Kahana E - Search Results

1

Snord 3A: a molecular marker and modulator of prion disease progression.

Cohen E, Avrahami D, Frid K, Canello T, Levy Lahad E, Zeligson S, Perlberg S, Chapman J, Cohen OS, Kahana E, Lavon I, Gabizon R. Cohen E, et al. Among authors: kahana e. PLoS One. 2013;8(1):e54433. doi: 10.1371/journal.pone.0054433. Epub 2013 Jan 21. PLoS One. 2013. PMID: 23349890 Free PMC article.

2

Dimethyl sulfoxide delays PrP sc accumulation and disease symptoms in prion-infected hamsters.

Shaked GM, Engelstein R, Avraham I, Kahana E, Gabizon R. Shaked GM, et al. Among authors: kahana e. Brain Res. 2003 Sep 5;983(1-2):137-43. doi: 10.1016/s0006-8993(03)03045-2. Brain Res. 2003. PMID: 12914974

3

Thalamo-striatal diffusion reductions precede disease onset in prion mutation carriers.

Lee H, Rosenmann H, Chapman J, Kingsley PB, Hoffmann C, Cohen OS, Kahana E, Korczyn AD, Prohovnik I. Lee H, et al. Among authors: kahana e. Brain. 2009 Oct;132(Pt 10):2680-7. doi: 10.1093/brain/awp064. Epub 2009 Mar 24. Brain. 2009. PMID: 19321460 Free PMC article.

4

Tau and 14-3-3 of genetic and sporadic Creutzfeldt-Jakob disease patients in Israel.

Meiner Z, Kahana E, Baitcher F, Korczyn AD, Chapman J, Cohen OS, Milo R, Aharon-Perez J, Abramsky O, Gabizon R, Rosenmann H. Meiner Z, et al. Among authors: kahana e. J Neurol. 2011 Feb;258(2):255-62. doi: 10.1007/s00415-010-5738-6. Epub 2010 Sep 9. J Neurol. 2011. PMID: 20827556

5

Characterization of sleep disorders in patients with E200K familial Creutzfeldt-Jakob disease.

Cohen OS, Chapman J, Korczyn AD, Warman-Alaluf N, Orlev Y, Givaty G, Nitsan Z, Appel S, Rosenmann H, Kahana E, Shechter-Amir D. Cohen OS, et al. Among authors: kahana e. J Neurol. 2015 Feb;262(2):443-50. doi: 10.1007/s00415-014-7593-3. Epub 2014 Dec 2. J Neurol. 2015. PMID: 25451855

6

Familial Creutzfeldt-Jakob disease with the E200K mutation: longitudinal neuroimaging from asymptomatic to symptomatic CJD.

Cohen OS, Chapman J, Korczyn AD, Nitsan Z, Appel S, Hoffmann C, Rosenmann H, Kahana E, Lee H. Cohen OS, et al. Among authors: kahana e. J Neurol. 2015 Mar;262(3):604-13. doi: 10.1007/s00415-014-7615-1. Epub 2014 Dec 19. J Neurol. 2015. PMID: 25522698

7

Clinical radiological correlation in E200K familial Creutzfeldt-Jakob disease.

Cohen OS, Chapman J, Korczyn AD, Siaw OL, Warman-Alaluf N, Nitsan Z, Appel S, Kahana E, Rosenmann H, Hoffmann C. Cohen OS, et al. Among authors: kahana e. J Neural Transm (Vienna). 2016 Dec;123(12):1457-1462. doi: 10.1007/s00702-016-1617-3. Epub 2016 Sep 13. J Neural Transm (Vienna). 2016. PMID: 27624725

8

CSF tau correlates with the degree of cortical involvement in E200K familial Creutzfeldt-Jakob disease.

Cohen OS, Chapman J, Korczyn AD, Siaw OL, Warman-Alaluf N, Nitsan Z, Appel S, Kahana E, Rosenmann H, Hoffmann C. Cohen OS, et al. Among authors: kahana e. Neurosci Lett. 2016 Nov 10;634:76-78. doi: 10.1016/j.neulet.2016.10.012. Epub 2016 Oct 6. Neurosci Lett. 2016. PMID: 27721036

9

Disease duration in E200K familial Creutzfeldt-Jakob disease is correlated with clinical, radiological, and laboratory variables.

Cohen OS, Chapman J, Korczyn AD, Nitsan Z, Appel S, Kahana E, Rosenmann H, Hoffmann C. Cohen OS, et al. Among authors: kahana e. J Neural Transm (Vienna). 2019 May;126(5):607-611. doi: 10.1007/s00702-018-1958-1. Epub 2018 Nov 29. J Neural Transm (Vienna). 2019. PMID: 30498951

10

Familial Creutzfeldt-Jakob disease homozygous to the E200K mutation: clinical characteristics and disease course.

Nitsan Z, Cohen OS, Chapman J, Kahana E, Korczyn AD, Appel S, Osherov M, Rosenmann H, Milo R. Nitsan Z, et al. Among authors: kahana e. J Neurol. 2020 Aug;267(8):2455-2458. doi: 10.1007/s00415-020-09826-z. Epub 2020 May 4. J Neurol. 2020. PMID: 32367297

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