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Serum miRNAs as biomarkers for the rare types of muscular dystrophy.
Koutsoulidou A, Koutalianos D, Georgiou K, Kakouri AC, Oulas A, Tomazou M, Kyriakides TC, Roos A, Papadimas GK, Papadopoulos C, Kararizou E, Spyrou GM, Zamba Papanicolaou E, Lochmüller H, Phylactou LA. Koutsoulidou A, et al. Among authors: phylactou la. Neuromuscul Disord. 2022 Apr;32(4):332-346. doi: 10.1016/j.nmd.2022.03.003. Epub 2022 Mar 11. Neuromuscul Disord. 2022. PMID: 35393236 Free article.
High carrier frequency of 21-hydroxylase deficiency in Cyprus.
Phedonos AA, Shammas C, Skordis N, Kyriakides TC, Neocleous V, Phylactou LA. Phedonos AA, et al. Among authors: phylactou la. Clin Genet. 2013 Dec;84(6):585-8. doi: 10.1111/cge.12153. Epub 2013 Apr 22. Clin Genet. 2013. PMID: 23600966
Familial Mediterranean fever associated with MEFV mutations in a large cohort of Cypriot patients.
Neocleous V, Costi C, Kyriakou C, Kyriakides TC, Shammas C, Skordis N, Toumba M, Kyriakou S, Koliou M, Kousparou M, Onoufriou M, Hadjipanayis A, Iasonides M, Atamyan VN, Pierides A, Christophidou-Anastasiadou V, Tanteles GA, Phylactou LA. Neocleous V, et al. Among authors: phylactou la. Ann Hum Genet. 2015 Jan;79(1):20-7. doi: 10.1111/ahg.12087. Epub 2014 Nov 13. Ann Hum Genet. 2015. PMID: 25393764
109 results