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FCGR3A-V158F polymorphism is a disease-specific pharmacogenetic marker for the treatment of psoriasis with Fc-containing TNFα inhibitors.
Mendrinou E, Patsatsi A, Zafiriou E, Papadopoulou D, Aggelou L, Sarri C, Mamuris Z, Kyriakou A, Sotiriadis D, Roussaki-Schulze A, Sarafidou T, Vasilopoulos Y. Mendrinou E, et al. Among authors: sarri c. Pharmacogenomics J. 2017 Jun;17(3):237-241. doi: 10.1038/tpj.2016.16. Epub 2016 Apr 5. Pharmacogenomics J. 2017. PMID: 27044681
A pharmacogenetic study of ABCB1 polymorphisms and cyclosporine treatment response in patients with psoriasis in the Greek population.
Vasilopoulos Y, Sarri C, Zafiriou E, Patsatsi A, Stamatis C, Ntoumou E, Fassos I, Tsalta A, Karra A, Roussaki-Schulze A, Sotiriadis D, Mamuris Z, Sarafidou T. Vasilopoulos Y, et al. Among authors: sarri c. Pharmacogenomics J. 2014 Dec;14(6):523-5. doi: 10.1038/tpj.2014.23. Epub 2014 Jun 3. Pharmacogenomics J. 2014. PMID: 24889923
Netherton Syndrome: A Genotype-Phenotype Review.
Sarri CA, Roussaki-Schulze A, Vasilopoulos Y, Zafiriou E, Patsatsi A, Stamatis C, Gidarokosta P, Sotiriadis D, Sarafidou T, Mamuris Z. Sarri CA, et al. Mol Diagn Ther. 2017 Apr;21(2):137-152. doi: 10.1007/s40291-016-0243-y. Mol Diagn Ther. 2017. PMID: 27905021 Review.
Corrigendum to "Netherton Syndrome in a Neonate with Possible Growth Hormone Deficiency and Transient Hyperaldosteronism".
Chatziioannidis I, Babatseva E, Patsatsi A, Galli-Tsinopoulou A, Sarri C, Lithoxopoulou M, Mitsiakos G, Karagianni P, Tsakalidis C, Mamuris Z, Nikolaidis N. Chatziioannidis I, et al. Among authors: sarri c. Case Rep Pediatr. 2015;2015:328717. doi: 10.1155/2015/328717. Epub 2015 Oct 13. Case Rep Pediatr. 2015. PMID: 26550512 Free PMC article. No abstract available.
41 results