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Mild Phenotype in a Patient with a De Novo 6.3 Mb Distal Deletion at 10q26.2q26.3.
Tanteles GA, Nikolaou E, Christou Y, Alexandrou A, Evangelidou P, Christophidou-Anastasiadou V, Sismani C, Papacostas SS. Tanteles GA, et al. Among authors: christou y. Case Rep Genet. 2015;2015:242891. doi: 10.1155/2015/242891. Epub 2015 Jul 29. Case Rep Genet. 2015. PMID: 26294985 Free PMC article.
Pathogenic and Low-Frequency Variants in Children With Central Precocious Puberty.
Neocleous V, Fanis P, Toumba M, Gorka B, Kousiappa I, Tanteles GA, Iasonides M, Nicolaides NC, Christou YP, Michailidou K, Nicolaou S, Papacostas SS, Christoforidis A, Kyriakou A, Vlachakis D, Skordis N, Phylactou LA. Neocleous V, et al. Among authors: christou yp. Front Endocrinol (Lausanne). 2021 Sep 24;12:745048. doi: 10.3389/fendo.2021.745048. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34630334 Free PMC article.
Quality of Life of Cypriot Patients Suffering with Huntington's Disease.
Varda E, Demetriou CA, Heraclides A, Christou YP, Zamba-Papanicolaou E. Varda E, et al. PLoS Curr. 2016 Oct 25;8:ecurrents.hd.270776c4fdd7776499dd45bf47049a75. doi: 10.1371/currents.hd.270776c4fdd7776499dd45bf47049a75. PLoS Curr. 2016. PMID: 27917304 Free PMC article.
Identification of exosomal muscle-specific miRNAs in serum of myotonic dystrophy patients relating to muscle disease progress.
Koutsoulidou A, Photiades M, Kyriakides TC, Georgiou K, Prokopi M, Kapnisis K, Lusakowska A, Nearchou M, Christou Y, Papadimas GK, Anayiotos A, Kyriakou K, Kararizou E, Zamba Papanicolaou E, Phylactou LA. Koutsoulidou A, et al. Among authors: christou y. Hum Mol Genet. 2017 Sep 1;26(17):3285-3302. doi: 10.1093/hmg/ddx212. Hum Mol Genet. 2017. PMID: 28637233
33 results