Fatma Tuğba Eminoğlu

19PUBLICATIONS
169CO-AUTHORS
Paediatrics not elsewhere classifiedMedical biochemistry - inorganic elements and compoundsDevelopmental genetics (incl. sex determination)Infant and child healthEpigenetics (incl. genome methylation and epigenomics)
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Publications (19)

|Jun 02, 2026
When It's Not Phenylketonuria: Alternative Diagnoses Revealed by Newborn Screening for Hyperphenylalaninemia.

|Feb 09, 2026
Cardiac involvement in pediatric patients with inherited metabolic disease.

Gamzegül Gözen Bayramoğlu, Engin Köse, Ümmühan Öncül

|Jul 31, 2025
Pseudohypertriglyceridemia as a clue: clinical and genetic spectrum of glycerol kinase deficiency in three pediatric cases.

Cemre Kara, Pınar Kılıçdağı Çanakcı, Engin Köse

|Jul 21, 2025
Expert opinion on clinical presentation, diagnosis, and treatment of infantile-onset Pompe disease: a Delphi study in Türkiye.

Ekin Özsaydi Aktaşoğlu, Aslı Inci, Rıdvan Murat Öktem

|Jun 25, 2025
NOD-m: a novel clinical score for predicting hearing loss in inherited metabolic disorders.

Merve Koç Yekedüz, İlayda Kütükkiran, İlknur Sürücü Kara

|May 28, 2025
Wolcott-Rallison syndrome: late-onset diabetes, multiple epiphyseal dysplasia, and acute liver failure - a case report.

Selçuk Teke, Zarife Kuloğlu, Arzu Meltem Demir

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Frequent Collaborators

15 joint publications

Engin Köse

9 joint publications

Merve Koç Yekedüz

5 joint publications

İlknur Sürücü Kara

4 joint publications

Ümmühan Öncül