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Page 1
Eight novel mutations in MLC1 from 18 Iranian patients with megalencephalic leukoencephalopathy with subcortical cysts.
Kariminejad A, Rajaee A, Ashrafi MR, Alizadeh H, Tonekaboni SH, Malamiri RA, Ghofrani M, Karimzadeh P, Mohammadi MM, Baghalshooshtari A, Bozorgmehr B, Kariminejad MH, Postma N, Abbink TE, van der Knaap MS. Kariminejad A, et al. Among authors: tonekaboni sh. Eur J Med Genet. 2015 Feb;58(2):71-4. doi: 10.1016/j.ejmg.2014.12.004. Epub 2014 Dec 11. Eur J Med Genet. 2015. PMID: 25497041
Evaluation of one hundred pediatric muscle biopsies during a 2-year period in mofid children and toos hospitals.
Nilipor Y, Shariatmadari F, Abdollah Gorji F, Rouzrokh M, Ghofrani M, Karimzadeh P, Taghdiri MM, Delavarkasmaei H, Ahmadabadi F, Bakhshandeh Bali MK, Nemati H, Saket S, Jafari N, Yaghini O, Tonekaboni SH. Nilipor Y, et al. Among authors: tonekaboni sh. Iran J Child Neurol. 2013 Spring;7(2):17-21. Iran J Child Neurol. 2013. PMID: 24665292 Free PMC article.
LGMD2E is the most common type of sarcoglycanopathies in the Iranian population.
Alavi A, Esmaeili S, Nilipour Y, Nafissi S, Tonekaboni SH, Zamani G, Ashrafi MR, Kahrizi K, Najmabadi H, Jazayeri F. Alavi A, et al. Among authors: tonekaboni sh. J Neurogenet. 2017 Sep;31(3):161-169. doi: 10.1080/01677063.2017.1346093. Epub 2017 Jul 7. J Neurogenet. 2017. PMID: 28687063
65 results