Evangelia Charmandari, MD, PhD - Publications

Affiliations: 
2011- Medical School National and Kapodistrian University of Athens 
Area:
Endocrinology, Metabolism, Diabetes
Website:
http://www.echarmandari.gr/

82 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Nicolaides NC, Makridakis M, Stroggilos R, Lygirou V, Koniari E, Papageorgiou I, Sertedaki A, Zoidakis J, Charmandari E. Plasma Proteomics in Healthy Subjects with Differences in Tissue Glucocorticoid Sensitivity Identifies A Novel Proteomic Signature. Biomedicines. 10. PMID 35052863 DOI: 10.3390/biomedicines10010184  0.635
2021 Nicolaides NC, Charmandari E. Primary Generalized Glucocorticoid Resistance and Hypersensitivity Syndromes: A 2021 Update. International Journal of Molecular Sciences. 22. PMID 34639183 DOI: 10.3390/ijms221910839  0.674
2021 Paltoglou G, Raftopoulou C, Nicolaides NC, Genitsaridi SM, Karampatsou SI, Papadopoulou M, Kassari P, Charmandari E. A Comprehensive, Multidisciplinary, Personalized, Lifestyle Intervention Program Is Associated with Increased Leukocyte Telomere Length in Children and Adolescents with Overweight and Obesity. Nutrients. 13. PMID 34444842 DOI: 10.3390/nu13082682  0.635
2021 Nicolaides NC, Ioannidi MK, Koniari E, Papageorgiou I, Bartzeliotou A, Sertedaki A, Klapa MI, Charmandari E. Untargeted Plasma Metabolomics Unravels a Metabolic Signature for Tissue Sensitivity to Glucocorticoids in Healthy Subjects: Its Implications in Dietary Planning for a Healthy Lifestyle. Nutrients. 13. PMID 34205537 DOI: 10.3390/nu13062120  0.641
2020 Tragomalou A, Moschonis G, Kassari P, Papageorgiou I, Genitsaridi SM, Karampatsou S, Manios Y, Charmandari E. A National e-Health Program for the Prevention and Management of Overweight and Obesity in Childhood and Adolescence in Greece. Nutrients. 12. PMID 32961973 DOI: 10.3390/Nu12092858  0.323
2020 Genitsaridi SM, Giannios C, Karampatsou S, Papageorgiou I, Papadopoulos G, Farakla I, Koui E, Georgiou A, Romas S, Terzioglou E, Papathanasiou C, Kassari P, Manios Y, Charmandari E. A Comprehensive Multidisciplinary Management Plan Is Effective in Reducing the Prevalence of Overweight and Obesity in Childhood and Adolescence. Hormone Research in Paediatrics. 1-14. PMID 32580197 DOI: 10.1159/000507760  0.743
2020 Tragomalou A, Moschonis G, Manios Y, Kassari P, Ioakimidis I, Diou C, Stefanopoulos L, Lekka E, Maglaveras N, Delopoulos A, Charmandari E. Novel e-Health Applications for the Management of Cardiometabolic Risk Factors in Children and Adolescents in Greece. Nutrients. 12. PMID 32408523 DOI: 10.3390/Nu12051380  0.329
2019 Genitsaridi SM, Karampatsou S, Papageorgiou I, Mantzou A, Papathanasiou C, Kassari P, Paltoglou G, Kourkouti C, Charmandari E. Hair Cortisol Concentrations in Overweight and Obese Children and Adolescents. Hormone Research in Paediatrics. 1-8. PMID 31851969 DOI: 10.1159/000504913  0.309
2019 Lamprokostopoulou A, Moschonis G, Manios Y, Critselis E, Nicolaides NC, Stefa A, Koniari E, Gagos S, Charmandari E. Childhood obesity and leukocyte telomere length. European Journal of Clinical Investigation. e13178. PMID 31610015 DOI: 10.1111/Eci.13178  0.647
2019 Nicolaides NC, Charmandari E. Glucocorticoid Resistance. Experientia Supplementum (2012). 111: 85-102. PMID 31588529 DOI: 10.1007/978-3-030-25905-1_6  0.656
