Çamtosun E - Search Results

1

Clinical Characteristics and Genetic Analyses of Patients with Idiopathic Hypogonadotropic Hypogonadism.

Çiftci N, Akıncı A, Akbulut E, Çamtosun E, Dündar İ, Doğan M, Kayaş L. Çiftci N, et al. Among authors: camtosun e. J Clin Res Pediatr Endocrinol. 2023 May 29;15(2):160-171. doi: 10.4274/jcrpe.galenos.2023.2022-10-14. Epub 2023 Jan 26. J Clin Res Pediatr Endocrinol. 2023. PMID: 36700485 Free PMC article.

2

ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity.

Kocaay P, Şıklar Z, Çamtosun E, Kendirli T, Berberoğlu M. Kocaay P, et al. Among authors: camtosun e. J Clin Res Pediatr Endocrinol. 2014 Dec;6(4):254-7. doi: 10.4274/Jcrpe.1432. J Clin Res Pediatr Endocrinol. 2014. PMID: 25541898 Free PMC article.

3

The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels.

Şıklar Z, Kocaay P, Çamtosun E, İsakoca M, Hacıhamdioğlu B, Savaş Erdeve Ş, Berberoğlu M. Şıklar Z, et al. Among authors: camtosun e. J Clin Res Pediatr Endocrinol. 2015 Dec;7(4):301-6. doi: 10.4274/jcrpe.2111. J Clin Res Pediatr Endocrinol. 2015. PMID: 26777041 Free PMC article.

4

Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign.

Çamtosun E, Şıklar Z, Ceylaner S, Kocaay P, Berberoğlu M. Çamtosun E, et al. J Clin Res Pediatr Endocrinol. 2017 Jun 1;9(2):163-167. doi: 10.4274/jcrpe.3839. Epub 2016 Dec 23. J Clin Res Pediatr Endocrinol. 2017. PMID: 28008861 Free PMC article.

5

Prospective Follow-up of Children with Idiopathic Growth Hormone Deficiency After Termination of Growth Hormone Treatment: Is There Really Need for Treatment at Transition to Adulthood?

Çamtosun E, Şıklar Z, Berberoğlu M. Çamtosun E, et al. J Clin Res Pediatr Endocrinol. 2018 Jul 31;10(3):247-255. doi: 10.4274/jcrpe.0010. Epub 2018 Mar 19. J Clin Res Pediatr Endocrinol. 2018. PMID: 29553045 Free PMC article.

6

A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment.

Çamtosun E, Akıncı A, Demiral E, Tekedereli İ, Sığırcı A. Çamtosun E, et al. J Clin Res Pediatr Endocrinol. 2019 Sep 3;11(3):301-305. doi: 10.4274/jcrpe.galenos.2018.2018.0211. Epub 2018 Nov 23. J Clin Res Pediatr Endocrinol. 2019. PMID: 30468148 Free PMC article.

7

Autosomal recessive cutis laxa: a novel mutation in the FBLN5 gene in a family.

Tekedereli I, Demiral E, Gokce IK, Esener Z, Camtosun E, Akinci A. Tekedereli I, et al. Among authors: camtosun e. Clin Dysmorphol. 2019 Apr;28(2):63-65. doi: 10.1097/MCD.0000000000000258. Clin Dysmorphol. 2019. PMID: 30640789

8

Laron syndrome related to homozygous growth hormone receptor c.784>C mutation in a patient with hypoplastic pulmonary arteries.

Akinci A, Karakurt C, Hwa V, Dündar I, Çamtosun E. Akinci A, et al. Among authors: camtosun e. Cardiovasc J Afr. 2019 Mar/Apr 23;30(2):e7-e8. doi: 10.5830/CVJA-2019-002. Epub 2019 Jan 22. Cardiovasc J Afr. 2019. PMID: 30720842

9

Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study.

Akıncı A, Türkkahraman D, Tekedereli İ, Özer L, Evren B, Şahin İ, Kalkan T, Çürek Y, Çamtosun E, Döğer E, Bideci A, Güven A, Eren E, Sangün Ö, Çayır A, Bilir P, Törel Ergür A, Ercan O. Akıncı A, et al. Among authors: camtosun e. J Clin Res Pediatr Endocrinol. 2019 Nov 22;11(4):341-349. doi: 10.4274/jcrpe.galenos.2019.2019.0021. Epub 2019 Apr 17. J Clin Res Pediatr Endocrinol. 2019. PMID: 30991789 Free PMC article.

10

Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience.

Çamtosun E, Dündar İ, Akıncı A, Kayaş L, Çiftci N. Çamtosun E, et al. J Clin Res Pediatr Endocrinol. 2021 Feb 26;13(1):88-99. doi: 10.4274/jcrpe.galenos.2020.2020.0132. Epub 2020 Sep 17. J Clin Res Pediatr Endocrinol. 2021. PMID: 32938577 Free PMC article.

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