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92 results
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A dual role for interleukin-1 in hippocampal-dependent memory processes.
Goshen I, Kreisel T, Ounallah-Saad H, Renbaum P, Zalzstein Y, Ben-Hur T, Levy-Lahad E, Yirmiya R. Goshen I, et al. Among authors: renbaum p. Psychoneuroendocrinology. 2007 Sep-Nov;32(8-10):1106-15. doi: 10.1016/j.psyneuen.2007.09.004. Epub 2007 Oct 31. Psychoneuroendocrinology. 2007. PMID: 17976923
Vesicular acetylcholine transporter defect underlies devastating congenital myasthenia syndrome.
Aran A, Segel R, Kaneshige K, Gulsuner S, Renbaum P, Oliphant S, Meirson T, Weinberg-Shukron A, Hershkovitz Y, Zeligson S, Lee MK, Samson AO, Parsons SM, King MC, Levy-Lahad E, Walsh T. Aran A, et al. Among authors: renbaum p. Neurology. 2017 Mar 14;88(11):1021-1028. doi: 10.1212/WNL.0000000000003720. Epub 2017 Feb 10. Neurology. 2017. PMID: 28188302 Free PMC article.
Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewish population.
Horowitz M, Pasmanik-Chor M, Borochowitz Z, Falik-Zaccai T, Heldmann K, Carmi R, Parvari R, Beit-Or H, Goldman B, Peleg L, Levy-Lahad E, Renbaum P, Legum S, Shomrat R, Yeger H, Benbenisti D, Navon R, Dror V, Shohat M, Magal N, Navot N, Eyal N. Horowitz M, et al. Among authors: renbaum p. Hum Mutat. 1998;12(4):240-4. doi: 10.1002/(SICI)1098-1004(1998)12:4<240::AID-HUMU4>3.0.CO;2-J. Hum Mutat. 1998. PMID: 9744474
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