2019 Nicolaides NC, Polyzos A, Koniari E, Lamprokostopoulou A, Papageorgiou I, Golfinopoulou E, Papathanasiou C, Sertedaki A, Thanos D, Chrousos GP, Charmandari E. Transcriptomics in Tissue Glucocorticoid Sensitivity. European Journal of Clinical Investigation. e13129. PMID 31091335 DOI: 10.1111/Eci.13129  0.653
2019 Moschonis G, Michalopoulou M, Tsoutsoulopoulou K, Vlachopapadopoulou E, Michalacos S, Charmandari E, Chrousos GP, Manios Y. Assessment of the Effectiveness of a Computerised Decision-Support Tool for Health Professionals for the Prevention and Treatment of Childhood Obesity. Results from a Randomised Controlled Trial. Nutrients. 11. PMID 30917561 DOI: 10.3390/Nu11030706  0.306
2018 Farakla I, Koui E, Arditi J, Papageorgiou I, Bartzeliotou A, Papadopoulos GE, Mantzou A, Papathanasiou C, Dracopoulou M, Papastamataki M, Moutsatsou P, Papassotiriou I, Chrousos GP, Charmandari E. Effect of Honey on Glucose and Insulin Concentrations in Obese Girls. European Journal of Clinical Investigation. e13042. PMID 30368796 DOI: 10.1111/Eci.13042  0.744
2018 Adlbrecht C, Blanco-Verea A, Bouzas-Mosquera MC, Brion M, Burtscher M, Carbone F, Chang TT, Charmandari E, Chen JW, Correia-Costa L, Dullaart RPF, Eleftheriades M, Fernandez-Fernandez B, Goliasch G, Gremmel T, et al. Research update for articles published in EJCI in 2016. European Journal of Clinical Investigation. e13016. PMID 30099749 DOI: 10.1111/eci.13016  0.596
2018 Emmanouil CC, Pervanidou P, Charmandari E, Darviri C, Chrousos GP. The effectiveness of a health promotion and stress-management intervention program in a sample of obese children and adolescents. Hormones (Athens, Greece). 17: 405-413. PMID 30099726 DOI: 10.1007/S42000-018-0052-2  0.324
2018 Kassari P, Papaioannou P, Billiris A, Karanikas H, Eleftheriou S, Thireos E, Manios Y, Chrousos GP, Charmandari E. Electronic registry for the management of childhood obesity in Greece. European Journal of Clinical Investigation. 48. PMID 29327339 DOI: 10.1111/Eci.12887  0.317
2017 Papageorgiou L, Vlachakis C, Dragoumani K, Raftopoulou S, Brouzas D, Nicolaides NC, Chrousos GP, Charmandari E, Megalooikonomou V, Vlachakis D. HCV genetics and genotypes dictate future antiviral strategies. Journal of Molecular Biochemistry. 6: 33-40. PMID 29387656  0.568
2017 Al-Daghri NM, Batzel JJ, Burgmann H, Carbone F, Charmandari E, Chrousos GP, Distelmaier K, Cvirn G, Dullaart RPF, Dumitrascu DL, Esteve-Pastor MA, Gervasini G, Goliasch G, Goswami N, Gruppen EG, et al. Research update for articles published in EJCI in 2015. European Journal of Clinical Investigation. 47: 775-788. PMID 28960328 DOI: 10.1111/eci.12819  0.558
2017 Nicolaides NC, Kino T, Roberts ML, Katsantoni E, Sertedaki A, Moutsatsou P, Psarra AG, Chrousos GP, Charmandari E. The Role of S-Palmitoylation of the Human Glucocorticoid Receptor (hGR) in Mediating the Nongenomic Glucocorticoid Actions. Journal of Molecular Biochemistry. 6: 3-12. PMID 28775968  0.607
2017 Nicolaides NC, Charmandari E. Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes. Hormones (Athens, Greece). 16: 124-138. PMID 28742501 DOI: 10.14310/Horm.2002.1728  0.678
2017 Nicolaides NC, Charmandari E, Kino T, Chrousos GP. Stress-Related and Circadian Secretion and Target Tissue Actions of Glucocorticoids: Impact on Health. Frontiers in Endocrinology. 8: 70. PMID 28503165 DOI: 10.3389/Fendo.2017.00070  0.664
2017 Kyritsi EM, Koltsida G, Farakla I, Papanikolaou A, Critselis E, Mantzou E, Zoumakis E, Kolaitis G, Chrousos GP, Charmandari E. Psychological vulnerability to stress in carriers of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Hormones (Athens, Greece). 16: 42-53. PMID 28500827 DOI: 10.14310/Horm.2002.1718  0.753
