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Genetic IGF1R defects: new cases expand the spectrum of clinical features.
Gonc EN, Ozon ZA, Oguz S, Kabacam S, Taskiran EZ, Kiper POS, Utine GE, Alikasifoglu A, Kandemir N, Boduroglu OK, Alikasifoglu M. Gonc EN, et al. Among authors: kiper pos. J Endocrinol Invest. 2020 Dec;43(12):1739-1748. doi: 10.1007/s40618-020-01264-y. Epub 2020 Apr 30. J Endocrinol Invest. 2020. PMID: 32356191
Recurrent fractures and an unusual diagnosis: Pycnodysostosis.
Gurbanov A, Kiper PÖŞ, Tekşam Ö. Gurbanov A, et al. Among authors: kiper pos. J Natl Med Assoc. 2022 Jun;114(3):295-297. doi: 10.1016/j.jnma.2022.02.008. Epub 2022 Mar 8. J Natl Med Assoc. 2022. PMID: 35272848 No abstract available.
Novel insights into diabetes mellitus due to DNAJC3-defect: Evolution of neurological and endocrine phenotype in the pediatric age group.
Ozon ZA, Alikasifoglu A, Kandemir N, Aydin B, Gonc EN, Karaosmanoglu B, Celik NB, Eroglu-Ertugrul NG, Taskiran EZ, Haliloglu G, Oguz KK, Kiper PO, Yalnizoglu D, Utine GE, Alikasifoglu M. Ozon ZA, et al. Among authors: kiper po. Pediatr Diabetes. 2020 Nov;21(7):1176-1182. doi: 10.1111/pedi.13098. Epub 2020 Sep 10. Pediatr Diabetes. 2020. PMID: 32738013
25 results