Kahana E - Search Results

1

Multiplex families with epilepsy: Success of clinical and molecular genetic characterization.

Afawi Z, Oliver KL, Kivity S, Mazarib A, Blatt I, Neufeld MY, Helbig KL, Goldberg-Stern H, Misk AJ, Straussberg R, Walid S, Mahajnah M, Lerman-Sagie T, Ben-Zeev B, Kahana E, Masalha R, Kramer U, Ekstein D, Shorer Z, Wallace RH, Mangelsdorf M, MacPherson JN, Carvill GL, Mefford HC, Jackson GD, Scheffer IE, Bahlo M, Gecz J, Heron SE, Corbett M, Mulley JC, Dibbens LM, Korczyn AD, Berkovic SF. Afawi Z, et al. Among authors: kahana e. Neurology. 2016 Feb 23;86(8):713-22. doi: 10.1212/WNL.0000000000002404. Epub 2016 Jan 22. Neurology. 2016. PMID: 26802095 Free PMC article.

2

Epidemiology of dementia in Ashkelon: the influence of education.

Kahana E, Galper Y, Zilber N, Korczyn AD. Kahana E, et al. J Neurol. 2003 Apr;250(4):424-8. doi: 10.1007/s00415-003-0999-y. J Neurol. 2003. PMID: 12700906

3

Prevalence of myotonic dystrophy in Israeli Jewish communities: inter-community variation and founder premutations.

Segel R, Silverstein S, Lerer I, Kahana E, Meir R, Sagi M, Zilber N, Korczyn AD, Shapira Y, Argov Z, Abeliovich D. Segel R, et al. Among authors: kahana e. Am J Med Genet A. 2003 Jun 15;119A(3):273-8. doi: 10.1002/ajmg.a.20177. Am J Med Genet A. 2003. PMID: 12784291

4

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.

5

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

6

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy.

Heron SE, Smith KR, Bahlo M, Nobili L, Kahana E, Licchetta L, Oliver KL, Mazarib A, Afawi Z, Korczyn A, Plazzi G, Petrou S, Berkovic SF, Scheffer IE, Dibbens LM. Heron SE, et al. Among authors: kahana e. Nat Genet. 2012 Nov;44(11):1188-90. doi: 10.1038/ng.2440. Epub 2012 Oct 21. Nat Genet. 2012. PMID: 23086396

7

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

8

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

9

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

10

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

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