Ezgu F - Search Results

1

Ezgu F. Ezgu F. Adv Clin Chem. 2016;73:195-250. doi: 10.1016/bs.acc.2015.12.001. Epub 2016 Jan 23. Adv Clin Chem. 2016. PMID: 26975974 Review.

2

Recent advances in the molecular diagnosis of inborn errors of metabolism.

Ezgu F. Ezgu F. Clin Biochem. 2014 Jun;47(9):759-60. doi: 10.1016/j.clinbiochem.2014.05.048. Epub 2014 May 21. Clin Biochem. 2014. PMID: 24858207 No abstract available.

3

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: ezgu f. 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

4

Very long-chain acyl CoA dehydrogenase deficiency which was accepted as infanticide.

Eminoglu TF, Tumer L, Okur I, Ezgu FS, Biberoglu G, Hasanoglu A. Eminoglu TF, et al. Among authors: ezgu fs. Forensic Sci Int. 2011 Jul 15;210(1-3):e1-3. doi: 10.1016/j.forsciint.2011.04.003. Epub 2011 Apr 30. Forensic Sci Int. 2011. PMID: 21531094

5

Rapid molecular diagnosis of genetic diseases by high resolution melting analysis: fabry and glycogen storage 1A diseases.

Ezgu F, Divanoglu Y, Polat M, Bahceci S, Hasanoglu A, Desnick RJ. Ezgu F, et al. Genet Test Mol Biomarkers. 2014 Jan;18(1):3-7. doi: 10.1089/gtmb.2013.0371. Epub 2013 Dec 17. Genet Test Mol Biomarkers. 2014. PMID: 24341606

6

Diagnosis of glycine encephalopathy in a pediatric patient by detection of a GLDC mutation during initial next generation DNA sequencing.

Ezgu F, Çiftci B, Topçu B, Adıyaman G, Gökmenoğlu H, Küçükçongar A, Kasapkara Ç, Biberoğlu G, Tümer L, Hasanoğlu A. Ezgu F, et al. Metab Brain Dis. 2014 Mar;29(1):211-3. doi: 10.1007/s11011-014-9482-y. Epub 2014 Jan 11. Metab Brain Dis. 2014. PMID: 24407464

7

Hematologic Findings of Inherited Metabolic Disease: They are More Than Expected.

Sal E, Yenicesu I, Okur I, Kaya Z, Ezgu FS, Kocak U, Tumer L, Gursel T, Hasanoglu A. Sal E, et al. J Pediatr Hematol Oncol. 2018 Jul;40(5):355-359. doi: 10.1097/MPH.0000000000001206. J Pediatr Hematol Oncol. 2018. PMID: 29746437

8

Clinical and genetic spectrum of glycogen storage disease in Iranian population using targeted gene sequencing.

Beyzaei Z, Ezgu F, Geramizadeh B, Imanieh MH, Haghighat M, Dehghani SM, Honar N, Zahmatkeshan M, Jassbi A, Mahboubifar M, Alborzi A. Beyzaei Z, et al. Among authors: ezgu f. Sci Rep. 2021 Mar 29;11(1):7040. doi: 10.1038/s41598-021-86338-4. Sci Rep. 2021. PMID: 33782433 Free PMC article.

9

Glycogen storage disorder types IX: the mutation spectrum and ethnic distribution.

Geramizadeh B, Ezgu F, Beyzaei Z. Geramizadeh B, et al. Among authors: ezgu f. Orphanet J Rare Dis. 2024 Dec 20;19(1):475. doi: 10.1186/s13023-024-03488-0. Orphanet J Rare Dis. 2024. PMID: 39707443 Free PMC article. Review.

10

Severe renal tubulopathy in a newborn due to BCS1L gene mutation: effects of different treatment modalities on the clinical course.

Ezgu F, Senaca S, Gunduz M, Tumer L, Hasanoglu A, Tiras U, Unsal R, Bakkaloglu SA. Ezgu F, et al. Gene. 2013 Oct 10;528(2):364-6. doi: 10.1016/j.gene.2013.07.007. Epub 2013 Jul 26. Gene. 2013. PMID: 23892085

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