Özkan B - Search Results

1

Two different patterns of mini-puberty in two 46,XY newborns with 17β-hydroxysteroid dehydrogenase type 3 deficiency.

Demir K, Yıldız M, Elmas ÖN, Korkmaz HA, Tunç S, Olukman Ö, Hazan F, Özkan KU, Özkan B. Demir K, et al. Among authors: ozkan ku, ozkan b. J Pediatr Endocrinol Metab. 2015 Jul;28(7-8):961-5. doi: 10.1515/jpem-2014-0365. J Pediatr Endocrinol Metab. 2015. PMID: 25879310

2

A case of Turner syndrome with concomitant transient hypogammaglobulinaemia of infancy and central diabetes insipidus.

Korkmaz HA, Özkan B, Hazan F, Büyükinan M, Çelik T. Korkmaz HA, et al. Among authors: ozkan b. J Clin Res Pediatr Endocrinol. 2013;5(1):62-4. doi: 10.4274/Jcrpe.880. Epub 2013 Jun 29. J Clin Res Pediatr Endocrinol. 2013. PMID: 23419422 Free PMC article.

3

Neonatal seizure as a manifestation of unrecognized maternal hyperparathyroidism.

Korkmaz HA, Ozkan B, Terek D, Dizdarer C, Arslanoğlu S. Korkmaz HA, et al. Among authors: ozkan b. J Clin Res Pediatr Endocrinol. 2013 Sep 10;5(3):206-8. doi: 10.4274/Jcrpe.1037. J Clin Res Pediatr Endocrinol. 2013. PMID: 24072092 Free PMC article.

4

Management of central diabetes insipidus with oral desmopressin lyophilisate in infants.

Korkmaz HA, Demir K, Kılıç FK, Terek D, Arslanoğlu S, Dizdarer C, Ozkan B. Korkmaz HA, et al. Among authors: ozkan b. J Pediatr Endocrinol Metab. 2014 Sep;27(9-10):923-7. doi: 10.1515/jpem-2013-0368. J Pediatr Endocrinol Metab. 2014. PMID: 24854529

5

GPR30 Gene Polymorphisms Are Associated with Gynecomastia Risk in Adolescents.

Korkmaz HA, Edgünlü T, Eren E, Demir K, Çakir ED, Çelik SK, Özkan B. Korkmaz HA, et al. Among authors: ozkan b. Horm Res Paediatr. 2015;83(3):177-82. doi: 10.1159/000369013. Epub 2014 Dec 18. Horm Res Paediatr. 2015. PMID: 25531203 Clinical Trial.

6

Importance of insulin immunoassays in the diagnosis of factitious hypoglycemia.

Nalbantoğlu Elmas Ö, Demir K, Soylu N, Çelik N, Özkan B. Nalbantoğlu Elmas Ö, et al. Among authors: ozkan b. J Clin Res Pediatr Endocrinol. 2014 Dec;6(4):258-61. doi: 10.4274/Jcrpe.1492. J Clin Res Pediatr Endocrinol. 2014. PMID: 25541899 Free PMC article.

7

Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A.

Demir K, Kattan WE, Zou M, Durmaz E, BinEssa H, Nalbantoğlu Ö, Al-Rijjal RA, Meyer B, Özkan B, Shi Y. Demir K, et al. Among authors: ozkan b. PLoS One. 2015 Jul 1;10(7):e0131376. doi: 10.1371/journal.pone.0131376. eCollection 2015. PLoS One. 2015. PMID: 26132292 Free PMC article.

8

A novel mutation of AMH in three siblings with persistent Mullerian duct syndrome.

Nalbantoğlu Ö, Demir K, Korkmaz HA, Büyükinan M, Yıldız M, Tunç S, Özkan B. Nalbantoğlu Ö, et al. Among authors: ozkan b. J Pediatr Endocrinol Metab. 2015 Nov 1;28(11-12):1379-82. doi: 10.1515/jpem-2014-0501. J Pediatr Endocrinol Metab. 2015. PMID: 26181047

9

Molecular diagnosis of maturity-onset diabetes of the young (MODY) in Turkish children by using targeted next-generation sequencing.

Anık A, Çatlı G, Abacı A, Sarı E, Yeşilkaya E, Korkmaz HA, Demir K, Altıncık A, Tuhan HÜ, Kızıldağ S, Özkan B, Ceylaner S, Böber E. Anık A, et al. Among authors: ozkan b. J Pediatr Endocrinol Metab. 2015 Nov 1;28(11-12):1265-71. doi: 10.1515/jpem-2014-0430. J Pediatr Endocrinol Metab. 2015. PMID: 26226118

10

Factors Influencing Serum Vitamin D Concentration in Turkish Children Residing in İzmir: A Single-Center Experience.

Gülez P, Korkmaz HA, Özkök D, Can D, Özkan B. Gülez P, et al. Among authors: ozkan b. J Clin Res Pediatr Endocrinol. 2015 Dec;7(4):294-300. doi: 10.4274/jcrpe.1938. J Clin Res Pediatr Endocrinol. 2015. PMID: 26777040 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

534 results

Search Page

Filters