Beken S - Search Results

1

Interleukin-8 and Its Receptors in Human Milk from Mothers of Full-Term and Premature Infants.

Polat A, Tunc T, Erdem G, Yerebasmaz N, Tas A, Beken S, Basbozkurt G, Saldir M, Zenciroglu A, Yaman H. Polat A, et al. Among authors: beken s. Breastfeed Med. 2016 Jun;11:247-51. doi: 10.1089/bfm.2015.0186. Epub 2016 Apr 22. Breastfeed Med. 2016. PMID: 27105439

2

Can intrauterine death of a co-twin result in renal failure in the survivor?

Aydın B, Dilli D, Zenciroğlu A, Aydoğ O, Beken S, Uzunalıç N, Cınar HG, Akyüz SG, Okumuş N. Aydın B, et al. Among authors: beken s. Ren Fail. 2013;35(4):544-6. doi: 10.3109/0886022X.2013.766565. Epub 2013 Feb 14. Ren Fail. 2013. PMID: 23406005 Free article.

3

Fibrinolytic therapy of thrombosis in 27 newborns followed-up in neonatal intensive care unit.

Aydın B, Beken S, Dilli D, Çınar HG, Özkan E, Zenciroğlu A, Okumus N. Aydın B, et al. Among authors: beken s. Pediatr Hematol Oncol. 2013 Nov;30(8):705-16. doi: 10.3109/08880018.2013.793756. Epub 2013 May 7. Pediatr Hematol Oncol. 2013. PMID: 23647504 Clinical Trial.

4

Successful hypothermia treatment of hypoxic-ischemic encephalopathy in a neonate with epidermolysis bullosa.

Karadag N, Beken S, Dilli D, Zenciroglu A, Okumus N. Karadag N, et al. Among authors: beken s. Indian J Pediatr. 2014 Aug;81(8):803-4. doi: 10.1007/s12098-013-1182-9. Epub 2013 Aug 11. Indian J Pediatr. 2014. PMID: 23934101

5

A novel mutation of laminin β-2 gene in Pierson syndrome manifested with nephrotic syndrome in the early neonatal period.

Aydin B, Ipek MS, Ozaltin F, Zenciroğlu A, Dilli D, Beken S, Okumuş N, Hoşağasi N, Saygili-Karagöl B, Kundak A, Renda R, Aydog O. Aydin B, et al. Among authors: beken s. Genet Couns. 2013;24(2):141-7. Genet Couns. 2013. PMID: 24032283

6

Crisponi syndrome: a new mutation in CRLF1 gene associated with moderate outcome.

Uzunalic N, Zenciroglu A, Beken S, Piras R, Dilli D, Aydin B, Chiappe F, Okumus N, Crisponi L. Uzunalic N, et al. Among authors: beken s. Genet Couns. 2013;24(2):161-6. Genet Couns. 2013. PMID: 24032286

7

Papillorenal syndrome with de novo reciprocal translocation t(2;15) (q31; q26).

Aydin B, Dilli D, Beken S, Zenciroglu A, Uzunalic N, Yuksekkaya P, Akyuz SG, Aydog O, Okumus N. Aydin B, et al. Among authors: beken s. Genet Couns. 2013;24(2):201-5. Genet Couns. 2013. PMID: 24032291

8

Treatment outcomes of infants with cyanotic congenital heart disease treated with synbiotics.

Dilli D, Aydin B, Zenciroğlu A, Özyazici E, Beken S, Okumuş N. Dilli D, et al. Among authors: beken s. Pediatrics. 2013 Oct;132(4):e932-8. doi: 10.1542/peds.2013-1262. Epub 2013 Sep 16. Pediatrics. 2013. PMID: 24043284 Clinical Trial.

9

Distribution of congenital anomalies in a neonatal intensive care unit in Turkey.

Dursun A, Zenciroglu A, Hakan N, Karadag N, Karagol BS, Aydin B, Dilli D, Okumus N, Beken S. Dursun A, et al. Among authors: beken s. J Matern Fetal Neonatal Med. 2014 Jul;27(10):1069-74. doi: 10.3109/14767058.2013.847420. Epub 2013 Oct 17. J Matern Fetal Neonatal Med. 2014. PMID: 24059457

10

Comparison of a rapid bed-side test with a central laboratory analysis for C-reactive protein in newborn infants with suspicion of sepsis.

Aydin B, Dilli D, Zenciroğlu A, Kaya O, Bilaloğlu E, Okumuş N, Beken S. Aydin B, et al. Among authors: beken s. Clin Lab. 2013;59(9-10):1045-51. doi: 10.7754/clin.lab.2012.120923. Clin Lab. 2013. PMID: 24273927

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