| 2022 |
Campbell D, Reyes M, Kaygusuz SB, Abali S, Guran T, Bereket A, Kagami M, Turan S, Jüppner H. A novel deletion involving the first GNAS exon encoding Gsα causes PHP1A without methylation changes at exon A/B. Bone. April 2022;157:116344. |
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| 2023 |
Turan S. Osteopetrosis: gene-based nosology and significance dysosteosclerosis. Bone. February 2023;167:116615. |
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| 2020 |
Bayramli R, Cevlik T, Guran T, Atay Z, Bas S, Haklar G, Bereket A, Turan S. Clinical significance of hypophosphatasemia in children. Calcif Tiss Int. June 2020;106(6):608-615. |
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| 2020 |
Eltan M, Alavanda C, Abali ZY, Ergenekon P, Ozturk NY, Sakar M, Dagcinar A, Kirkgoz T, Kaygusuz SB, Gokdemir Y, Elcioglu HN, Guran T, Bereket A, Ata P, Turan S. A rare cause of hypophosphatemia: raine syndrome changing clinical features with age. Calcif Tiss Int. July 2020;107(1):96-103. |
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| 2021 |
Kaygusuz SB, Alavanda C, Kirkgoz T, Eltan M, Abali ZY, Helvacioglu D, Guran T, Ata P, Bereket A, Turan S. Does genotype–phenotype correlation exist in vitamin D-dependent rickets type IA: report of 13 new cases and review of the literature. Calcif Tiss Int. May 2021;108(5):576-586. |
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