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Ayşe Ergül Bozacı

Observed names: A. Ergul Bozaci, A.E. Bozaci, AYŞE ERGÜL BOZACI, Ayse Ergul Bozaci, Ayse Ergul Bozacı, Ayse Ergül Bozaci, Ayse Ergül Bozacı, Ayşe E Bozacı, Ayşe Ergul Bozaci, Ayşe Ergul Bozaco, Ergül Bozacı
Institution: Akdeniz University
ORCID: 0000-0002-9783-1016
Observed ORCID: 0000-0002-9783-1016
OpenAlex ID: A5074597195
Clinical and genetic features of 13 patients with mucopolysaccarhidosis type IIIB: Description of two novel NAGLU gene mutations
2021 · F. Ozkinay, D.A. Emecen, et al. · Molecular Genetics and Metabolism Reports · 21
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Three-Country Snapshot of Ornithine Transcarbamylase Deficiency
2022 · Berna Seker Yilmaz, Julien Baruteau, et al. · Life · 19
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Tetrahydrobiopterin deficiencies: Lesson from clinical experience
2021 · Ayse Ergul Bozaci, Esra Er, et al. · JIMD Reports · 17
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Glutaric aciduria and L-2-hydroxyglutaric aciduria: Clinical and molecular findings of 35 patients from Turkey
2023 · Ayse Ergül Bozaci, Esra Er, et al. · Molecular Genetics and Metabolism Reports · 15
Rare cause of ketolysis: Monocarboxylate transporter 1 deficiency
2022 · Ayşe Ergül Bozacı, Aysel Tekmenuray Ünal · The Turkish Journal of Pediatrics · 6
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Evaluation of cardiac function in pediatric patients diagnosed with mucopolysaccharidosis (MPS) and use of annular plane systolic excursion (APSE) to evaluate systolic function
2025 · Kerem Ertaş, Özlem Gül, et al. · Molecular Genetics and Metabolism · 5
The evaluation of inherited metabolic diseases presenting with rhabdomyolysis from Turkey: Single center experience
2024 · Huseyin Bilgin, Ayse Ergul Bozaci · Molecular Genetics and Metabolism Reports · 4
Evaluation of serum 25-hidroxy vitamin D and zinc levels in asthmatic patients
2017 · Murat Elevli, Ayşe Ergül Bozacı, et al. · Turkish Journal of Biochemistry · 4
Long-term follow-up of alkaptonuria patients: single center experience
2022 · Ayse Ergul Bozaci, Havva Yazici, et al. · Journal of Pediatric Endocrinology and Metabolism · 3
Clinical and laboratory outcomes of ketogenic versus glycine-restricted diet in nonketotic hyperglycinemia: A comparative study
2026 · Ayşe Ergül Bozacı, İzzet Erdal, et al. · Molecular Genetics and Metabolism · 2
Evaluation of aortic elasticity properties in mucopolysaccharidosis patients; effect of enzyme replacement therapy (ERT) on aortic stiffness
2024 · Kerem Ertas, Ozlem Gul, et al. · Journal of Pediatric Endocrinology and Metabolism · 2
Mitochondrial DNA Depletion Syndromes Gene Panel versus Clinical Exome Sequencing in Children with Suspected Mitochondrial Hepatopathies
2024 · Neslihan Doğulu, Engin Köse, et al. · Molecular Syndromology · 2
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Experience with carnitine palmitoyltransferase II deficiency: diagnostic challenges in the myopathic form
2023 · Havva Yazıcı, Gunes Ak, et al. · Journal of Pediatric Endocrinology and Metabolism · 2
Evaluation of the Neurodevelopmental Status for Urea Cycle Disorders: Based on Clinical Experience
2023 · Ayşe Ergül Bozacı, Emine Göksoy, et al. · The Journal of Pediatric Research · 2
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Radiographic Findings of Mucopolysaccharidosis and Comparison with Bone Mineral Density: A Study from Southeastern Turkey
2022 · Ercan Ayaz, Ayse Ergul Bozaci · Journal of Clinical Densitometry · 2
Rare coexistence of Tay-Sachs disease, coarctation of the aorta and grade V vesicoureteral reflux
2022 · Murat Ç Karataş, Havva Yazıcı, et al. · Archivos Argentinos de Pediatria · 2
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Expert opinion on clinical presentation, diagnosis and treatment of infantile onset pompe disease: a delphi study in Türkiye
2025 · EKİN ÖZSAYDI AKTAŞOĞLU, ASLI İNCİ, et al. · TURKISH JOURNAL OF MEDICAL SCIENCES · 1
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
2023 · Gültaç Evren, Ayşe Ergül Bozacı · Trends in Pediatrics · 1
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The role of inborn errors of metabolism in the etiology of neonatal cholestasis: A single center experience
2023 · Ayse Ergül Bozacı, Fatma Demirbaş Ar, et al. · Trends in Pediatrics · 1
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First Case Report of McArdle Disease and Alive Renal Transplantation
2022 · Ramazan Danis, Jehat Kılıc, et al. · Turkish Journal of Nephrology · 1
OP–137 Pediatric succinic semialdehyde dehydrogenase deficiency: clinical spectrum and treatment responses
2026 · Ayşe Sandıkkaya, Cengiz Havalı, et al. · BMJ Paediatrics Open
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Development and Validation of a Multiplex LC-MS/MS Assay for Lysosphingolipid Quantification in the Diagnosis of Gaucher and Fabry Diseases
2026 · Halide Akbaş, Ayşe Ergül Bozacı, et al. · Inherited Metabolic Disorders and Nutrition
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CAPOS and Beyond: ATP1A3 Variants in Pediatric Movement Disorders – Case Reports
2025 · Mehpare Sarı Yanartaş, Özlem Yayıcı Köken, et al. · Molecular Syndromology
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Arg339Gln Is a Recurrent Variant in Rare Combined Oxidative Phosphorylation Deficiency 4: A New Patient with Biallelic TUFM Gene Variant
2025 · Aysel Tekmenuray-Unal, Muhammet Tas, et al. · Molecular Syndromology
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Analysis of Laboratory and Demographic Data of Late Diagnosed Phenylketonuria Cases
2025 · Hüseyin Bilgin, Ayşe Ergül Bozacı · Inherited Metabolic Disorders and Nutrition
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Works count: 28
Citation count: 112
H-index: 5
I10-index: 4
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