2017 Stavrou S, Nicolaides NC, Critselis E, Darviri C, Charmandari E, Chrousos GP. Paediatric stress: from neuroendocrinology to contemporary disorders. European Journal of Clinical Investigation. 47: 262-269. PMID 28074555 DOI: 10.1111/Eci.12724  0.654
2016 Stavrou S, Nicolaides NC, Papageorgiou I, Papadopoulou P, Terzioglou E, Chrousos GP, Darviri C, Charmandari E. The effectiveness of a stress-management intervention program in the management of overweight and obesity in childhood and adolescence. Journal of Molecular Biochemistry. 5: 63-70. PMID 27570747  0.638
2016 Nicolaides N, Lamprokostopoulou A, Sertedaki A, Charmandari E. Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance. Hormones (Athens, Greece). 15: 23-34. PMID 27086682 DOI: 10.14310/Horm.2002.1660  0.677
2016 Nicolaides NC, Skyrla E, Vlachakis D, Psarra AM, Moutsatsou P, Sertedaki A, Kossida S, Charmandari E. Functional characterization of the hGRαT556I causing Chrousos syndrome. European Journal of Clinical Investigation. 46: 42-9. PMID 26541474 DOI: 10.1111/Eci.12563  0.667
2015 Charmandari E, Zhang RG, Silveira LG, Fan QR, Chrousos GP, Sertedaki A, Latronico AC, Segaloff DL. Misfolding Ectodomain Mutations of the Lutropin Receptor Increase Efficacy of Hormone Stimulation. Molecular Endocrinology (Baltimore, Md.). me20151205. PMID 26554443 DOI: 10.1210/Me.2015-1205  0.304
2015 Nicolaides NC, Lamprokostopoulou A, Polyzos A, Kino T, Katsantoni E, Triantafyllou P, Christophoridis A, Katzos G, Dracopoulou M, Sertedaki A, Chrousos GP, Charmandari E. Transient generalized glucocorticoid hypersensitivity. European Journal of Clinical Investigation. 45: 1306-15. PMID 26479047 DOI: 10.1111/Eci.12554  0.67
2015 Nicolaides NC, Geer EB, Vlachakis D, Roberts ML, Psarra AM, Moutsatsou P, Sertedaki A, Kossida S, Charmandari E. A novel mutation of the hGR gene causing Chrousos syndrome. European Journal of Clinical Investigation. 45: 782-91. PMID 26031419 DOI: 10.1111/Eci.12470  0.662
2015 Markou A, Sertedaki A, Kaltsas G, Androulakis I, Marakaki C, Pappa T, Gouli A, Papanastasiou L, Fountoulakis S, Zacharoulis A, Karavidas A, Ragkou D, Charmandari E, Chrousos GP, Piaditis GP. STRESS-INDUCED ALDOSTERONE HYPER-SECRETION IN A SUBSTANTIAL SUBSET OF PATIENTS WITH ESSENTIAL HYPERTENSION. The Journal of Clinical Endocrinology and Metabolism. jc20151268. PMID 25974737 DOI: 10.1210/Jc.2015-1268  0.316
2015 Nicolaides NC, Charmandari E. Chrousos syndrome: from molecular pathogenesis to therapeutic management. European Journal of Clinical Investigation. 45: 504-14. PMID 25715669 DOI: 10.1111/Eci.12426  0.662
2015 Hindmarsh PC, Charmandari E. Variation in absorption and half-life of hydrocortisone influence plasma cortisol concentrations. Clinical Endocrinology. 82: 557-61. PMID 25369980 DOI: 10.1111/Cen.12653  0.495
2015 Nicolaides NC, Kyratzi E, Lamprokostopoulou A, Chrousos GP, Charmandari E. Stress, the stress system and the role of glucocorticoids. Neuroimmunomodulation. 22: 6-19. PMID 25227402 DOI: 10.1159/000362736  0.656
2014 Nicolaides NC, Charmandari E, Chrousos GP, Kino T. Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor. Bmc Endocrine Disorders. 14: 71. PMID 25155432 DOI: 10.1186/1472-6823-14-71  0.671
