Kahana E - Search Results

1

Juvenile multiple sclerosis similar to type I diabetes mellitus has a seasonality of month of birth which differs from that in the general population.

Lewy H, Rotstein A, Kahana E, Marrosu MG, Cocco E, Laron Z. Lewy H, et al. Among authors: kahana e. J Pediatr Endocrinol Metab. 2008 May;21(5):473-7. doi: 10.1515/jpem.2008.21.5.473. J Pediatr Endocrinol Metab. 2008. PMID: 18655530 No abstract available.

2

Multiple sclerosis: geoepidemiology, genetics and the environment.

Milo R, Kahana E. Milo R, et al. Among authors: kahana e. Autoimmun Rev. 2010 Mar;9(5):A387-94. doi: 10.1016/j.autrev.2009.11.010. Epub 2009 Nov 20. Autoimmun Rev. 2010. PMID: 19932200 Review.

3

The frequency of multiple sclerosis in jewish and arab populations in greater jerusalem.

Karni A, Kahana E, Zilber N, Abramsky O, Alter M, Karussis D. Karni A, et al. Among authors: kahana e. Neuroepidemiology. 2003 Jan-Feb;22(1):82-6. doi: 10.1159/000067101. Neuroepidemiology. 2003. PMID: 12566958

4

Epidemiologic studies of multiple sclerosis: a review.

Kahana E. Kahana E. Biomed Pharmacother. 2000 Mar;54(2):100-2. doi: 10.1016/S0753-3322(00)88859-9. Biomed Pharmacother. 2000. PMID: 10759294 Review.

5

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

6

Genetic Creutzfeldt-Jakob disease in Turkish Jews-demographic and clinical features.

Menendez L, Milo R, Cohen OS, Chapman J, Rosenmann H, Nitsan Z, Kahana E, Appel S. Menendez L, et al. Among authors: kahana e. Acta Neurol Scand. 2022 Nov;146(5):586-589. doi: 10.1111/ane.13684. Epub 2022 Aug 16. Acta Neurol Scand. 2022. PMID: 35974683

7

Multiple sclerosis frequency in Israel's diverse populations.

Alter M, Kahana E, Zilber N, Miller A. Alter M, et al. Among authors: kahana e. Neurology. 2006 Apr 11;66(7):1061-6. doi: 10.1212/01.wnl.0000204194.47925.0d. Neurology. 2006. PMID: 16606919

8

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

9

The Fas promoter polymorphism at position -670 is not associated with late-onset sporadic Alzheimer's disease.

Rosenmann H, Meiner Z, Kahana E, Aladjem Z, Friedman G, Ben-Yehuda A, Grenader T, Wertman E, Abramsky O. Rosenmann H, et al. Among authors: kahana e. Dement Geriatr Cogn Disord. 2004;17(3):143-6. doi: 10.1159/000076347. Epub 2004 Jan 20. Dement Geriatr Cogn Disord. 2004. PMID: 14739535

10

Lack of association of interleukin-1beta polymorphism with Alzheimer's disease in the Jewish population.

Rosenmann H, Meiner Z, Dresner-Pollak R, Kahana E, Aladjem Z, Grenader T, Wertman E, Abramsky O. Rosenmann H, et al. Among authors: kahana e. Neurosci Lett. 2004 Jun 10;363(2):131-3. doi: 10.1016/j.neulet.2004.03.063. Neurosci Lett. 2004. PMID: 15172100

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