Özlem Nalbantoğlu, M.D.
14.12.2018

Özlem Nalbantoğlu.jpg

Department of Pediatric Endocrinology

Name: Özlem Nalbantoğlu

Prof of Pediatrics, MD, Division of Pediatric Endocrinology, Dept of Pediatrics, Behçet Uz Childrens Hospital, İzmir.

Birth date and place: Erciş/Van, 28/04/1977

Education

1995-2001: Dokuz Eylül Unv. Faculty of Medicine, İzmir

2002-2007: Yüzüncü yıl  Unv. Faculty of Medicine, Pediatric  Assistant ,Van
2008-2011: İnönü Unv. Pediatric Endocrinology fellowship, Malatya

2011-2013: Malataya State Hospital, Pediatric Endocrinologist

2013-…….: Dr. Behçet Uz Children and Pediatric Surgery Traning Hospital, Pediatric Endocrinologist

Members of foundation

        

         “The Endocrine Society“

   

 SOME PUBLİCATİONS  IN JOURNAL of SCI

  1. Abacı A, Çatlı G, Kırbıyık Ö, Şahin NM, Abalı ZY, Ünal E, Şıklar Z, Mengen E, Özen S, Güran T, Kara C, Yıldız M, Eren E, Nalbantoğlu Ö, Güven A, Çayır A, Akbaş ED, Kor Y, Çürek Y, Aycan Z, Baş F, Darcan Ş, Berberoğlu M. Genotype-phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey.J Endocrinol Invest. 2018 Aug 21
  2. Tuhan H, Ceylaner S, Nalbantoğlu Ö, Acar S, Abacı A, Böber E, Demir K. A Mutation in INSR in a Child Presenting with Severe Acanthosis Nigricans. J Clin Res Pediatr Endocrinol. 2017 Dec 15;9(4):371-374.
  3. Aral CA, Nalbantoğlu Ö, Nur BG, Altunsoy M, Aral K. Metabolic control and periodontal treatment decreases elevated oxidative stress in the early phases of type 1 diabetes onset. Arch Oral Biol. 2017 Oct;82:115-120.
  4. Karti O, Nalbantoglu O, Abali S, Ayhan Z, Tunc S, Kusbeci T, Ozkan B. Retinal Ganglion Cell Loss in Children With Type 1 Diabetes Mellitus Without Diabetic Retinopathy. Ophthalmic Surg Lasers Imaging Retina. 2017 Jun 1;48(6):473-477. 
  5. Katipoğlu N, Karapinar TH, Demir K, Aydin Köker S, Nalbantoğlu Ö, Ay Y, Korkmaz HA, Oymak Y, Yıldız M, Tunç S, Hazan F, Vergin C, Ozkan B. Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report. Arch Argent Pediatr. 2017 Jun 1;115(3):e153-e156. 
  6. Tunç S, Demir K, Tükün FA, Topal C, Hazan F, Sağlam B, Nalbantoğlu Ö, Yıldız M, Özkan B. Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents. J Clin Res Pediatr Endocrinol. 2017 Sep 1;9(3):216-221. D
  7. Bağ Ö, Tunç S, Nalbantoğlu Ö, Ecevit Ç, Öztürk A, Özkan B, Demir K.Higher-Than-Conventional Subcutaneous Regular Insulin Doses Following Diabetic Ketoacidosis in Children and Adolescents J Clin Res Pediatr Endocrinol. 2017 Jun 1;9(2):132-137.
  8. Karti O, Nalbantoglu O, Abali S, Tunc S, Ozkan B. The assessment of peripapillary retinal nerve fiber layer and macular ganglion cell layer changes in obese children: a cross-sectional study using optical coherencetomography.Int Ophthalmol. 2017 Aug;37(4):1031-1038.
  9. Demir K, Nalbantoğlu Ö, Karaer K, Korkmaz HA, Yıldız M, Tunç S, Özkan B. Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy. J Clin Res Pediatr Endocrinol. 2015 Dec;7(4):356-7.
  10. Yıldız M, İşleten F, Demir K, Çelik N, Korkmaz HA, Tuğlu B, Nalbantoğlu Ö, Özkan B. Anti-cyclic citrullinated peptide antibodies are not frequently observed in children with type 1 diabetes mellitus: a single-center study. Turk J Pediatr. 2016;58(4):395-399.
  11. Mengen E, Tunc S, Kotan LD, Nalbantoglu O, Demir K, Gurbuz F, Turan I, Seker G, Yuksel B, Topaloglu AK. Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide. Horm Res Paediatr. 2016;85(2):107-11.
  12. Nalbantoğlu Ö, Demir K, Korkmaz HA, Büyükinan M, Yıldız M, Tunç S, Özkan B.  A novel mutation of AMH in three siblings with persistent Mullerian duct syndrome. J Pediatr Endocrinol Metab. 2015 Nov 1;28(11-12):1379-82. 
  13. Demir K, Kattan WE, Zou M, Durmaz E, BinEssa H, Nalbantoğlu Ö, Al-Rijjal RA, Meyer B, Özkan B, Shi Y. Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A. PLoS One. 2015 Jul 1;10(7):e0131376.
  14. Aknc A, Karakurt C, Gurbuz S, Elkran O, Nalbantoglu O, Kocak G, Guldur T, Yologlu S. Association of cardiac changes with serum adiponectin and resistin levels in obese and overweight children.J Cardiovasc Med (Hagerstown). 2013 Mar;14(3):228-34. 
  15. Korkmaz HA, Demir K, Hazan F, Yıldız M, Elmas ÖN, Özkan B.Association of Wolfram syndrome with Fallot tetralogy in a girl. Arch Argent Pediatr. 2016 Jun 1;114(3):e163-6.
  16. Demir K, Yıldız M, Elmas ÖN, Korkmaz HA, Tunç S, Olukman Ö, Hazan F, Özkan KU, Özkan B. Two different patterns of mini-puberty in two 46,XY newborns with 17β-hydroxysteroid dehydrogenase type 3 deficiency.J Pediatr Endocrinol Metab. 2015 Jul;28(7-8):961-5. 
  17. Elmas AT, Tabel Y, Elmas ON. Reference intervals of serum cystatin C for determining cystatin C-based glomerular filtration rates in preterm neonates.J Matern Fetal Neonatal Med. 2013 Oct;26(15):1474-8.
  18. Elmas AT, Tabel Y, Elmas ON.Serum cystatin C predicts acute kidney injury in preterm neonates with respiratory distress syndrome. Pediatr Nephrol. 2013 Mar;28(3):477-84. 
  19. Elmas AT, Tabel Y, Elmas ON. Short- and long-term efficacy of levamisole in children with steroid-sensitive nephrotic syndrome.Int Urol Nephrol. 2013 Aug;45(4):1047-5
  20. Elmas ÖN, Akıncı A, Bilir P. Tuberculous meningitis associated with diabetic ketoacidosis.J Clin Res Pediatr Endocrinol. 2011;3(4):222-4. D
  21. Bay A, Yilmaz N, Nalbantoglu O, Yilmaz C, Etlik O, Faik Oner A. Multiple brain abscesses in a child with autoimmune hemolytic anemia.Pediatr Blood Cancer. 2007 Dec;49(7):1034-6.