg R. Cohen R, et al. Eur J Paediatr Neurol. 2014 Nov;18(6):801-5. doi: 10.1016/j.ejpn.2014.06.007. Epub 2014 Jul 5. Eur J Paediatr Neurol. 2014. PMID: 25033742

5

Novel EXOSC3 mutation causes complicated hereditary spastic paraplegia.

Halevy A, Lerer I, Cohen R, Kornreich L, Shuper A, Gamliel M, Zimerman BE, Korabi I, Meiner V, Straussberg R, Lossos A. Halevy A, et al. Among authors: cohen r. J Neurol. 2014 Nov;261(11):2165-9. doi: 10.1007/s00415-014-7457-x. Epub 2014 Aug 23. J Neurol. 2014. PMID: 25149867

6

Development of Infants With Idiopathic External Hydrocephalus.

Halevy A, Cohen R, Viner I, Diamond G, Shuper A. Halevy A, et al. Among authors: cohen r. J Child Neurol. 2015 Jul;30(8):1044-7. doi: 10.1177/0883073814553273. Epub 2014 Oct 27. J Child Neurol. 2015. PMID: 25348416

7

Polymicrogyria and myoclonic epilepsy in autosomal recessive cutis laxa type 2A.

Cohen R, Halevy A, Aharoni S, Kraus D, Konen O, Basel-Vanagaite L, Goldberg-Stern H, Straussberg R. Cohen R, et al. Neurogenetics. 2016 Oct;17(4):251-257. doi: 10.1007/s10048-016-0491-3. Epub 2016 Sep 8. Neurogenetics. 2016. PMID: 27631729

8

Congenital myasthenic syndrome in Israel: Genetic and clinical characterization.

Aharoni S, Sadeh M, Shapira Y, Edvardson S, Daana M, Dor-Wollman T, Mimouni-Bloch A, Halevy A, Cohen R, Sagie L, Argov Z, Rabie M, Spiegel R, Chervinsky I, Orenstein N, Engel AG, Nevo Y. Aharoni S, et al. Among authors: cohen r. Neuromuscul Disord. 2017 Feb;27(2):136-140. doi: 10.1016/j.nmd.2016.11.014. Epub 2016 Nov 24. Neuromuscul Disord. 2017. PMID: 28024842 Free PMC article.

9

Thick Corpus Callosum in Children.

Schupper A, Konen O, Halevy A, Cohen R, Aharoni S, Shuper A. Schupper A, et al. Among authors: cohen r. J Clin Neurol. 2017 Apr;13(2):170-174. doi: 10.3988/jcn.2017.13.2.170. J Clin Neurol. 2017. PMID: 28406584 Free PMC article.

10

Attention Deficit Hyperactivity Disorder in Neurofibromatosis Type 1: Evaluation with a Continuous Performance Test.

Cohen R, Halevy A, Aharon S, Shuper A. Cohen R, et al. J Clin Neurol. 2018 Apr;14(2):153-157. doi: 10.3988/jcn.2018.14.2.153. J Clin Neurol. 2018. PMID: 29629523 Free PMC article.

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