Delil K - Search Results

1

Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature.

Delil K, Karabulut HG, Hacıhamdioğlu B, Şıklar Z, Berberoğlu M, Öçal G, Tükün A, Ruhi HI. Delil K, et al. J Clin Res Pediatr Endocrinol. 2016 Jun 5;8(2):144-9. doi: 10.4274/jcrpe.2307. Epub 2015 Dec 18. J Clin Res Pediatr Endocrinol. 2016. PMID: 26758084 Free PMC article.

2

Homozygous Mutation in the Insulin Receptor Gene Associated with Mild Type A Insulin Resistance Syndrome: A Case Report.

Hacıhamdioğlu B, Baş EG, Delil K. Hacıhamdioğlu B, et al. Among authors: delil k. J Clin Res Pediatr Endocrinol. 2020 Feb 5;13(1):100-103. doi: 10.4274/jcrpe.galenos.2020.2019.0213. Online ahead of print. J Clin Res Pediatr Endocrinol. 2020. PMID: 32018348 Free PMC article.

3

22q11 deletion syndrome: current perspective.

Hacıhamdioğlu B, Hacıhamdioğlu D, Delil K. Hacıhamdioğlu B, et al. Among authors: delil k. Appl Clin Genet. 2015 May 18;8:123-32. doi: 10.2147/TACG.S82105. eCollection 2015. Appl Clin Genet. 2015. PMID: 26056486 Free PMC article. Review.

4

Vitamin D receptor gene polymorphisms in children with kidney stone disease.

Subaşı B, Gökçe İ, Delil K, Alpay H. Subaşı B, et al. Among authors: delil k. Turk J Pediatr. 2017;59(4):404-409. doi: 10.24953/turkjped.2017.04.006. Turk J Pediatr. 2017. PMID: 29624220 Free article.

5

Biallelic Mutations in DNAJB11 are Associated with Prenatal Polycystic Kidney Disease in a Turkish Family.

Ateş EA, Turkyilmaz A, Delil K, Alavanda C, Söylemez MA, Geçkinli BB, Ata P, Arman A. Ateş EA, et al. Among authors: delil k. Mol Syndromol. 2021 Jun;12(3):179-185. doi: 10.1159/000513611. Epub 2021 Apr 1. Mol Syndromol. 2021. PMID: 34177435 Free PMC article.

6

JAGN1 Deficient Severe Congenital Neutropenia: Two Cases from the Same Family.

Baris S, Karakoc-Aydiner E, Ozen A, Delil K, Kiykim A, Ogulur I, Baris I, Barlan IB. Baris S, et al. Among authors: delil k. J Clin Immunol. 2015 May;35(4):339-43. doi: 10.1007/s10875-015-0156-2. Epub 2015 Apr 8. J Clin Immunol. 2015. PMID: 25851723

7

Challenges in the treatment of fibrodysplasia ossificans progressiva.

Gencer-Atalay K, Ozturk EC, Yagci I, Ata P, Delil K, Ozgen Z, Akyuz G. Gencer-Atalay K, et al. Among authors: delil k. Rheumatol Int. 2019 Mar;39(3):569-576. doi: 10.1007/s00296-018-4179-x. Epub 2018 Oct 20. Rheumatol Int. 2019. PMID: 30343406 Review.

8

Case of fatal heart failure with biventricular noncompaction, genital skeletal abnormalities and mental retardation.

Ataş H, Samadov F, Sarı İ, Delil K. Ataş H, et al. Among authors: delil k. Anatol J Cardiol. 2015 Jan;15(1):71-2. doi: 10.5152/akd.2014.5722. Epub 2014 Dec 25. Anatol J Cardiol. 2015. PMID: 25550252 Free PMC article. No abstract available.

9

CLINICAL REPORT OF A PATIENT WITH DE NOVO TRISOMY 12q23.1q24.33.

Geckinli BB, Aydin H, Karaman A, Delil K, Simsek H, Gokmeydan E, Turkdogan D. Geckinli BB, et al. Among authors: delil k. Genet Couns. 2015;26(4):393-400. Genet Couns. 2015. PMID: 26852509

10

Acute inferior myocardial infarction in a patient with a prosthetic aortic valve and high international normalized ratio.

Atas H, Sari I, Delil K, Ileri C, Samadov F. Atas H, et al. Among authors: delil k. Postepy Kardiol Interwencyjnej. 2014;10(1):63-5. doi: 10.5114/pwki.2014.41475. Epub 2014 Mar 23. Postepy Kardiol Interwencyjnej. 2014. PMID: 24799934 Free PMC article.

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