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Vanishing urate, acute kidney injury episodes and a homozygous SLC2A9 mutation.
Androvitsanea A, Stylianou K, Maragkaki E, Tzanakakis M, Stratakis S, Petrakis I, Giatzakis C, Daphnis E. Androvitsanea A, et al. Among authors: giatzakis c. Int Urol Nephrol. 2015 Jun;47(6):1035-6. doi: 10.1007/s11255-015-1005-1. Epub 2015 May 13. Int Urol Nephrol. 2015. PMID: 25966807 No abstract available.
Corrigendum to "Mutation Spectrum of the ABCA4 Gene in a Greek Cohort with Stargardt Disease: Identification of Novel Mutations and Evidence of Three Prevalent Mutated Alleles".
Kamakari S, Kokkinou V, Koutsodontis G, Stamatiou P, Giatzakis C, Anastasakis A, Aslanides IM, Koukoula S, Panagiotoglou T, Datseris I, Tsilimbaris MK. Kamakari S, et al. Among authors: giatzakis c. J Ophthalmol. 2018 Dec 16;2018:3039672. doi: 10.1155/2018/3039672. eCollection 2018. J Ophthalmol. 2018. PMID: 30647958 Free PMC article.
Does somatostatin have a role in the regulation of cortisol secretion in primary pigmented nodular adrenocortical disease (ppnad)? a clinical and in vitro investigation.
Bram Z, Xekouki P, Louiset E, Keil MF, Avgeropoulos D, Giatzakis C, Nesterova M, Sinaii N, Hofland LJ, Cherqaoui R, Lefebvre H, Stratakis CA. Bram Z, et al. Among authors: giatzakis c. J Clin Endocrinol Metab. 2014 May;99(5):E891-901. doi: 10.1210/jc.2013-2657. Epub 2014 Feb 10. J Clin Endocrinol Metab. 2014. PMID: 24512486 Free PMC article. Clinical Trial.
A cAMP-specific phosphodiesterase (PDE8B) that is mutated in adrenal hyperplasia is expressed widely in human and mouse tissues: a novel PDE8B isoform in human adrenal cortex.
Horvath A, Giatzakis C, Tsang K, Greene E, Osorio P, Boikos S, Libè R, Patronas Y, Robinson-White A, Remmers E, Bertherat J, Nesterova M, Stratakis CA. Horvath A, et al. Among authors: giatzakis c. Eur J Hum Genet. 2008 Oct;16(10):1245-53. doi: 10.1038/ejhg.2008.85. Epub 2008 Apr 23. Eur J Hum Genet. 2008. PMID: 18431404 Free PMC article.
21 results