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Early diagnostic clues of mucolipidosis type II: Significance of radiological findings.
Burgac E, Kaplan İ, Köseci B, Kara E, Kor D, Bulut FD, Atmış A, Pişkin F, Tuğ Bozdoğan S, Urel Demir G, İncecik F, Önenli Mungan N. Burgac E, et al. Among authors: onenli mungan n. Am J Med Genet A. 2024 Jun;194(6):e63545. doi: 10.1002/ajmg.a.63545. Epub 2024 Jan 24. Am J Med Genet A. 2024. PMID: 38264826
Expanding the phenotypic landscape of Gaucher disease type 3c with a novel entity - Transient neonatal cholestasis.
Bulut FD, Kor D, Kılavuz S, Şeker Yılmaz B, Kaplan İ, Ekinci F, Burgaç E, Varol İ, Köşeci B, Tuğ Bozdoğan S, Kara E, Demir F, Deniz A, Temiz F, Önenli Mungan N. Bulut FD, et al. Among authors: onenli mungan n. Eur J Med Genet. 2023 Jun;66(6):104764. doi: 10.1016/j.ejmg.2023.104764. Epub 2023 Apr 13. Eur J Med Genet. 2023. PMID: 37061027
Evaluation of bone health in patients with mucopolysaccharidosis.
Kor D, Bulut FD, Kılavuz S, Şeker Yılmaz B, Köşeci B, Kara E, Kaya Ö, Başaran S, Seydaoğlu G, Önenli Mungan N. Kor D, et al. Among authors: onenli mungan n. J Bone Miner Metab. 2022 May;40(3):498-507. doi: 10.1007/s00774-021-01304-4. Epub 2022 Jan 23. J Bone Miner Metab. 2022. PMID: 35066680
Impaired glucose tolerance in Fanconi-Bickel syndrome: Eight patients with two novel mutations.
Şeker-Yılmaz B, Kör D, Bulut FD, Yüksel B, Karabay-Bayazıt A, Topaloğlu AK, Ceylaner G, Önenli-Mungan N. Şeker-Yılmaz B, et al. Among authors: onenli mungan n. Turk J Pediatr. 2017;59(4):434-441. doi: 10.24953/turkjped.2017.04.010. Turk J Pediatr. 2017. PMID: 29624224 Free article.
Seker-Yilmaz B, Kor D, Bulut FD, Yuksel B, Karabay-Bayazit A, Topaloglu AK, Ceylaner G, Onenli-Mungan N. Impaired glucose tolerance in Fanconi-Bickel syndrome: Eight patients with two novel mutations. ...
Seker-Yilmaz B, Kor D, Bulut FD, Yuksel B, Karabay-Bayazit A, Topaloglu AK, Ceylaner G, Onenli-Mungan N. Impaired gluco …
35 results