Aydilek D. Cakir
Sisli, Turkey
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 14 publications
The first report of a gross deletion in the SCNN1G gene in a case presenting with hyponatremic convulsion at fifth year of treatment.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: July 01, 2025
Comparative Analysis of Girls With Slowly Progressive Central Precocious Puberty Vs. Rapidly Progressive Central Precocious Puberty: Single-Center Experience.
Journal: Sisli Etfal Hastanesi tip bulteni
Published: December 30, 2024
Successful Management of an Infant with Congenital Focal Hyperinsulinism with No Apparent Lesion During Surgery.
Journal: Sisli Etfal Hastanesi tip bulteni
Published: May 09, 2024
Determination of the cryoprotective effect of n-methylacetamide in rabbit semen.
Journal: Cryo letters
Published: February 05, 2024
Correction: Clinical indicators that influence a clinician's decision to start L-thyroxine treatment in prematurity with transient hypothyroxinemia.
Journal: Italian journal of pediatrics
Published: September 29, 2023
Clinical indicators that influence a clinician's decision to start L-thyroxine treatment in prematurity with transient hypothyroxinemia.
Journal: Italian journal of pediatrics
Published: April 10, 2023
Differentiated Thyroid Cancer in Children and Adolescents: Clinicopathological Characteristics of 32 Patients Followed up in our Pediatric Endocrinology Unit.
Journal: Sisli Etfal Hastanesi tip bulteni
Published: December 21, 2022
The association of metabolic syndrome status with sensorineural hearing loss in pediatric obese patients.
Journal: International journal of pediatric otorhinolaryngology
Published: November 09, 2022
Comparative analyses of surrogates of metabolic syndrome in children and adolescents with metabolically healthy obesity vs. metabolically unhealthy obesity according to Damanhoury's criteria.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: September 23, 2022
Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 11, 2020
Evaluation of the thyroid disorders in children with familial Mediterranean fever.
Journal: Clinical rheumatology
Published: June 29, 2020
Factors influencing blood pressure and microalbuminuria in children with type 1 diabetes mellitus: salt or sugar?
Journal: Pediatric nephrology (Berlin, Germany)
Published: November 06, 2019
Last Updated: 09/26/2026