Akademisyen
AYŞE ERGÜL BOZACI
DOÇENT
AKDENİZ ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Çocuk Metabolizma Hastalıkları (Çocuk Sağlığı ve Hastalıkları)
Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.
- Makale 25
- Proje 0
- Kitap 3
- Bildiri 41
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
2
Q2
5
Q3
11
Q4
3
WoS (JCR)
Q1
0
Q2
4
Q3
5
Q4
14
TR Index
7
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
0
Üst %10 makale
0
Ort. yüzdelik
74.9%
Üst %1 payı
0.0%
Üst %10 payı
0.0%
Makaleler
YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.
Makale listesi
- 2026 Clinical and laboratory outcomes of ketogenic versus glycine-restricted diet in nonketotic hyperglycinemia: A comparative study YÖKSİS SJR Q1 JCR Q2
- 2026 Development and Validation of a Multiplex LC-MS/MS Assay for Lysosphingolipid Quantification in the Diagnosis of Gaucher and Fabry Diseases YÖKSİS
- 2025 CAPOS and Beyond: ATP1A3 Variants in Pediatric Movement Disorders – Case Reports YÖKSİS SJR Q3 JCR Q4
- 2025 Expert opinion on clinical presentation, diagnosis and treatment of infantile onset pompe disease: a delphi study in Türkiye YÖKSİS TR Index SJR Q3 JCR Q2
- 2025 Evaluation of cardiac function in pediatric patients diagnosed with mucopolysaccharidosis (MPS) and use of annular plane systolic excursion (APSE) to evaluate systolic function YÖKSİS SJR Q1 JCR Q2 OpenAlex 87.2%
- 2025 Analysis of Laboratory and Demographic Data of Late Diagnosed Phenylketonuria Cases YÖKSİS
- 2025 Clinical Features, Genetic Spectrum, and Outcome of Hereditary Tyrosinemia Type 1: A Multicenter Study from Southeastern Türkiye YÖKSİS TR Index JCR Q4
- 2024 Evaluation of aortic elasticity properties in mucopolysaccharidosis patients; effect of enzyme replacement therapy (ERT) on aortic stiffness YÖKSİS SJR Q2 JCR Q3 OpenAlex 62.6%
- 2024 Mitochondrial DNA Depletion Syndromes Gene Panel versus Clinical Exome Sequencing in Children with Suspected Mitochondrial Hepatopathies YÖKSİS SJR Q3 JCR Q4
- 2024 Experience with carnitine palmitoyltransferase II deficiency: diagnostic challenges in the myopathic form YÖKSİS SJR Q2 JCR Q3
- 2024 The evaluation of inherited metabolic diseases presenting with rhabdomyolysis from Turkey: Single center experience YÖKSİS SJR Q3 JCR Q3
- 2023 Glutaric aciduria and L-2-hydroxyglutaric aciduria: Clinical and molecular findings of 35 patients from Turkey YÖKSİS SJR Q3 JCR Q3
- 2023 The role of inborn errors of metabolism in the etiology of neonatal cholestasis: A single center experience YÖKSİS TR Index SJR Q4 JCR Q4
- 2023 Genetic spectrum of familial hypertriglyceridemia from the southeastern region of Turkey YÖKSİS JCR Q4
- 2023 The prevalence, results, and treatments of the patients followed up with a diagnosis of metabolic disease in the pediatric intensive care unit: A single-center experience YÖKSİS TR Index SJR Q4 JCR Q4
- 2023 Evaluation of the Neurodevelopmental Status for Urea Cycle Disorders: Based on Clinical Experience YÖKSİS TR Index SJR Q3 JCR Q4
- 2022 Three-Country Snapshot of Ornithine Transcarbamylase Deficiency YÖKSİS SJR Q2 JCR Q2
- 2022 Long-term follow-up of alkaptonuria patients: single center experience YÖKSİS SJR Q2 JCR Q4
- 2022 Rare coexistence of Tay-Sachs disease, coarctation of the aorta and grade V vesicoureteral reflux. YÖKSİS SJR Q3 JCR Q4
- 2022 Rare cause of ketolysis: Monocarboxylate transporter 1 deficiency YÖKSİS TR Index SJR Q3 JCR Q4