Publications by authors named "Ovidia Golea"

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International evaluation of unrecognizably uglifying human faces in late and severe secondary hyperparathyroidism in chronic kidney disease. Sagliker syndrome. A unique catastrophic entity, cytogenetic studies for chromosomal abnormalities, calcium-sensing receptor gene and GNAS1 mutations. Striking and promising missense mutations on the GNAS1 gene exons 1, 4, 10, 4.
Ismail Yildiz, Yahya Sagliker, Osman Demirhan, Erdal Tunc, Nihal Inandiklioglu, Ovidia Golea

J Ren Nutr· January 2012

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Is survival enough for quality of life in Sagliker Syndrome-uglifying human face appearances in chronic kidney disease?
Yahya Sagliker, Vidya Acharya, Ovidia Golea, Alaa Sabry, Musa Bali

J Nephrol· September 2008

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International study on Sagliker syndrome and uglifying human face appearance in severe and late secondary hyperparathyroidism in chronic kidney disease patients.
Yahya Sagliker, Vidya Acharya, Zhang Ling, Ovidia Golea, Alaa Sabry

J Ren Nutr· January 2008

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