Okur I - Search Results

1

Structure-function analyses of microsomal triglyceride transfer protein missense mutations in abetalipoproteinemia and hypobetalipoproteinemia subjects.

Walsh MT, Di Leo E, Okur I, Tarugi P, Hussain MM. Walsh MT, et al. Among authors: okur i. Biochim Biophys Acta. 2016 Nov;1861(11):1623-1633. doi: 10.1016/j.bbalip.2016.07.015. Epub 2016 Jul 31. Biochim Biophys Acta. 2016. PMID: 27487388

2

The Janus-faced manifestations of homozygous familial hypobetalipoproteinemia due to apolipoprotein B truncations.

Di Leo E, Eminoglu T, Magnolo L, Bolkent MG, Tümer L, Okur I, Tarugi P. Di Leo E, et al. Among authors: okur i. J Clin Lipidol. 2015 May-Jun;9(3):400-5. doi: 10.1016/j.jacl.2015.01.005. Epub 2015 Jan 28. J Clin Lipidol. 2015. PMID: 26073401

3

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: okur i. 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.

4

Screening for Fabry disease in patients undergoing dialysis for chronic renal failure in Turkey: identification of new case with novel mutation.

Okur I, Ezgu F, Biberoglu G, Tumer L, Erten Y, Isitman M, Eminoglu FT, Hasanoglu A. Okur I, et al. Gene. 2013 Sep 15;527(1):42-7. doi: 10.1016/j.gene.2013.05.050. Epub 2013 Jun 10. Gene. 2013. PMID: 23756194

5

The levels of asymmetric dimethylarginine, homocysteine and carotid intima-media thickness in hypercholesterolemic children.

Hasanoğlu A, Okur I, Oren AC, Biberoğlu G, Oktar S, Eminoğlu FT, Tümer L. Hasanoğlu A, et al. Among authors: okur i. Turk J Pediatr. 2011 Sep-Oct;53(5):522-7. Turk J Pediatr. 2011. PMID: 22272452

6

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: okur i. 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

7

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: okur i. Autism Res. 2021 May;14(5):887-896. doi: 10.1002/aur.2486. Epub 2021 Feb 19. Autism Res. 2021. PMID: 33605552

8

Vitamin D intoxication and hypercalcaemia in an infant treated with pamidronate infusions.

Ezgu FS, Buyan N, Gündüz M, Tümer L, Okur I, Hasanoglu A. Ezgu FS, et al. Among authors: okur i. Eur J Pediatr. 2004 Mar;163(3):163-5. doi: 10.1007/s00431-003-1387-4. Epub 2004 Jan 9. Eur J Pediatr. 2004. PMID: 14714183

9

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. Among authors: okur i. 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.

10

Multisystem involvement in a patient due to accumulation of amylopectin-like material with diminished branching enzyme activity.

Eminoglu TF, Tumer L, Okur I, Olgunturk R, Hasanoglu A, Gonul II, Dalgic B. Eminoglu TF, et al. Among authors: okur i. J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S255-9. doi: 10.1007/s10545-008-0819-8. Epub 2008 Apr 4. J Inherit Metab Dis. 2008. PMID: 18392749

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