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	1.	Juvenile Paget's disease: the second reported, oldest patient is homozygous for the TNFRSF11B "Balkan" mutation (966_969delTGACinsCTT), which elevates circulating immunoreactive osteoprotegerin levels. [electronic resource] by Whyte, Michael P Singhellakis, Panagiotis N Petersen, Michael B Davies, Michael Totty, William G Mumm, Steven Producer: 20070829 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Vitamin D deficiency in white, apparently healthy, free-living adults in a temperate region. [electronic resource] by Singhellakis, Panagiotis N Malandrinou, Fotini Ch Psarrou, Catherine J Danelli, Alexandra M Tsalavoutas, Sotirios D Constandellou, Evangelia S Producer: 20111027 In: Hormones (Athens, Greece) vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Denosumab treatment for juvenile Paget's disease: results from two adult patients with osteoprotegerin deficiency ("Balkan" mutation in the TNFRSF11B gene). [electronic resource] by Polyzos, Stergios A Singhellakis, Panagiotis N Naot, Dorit Adamidou, Fotini Malandrinou, Fotini C Anastasilakis, Athanasios D Polymerou, Vaia Kita, Marina Producer: 20140714 In: The Journal of clinical endocrinology and metabolism vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Association of prolactin receptor (PRLR) variants with prolactinomas. [electronic resource] by Gorvin, Caroline M Newey, Paul J Rogers, Angela Stokes, Victoria Neville, Matt J Lines, Kate E Ntali, Georgia Lees, Peter Morrison, Patrick J Singhellakis, Panagiotis N Malandrinou, Fotini Ch Karavitaki, Niki Grossman, Ashley B Karpe, Fredrik Thakker, Rajesh V Producer: 20200309 In: Human molecular genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Clinical variability of familial tumoral calcinosis caused by novel GALNT3 mutations. [electronic resource] by Ichikawa, Shoji Baujat, Geneviève Seyahi, Aksel Garoufali, Anastasia G Imel, Erik A Padgett, Leah R Austin, Anthony M Sorenson, Andrea H Pejin, Zagorka Topouchian, Vicken Quartier, Pierre Cormier-Daire, Valerie Dechaux, Michele Malandrinou, Fotini Ch Singhellakis, Panagiotis N Le Merrer, Martine Econs, Michael J Producer: 20100708 In: American journal of medical genetics. Part A vol. 152A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)