İnci A - Search Results

1

Quality of Life and Related Factors in Patients Diagnosed with Mucopolysaccharidosis and Their Caregivers.

Yekedüz MK, Cilesiz K, Kara İS, İnci A, Kose E, Tümer L, Eminoğlu FT. Yekedüz MK, et al. Among authors: inci a. Klin Padiatr. 2024 Dec 10. doi: 10.1055/a-2451-6562. Online ahead of print. Klin Padiatr. 2024. PMID: 39657772 English.

2

Long-term clinical evaluation of patients with alpha-mannosidosis - A multicenter study.

Köse E, Kasapkara ÇS, İnci A, Yıldız Y, Sürücü Kara İ, Kahraman AB, Tümer L, Dursun A, Eminoğlu FT. Köse E, et al. Among authors: inci a. Eur J Med Genet. 2024 Apr;68:104927. doi: 10.1016/j.ejmg.2024.104927. Epub 2024 Feb 19. Eur J Med Genet. 2024. PMID: 38382588 Free article.

3

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

4

Clinical and event-based outcomes of patients with mucopolysaccharidosis VI receiving enzyme replacement therapy in Turkey: a case series.

İnci A, Okur İ, Tümer L, Biberoğlu G, Öktem M, Ezgü F. İnci A, et al. Orphanet J Rare Dis. 2021 Oct 19;16(1):438. doi: 10.1186/s13023-021-02060-4. Orphanet J Rare Dis. 2021. PMID: 34666789 Free PMC article.

5

Clinical, biochemical, and molecular insights into Cerebrotendinous Xanthomatosis: A nationwide study of 100 Turkish individuals.

Zubarioglu T, Kıykım E, Köse E, Eminoğlu FT, Teke Kısa P, Balcı MC, Özer I, İnci A, Çilesiz K, Canda E, Yazıcı H, Öztürk-Hişmi B, Bulut FD, Dorum S, Akgun A, Yalçın-Çakmaklı G, Kılıç-Yıldırım G, Soyuçen E, Akçalı A, Güneş D, Durmuş A, Gündüz A, Kasapkara ÇS, Göksoy E, Akar HT, Ersoy M, Erdöl Ş, Yıldız Y, Hanağası HA, Arslan N, Aktuğlu-Zeybek Ç. Zubarioglu T, et al. Among authors: inci a. Mol Genet Metab. 2024 Jun;142(2):108493. doi: 10.1016/j.ymgme.2024.108493. Epub 2024 May 13. Mol Genet Metab. 2024. PMID: 38772327

6

A Patient with a Novel RARS2 Variant Exhibiting Liver Involvement as a New Clinical Feature and Review of the Literature.

Sevinç S, İnci A, Ezgü FS, Eminoğlu FT. Sevinç S, et al. Among authors: inci a. Mol Syndromol. 2022 May;13(3):226-234. doi: 10.1159/000519604. Epub 2022 Feb 1. Mol Syndromol. 2022. PMID: 35707589 Free PMC article.

7

Advances in Immune Tolerance Induction in Enzyme Replacement Therapy.

İnci A, Ezgü FS, Tümer L. İnci A, et al. Paediatr Drugs. 2024 May;26(3):287-308. doi: 10.1007/s40272-024-00627-9. Epub 2024 Apr 25. Paediatr Drugs. 2024. PMID: 38664313 Free PMC article. Review.

8

Vitamin D Levels and Bone Mineral Density in Inborn Errors of Metabolism Requiring Specialised Diets.

Olgac A, Inci A, Okur I, Ezgu F, Biberoglu G, Tumer L. Olgac A, et al. Among authors: inci a. J Coll Physicians Surg Pak. 2019 Dec;29(12):1207-1211. doi: 10.29271/jcpsp.2019.12.1207. J Coll Physicians Surg Pak. 2019. PMID: 31839097

9

Endocrinological, immunological and metabolic features of patients with Fabry disease under therapy.

Emecen Sanli M, Kilic A, Inci A, Okur I, Ezgu F, Tumer L. Emecen Sanli M, et al. Among authors: inci a. J Pediatr Endocrinol Metab. 2023 May 31;0(0):650-658. doi: 10.1515/jpem-2023-0105. Print 2023 Jul 26. J Pediatr Endocrinol Metab. 2023. PMID: 37257483

10

Intestinal microbiota composition of children with glycogen storage Type I patients.

Gokalp S, Dinleyici EC, Muluk C, Inci A, Aktas E, Okur I, Ezgu F, Tumer L. Gokalp S, et al. Among authors: inci a. Eur J Clin Nutr. 2024 May;78(5):407-412. doi: 10.1038/s41430-024-01412-0. Epub 2024 Feb 24. Eur J Clin Nutr. 2024. PMID: 38402355 Free PMC article.

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