Kose E - Search Results

1

Challenges Faced by Newborns with Inherited Metabolic Disorders and Their Mothers During Antepartum, Intrapartum, and Postpartum Periods.

Koç Yekedüz M, Yağci GN, Sürücü Kara İ, Evgin M, Kose E, Eminoğlu FT. Koç Yekedüz M, et al. Among authors: kose e. Fetal Pediatr Pathol. 2025 Jan 6:1-10. doi: 10.1080/15513815.2024.2447082. Online ahead of print. Fetal Pediatr Pathol. 2025. PMID: 39760466

2

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

3

A Patient with Recurrent Severe Hypoglycemic Attacks and Mitochondrial Complex III Deficiency, Nuclear Type 3: a Novel UQCRB Variant.

Koç Yekedüz M, Öncül Ü, Köse E, Ezgü F, Eminoğlu FT. Koç Yekedüz M, et al. Among authors: kose e. Mol Syndromol. 2022 Feb;13(1):64-68. doi: 10.1159/000517761. Epub 2021 Sep 9. Mol Syndromol. 2022. PMID: 35221877 Free PMC article.

4

Pros and Cons of Telemedicine for Inherited Metabolic Disorders in a Developing Country During the COVID-19 Pandemic.

Koç Yekedüz M, Doğulu N, Sürücü Kara İ, Öncül Ü, Bakirarar B, Kullu P, Ar Y, Köse E, Eminoğlu FT. Koç Yekedüz M, et al. Among authors: kose e. Telemed J E Health. 2022 Mar 30. doi: 10.1089/tmj.2021.0610. Online ahead of print. Telemed J E Health. 2022. PMID: 35363077

5

Early neuroimaging findings of infants diagnosed with inherited metabolic disorders in neonatal period: A case-control study.

Koç Yekedüz M, Şen Akova B, Köse E, Doğulu N, Öncül Ü, Okulu E, Arsan S, Fitöz S, Eminoğlu FT. Koç Yekedüz M, et al. Among authors: kose e. Clin Neurol Neurosurg. 2022 Nov;222:107474. doi: 10.1016/j.clineuro.2022.107474. Epub 2022 Oct 13. Clin Neurol Neurosurg. 2022. PMID: 36270219

6

A different approach to the evaluation of the genotype-phenotype relationship in biotinidase deficiency: repeated measurement of biotinidase enzyme activity.

Sürücü Kara İ, Köse E, Koç Yekedüz M, Eminoğlu FT. Sürücü Kara İ, et al. Among authors: kose e. J Pediatr Endocrinol Metab. 2023 Sep 20;36(11):1061-1071. doi: 10.1515/jpem-2023-0337. Print 2023 Nov 27. J Pediatr Endocrinol Metab. 2023. PMID: 37725148

7

IGAm: A novel index predicting long-term survival in patients with early-diagnosed inherited metabolic disorders.

Koç Yekedüz M, Köse E, Eminoğlu FT. Koç Yekedüz M, et al. Among authors: kose e. J Pediatr Endocrinol Metab. 2023 Oct 5;36(11):1100-1108. doi: 10.1515/jpem-2023-0272. Print 2023 Nov 27. J Pediatr Endocrinol Metab. 2023. PMID: 37788389

8

Neuronal ceroid lipofuscinosis type 11 diagnosed patient with bi-allelic variants in GRN gene: case report and review of literature.

Sürücü Kara İ, Köse E, Çavdarlı B, Eminoğlu FT. Sürücü Kara İ, et al. Among authors: kose e. J Pediatr Endocrinol Metab. 2024 Jan 23;37(3):280-288. doi: 10.1515/jpem-2023-0411. Print 2024 Mar 25. J Pediatr Endocrinol Metab. 2024. PMID: 38253347 Review.

9

Two Turkish patients with Primary Coenzyme Q10 Deficiency-7: case report and literature review.

Sonuç Kartal G, Koç Yekedüz M, Köse E, Eminoğlu FT. Sonuç Kartal G, et al. Among authors: kose e. J Pediatr Endocrinol Metab. 2024 Feb 2;37(3):260-270. doi: 10.1515/jpem-2023-0490. Print 2024 Mar 25. J Pediatr Endocrinol Metab. 2024. PMID: 38353291 Review.

10

Is Ultrasonography a Reliable Approach for the Evaluation of Carpal Tunnel Syndrome in Patients With Mucopolysaccharidosis?

Koç Yekedüz M, Köse E, İnci A, Yüksel MF, Doğulu N, Şen Akova B, Yeniay Süt N, Öncül Ü, Yildirim M, Fitoz S, Teber S, Tümer L, Eminoğlu FT. Koç Yekedüz M, et al. Among authors: kose e. Pediatr Neurol. 2024 Jun;155:171-176. doi: 10.1016/j.pediatrneurol.2024.03.032. Epub 2024 Apr 5. Pediatr Neurol. 2024. PMID: 38669799

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