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The last 5 uploaded publications
Metabolism and skin diseases
Christos C. Zouboulis, Constantine A. Stratakis, George Chrousos, Christian A. Koch (2016). Metabolism and skin diseases. , 17(3), DOI: https://doi.org/10.1007/s11154-016-9396-6.
Article163 days agoMetabolism and skin diseases
Christos C. Zouboulis, Constantine A. Stratakis, George Chrousos, Christian A. Koch (2016). Metabolism and skin diseases. , 17(3), DOI: https://doi.org/10.1007/s11154-016-9396-6.
Article163 days agoFunctional characterization of two novel germline mutations of the <i><scp>KCNJ</scp>5</i> gene in hypertensive patients without primary aldosteronism but with <scp>ACTH</scp>‐dependent aldosterone hypersecretion
Amalia Sertedaki, Αthina Markou, Dimitriοs Vlachakis, Σοφία Κοσσίδα, Emilie Campanac, Dax A. Hoffman, Maria De La Luz Sierra, Paraskevi Xekouki, Constantine A. Stratakis, Gregory Kaltsas, George Piaditis, George Chrousos, Evangelia Charmandari (2016). Functional characterization of two novel germline mutations of the <i><scp>KCNJ</scp>5</i> gene in hypertensive patients without primary aldosteronism but with <scp>ACTH</scp>‐dependent aldosterone hypersecretion. , 85(6), DOI: https://doi.org/10.1111/cen.13132.
Article163 days agoFamilial pituitary apoplexy as the only presentation of a novel AIP mutation
Paraskevi Xekouki, Spyridon A Mastroyiannis, Dimitrios Avgeropoulos, Maria De La Luz Sierra, Giampaolo Trivellin, Evgenia Gourgari, Charalampos Lyssikatos, Martha Quezado, Nicholas J. Patronas, Christina Kanaka‐Gantenbein, George Chrousos, Constantine A. Stratakis (2013). Familial pituitary apoplexy as the only presentation of a novel AIP mutation. , 20(5), DOI: https://doi.org/10.1530/erc-13-0218.
Letter163 days agoA Novel Point Mutation in the KCNJ5 Gene Causing Primary Hyperaldosteronism and Early-Onset Autosomal Dominant Hypertension
Amalia Sertedaki, Tomoshige Kino, Christina Merakou, Dax A. Hoffman, Michael M. Hatch, Darrell E. Hurt, Lin Lin, Paraskevi Xekouki, Constantine A. Stratakis, George Chrousos, Evangelia Charmandari (2012). A Novel Point Mutation in the KCNJ5 Gene Causing Primary Hyperaldosteronism and Early-Onset Autosomal Dominant Hypertension. , 97(8), DOI: https://doi.org/10.1210/jc.2012-1334.
Article163 days ago