Koç Yekedüz M - 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. 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

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. Pediatr Neurol. 2024 Jun;155:171-176. doi: 10.1016/j.pediatrneurol.2024.03.032. Epub 2024 Apr 5. Pediatr Neurol. 2024. PMID: 38669799

3

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: koc yekeduz m. 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.

4

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. 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

5

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: koc yekeduz m. 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

6

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. Clin Neurol Neurosurg. 2022 Nov;222:107474. doi: 10.1016/j.clineuro.2022.107474. Epub 2022 Oct 13. Clin Neurol Neurosurg. 2022. PMID: 36270219

7

Unmet Needs of Children with Inherited Metabolic Disorders in the COVID-19 Pandemic.

Özalp Akın E, Eminoğlu FT, Doğulu N, Koç Yekeduz M, Öncül U, Akpınar F, Hayran G. Özalp Akın E, et al. Among authors: koc yekeduz m. Turk Arch Pediatr. 2022 May;57(3):335-341. doi: 10.5152/TurkArchPediatr.2022.21367. Turk Arch Pediatr. 2022. PMID: 35781238 Free PMC article.

8

Probable Miglustat-Induced Psychosis in a Child With Niemann-Pick Type C.

Koç Yekedüz M, Öncül Ü, Köse E, Eminoğlu FT. Koç Yekedüz M, et al. Clin Neuropharmacol. 2022 Jul-Aug 01;45(4):107-109. doi: 10.1097/WNF.0000000000000511. Epub 2022 Jun 11. Clin Neuropharmacol. 2022. PMID: 35696615

9

An Atypical Presentation of Mevalonate Kinase Deficiency in Response to Colchicine Treatment.

Koç Yekedüz M, Doğulu N, Öncül Ü, Köse E, Ceylaner S, Eminoğlu FT. Koç Yekedüz M, et al. Mol Syndromol. 2022 Feb;13(2):146-151. doi: 10.1159/000518825. Epub 2021 Oct 25. Mol Syndromol. 2022. PMID: 35418827 Free PMC article.

10

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. Telemed J E Health. 2022 Mar 30. doi: 10.1089/tmj.2021.0610. Online ahead of print. Telemed J E Health. 2022. PMID: 35363077

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