Köse E - Search Results

1

Mitochondrial DNA Depletion Syndromes Gene Panel versus Clinical Exome Sequencing in Children with Suspected Mitochondrial Hepatopathies.

Doğulu N, Köse E, Ceylaner S, Kasapkara ÇS, Bozaci AE, Oncul U, Eminoğlu FT. Doğulu N, et al. Among authors: kose e. Mol Syndromol. 2024 Dec;15(6):450-463. doi: 10.1159/000539034. Epub 2024 Jun 17. Mol Syndromol. 2024. PMID: 39634245 Free article.

2

Pyruvate carboxylase deficiency type C as a differential diagnosis of diabetic ketoacidosis.

Doğulu N, Öncül Ü, Köse E, Aycan Z, Eminoğlu FT. Doğulu N, et al. Among authors: kose e. J Pediatr Endocrinol Metab. 2021 Apr 16;34(7):947-950. doi: 10.1515/jpem-2020-0646. Print 2021 Jul 27. J Pediatr Endocrinol Metab. 2021. PMID: 33860652

3

A case with Gaucher disease unable to reach enzyme replacement therapy because of COVID-19 quarantine: The first case from Turkey.

Yekedüz MK, Köse E, Eminoğlu FT. Yekedüz MK, et al. Among authors: kose e. Turk Arch Pediatr. 2021 May 1;56(3):270-271. doi: 10.5152/TurkArchPediatr.2021.21023. eCollection 2021. Turk Arch Pediatr. 2021. PMID: 34104921 Free PMC article. No abstract available.

4

The clinical variations and diagnostic challenges of deoxyguanosine kinase deficiency: a descriptive case series.

Doğulu N, Tuna Kırsaçlıoğlu C, Köse E, Ünlüsoy Aksu A, Kuloğlu Z, Kansu A, Eminoğlu FT. Doğulu N, et al. Among authors: kose e. J Pediatr Endocrinol Metab. 2021 Jun 28;34(10):1341-1347. doi: 10.1515/jpem-2021-0108. Print 2021 Oct 26. J Pediatr Endocrinol Metab. 2021. PMID: 34167177

5

Inherited metabolic disorders in the neonatal intensive care unit: Red flags to look out for.

Eminoğlu FT, Koç Yekedüz M, Doğulu N, Öncül Ü, Köse E, Okulu E, Erdeve Ö, Atasay B, Arsan S. Eminoğlu FT, et al. Among authors: kose e. Pediatr Int. 2022 Jan;64(1):e14953. doi: 10.1111/ped.14953. Pediatr Int. 2022. PMID: 34390086

6

A Mild Phenotype of Mitochondrial DNA Depletion Syndrome Type 13 with a Novel FBXL4 Variant.

Oncul U, Kose E, Eminoglu FT. Oncul U, et al. Among authors: kose e. Mol Syndromol. 2021 Aug;12(5):294-299. doi: 10.1159/000515928. Epub 2021 Jul 19. Mol Syndromol. 2021. PMID: 34602956 Free PMC article.

7

Characteristics of continuous venovenous hemodiafiltration in the acute treatment of inherited metabolic disorders.

Eminoğlu FT, Öncül Ü, Kahveci F, Okulu E, Kraja E, Köse E, Kendirli T. Eminoğlu FT, et al. Among authors: kose e. Pediatr Nephrol. 2022 Jun;37(6):1387-1397. doi: 10.1007/s00467-021-05329-9. Epub 2021 Oct 25. Pediatr Nephrol. 2022. PMID: 34693482 Free PMC article.

8

Serum biotin interference: A troublemaker in hormone immunoassays.

Öncül Ü, Eminoğlu FT, Köse E, Doğan Ö, Özsu E, Aycan Z. Öncül Ü, et al. Among authors: kose e. Clin Biochem. 2022 Jan;99:97-102. doi: 10.1016/j.clinbiochem.2021.10.011. Epub 2021 Nov 1. Clin Biochem. 2022. PMID: 34736903 Clinical Trial.

9

Does Metformin Treatment in Pediatric Population Cause Vitamin B12 Deficiency?

Taş Ö, Kontbay T, Dogan O, Kose E, Berberoglu M, Siklar Z, Tumer L, Eminoglu FT. Taş Ö, et al. Among authors: kose e. Klin Padiatr. 2022 Jul;234(4):221-227. doi: 10.1055/a-1702-2614. Epub 2022 Feb 3. Klin Padiatr. 2022. PMID: 35114702 English.

10

Correction: Does Metformin Treatment in Pediatric Population Cause Vitamin B12 Deficiency?

Taş Ö, Kontbay T, Dogan O, Kose E, Berberoglu M, Siklar Z, Tumer L, Eminoglu FT. Taş Ö, et al. Among authors: kose e. Klin Padiatr. 2022 Feb 16. doi: 10.1055/a-1766-2824. Online ahead of print. Klin Padiatr. 2022. PMID: 35172352 English. No abstract available.

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