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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: kandemir n. Pediatr Diabetes. 2020 Nov;21(7):1176-1182. doi: 10.1111/pedi.13098. Epub 2020 Sep 10. Pediatr Diabetes. 2020. PMID: 32738013
Neuroleptic malignant syndrome in a patient with citrullinaemia.
Dursun A, Yilma Y, Ozsari M, Kandemir N, Coşkun T. Dursun A, et al. Among authors: kandemir n. J Inherit Metab Dis. 2000 Dec;23(8):841-2. doi: 10.1023/a:1026716820324. J Inherit Metab Dis. 2000. PMID: 11196110 No abstract available.
Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome.
Vurallı D, Gönç N, Vidaud D, Özön A, Alikaşifoğlu A, Kandemir N. Vurallı D, et al. Among authors: kandemir n. J Clin Res Pediatr Endocrinol. 2016 Mar 5;8(1):96-100. doi: 10.4274/jcrpe.2070. Epub 2015 Dec 18. J Clin Res Pediatr Endocrinol. 2016. PMID: 26758488 Free PMC article.
Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes.
Bertko E, Klammt J, Dusatkova P, Bahceci M, Gonc N, Ten Have L, Kandemir N, Mansmann G, Obermannova B, Oostdijk W, Pfäffle H, Rockstroh-Lippold D, Schlicke M, Tuzcu AK, Pfäffle R. Bertko E, et al. Among authors: kandemir n. J Hum Genet. 2017 Aug;62(8):755-762. doi: 10.1038/jhg.2017.34. Epub 2017 Mar 30. J Hum Genet. 2017. PMID: 28356564 Free PMC article.
157 results