2014 Nicolaides NC, Charmandari E, Chrousos GP, Kino T. Circadian endocrine rhythms: the hypothalamic-pituitary-adrenal axis and its actions. Annals of the New York Academy of Sciences. 1318: 71-80. PMID 24890877 DOI: 10.1111/Nyas.12464  0.666
2014 Charmandari E, Nicolaides NC, Chrousos GP. Adrenal insufficiency. Lancet (London, England). 383: 2152-67. PMID 24503135 DOI: 10.1016/S0140-6736(13)61684-0  0.637
2014 Nicolaides NC, Roberts ML, Kino T, Braatvedt G, Hurt DE, Katsantoni E, Sertedaki A, Chrousos GP, Charmandari E. A novel point mutation of the human glucocorticoid receptor gene causes primary generalized glucocorticoid resistance through impaired interaction with the LXXLL motif of the p160 coactivators: dissociation of the transactivating and transreppressive activities. The Journal of Clinical Endocrinology and Metabolism. 99: E902-7. PMID 24483153 DOI: 10.1210/Jc.2013-3005  0.675
2013 Roberts ML, Kino T, Nicolaides NC, Hurt DE, Katsantoni E, Sertedaki A, Komianou F, Kassiou K, Chrousos GP, Charmandari E. A novel point mutation in the DNA-binding domain (DBD) of the human glucocorticoid receptor causes primary generalized glucocorticoid resistance by disrupting the hydrophobic structure of its DBD. The Journal of Clinical Endocrinology and Metabolism. 98: E790-5. PMID 23426617 DOI: 10.1210/Jc.2012-3549  0.682
2013 Charmandari E, Kino T, Chrousos GP. Primary generalized familial and sporadic glucocorticoid resistance (Chrousos syndrome) and hypersensitivity. Endocrine Development. 24: 67-85. PMID 23392096 DOI: 10.1159/000342505  0.378
2013 Peters CJ, Hill N, Dattani MT, Charmandari E, Matthews DR, Hindmarsh PC. Deconvolution analysis of 24-h serum cortisol profiles informs the amount and distribution of hydrocortisone replacement therapy. Clinical Endocrinology. 78: 347-51. PMID 22803584 DOI: 10.1111/J.1365-2265.2012.04502.X  0.493
2012 Charmandari E, Achermann JC, Carel JC, Soder O, Chrousos GP. Stress response and child health. Science Signaling. 5: mr1. PMID 23112343 DOI: 10.1126/Scisignal.2003595  0.341
2012 Charmandari E. Primary generalized glucocorticoid resistance and hypersensitivity: the end-organ involvement in the stress response. Science Signaling. 5: pt5. PMID 23033539 DOI: 10.1126/Scisignal.2003337  0.413
2011 Charmandari E, Chrousos GP, Lambrou GI, Pavlaki A, Koide H, Ng SS, Kino T. Peripheral CLOCK regulates target-tissue glucocorticoid receptor transcriptional activity in a circadian fashion in man. Plos One. 6: e25612. PMID 21980503 DOI: 10.1371/Journal.Pone.0025612  0.307
2011 Charmandari E. Primary generalized glucocorticoid resistance and hypersensitivity. Hormone Research in Paediatrics. 76: 145-55. PMID 21912096 DOI: 10.1159/000330759  0.354
2011 Galata Z, Moschonis G, Makridakis M, Dimitraki P, Nicolaides NC, Manios Y, Bartzeliotou A, Chrousos GP, Charmandari E. Plasma proteomic analysis in obese and overweight prepubertal children. European Journal of Clinical Investigation. 41: 1275-83. PMID 21569026 DOI: 10.1111/J.1365-2362.2011.02536.X  0.649
2010 Charmandari E, Kino T. Chrousos syndrome: a seminal report, a phylogenetic enigma and the clinical implications of glucocorticoid signalling changes. European Journal of Clinical Investigation. 40: 932-42. PMID 20649902 DOI: 10.1111/J.1365-2362.2010.02336.X  0.342
2010 Nicolaides NC, Galata Z, Kino T, Chrousos GP, Charmandari E. The human glucocorticoid receptor: molecular basis of biologic function. Steroids. 75: 1-12. PMID 19818358 DOI: 10.1016/J.Steroids.2009.09.002  0.66
