Fatma Derya Bulut

20PUBLICATIONS
89CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Central nervous systemAutoimmunityCardiology (incl. cardiovascular diseases)Medical biochemistry - proteins and peptides (incl. medical proteomics)
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Publications (20)

|Oct 29, 2026
Next-Generation Sequencing in Pediatric Lipid Disorders: Expanding the Genetic Landscape and Clinical Understanding.

|Jul 28, 2026
Creatine Deficiency Syndromes: Clinical Spectrum, Neuroimaging Features and Treatment Response.

|May 05, 2026
Mucolipidosis Type III: A Hidden Challenge in the Differential Diagnosis of Rheumatological Disorders.

|May 03, 2026
Shifting Towards Empagliflozin First-Line Therapy in Glycogen Storage Disease Type Ib: A Nationwide Real-World Study.

|Nov 13, 2025
Genotype-Phenotype Correlations and Shifting Diagnosis Age in Turkish Mucopolysaccharidosis Type II Patients: A Multicenter Retrospective Study.

Havva Yazıcı, Esra Kara, Fatma Derya Bulut

|Sep 27, 2025
Feeding Models in Classical Phenylketonuria: Do They Make a Difference in Infant Sleep?

Ezgi Burgaç, Ebru Çiçek Türköz, Adnan Barutçu

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Frequent Collaborators

13 joint publications

Neslihan Önenli-Mungan

9 joint publications

Deniz Kor

8 joint publications

Ezgi Burgac

7 joint publications

Esra Kara