Inzelberg R - Search Results

1

Do tardive dyskinesia and L-dopa induced dyskinesia share common genetic risk factors? An exploratory study.

Greenbaum L, Goldwurm S, Zozulinsky P, Lifschytz T, Cohen OS, Yahalom G, Cilia R, Tesei S, Asselta R, Inzelberg R, Kohn Y, Hassin-Baer S, Lerer B. Greenbaum L, et al. Among authors: inzelberg r. J Mol Neurosci. 2013 Oct;51(2):380-8. doi: 10.1007/s12031-013-0020-x. Epub 2013 May 12. J Mol Neurosci. 2013. PMID: 23666822

2

Sequence variants in SLC6A3, DRD2, and BDNF genes and time to levodopa-induced dyskinesias in Parkinson's disease.

Kaplan N, Vituri A, Korczyn AD, Cohen OS, Inzelberg R, Yahalom G, Kozlova E, Milgrom R, Laitman Y, Friedman E, Rosset S, Hassin-Baer S. Kaplan N, et al. Among authors: inzelberg r. J Mol Neurosci. 2014 Jun;53(2):183-8. doi: 10.1007/s12031-014-0276-9. Epub 2014 Mar 15. J Mol Neurosci. 2014. PMID: 24633632

3

The melanocortin 1 receptor (Mc1r) variants do not account for the co-occurrence of Parkinson's disease and malignant melanoma.

Elincx-Benizri S, Inzelberg R, Greenbaum L, Cohen OS, Yahalom G, Laitman Y, Djaldetti R, Orlev Y, Scope A, Azizi E, Friedman E, Hassin-Baer S. Elincx-Benizri S, et al. Among authors: inzelberg r. J Mol Neurosci. 2014 Dec;54(4):820-5. doi: 10.1007/s12031-014-0425-1. Epub 2014 Oct 5. J Mol Neurosci. 2014. PMID: 25284244

4

Dyskinesias in patients with Parkinson's disease: effect of the leucine-rich repeat kinase 2 (LRRK2) G2019S mutation.

Yahalom G, Kaplan N, Vituri A, Cohen OS, Inzelberg R, Kozlova E, Korczyn AD, Rosset S, Friedman E, Hassin-Baer S. Yahalom G, et al. Among authors: inzelberg r. Parkinsonism Relat Disord. 2012 Nov;18(9):1039-41. doi: 10.1016/j.parkreldis.2012.05.014. Epub 2012 Jun 13. Parkinsonism Relat Disord. 2012. PMID: 22703868

5

Genetic movement disorders in patients of Jewish ancestry.

Inzelberg R, Hassin-Baer S, Jankovic J. Inzelberg R, et al. JAMA Neurol. 2014 Dec;71(12):1567-72. doi: 10.1001/jamaneurol.2014.1364. JAMA Neurol. 2014. PMID: 25347348 Review.

6

Motor progression of Parkinson's disease with the leucine-rich repeat kinase 2 G2019S mutation.

Yahalom G, Orlev Y, Cohen OS, Kozlova E, Friedman E, Inzelberg R, Hassin-Baer S. Yahalom G, et al. Among authors: inzelberg r. Mov Disord. 2014 Jul;29(8):1057-60. doi: 10.1002/mds.25931. Epub 2014 Jun 5. Mov Disord. 2014. PMID: 24903616

7

Parkinson's disease genes do not segregate with breast cancer genes' loci.

Kravitz E, Laitman Y, Hassin-Baer S, Inzelberg R, Friedman E. Kravitz E, et al. Among authors: inzelberg r. Cancer Epidemiol Biomarkers Prev. 2013 Aug;22(8):1464-72. doi: 10.1158/1055-9965.EPI-13-0472. Epub 2013 Jun 13. Cancer Epidemiol Biomarkers Prev. 2013. PMID: 23765085

8

The LRRK2 G2019S mutation status does not affect the outcome of subthalamic stimulation in patients with Parkinson's disease.

Greenbaum L, Israeli-Korn SD, Cohen OS, Elincx-Benizri S, Yahalom G, Kozlova E, Strauss H, Molshatzki N, Inzelberg R, Spiegelmann R, Israel Z, Hassin-Baer S. Greenbaum L, et al. Among authors: inzelberg r. Parkinsonism Relat Disord. 2013 Nov;19(11):1053-6. doi: 10.1016/j.parkreldis.2013.07.005. Epub 2013 Aug 6. Parkinsonism Relat Disord. 2013. PMID: 23932063

9

Subthalamic nucleus deep brain stimulation does not improve visuo-motor impairment in Parkinson's disease.

Israeli-Korn SD, Hocherman S, Hassin-Baer S, Cohen OS, Inzelberg R. Israeli-Korn SD, et al. Among authors: inzelberg r. PLoS One. 2013 Jun 11;8(6):e65270. doi: 10.1371/journal.pone.0065270. Print 2013. PLoS One. 2013. PMID: 23776460 Free PMC article. Clinical Trial.

10

Phenotype of the 202 adenine deletion in the parkin gene: 40 years of follow-up.

Hassin-Baer S, Hattori N, Cohen OS, Massarwa M, Israeli-Korn SD, Inzelberg R. Hassin-Baer S, et al. Among authors: inzelberg r. Mov Disord. 2011 Mar;26(4):719-22. doi: 10.1002/mds.23456. Epub 2011 Jan 21. Mov Disord. 2011. PMID: 21506149

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