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Cephalometric evaluation of patients with Sagliker syndrome: uglifying human face appearance in severe and late secondary hyperparathyroidism in chronic renal failure patients.
Uzel A, Uzel I, Sagliker Y, Yildiz I, Halvaci I, Paylar N, Ocal F, Balal M, Ozkaynak PS, Paydas S, Sagliker C, Sagliker HS, Kiralp N, Adam SM, Esenturk M, Gocmez E, Taskapan H, Yuksekgonul M, Emir I, Guler T, Yakar H, Sekin O, Kayali E, Caliskan S, Eskiocak AF, Ogruk B, Guzelyurt T, Kurt C. Uzel A, et al. Among authors: paylar n. J Ren Nutr. 2006 Jul;16(3):229-32. doi: 10.1053/j.jrn.2006.04.019. J Ren Nutr. 2006. PMID: 16825025
Neurologic manifestations in Sagliker syndrome: uglifying human face appearance in severe and late secondary hyperparathyroidism in chronic renal failure patients.
Giray S, Sagliker Y, Yildiz I, Halvaci I, Paylar N, Ocal F, Balal M, Ozkaynak PS, Paydas S, Sagliker C, Sagliker HS, Kiralp N, Adam SM, Esenturk M, Gocmez E, Taskapan H, Yuksekgonul M, Emir I, Guler T, Yakar H, Sekin O, Kayali E, Caliskan S, Eskiocak AF, Ogruk B, Guzelyurt T, Kurt C. Giray S, et al. Among authors: paylar n. J Ren Nutr. 2006 Jul;16(3):233-6. doi: 10.1053/j.jrn.2006.04.018. J Ren Nutr. 2006. PMID: 16825026
International study on Sagliker syndrome and uglifying human face appearance in severe and late secondary hyperparathyroidism in chronic kidney disease patients.
Sagliker Y, Acharya V, Ling Z, Golea O, Sabry A, Eyupoglu K, Ookalkar DS, Tapiawala S, Durugkar S, Khetan P, Capusa C, Univar R, Yildiz I, Cengiz K, Bali M, Ozkaynak PS, Sagliker HS, Paylar N, Adam SM, Balal M, Paydas S, Demirhan O, Tasdemir D, Ben Maiz H, Redulescu D, Garneata L, Mircescu G, Hong-Liang R, Lun L, Yildizer K, Emir I, Yuksekgonul M, Yenicerioglu Y, Akar H, Sagliker C, Esenturk M, Kiralp N. Sagliker Y, et al. Among authors: paylar n. J Ren Nutr. 2008 Jan;18(1):114-7. doi: 10.1053/j.jrn.2007.10.023. J Ren Nutr. 2008. PMID: 18089456
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.
Yildiz I, Sagliker Y, Demirhan O, Tunc E, Inandiklioglu N, Tasdemir D, Acharya V, Zhang L, Golea O, Sabry A, Ookalkar DS, Capusa C, Radulescu D, Garneata L, Mircescu G, Ben Maiz H, Chen CH, Prado Rome J, Benzegoutta M, Paylar N, Eyuboglu K, Karatepe E, Esenturk M, Yavascan O, Grzegorzevska A, Shilo V, Mazdeh MM, Francesco RC, Gouda Z, Adam SM, Emir I, Ocal F, Usta E, Kiralp N, Sagliker C, Ozkaynak PS, Sagliker HS, Bassuoni M, Sekin O. Yildiz I, et al. Among authors: paylar n. J Ren Nutr. 2012 Jan;22(1):157-61. doi: 10.1053/j.jrn.2011.10.030. J Ren Nutr. 2012. PMID: 22200434 Review.
Is survival enough for quality of life in Sagliker Syndrome-uglifying human face appearances in chronic kidney disease?
Sagliker Y, Acharya V, Golea O, Sabry A, Bali M, Eyupoglu K, Ookalkar D, Tapiawala S, Durugkar S, Khetan P, Capusa C, Univar R, Yildiz I, Cengiz K, Akar H, Yenicerioglu Y, Sagliker Ozkaynak P, Sabit Sagliker H, Paylar N. Sagliker Y, et al. Among authors: paylar n. J Nephrol. 2008 Mar-Apr;21 Suppl 13:S134-8. J Nephrol. 2008. PMID: 18446747