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Page 1
Retrospective analysis of persistent HyperCKemia with or without muscle weakness in a case series from Greece highlights vast DMD variant heterogeneity.
Kekou K, Svingou M, Vogiatzakis N, Nitsa E, Veltra D, Marinakis NM, Tilemis FN, Tzetis M, Mitrakos A, Tsaroucha C, Selenti N, Papadimas GK, Papadopoulos C, Traeger-Synodinos J, Lochmuller H, Sofocleous C. Kekou K, et al. Among authors: tzetis m. Expert Rev Mol Diagn. 2023 Jul-Dec;23(11):999-1010. doi: 10.1080/14737159.2023.2264181. Epub 2023 Oct 24. Expert Rev Mol Diagn. 2023. PMID: 37754746
Characteristics of Café-au-lait Macules and their Association with the Neurofibromatosis type I Genotype in a Cohort of Greek Children.
Nasi L, Alexopoulos A, Kokkinou E, Roka K, Tzetis M, Tsipi M, Kakourou T, Kanaka-Gantenbein C, Chrousos G, Kattamis A, Pons R; Agia Sophia Neurocutaneous Group. Nasi L, et al. Among authors: tzetis m. Acta Derm Venereol. 2023 Jun 5;103:adv5758. doi: 10.2340/actadv.v103.5758. Acta Derm Venereol. 2023. PMID: 37272364 Free PMC article.
Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children.
Christodoulaki V, Kosma K, Marinakis NM, Tilemis FN, Stergiou N, Kampouraki A, Kapogiannis C, Karava V, Mitsioni A, Mila M, Kanaka-Gantenbein C, Makrythanasis P, Tzetis M, Traeger-Synodinos J. Christodoulaki V, et al. Among authors: tzetis m. Genes (Basel). 2024 Aug 2;15(8):1016. doi: 10.3390/genes15081016. Genes (Basel). 2024. PMID: 39202375 Free PMC article.
133 results