Hale U. Tuhan
Antalya, Turkey
Last Updated: 09/26/2026
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Found 49 publications
Longitudinal changes in nonfunctioning pituitary neuroendocrine tumors in children receiving growth hormone therapy: A comparison with untreated patients.
Journal: Archivos argentinos de pediatria
Published: July 28, 2026
Evaluation of retinochoroidal microvascular parameters and biochemical markers in childhood obesity.
Evaluation of retinochoroidal microvascular parameters and biochemical markers in childhood obesity.
Journal: Microvascular research
Published: May 04, 2026
Automatic bone age assessment for adult height prediction in children with congenital adrenal hyperplasia.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: February 13, 2026
Evaluation of Muscle Mass and Strength in Children and Adolescents with Disorders of Sex Development.
Journal: Journal of clinical research in pediatric endocrinology
Published: January 07, 2026
Single-Center Experience in Five Patients Diagnosed with Lipoid Congenital Adrenal Hyperplasia due to Steroidogenic Acute Regulatory Protein (STAR) Gene Variants: A Rare Cause of Adrenal Insufficiency
Journal: Journal of clinical research in pediatric endocrinology
Published: November 20, 2025
A Rare Endocrinological Emergency in Children with Hypothyroidism: Clinical Evaluation of Cases Presenting with Myxedema Coma.
Journal: Turkish archives of pediatrics
Published: September 17, 2025
Can uric acid levels be helpful for the diagnosis of CPP in girls?
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: August 27, 2025
Evaluation of the genetic alterations landscape of differentiated thyroid cancer in children.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: June 24, 2025
A Case of Adolescent Girl with Hypercalcemia Resistant to Medical Treatment Due to Giant Breast Fibroadenoma.
Journal: Journal of clinical research in pediatric endocrinology
Published: June 12, 2025
Growth Hormone Therapy in Neurosecretory Dysfunction.
Journal: Turkish archives of pediatrics
Published: May 12, 2025
A RARE CAUSE OF NEONATAL SALT WASTING: CLINICAL MANAGEMENT OF A CASE WITH PSEUDOHYPOALDOSTERONISM DETECTED WITH A NOVEL HOMOZYGOUS VARIANT IN THE SCNN1A GENE.
Journal: Acta endocrinologica (Bucharest, Romania : 2005)
Published: April 01, 2025
CONCURRENT OCCURRENCE OF NEUROFIBROMATOSIS TYPE 1 AND TURNER SYNDROME: A PEDIATRIC CASE REPORT WITH COMPREHENSIVE LITERATURE REVIEW.
Journal: Acta endocrinologica (Bucharest, Romania : 2005)
Published: January 01, 2025
Last Updated: 09/26/2026