Two Cases of Acute Myocarditis with Multiple Intracardiac Thrombi: The Role of Hypercoagulable States.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
Works by Delil, Kenan
Results: 12
1
2
Homozygous Mutation in the Insulin Receptor Gene Associated with Mild Type A Insulin Resistance Syndrome: A Case Report.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 100, doi. 10.4274/jcrpe.galenos.2020.2019.0213
- By:
- Publication type:
- Article
3
Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2016, v. 8, n. 2, p. 144, doi. 10.4274/jcrpe.2307
- By:
- Publication type:
- Article
4
Challenges in the treatment of fibrodysplasia ossificans progressiva.
- Published in:
- Rheumatology International, 2019, v. 39, n. 3, p. 569, doi. 10.1007/s00296-018-4179-x
- By:
- Publication type:
- Article
5
Biallelic Mutations in DNAJB11are Associated with Prenatal Polycystic Kidney Disease in a Turkish Family.
- Published in:
- Molecular Syndromology, 2021, v. 12, n. 3, p. 179, doi. 10.1159/000513611
- By:
- Publication type:
- Article
6
22q11 deletion syndrome: current perspective.
- Published in:
- Application of Clinical Genetics, 2015, v. 8, p. 123, doi. 10.2147/TACG.S82105
- By:
- Publication type:
- Article
7
Acute inferior myocardial infarction in a patient with a prosthetic aortic valve and high international normalized ratio.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
8
Author`s Reply.
- Published in:
- Anatolian Journal of Cardiology / Anadolu Kardiyoloji Dergisi, 2015, v. 15, n. 5, p. 434
- By:
- Publication type:
- Article
9
Noncompaction with dysmorphism, mental retardation, general wasting, and hypogonadism requires neurologic and sophisticated cytogenetic investigations.
- Published in:
- 2015
- By:
- Publication type:
- Letter to the Editor
10
Case of fatal heart failure with biventricular noncompaction, genital skeletal abnormalities and mental retardation.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
11
Vitamin D receptor gene polymorphisms in children with kidney stone disease.
- Published in:
- Turkish Journal of Pediatrics, 2017, v. 59, n. 4, p. 404, doi. 10.24953/turkjped.2017.04.006
- By:
- Publication type:
- Article
12
Functionally stable plasminogen activator inhibitor-1 in a family with cardiovascular disease and vitiligo.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2014, v. 38, n. 1, p. 50, doi. 10.1007/s11239-013-1021-x
- By:
- Publication type:
- Article