2009 Charmandari E, Chrousos GP, Kino T. Identification of natural human glucocorticoid receptor (hGR) mutations or polymorphisms and their functional consequences at the hormone-receptor interaction level. Methods in Molecular Biology (Clifton, N.J.). 590: 33-60. PMID 19763496 DOI: 10.1007/978-1-60327-378-7_3  0.381
2009 Chrousos GP, Kino T, Charmandari E. Evaluation of the hypothalamic-pituitary-adrenal axis function in childhood and adolescence. Neuroimmunomodulation. 16: 272-83. PMID 19571588 DOI: 10.1159/000216185  0.382
2008 Charmandari E, Ichijo T, Jubiz W, Baid S, Zachman K, Chrousos GP, Kino T. A novel point mutation in the amino terminal domain of the human glucocorticoid receptor (hGR) gene enhancing hGR-mediated gene expression. The Journal of Clinical Endocrinology and Metabolism. 93: 4963-8. PMID 18827003 DOI: 10.1210/Jc.2008-0892  0.316
2008 Charmandari E, Kino T, Ichijo T, Chrousos GP. Generalized glucocorticoid resistance: clinical aspects, molecular mechanisms, and implications of a rare genetic disorder. The Journal of Clinical Endocrinology and Metabolism. 93: 1563-72. PMID 18319312 DOI: 10.1210/Jc.2008-0040  0.303
2007 Charmandari E, Kino T, Ichijo T, Jubiz W, Mejia L, Zachman K, Chrousos GP. A novel point mutation in helix 11 of the ligand-binding domain of the human glucocorticoid receptor gene causing generalized glucocorticoid resistance. The Journal of Clinical Endocrinology and Metabolism. 92: 3986-90. PMID 17635946 DOI: 10.1210/Jc.2006-2830  0.383
2007 Charmandari E, Kino T. Novel causes of generalized glucocorticoid resistance. Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme. 39: 445-50. PMID 17578762 DOI: 10.1055/S-2007-980196  0.402
2006 Charmandari E, Chrousos GP. Metabolic syndrome manifestations in classic congenital adrenal hyperplasia: do they predispose to atherosclerotic cardiovascular disease and secondary polycystic ovary syndrome? Annals of the New York Academy of Sciences. 1083: 37-53. PMID 17148732 DOI: 10.1196/Annals.1367.005  0.377
2006 Kino T, Souvatzoglou E, Charmandari E, Ichijo T, Driggers P, Mayers C, Alatsatianos A, Manoli I, Westphal H, Chrousos GP, Segars JH. Rho family Guanine nucleotide exchange factor Brx couples extracellular signals to the glucocorticoid signaling system. The Journal of Biological Chemistry. 281: 9118-26. PMID 16469733 DOI: 10.1074/Jbc.M509339200  0.308
2006 Charmandari E, Kino T, Ichijo T, Zachman K, Alatsatianos A, Chrousos GP. Functional characterization of the natural human glucocorticoid receptor (hGR) mutants hGRalphaR477H and hGRalphaG679S associated with generalized glucocorticoid resistance. The Journal of Clinical Endocrinology and Metabolism. 91: 1535-43. PMID 16449337 DOI: 10.1210/Jc.2005-1893  0.334
2005 Charmandari E, Raji A, Kino T, Ichijo T, Tiulpakov A, Zachman K, Chrousos GP. A novel point mutation in the ligand-binding domain (LBD) of the human glucocorticoid receptor (hGR) causing generalized glucocorticoid resistance: the importance of the C terminus of hGR LBD in conferring transactivational activity. The Journal of Clinical Endocrinology and Metabolism. 90: 3696-705. PMID 15769988 DOI: 10.1210/Jc.2004-1920  0.353
2005 Charmandari E, Tsigos C, Chrousos G. Endocrinology of the stress response. Annual Review of Physiology. 67: 259-84. PMID 15709959 DOI: 10.1146/Annurev.Physiol.67.040403.120816  0.341
