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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: doulgeraki a. Horm Res Paediatr. 2014;82(3):206-12. doi: 10.1159/000362618. Epub 2014 Jul 23. Horm Res Paediatr. 2014. PMID: 25060608
Hypophosphatasia.
Tournis S, Yavropoulou MP, Polyzos SA, Doulgeraki A. Tournis S, et al. Among authors: doulgeraki a. J Clin Med. 2021 Dec 1;10(23):5676. doi: 10.3390/jcm10235676. J Clin Med. 2021. PMID: 34884378 Free PMC article. Review.
Circulating Irisin Levels in Preadolescents and Adolescents Born Preterm.
Koutroumpa A, Kanaka Gantenbein C, Mantzou A, Doulgeraki A, Bacopoulou F, Bouza H, Chrousos G, Siahanidou T. Koutroumpa A, et al. Among authors: doulgeraki a. Horm Res Paediatr. 2021;94(11-12):416-425. doi: 10.1159/000521265. Epub 2021 Dec 2. Horm Res Paediatr. 2021. PMID: 34856543
Editorial: Rickets and osteomalacia, from genes to nutrition.
Doulgeraki A, Laurent MR. Doulgeraki A, et al. Front Endocrinol (Lausanne). 2023 Jan 19;14:1141888. doi: 10.3389/fendo.2023.1141888. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 36742385 Free PMC article. No abstract available.
A novel frameshift deletion in PLS3 causing severe primary osteoporosis.
Costantini A, Krallis PΝ, Kämpe A, Karavitakis EM, Taylan F, Mäkitie O, Doulgeraki A. Costantini A, et al. Among authors: doulgeraki a. J Hum Genet. 2018 Aug;63(8):923-926. doi: 10.1038/s10038-018-0472-5. Epub 2018 Jun 8. J Hum Genet. 2018. PMID: 29884797
Denosumab for the treatment of primary pediatric osteoporosis.
Anastasilakis AD, Makras P, Doulgeraki A, Polyzos SA, Guarnieri V, Papapoulos SE. Anastasilakis AD, et al. Among authors: doulgeraki a. Osteoporos Int. 2021 Nov;32(11):2377-2381. doi: 10.1007/s00198-021-06002-5. Epub 2021 May 13. Osteoporos Int. 2021. PMID: 33987688
73 results