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Year Number of Results
1966 1
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1970 2
1972 1
1973 1
1977 2
1983 3
1984 1
1985 3
1986 3
1990 1
1997 3
1999 3
2000 1
2001 1
2002 1
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2010 1
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41 results

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Page 1
Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54.
Smith TB, Rea A, Thomas HB, Thompson K, Oláhová M, Maroofian R, Zamani M, He L, Sadeghian S, Galehdari H, Lotan NS, Gilboa T, Herman KC, McCorvie TJ, Yue WW, Houlden H, Taylor RW, Newman WG, O'Keefe RT. Smith TB, et al. Among authors: lotan ns. Eur J Hum Genet. 2023 Oct;31(10):1190-1194. doi: 10.1038/s41431-023-01437-2. Epub 2023 Aug 9. Eur J Hum Genet. 2023. PMID: 37558808 Free PMC article.
Social world knowledge: Modeling and applications.
Lotan N, Minkov E. Lotan N, et al. PLoS One. 2023 Jul 7;18(7):e0283700. doi: 10.1371/journal.pone.0283700. eCollection 2023. PLoS One. 2023. PMID: 37418393 Free PMC article.
Memorial - Professor Samuel Sideman.
Beyar R, Landesberg A, Lotan N. Beyar R, et al. Among authors: lotan n. Artif Cells Nanomed Biotechnol. 2016 Jun;44(4):1050. doi: 10.3109/21691401.2016.1154281. Epub 2016 Mar 9. Artif Cells Nanomed Biotechnol. 2016. PMID: 26961719 No abstract available.
Large porous particles for pulmonary drug delivery.
Edwards DA, Hanes J, Caponetti G, Hrkach J, Ben-Jebria A, Eskew ML, Mintzes J, Deaver D, Lotan N, Langer R. Edwards DA, et al. Among authors: lotan n. Science. 1997 Jun 20;276(5320):1868-71. doi: 10.1126/science.276.5320.1868. Science. 1997. PMID: 9188534
Intellectual disability syndrome associated with a homozygous founder variant in SGSM3 in Ashkenazi Jews.
Birnbaum R, Ezer S, Lotan NS, Eilat A, Sternlicht K, Benyamini L, Reish O, Falik-Zaccai T, Ben-Gad G, Rod R, Segel R, Kim K, Burton B, Keegan CE, Wagner M, Henderson LB, Mor N, Barel O, Hirsch Y, Meiner V, Elpeleg O, Harel T, Mor-Shakad H. Birnbaum R, et al. Among authors: lotan ns. J Med Genet. 2024 Feb 21;61(3):289-293. doi: 10.1136/jmg-2023-109504. J Med Genet. 2024. PMID: 37833060
41 results