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, Deniz Tasdemir, Vidya Acharya, Ling Zhang, Ovidia Golea, Alaa Sabry, Dhananjay S Ookalkar, Cristina Capusa, Dana Radulescu, Liliana Garneata, Gabriel Mircescu, Hedi Ben Maiz, Cheng Hsu Chen, Jorge Prado Rome, Mansour Benzegoutta, Nuray Paylar, Kamil Eyuboglu, Ersin Karatepe, Mustafa Esenturk, Onder Yavascan, Alicza Grzegorzevska, Valery Shilo, Mitra Mahdavi Mazdeh, Ramos Carillo Francesco, Zaghloul Gouda, Siddik Momin Adam, Idris Emir, Faith Ocal, Erol Usta, Necati Kiralp, Cemal Sagliker, Piril Sagliker Ozkaynak, Hasan Sabit Sagliker, Mahmoud Bassuoni, Oktay Sekin
Journal of renal nutrition : the official journal of the Council on Renal Nutrition of the National Kidney Foundation 2012;22(1):157-61