Gole E - Search Results

1

Hereditary rickets. How genetic alterations explain the biochemical and clinical phenotypes.

Papadopoulou A, Gole E, Nicolaidou P. Papadopoulou A, et al. Among authors: gole e. Endocr Metab Immune Disord Drug Targets. 2013 Dec;13(4):324-34. doi: 10.2174/1871530313666131224114530. Endocr Metab Immune Disord Drug Targets. 2013. PMID: 24365280 Review.

2

Calcium sensing receptor in pregnancies complicated by gestational diabetes mellitus.

Papadopoulou A, Gole E, Moutafi A, Sfikas C, Oehrl W, Samiotaki M, Papadimitriou A, Papaevagelou V, Nicolaidou P. Papadopoulou A, et al. Among authors: gole e. Placenta. 2014 Aug;35(8):632-8. doi: 10.1016/j.placenta.2014.05.001. Epub 2014 Jun 2. Placenta. 2014. PMID: 24930987

3

Effect of Leflunomide on Treatment of Pediatric Renal Transplant Recipients With BK Virus Infection.

Gole E, Mitsioni A, Darema M, Malakasioti G, Askiti V. Gole E, et al. Exp Clin Transplant. 2023 Oct;21(10):826-830. doi: 10.6002/ect.2023.0258. Exp Clin Transplant. 2023. PMID: 37965958 Free article.

4

Osteoporosis-pseudoglioma syndrome: clinical, genetic, and treatment-response study of 10 new cases in Greece.

Papadopoulos I, Bountouvi E, Attilakos A, Gole E, Dinopoulos A, Peppa M, Nikolaidou P, Papadopoulou A. Papadopoulos I, et al. Among authors: gole e. Eur J Pediatr. 2019 Mar;178(3):323-329. doi: 10.1007/s00431-018-3299-3. Epub 2018 Nov 29. Eur J Pediatr. 2019. PMID: 30499050

5

A Novel KCNJ11 Mutation Associated with Transient Neonatal Diabetes.

Gole E, Oikonomou S, Ellard S, De Franco E, Karavanaki K. Gole E, et al. J Clin Res Pediatr Endocrinol. 2018 Jun 1;10(2):175-178. doi: 10.4274/jcrpe.5166. Epub 2017 Sep 25. J Clin Res Pediatr Endocrinol. 2018. PMID: 28943514 Free PMC article.

6

Clinical characterization of a novel calcium sensing receptor genetic alteration in a Greek patient with autosomal dominant hypocalcemia type 1.

Papadopoulou A, Gole E, Melachroinou K, Trangas T, Bountouvi E, Papadimitriou A. Papadopoulou A, et al. Among authors: gole e. Hormones (Athens). 2017 Apr;16(2):200-204. doi: 10.14310/horm.2002.1734. Hormones (Athens). 2017. PMID: 28742508 Free article.

7

Identification and Functional Characterization of a Calcium-Sensing Receptor Mutation in an Infant with Familial Hypocalciuric Hypercalcemia.

Papadopoulou A, Gole E, Melachroinou K, Meristoudis C, Siahanidou T, Papadimitriou A. Papadopoulou A, et al. Among authors: gole e. J Clin Res Pediatr Endocrinol. 2016 Sep 1;8(3):341-6. doi: 10.4274/jcrpe.2800. Epub 2016 Apr 18. J Clin Res Pediatr Endocrinol. 2016. PMID: 27087013 Free PMC article.

8

Identification of a novel nonsense mutation in the ligand-binding domain of the vitamin d receptor gene and clinical description of two greek patients with hereditary vitamin d-resistant rickets and alopecia.

Papadopoulou A, Bountouvi E, Gole E, Doulgeraki A, Tournis S, Papadimitriou A, Nicolaidou P. Papadopoulou A, et al. Among authors: gole e. Horm Res Paediatr. 2014;82(3):206-12. doi: 10.1159/000362618. Epub 2014 Jul 23. Horm Res Paediatr. 2014. PMID: 25060608

9

Expanding the spectrum of genetic mutations in antenatal Bartter syndrome type II.

Fretzayas A, Gole E, Attilakos A, Daskalaki A, Nicolaidou P, Papadopoulou A. Fretzayas A, et al. Among authors: gole e. Pediatr Int. 2013 Jun;55(3):371-3. doi: 10.1111/j.1442-200X.2012.03716.x. Pediatr Int. 2013. PMID: 23782368

10

Phenotypic spectrum of 80 Greek patients referred as Noonan syndrome and PTPN11 mutation analysis: the value of initial clinical assessment.

Papadopoulou A, Issakidis M, Gole E, Kosma K, Fryssira H, Fretzayas A, Nicolaidou P, Kitsiou-Tzeli S. Papadopoulou A, et al. Among authors: gole e. Eur J Pediatr. 2012 Jan;171(1):51-8. doi: 10.1007/s00431-011-1487-5. Epub 2011 May 18. Eur J Pediatr. 2012. PMID: 21590266

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