2005 Charmandari E, Chrousos GP, Merke DP. Adrenocorticotropin hypersecretion and pituitary microadenoma following bilateral adrenalectomy in a patient with classic 21-hydroxylase deficiency. Journal of Pediatric Endocrinology & Metabolism : Jpem. 18: 97-101. PMID 15679075 DOI: 10.1515/Jpem.2005.18.1.97  0.346
2004 Kino T, Liou SH, Charmandari E, Chrousos GP. Glucocorticoid receptor mutants demonstrate increased motility inside the nucleus of living cells: time of fluorescence recovery after photobleaching (FRAP) is an integrated measure of receptor function. Molecular Medicine (Cambridge, Mass.). 10: 80-8. PMID 16307173 DOI: 10.2119/2005-00026.Kino  0.316
2004 Charmandari E, Brook CG, Hindmarsh PC. Classic congenital adrenal hyperplasia and puberty. European Journal of Endocrinology. 151: U77-82. PMID 15554890 DOI: 10.1530/Eje.0.151U077  0.754
2004 Charmandari E, Kino T, Chrousos GP. Familial/sporadic glucocorticoid resistance: clinical phenotype and molecular mechanisms. Annals of the New York Academy of Sciences. 1024: 168-81. PMID 15265781 DOI: 10.1196/Annals.1321.014  0.373
2004 Charmandari E, Merke DP, Negro PJ, Keil MF, Martinez PE, Haim A, Gold PW, Chrousos GP. Endocrinologic and psychologic evaluation of 21-hydroxylase deficiency carriers and matched normal subjects: evidence for physical and/or psychologic vulnerability to stress. The Journal of Clinical Endocrinology and Metabolism. 89: 2228-36. PMID 15126546 DOI: 10.1210/Jc.2003-031322  0.346
2004 Charmandari E, Kino T, Souvatzoglou E, Vottero A, Bhattacharyya N, Chrousos GP. Natural glucocorticoid receptor mutants causing generalized glucocorticoid resistance: molecular genotype, genetic transmission, and clinical phenotype. The Journal of Clinical Endocrinology and Metabolism. 89: 1939-49. PMID 15070967 DOI: 10.1210/Jc.2003-030450  0.345
2004 Weise M, Mehlinger SL, Drinkard B, Rawson E, Charmandari E, Hiroi M, Eisenhofer G, Yanovski JA, Chrousos GP, Merke DP. Patients with classic congenital adrenal hyperplasia have decreased epinephrine reserve and defective glucose elevation in response to high-intensity exercise. The Journal of Clinical Endocrinology and Metabolism. 89: 591-7. PMID 14764767 DOI: 10.1210/Jc.2003-030634  0.302
2003 Charmandari E, Pincus SM, Matthews DR, Johnston A, Brook CGD, Hindmarsh PC. Sexual dimorphism in the synchrony of joint growth hormone and cortisol dynamics in children with classic 21-hydroxylase deficiency Journal of Pediatric Endocrinology and Metabolism. 16: 1119-1130. PMID 14594172 DOI: 10.1515/Jpem.2003.16.8.1119  0.503
2003 Kino T, De Martino MU, Charmandari E, Mirani M, Chrousos GP. Tissue glucocorticoid resistance/hypersensitivity syndromes Journal of Steroid Biochemistry and Molecular Biology. 85: 457-467. PMID 12943736 DOI: 10.1016/S0960-0760(03)00218-8  0.372
2003 Roche EF, Charmandari E, Dattani MT, Hindmarsh PC. Blood pressure in children and adolescents with congenital adrenal hyperplasia (21-hydroxylase deficiency): a preliminary report. Clinical Endocrinology. 58: 589-96. PMID 12699440 DOI: 10.1046/J.1365-2265.2003.01757.X  0.563
2003 Charmandari E, Kino T, Souvatzoglou E, Chrousos GP. Pediatric stress: hormonal mediators and human development. Hormone Research. 59: 161-79. PMID 12649570 DOI: 10.1159/000069325  0.395
2002 Kino T, Vottero A, Charmandari E, Chrousos GP. Familial/sporadic glucocorticoid resistance syndrome and hypertension. Annals of the New York Academy of Sciences. 970: 101-11. PMID 12381545 DOI: 10.1111/J.1749-6632.2002.Tb04416.X  0.385
