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Items: 16

1.

Anti-Müllerian Hormone in Girls with Premature Adrenarche: The Impact of Polycystic Ovary Syndrome History in their Mothers.

Efthymiadou A, Bogiatzidou M, Kritikou D, Chrysis D.

J Pediatr. 2019 Feb;205:190-194. doi: 10.1016/j.jpeds.2018.09.064. Epub 2018 Oct 24.

PMID:
30529136
2.

Anemia in Patients With Resistance to Thyroid Hormone α: A Role for Thyroid Hormone Receptor α in Human Erythropoiesis.

van Gucht ALM, Meima ME, Moran C, Agostini M, Tylki-Szymanska A, Krajewska MW, Chrzanowska K, Efthymiadou A, Chrysis D, Demir K, Visser WE, Visser TJ, Chatterjee K, van Dijk TB, Peeters RP.

J Clin Endocrinol Metab. 2017 Sep 1;102(9):3517-3525. doi: 10.1210/jc.2017-00840.

3.

A Case of Vitamin-D-Dependent Rickets Type 1A with Normal 1,25-Dihydroxyvitamin D Caused by Two Novel Mutations of the CYP27B1 Gene.

Giannakopoulos A, Efthymiadou A, Chrysis D.

Horm Res Paediatr. 2017;87(1):58-63. doi: 10.1159/000446774. Epub 2016 Jun 11.

PMID:
27287609
4.

Osteoprotegerin, RANKL, ADMA, and Fetuin-A serum levels in children with type I diabetes mellitus.

Chrysis D, Efthymiadou A, Mermigka A, Kritikou D, Spiliotis BE.

Pediatr Diabetes. 2017 Jun;18(4):277-282. doi: 10.1111/pedi.12384. Epub 2016 Mar 29.

PMID:
27028343
5.

The effect of GH treatment on serum FGF23 and Klotho in GH-deficient children.

Efthymiadou A, Kritikou D, Mantagos S, Chrysis D.

Eur J Endocrinol. 2016 Apr;174(4):473-9. doi: 10.1530/EJE-15-1018. Epub 2016 Jan 13.

PMID:
26764419
6.

Resistance to thyroid hormone caused by a mutation in thyroid hormone receptor (TR)α1 and TRα2: clinical, biochemical, and genetic analyses of three related patients.

Moran C, Agostini M, Visser WE, Schoenmakers E, Schoenmakers N, Offiah AC, Poole K, Rajanayagam O, Lyons G, Halsall D, Gurnell M, Chrysis D, Efthymiadou A, Buchanan C, Aylwin S, Chatterjee KK.

Lancet Diabetes Endocrinol. 2014 Aug;2(8):619-26. doi: 10.1016/S2213-8587(14)70111-1. Epub 2014 Jun 23. Erratum in: Lancet Diabetes Endocrinol. 2014 Aug;2(8):e14.

7.

Fibroblast growth factor 23 and Klotho serum levels in healthy children.

Gkentzi D, Efthymiadou A, Kritikou D, Chrysis D.

Bone. 2014 Sep;66:8-14. doi: 10.1016/j.bone.2014.05.012. Epub 2014 May 29.

PMID:
24880094
8.

Hypercalcemia and osteolytic lesions as presenting symptoms of acute lymphoblastic leukemia in childhood. The use of zoledronic acid and review of the literature.

Kolyva S, Efthymiadou A, Gkentzi D, Karana-Ginopoulou A, Varvarigou A.

J Pediatr Endocrinol Metab. 2014 Mar;27(3-4):349-54. doi: 10.1515/jpem-2013-0244. Review.

PMID:
23934636
9.

45,X/46,XY mosaicism: a cause of short stature in males.

Efthymiadou A, Stefanou EG, Chrysis D.

Hormones (Athens). 2012 Oct-Dec;11(4):501-4.

10.

Can Kallmann syndrome be occasionally diagnosed during childhood? Genetic diagnosis in a child with associated renal agenesis and mirror movements.

Georgopoulos NA, Koika V, Varnavas P, Efthymiadou A, Marioli DJ, Mantagos S, Chrysis D.

Asian J Androl. 2009 Jul;11(4):521-3. doi: 10.1038/aja.2008.24. Epub 2009 Feb 23. No abstract available.

11.

Altered intrahepatic hematopoiesis in neonates from women with pregnancy induced hypertension/pre-eclampsia.

Tamiolakis D, Venizelos I, Lambropoulou M, Efthymiadou A, Arvanitidou V, Tsikouras P, Koutsougeras G, Chimonis G, Karamanidis D, Barbagadaki S, Nikolaidou S, Seliniotaki E, Boglou P, Papadopoulos N.

Acta Medica (Hradec Kralove). 2004;47(2):119-23.

PMID:
15446362
12.

CFTR localization in native airway cells and cell lines expressing wild-type or F508del-CFTR by a panel of different antibodies.

Carvalho-Oliveira I, Efthymiadou A, Malhó R, Nogueira P, Tzetis M, Kanavakis E, Amaral MD, Penque D.

J Histochem Cytochem. 2004 Feb;52(2):193-203.

PMID:
14729871
13.

Cystic fibrosis in Greece: molecular diagnosis, haplotypes, prenatal diagnosis and carrier identification amongst high-risk individuals.

Kanavakis E, Efthymiadou A, Strofalis S, Doudounakis S, Traeger-Synodinos J, Tzetis M.

Clin Genet. 2003 May;63(5):400-9.

PMID:
12752573
14.

New type of disease causing mutations: the example of the composite exonic regulatory elements of splicing in CFTR exon 12.

Pagani F, Stuani C, Tzetis M, Kanavakis E, Efthymiadou A, Doudounakis S, Casals T, Baralle FE.

Hum Mol Genet. 2003 May 15;12(10):1111-20.

PMID:
12719375
16.

CFTR gene mutations--including three novel nucleotide substitutions--and haplotype background in patients with asthma, disseminated bronchiectasis and chronic obstructive pulmonary disease.

Tzetis M, Efthymiadou A, Strofalis S, Psychou P, Dimakou A, Pouliou E, Doudounakis S, Kanavakis E.

Hum Genet. 2001 Mar;108(3):216-21.

PMID:
11354633

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