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83 results

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Page 1
Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutations.
Tajsharghi H, Hammans S, Lindberg C, Lossos A, Clarke NF, Mazanti I, Waddell LB, Fellig Y, Foulds N, Katifi H, Webster R, Raheem O, Udd B, Argov Z, Oldfors A. Tajsharghi H, et al. Among authors: fellig y. Eur J Hum Genet. 2014 Jun;22(6):801-8. doi: 10.1038/ejhg.2013.250. Epub 2013 Nov 6. Eur J Hum Genet. 2014. PMID: 24193343 Free PMC article.
Aggressive leptomeningeal gliomatosis in neurofibromatosis type 1.
Arkadir D, Fellig Y, Gomori MJ, Linetsky E, Shalom E, Lossos A. Arkadir D, et al. Among authors: fellig y. J Clin Oncol. 2012 Sep 20;30(27):e269-70. doi: 10.1200/JCO.2012.42.1719. Epub 2012 Aug 6. J Clin Oncol. 2012. PMID: 22869891 No abstract available.
Variable phenotypes of knockin mice carrying the M712T Gne mutation.
Sela I, Yakovlev L, Becker Cohen M, Elbaz M, Yanay N, Ben Shlomo U, Yotvat H, Fellig Y, Argov Z, Mitrani-Rosenbaum S. Sela I, et al. Among authors: fellig y. Neuromolecular Med. 2013 Mar;15(1):180-91. doi: 10.1007/s12017-012-8209-7. Epub 2012 Dec 13. Neuromolecular Med. 2013. PMID: 23238814
Congenital myopathy is caused by mutation of HACD1.
Muhammad E, Reish O, Ohno Y, Scheetz T, Deluca A, Searby C, Regev M, Benyamini L, Fellig Y, Kihara A, Sheffield VC, Parvari R. Muhammad E, et al. Among authors: fellig y. Hum Mol Genet. 2013 Dec 20;22(25):5229-36. doi: 10.1093/hmg/ddt380. Epub 2013 Aug 9. Hum Mol Genet. 2013. PMID: 23933735 Free PMC article.
Tumefactive demyelination following in vitro fertilization (IVF).
Vaknin-Dembinsky A, Bdolah Y, Karussis D, Rosenthal G, Petrou P, Fellig Y, Abramsky O, Lossos A. Vaknin-Dembinsky A, et al. Among authors: fellig y. J Neurol Sci. 2015 Jan 15;348(1-2):256-8. doi: 10.1016/j.jns.2014.11.016. Epub 2014 Nov 18. J Neurol Sci. 2015. PMID: 25499758
Nonsyndromic Early-Onset Cone-Rod Dystrophy and Limb-Girdle Muscular Dystrophy in a Consanguineous Israeli Family are Caused by Two Independent yet Linked Mutations in ALMS1 and DYSF.
Lazar CH, Kimchi A, Namburi P, Mutsuddi M, Zelinger L, Beryozkin A, Ben-Simhon S, Obolensky A, Ben-Neriah Z, Argov Z, Pikarsky E, Fellig Y, Marks-Ohana D, Ratnapriya R, Banin E, Sharon D, Swaroop A. Lazar CH, et al. Among authors: fellig y. Hum Mutat. 2015 Sep;36(9):836-41. doi: 10.1002/humu.22822. Epub 2015 Jul 14. Hum Mutat. 2015. PMID: 26077327 Free PMC article.
Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder.
Lossos A, Elazar N, Lerer I, Schueler-Furman O, Fellig Y, Glick B, Zimmerman BE, Azulay H, Dotan S, Goldberg S, Gomori JM, Ponger P, Newman JP, Marreed H, Steck AJ, Schaeren-Wiemers N, Mor N, Harel M, Geiger T, Eshed-Eisenbach Y, Meiner V, Peles E. Lossos A, et al. Among authors: fellig y. Brain. 2015 Sep;138(Pt 9):2521-36. doi: 10.1093/brain/awv204. Epub 2015 Jul 15. Brain. 2015. PMID: 26179919 Free PMC article.
83 results