Asburçe Olgaç

A rare case of primary coenzyme Q10 deficiency due to <i>COQ9</i> mutation

Asburçe Olgaç, Ülkühan Öztoprak, Çiğdem Seher Kasapkara et al. · Journal of Pediatric Endocrinology and Metabolism · 2019 · 23 citations

Life Sciences, Genetics, Pediatrics +17

Beneficial Effects of Modified Atkins Diet in Glycogen Storage Disease Type IIIa

Asburçe Olgaç, Aslı İnci, İlyas Okur et al. · Annals of Nutrition and Metabolism · 2020 · 16 citations

Agriculture, Nutrition, Nutritional Sciences +17

Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathy

Asburçe Olgaç, Çiğdem Seher Kasapkara, Ebru Yılmaz Keskin et al. · Journal of Pediatric Endocrinology and Metabolism · 2020 · 14 citations

Medicine, Molecular Genetics, Pediatrics +15

Multiplexed cell-based diagnostic devices for detection of renal biomarkers

Sıla Köse, Recep Erdem Ahan, İlkay Çisil Köksaldı et al. · Biosensors and Bioelectronics · 2022 · 12 citations

Medicine, Cell Biology, Nephrology +14

Recurrence of carbamoyl phosphate synthetase 1 (CPS1) deficiency in Turkish patients: Characterization of a founder mutation by use of recombinant CPS1 from insect cells expression

Liyan Hu, Carmen Dı́ez-Fernández, Véronique Rüfenacht et al. · Molecular Genetics and Metabolism · 2014 · 10 citations

Life Sciences, Genetics, Molecular Genetics +10