Results
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1370.
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1371.
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1372.
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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. [electronic resource] by
- Yildiz, Ismail
- Sagliker, Yahya
- Demirhan, Osman
- Tunc, Erdal
- Inandiklioglu, Nihal
- Tasdemir, Deniz
- Acharya, Vidya
- Zhang, Ling
- Golea, Ovidia
- Sabry, Alaa
- Ookalkar, Dhananjay S
- Capusa, Cristina
- Radulescu, Dana
- Garneata, Liliana
- Mircescu, Gabriel
- Ben Maiz, Hedi
- Chen, Cheng Hsu
- Prado Rome, Jorge
- Benzegoutta, Mansour
- Paylar, Nuray
- Eyuboglu, Kamil
- Karatepe, Ersin
- Esenturk, Mustafa
- Yavascan, Onder
- Grzegorzevska, Alicza
- Shilo, Valery
- Mazdeh, Mitra Mahdavi
- Francesco, Ramos Carillo
- Gouda, Zaghloul
- Adam, Siddik Momin
- Emir, Idris
- Ocal, Faith
- Usta, Erol
- Kiralp, Necati
- Sagliker, Cemal
- Ozkaynak, Piril Sagliker
- Sagliker, Hasan Sabit
- Bassuoni, Mahmoud
- Sekin, Oktay
Producer: 20120508
In:
Journal of renal nutrition : the official journal of the Council on Renal Nutrition of the National Kidney Foundation vol. 22
Availability: No items available.
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1378.
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1379.
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1380.
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