2002 Charmandari E, Calis KA, Keil MF, Mohassel MR, Remaley A, Merke DP. Flutamide decreases cortisol clearance in patients with congenital adrenal hyperplasia. The Journal of Clinical Endocrinology and Metabolism. 87: 3197-200. PMID 12107224 DOI: 10.1210/Jcem.87.7.8652  0.319
2002 Charmandari E, Johnston A, Honour JW, Brook CG, Hindmarsh PC. Treatment with flutamide decreases cortisol clearance: implications for therapy in congenital adrenal hyperplasia. Journal of Pediatric Endocrinology & Metabolism : Jpem. 15: 435-9. PMID 12008691 DOI: 10.1515/Jpem.2002.15.4.435  0.728
2002 Charmandari E, Pincus SM, Matthews DR, Johnston A, Brook CG, Hindmarsh PC. Oral hydrocortisone administration in children with classic 21-hydroxylase deficiency leads to more synchronous joint GH and cortisol secretion. The Journal of Clinical Endocrinology and Metabolism. 87: 2238-44. PMID 11994370 DOI: 10.1210/Jcem.87.5.8503  0.737
2002 Charmandari E, Weise M, Bornstein SR, Eisenhofer G, Keil MF, Chrousos GP, Merke DP. Children with classic congenital adrenal hyperplasia have elevated serum leptin concentrations and insulin resistance: potential clinical implications. The Journal of Clinical Endocrinology and Metabolism. 87: 2114-20. PMID 11994350 DOI: 10.1210/Jcem.87.5.8456  0.361
2002 Charmandari E, Brook CG, Hindmarsh PC. Why is management of patients with classical congenital adrenal hyperplasia more difficult at puberty? Archives of Disease in Childhood. 86: 266-9. PMID 11919101 DOI: 10.1136/Adc.86.4.266  0.745
2002 Charmandari E, Dattani MT, Perry LA, Hindmarsh PC, Brook CG. Kinetics and effect of percutaneous administration of dihydrotestosterone in children. Hormone Research. 56: 177-81. PMID 11910204 DOI: 10.1159/000048115  0.696
2001 Charmandari E, Matthews DR, Johnston A, Brook CGD, Hindmarsh PC. Serum cortisol and 17-hydroxyprogesterone interrelation in classic 21-hydroxylase deficiency: Is current replacement therapy satisfactory? Journal of Clinical Endocrinology and Metabolism. 86: 4679-4685. PMID 11600525 DOI: 10.1210/Jcem.86.10.7972  0.511
2001 Charmandari E, Pincus SM, Matthews DR, Dennison E, Fall CHD, Hindmarsh PC. Joint growth hormone and cortisol spontaneous secretion is more asynchronous in older females than in their male counterparts Journal of Clinical Endocrinology and Metabolism. 86: 3393-3399. PMID 11443216 DOI: 10.1210/Jcem.86.7.7695  0.512
2001 Charmandari E, Lichtarowicz-Krynska EJ, Hindmarsh PC, Johnston A, Aynsley-Green A, Brook CG. Congenital adrenal hyperplasia: management during critical illness. Archives of Disease in Childhood. 85: 26-8. PMID 11420193 DOI: 10.1136/Adc.85.1.26  0.496
2001 Charmandari E, Hindmarsh PC, Johnston A, Brook CG. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: alterations in cortisol pharmacokinetics at puberty. The Journal of Clinical Endocrinology and Metabolism. 86: 2701-8. PMID 11397874 DOI: 10.1210/Jcem.86.6.7522  0.721
2001 Charmandari E, Johnston A, Brook CG, Hindmarsh PC. Bioavailability of oral hydrocortisone in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. The Journal of Endocrinology. 169: 65-70. PMID 11250647 DOI: 10.1677/Joe.0.1690065  0.488
2000 Koziell A, Charmandari E, Hindmarsh PC, Rees L, Scambler P, Brook CG. Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy? Clinical Endocrinology. 52: 519-24. PMID 10762296 DOI: 10.1046/J.1365-2265.2000.052006801.X  0.524
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