Ezgü FS - Search Results

1

Neonatal multiple sulfatase deficiency with a novel mutation and review of the literature.

Nur BG, Mıhçı E, Pepe S, Biberoğlu G, Ezgü FS, Ballabio A, Öztekin O, Dursun O. Nur BG, et al. Among authors: ezgu fs. Turk J Pediatr. 2014 Jul-Aug;56(4):418-22. Turk J Pediatr. 2014. PMID: 25818962 Review.

2

Investigating for inborn errors of metabolism with tandem mass spectrometry in Ankara region, Turkey: a 2 years evaluation.

Tümer L, Biberoğlu G, Hasanoğlu A, Ezgu FS, Atalay Y. Tümer L, et al. Among authors: ezgu fs. J Trop Pediatr. 2004 Jun;50(3):189-90. doi: 10.1093/tropej/50.3.189. J Trop Pediatr. 2004. PMID: 15233202 No abstract available.

3

Severe infantile hypotonia with ethylmalonic aciduria: case report.

Okuyaz C, Ezgü FS, Biberoglu G, Zeviani M, Tiranti V, Yilgör E. Okuyaz C, et al. Among authors: ezgu fs. J Child Neurol. 2008 Jun;23(6):703-5. doi: 10.1177/0883073807313048. J Child Neurol. 2008. PMID: 18539996

4

N-carbamylglutamate treatment for acute neonatal hyperammonemia in isovaleric acidemia.

Kasapkara CS, Ezgu FS, Okur I, Tumer L, Biberoglu G, Hasanoglu A. Kasapkara CS, et al. Among authors: ezgu fs. Eur J Pediatr. 2011 Jun;170(6):799-801. doi: 10.1007/s00431-010-1362-9. Epub 2011 Jan 5. Eur J Pediatr. 2011. PMID: 21207059

5

Analysis of acylcarnitine levels by tandem mass spectrometry in epileptic children receiving valproate and oxcarbazepine.

Cansu A, Serdaroglu A, Biberoglu G, Tumer L, Hirfanoglu TL, Ezgu FS, Hasanoglu A. Cansu A, et al. Among authors: ezgu fs. Epileptic Disord. 2011 Dec;13(4):394-400. doi: 10.1684/epd.2011.0478. Epileptic Disord. 2011. PMID: 22258044 Free article.

6

Hypercalcemia in glycogen storage disease type I patients of Turkish origin.

Kasapkara CS, Tümer L, Okur I, Eminoğlu T, Ezgü FS, Hasanoğlu A. Kasapkara CS, et al. Among authors: ezgu fs. Turk J Pediatr. 2012 Jan-Feb;54(1):35-7. Turk J Pediatr. 2012. PMID: 22397040

7

Beneficial Effects of Modified Atkins Diet in Glycogen Storage Disease Type IIIa.

Olgac A, İnci A, Okur İ, Biberoğlu G, Oğuz D, Ezgü FS, Kasapkara ÇS, Aktaş E, Tümer L. Olgac A, et al. Among authors: ezgu fs. Ann Nutr Metab. 2020;76(4):233-241. doi: 10.1159/000509335. Epub 2020 Jul 24. Ann Nutr Metab. 2020. PMID: 32712609

8

Hypophosphatasia: is it an underdiagnosed disease even by expert physicians?

İnci A, Ergin FBC, Yüce BT, Çiftçi B, Demir E, Buyan N, Okur İ, Biberoğlu G, Öktem RM, Tümer L, Ezgü FS. İnci A, et al. Among authors: ezgu fs. J Bone Miner Metab. 2021 Jul;39(4):598-605. doi: 10.1007/s00774-020-01193-z. Epub 2021 Jan 6. J Bone Miner Metab. 2021. PMID: 33404770

9

Autism: Screening of inborn errors of metabolism and unexpected results.

İnci A, Özaslan A, Okur İ, Biberoğlu G, Güney E, Ezgü FS, Tümer L, İşeri E. İnci A, et al. Among authors: ezgu fs. Autism Res. 2021 May;14(5):887-896. doi: 10.1002/aur.2486. Epub 2021 Feb 19. Autism Res. 2021. PMID: 33605552

10

Two patients from Turkey with a novel variant in the GM2A gene and review of the literature.

İnci A, Cengiz Ergin FB, Biberoğlu G, Okur İ, Ezgü FS, Tümer L. İnci A, et al. Among authors: ezgu fs. J Pediatr Endocrinol Metab. 2021 Apr 6;34(6):805-812. doi: 10.1515/jpem-2020-0655. Print 2021 Jun 25. J Pediatr Endocrinol Metab. 2021. PMID: 33819415 Review.

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