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High Hereditary Transthyretin-Related Amyloidosis Prevalence in Crete: Genetic Heterogeneity and Distinct Phenotypes.
Tzagournissakis M, Foukarakis E, Samonakis D, Tsilimbaris M, Michaelidou K, Mathioudakis L, Marinis A, Giannakoudakis E, Spanaki C, Skoula I, Erimaki S, Amoiridis G, Koutsis G, Koukouraki S, Stylianou K, Plaitakis A, Mitsias PD, Zaganas I. Tzagournissakis M, et al. Among authors: stylianou k. Neurol Genet. 2022 Sep 9;8(5):e200013. doi: 10.1212/NXG.0000000000200013. eCollection 2022 Oct. Neurol Genet. 2022. PMID: 36101541 Free PMC article.
COVID-19 Vaccination and New Onset Glomerular Disease: Results from the IRocGN2 International Registry.
Waldman M, Sinaii N, Lerma EV, Kurien AA, Jhaveri KD, Uppal NN, Wanchoo R, Avasare R, Zuckerman JE, Liew A, Gallan AJ, El-Meanawy A, Yagil Y, Lebedev L, Baskaran K, Vilayur E, Cohen A, Weerasinghe N, Petrakis I, Stylianou K, Gakiopoulou H, Hamilton AJ, Edney N, Millner R, Marinaki S, Rein JL, Killen JP, Rodríguez Chagolla JM, Bassil C, Lopez Del Valle R, Evans J, Urisman A, Zawaideh M, Baxi PV, Rodby R, Vankalakunti M, Mejia Vilet JM, Ramirez Andrade SE, Homan MP, Vásquez Jiménez E, Perinpanayagam N, Velez JCQ, Mohamed MMB, Mohammed KMG, Sekar A, Ollila L, Aron AW, Arellano Arteaga KJ, Islam M, Berrio EM, Maoujoud O, Morales RR, Seipp R, Schulze CE, Yenchek RH, Vancea I, Muneeb M, Howard L, Caza TN. Waldman M, et al. Among authors: stylianou k. Kidney360. 2023 Mar 1;4(3):349-362. doi: 10.34067/KID.0006832022. Kidney360. 2023. PMID: 36996301 Free PMC article.
Human TTRV30M localization within podocytes in a transgenic mouse model of transthyretin related amyloidosis: does the environment play a role?
Petrakis I, Mavroeidi V, Stylianou K, Efthymiou G, Perakis K, Vardaki E, Stratigis S, Giannakakis K, Kourouniotis K, Amoiridis G, Plaitakis A, Saraiva MJ, Yamamura KI, Daphnis E. Petrakis I, et al. Among authors: stylianou k. Transgenic Res. 2013 Feb;22(1):101-16. doi: 10.1007/s11248-012-9632-0. Epub 2012 Jul 18. Transgenic Res. 2013. PMID: 22806634
The p.Pro482Ala Variant in the CNNM2 Gene Causes Severe Hypomagnesemia Amenable to Treatment with Spironolactone.
Petrakis I, Drosataki E, Stavrakaki I, Dermitzaki K, Lygerou D, Konidaki M, Pleros C, Kroustalakis N, Maragkou S, Androvitsanea A, Stylianou I, Zaganas I, Stylianou K. Petrakis I, et al. Among authors: stylianou i, stylianou k. Int J Mol Sci. 2022 Jun 30;23(13):7284. doi: 10.3390/ijms23137284. Int J Mol Sci. 2022. PMID: 35806288 Free PMC article.
150 results