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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2003 1
2004 3
2005 3
2006 2
2007 3
2008 3
2009 3
2010 3
2011 3
2012 6
2013 7
2014 8
2015 5
2016 6
2017 4
2018 5
2019 3
2021 1
2022 1
2024 0

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56 results

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Page 1
Homozygous MED25 mutation implicated in eye-intellectual disability syndrome.
Basel-Vanagaite L, Smirin-Yosef P, Essakow JL, Tzur S, Lagovsky I, Maya I, Pasmanik-Chor M, Yeheskel A, Konen O, Orenstein N, Weisz Hubshman M, Drasinover V, Magal N, Peretz Amit G, Zalzstein Y, Zeharia A, Shohat M, Straussberg R, Monté D, Salmon-Divon M, Behar DM. Basel-Vanagaite L, et al. Among authors: zeharia a. Hum Genet. 2015 Jun;134(6):577-87. doi: 10.1007/s00439-015-1541-x. Epub 2015 Mar 20. Hum Genet. 2015. PMID: 25792360 Clinical Trial.
MRI white matter lesions in pediatric migraine.
Eidlitz-Markus T, Zeharia A, Haimi-Cohen Y, Konen O. Eidlitz-Markus T, et al. Among authors: zeharia a. Cephalalgia. 2013 Aug;33(11):906-13. doi: 10.1177/0333102413480955. Epub 2013 Apr 10. Cephalalgia. 2013. PMID: 23575818
Defining the Phenotype and Assessing Severity in Phosphoglucomutase-1 Deficiency.
Wong SY, Beamer LJ, Gadomski T, Honzik T, Mohamed M, Wortmann SB, Brocke Holmefjord KS, Mork M, Bowling F, Sykut-Cegielska J, Koch D, Ackermann A, Stanley CA, Rymen D, Zeharia A, Al-Sayed M, Marquardt T, Jaeken J, Lefeber D, Conrad DF, Kozicz T, Morava E. Wong SY, et al. Among authors: zeharia a. J Pediatr. 2016 Aug;175:130-136.e8. doi: 10.1016/j.jpeds.2016.04.021. Epub 2016 May 17. J Pediatr. 2016. PMID: 27206562
Toward genotype phenotype correlations in GFM1 mutations.
Galmiche L, Serre V, Beinat M, Zossou R, Assouline Z, Lebre AS, Chretien F, Shenhav R, Zeharia A, Saada A, Vedrenne V, Boddaert N, de Lonlay P, Rio M, Munnich A, Rötig A. Galmiche L, et al. Among authors: zeharia a. Mitochondrion. 2012 Mar;12(2):242-7. doi: 10.1016/j.mito.2011.09.007. Epub 2011 Oct 1. Mitochondrion. 2012. PMID: 21986555
Classical Xanthinuria in Nine Israeli Families and Two Isolated Cases from Germany: Molecular, Biochemical and Population Genetics Aspects.
Peretz H, Lagziel A, Bittner F, Kabha M, Shtauber-Naamati M, Zhuravel V, Usher S, Rump S, Wollers S, Bork B, Mandel H, Falik-Zaccai T, Kalfon L, Graessler J, Zeharia A, Heib N, Shalev H, Landau D, Levartovsky D. Peretz H, et al. Among authors: zeharia a. Biomedicines. 2021 Jul 7;9(7):788. doi: 10.3390/biomedicines9070788. Biomedicines. 2021. PMID: 34356852 Free PMC article.
56 results