Fatih Suheyl Ezgu
Overview
Explore the profile of Fatih Suheyl Ezgu including associated specialties, affiliations and a list of published articles.
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Articles
48
Citations
177
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Recent Articles
1.
Ozata Uyar G, Yildiran H, Teker-Duztas D, Dalgic B, Karakas N, Camurdan M, et al.
Front Public Health
. 2025 Jan;
12:1435460.
PMID: 39744380
Introduction: Circadian Locomotor Output Cycles Kaput (CLOCK) is one of the transcription factors from the positive end of the molecular clock and regulates biological rhythm in mammals. Studies have shown...
2.
Ozsaydi Aktasoglu E, Kilic A, Emecen Sanli M, Inci A, Aktas E, Akdulum I, et al.
J Pediatr Endocrinol Metab
. 2024 Aug;
37(9):820-824.
PMID: 39101220
Objectives: Glycogen storage disease type V is caused by the mutations in muscle glycogen phosphorylase gene. This is the first report which DL-3-hydroxybutyric acid was used in combination with modified...
3.
Oktem R, Inci A, Bayrak H, Demir F, Biberoglu G, Mavis M, et al.
Mol Syndromol
. 2024 Jun;
15(3):185-193.
PMID: 38841329
Background: Hyperphenylalaninemia (HPA) is defined as blood phenylalanine (Phe) levels exceeding the normal values (>120 μmol/L or >2 mg/dL) and is caused by a deficiency in the enzyme phenylalanine hydroxylase...
4.
Inci A, Ezgu F, Tumer L
Paediatr Drugs
. 2024 Apr;
26(3):287-308.
PMID: 38664313
Inborn errors of metabolism (IEMs) are a group of genetic diseases that occur due to the either deficiency of an enzyme involved in a metabolic/biochemical pathway or other disturbances in...
5.
Kilic A, Emecen Sanli M, Ozsaydi Aktasoglu E, Gokalp S, Biberoglu G, Inci A, et al.
J Pediatr Endocrinol Metab
. 2024 Apr;
37(5):413-418.
PMID: 38624096
Objectives: Gaucher disease (GD) is a lysosomal storage disease caused by glucocerebrosidase (GCase) enzyme deficiency. Gaucher cells transformed from the macrophages by progressive sphingolipid accumulation and infiltrate bone marrow, spleen,...
6.
Sonmez A, Demirci I, Haymana C, Tasci I, Ayvali M, Ata N, et al.
Atherosclerosis
. 2023 May;
375:9-20.
PMID: 37216728
Background And Aims: Familial hypercholesterolemia (FH) is the most common cause of premature atherosclerotic cardiovascular disease (ASCVD). Türkiye is among the countries with the highest rate of ASCVD. However, no...
7.
Ertoy Karagol H, Inci A, Polat Terece S, Kilic A, Demir F, Yapar D, et al.
Int Arch Allergy Immunol
. 2023 Jan;
184(4):370-375.
PMID: 36623499
Background And Objective: Pompe disease (PD) is an inherited lysosomal storage disease that progresses with glycogen accumulation in many tissues, due to the deficiency of the acid-alpha glucosidase enzyme. Recombinant...
8.
Inci A, Yildirim G, Cengiz Ergin F, Sari S, Gurkan O, Okur I, et al.
J Pediatr Endocrinol Metab
. 2022 Jan;
35(4):451-462.
PMID: 35038814
Objectives: To reveal the different clinical presentations of liver glycogen storage disease type IX (GSD IX), which is a clinically and genetically heterogeneous type of glycogenosis. Methods: The data from...
9.
Inci A, Arslan B, Okur I, Biberoglu G, Sanli M, Aktasoglu E, et al.
Indian J Pediatr
. 2021 Apr;
88(7):723.
PMID: 33905091
No abstract available.
10.
Inci A, Aktas E, Cengiz Ergin F, Okur I, Biberoglu G, Ezgu F, et al.
JPEN J Parenter Enteral Nutr
. 2021 Apr;
45(8):1788-1792.
PMID: 33882172
Background: The ketogenic diet (KD) is a low-carbohydrate, high-fat diet that has been used as an effective nonpharmacological treatment in many neurological and metabolic disorders for a long time. The...