Ezgü F - Search Results

1

A new NBIA patient from Turkey with homozygous C19ORF12 mutation.

Kasapkara ÇS, Tümer L, Gregory A, Ezgü F, İnci A, Derinkuyu BE, Fox R, Rogers C, Hayflick S. Kasapkara ÇS, et al. Among authors: ezgu f. Acta Neurol Belg. 2019 Dec;119(4):623-625. doi: 10.1007/s13760-018-1026-5. Epub 2018 Oct 8. Acta Neurol Belg. 2019. PMID: 30298423 Free PMC article. No abstract available.

2

The co-existence of Fabry and celiac diseases: a case report.

Tümer L, Ezgü FS, Hasanoğlu A, Dalgiç B, Bakkaloğlu SA, Memiş L, Dursun A. Tümer L, et al. Pediatr Nephrol. 2004 Jun;19(6):679-81. doi: 10.1007/s00467-004-1462-8. Epub 2004 Apr 15. Pediatr Nephrol. 2004. PMID: 15085421

3

Serum carnitine levels in newborns with perinatal asphyxia and relation to neurologic prognosis.

Ezgü FS, Atalay Y, Hasanoğlu A, Gücüyener K, Biberoğlu G, Koç E, Ergenekon E, Tümer L. Ezgü FS, et al. Nutr Neurosci. 2004 Oct-Dec;7(5-6):351-6. doi: 10.1080/10284150400017280. Nutr Neurosci. 2004. PMID: 15682932

4

Effect of enteral and parenteral nutrition on growth parameters of hospitalized Turkish children.

Ezgu FS, Tumer L, Cinasal G, Hasanoglu A, Gunduz M. Ezgu FS, et al. Indian Pediatr. 2005 May;42(5):469-72. Indian Pediatr. 2005. PMID: 15923694

5

Cholesteryl ester storage disease in a young child presenting as isolated hepatomegaly treated with simvastatin.

Dalgiç B, Sari S, Gündüz M, Ezgü F, Tümer L, Hasanoğlu A, Akyol G. Dalgiç B, et al. Among authors: ezgu f. Turk J Pediatr. 2006 Apr-Jun;48(2):148-51. Turk J Pediatr. 2006. PMID: 16848116

6

Rapid screening of 10 common mutations in Turkish Gaucher patients using electronic DNA microarray.

Ezgu F, Hasanoglu A, Okur I, Biberoglu G, Tumer L, Eminoglu T, Dogan H. Ezgu F, et al. Blood Cells Mol Dis. 2008 Mar-Apr;40(2):246-7. doi: 10.1016/j.bcmd.2007.09.008. Epub 2007 Nov 26. Blood Cells Mol Dis. 2008. PMID: 18035560 No abstract available.

7

Homocysteine, fibrinogen and anti-ox-LDL antibody levels as markers of atherosclerosis in prepubertal obese children.

Ezgü F, Tümer L, Ozbay F, Hasanoglu A, Biberoğlu G, Aybay C. Ezgü F, et al. J Pediatr Endocrinol Metab. 2009 Oct;22(10):915-20. doi: 10.1515/jpem.2009.22.10.915. J Pediatr Endocrinol Metab. 2009. PMID: 20020579

8

Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R.

Hasanoglu A, Balwani M, Kasapkara CS, Ezgü FS, Okur I, Tümer L, Cakmak A, Nazarenko I, Yu C, Clavero S, Bishop DF, Desnick RJ. Hasanoglu A, et al. Among authors: ezgu fs. J Inherit Metab Dis. 2011 Feb;34(1):225-31. doi: 10.1007/s10545-010-9237-9. Epub 2010 Nov 20. J Inherit Metab Dis. 2011. PMID: 21103937 Free PMC article.

9

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

10

An infantile case of Zellweger syndrome presented with Kabuki-like phenotype.

Ezgu F, Eminoglu T, Okur I, Gunduz M, Tumer L, Hasanoglu A, Dalgic B. Ezgu F, et al. Genet Couns. 2011;22(2):217-20. Genet Couns. 2011. PMID: 21848015

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