T T. Eminoglu
Ankara, Turkey
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 22 publications
Optic Glioma in a Child With Alpha-Mannosidosis: A Previously Unreported Co-occurrence.
Journal: Pediatric blood & cancer
Published: April 24, 2026
Left Ventricular Global Longitudinal Strain as an Early Predictor of Disease Severity Progression in Gaucher Disease Type 1.
Journal: Echocardiography (Mount Kisco, N.Y.)
Published: March 12, 2026
Personalized Low Protein Products Produced with a 3D Food Printer for Inherited Metabolic Diseases on Restricted Diet.
Journal: Annals of nutrition & metabolism
Published: June 13, 2025
A Rare Pitfall in Bone Mineral Densitometry: Gaucher Disease.
Journal: Clinical nuclear medicine
Published: July 07, 2022
Severe rhabdomyolysis in neuronal ceroid lipofuscinosis type 7.
Journal: Clinical neurology and neurosurgery
Published: May 06, 2022
Early neuroimaging findings of infants diagnosed with inherited metabolic disorders in neonatal period: A case-control study.
Journal: Clinical neurology and neurosurgery
Published: November 02, 2021
Serum biotin interference: A troublemaker in hormone immunoassays.
Journal: Clinical biochemistry
Published: August 25, 2021
Characteristics of continuous venovenous hemodiafiltration in the acute treatment of inherited metabolic disorders.
Journal: Pediatric nephrology (Berlin, Germany)
Published: July 08, 2021
Genotype-Phenotype Correlation of the Childhood-Onset Bethlem Myopathy in the Mediterranean Region of Turkey.
Journal: Annals of Indian Academy of Neurology
Published: November 19, 2020
A Novel Variant of COL6A2 Gene Causing Bethlem Myopathy and Evaluation of Essential Hypertension.
Journal: Annals of Indian Academy of Neurology
Published: April 10, 2020
Effects of levetiracetam and valproic acid treatment on liver function tests, plasma free carnitine and lipid peroxidation in childhood epilepsies.
Journal: Epilepsy research
Published: December 18, 2018
The Metabolic Map into the Pathomechanism and Treatment of PGM1-CDG.
Journal: American journal of human genetics
Published: October 29, 2018
Last Updated: 09/26/2026