Ertuğrul Kıykım

Spondyloocular Syndrome: Novel Mutations in <i>XYLT2</i> Gene and Expansion of the Phenotypic Spectrum

Fulya Taylan, Alice Costantini, Nicole Coles et al. · Journal of Bone and Mineral Research · 2016 · 48 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Vitamin D levels in children and adolescents with autism

Esma Şengenç, Ertuğrul Kıykım, Sema Saltık · Journal of International Medical Research · 2020 · 31 citations · Full text

Medicine, Nutritional Sciences, Pediatrics +17

Telemedicine Applications in a Tertiary Pediatric Hospital in Turkey During COVID-19 Pandemic

Sezin Aydemir, Süheyla Ocak, Seha Saygılı et al. · Telemedicine Journal and e-Health · 2020 · 29 citations

Medicine, Child Health, Pediatrics +9

Clinical, biochemical, and molecular insights into Cerebrotendinous Xanthomatosis: A nationwide study of 100 Turkish individuals

Tanyel Zübarioğlu, Ertuğrul Kıykım, Engi̇n Köse et al. · Molecular Genetics and Metabolism · 2024 · 19 citations

Medicine, Molecular Medicine, Pathology +6

Cobalamin C defect‐hemolytic uremic syndrome caused by new mutation in <i>MMACHC</i>

Amra Adroviç, Nur Canpolat, Salim Çalışkan et al. · Pediatrics International · 2016 · 12 citations

Life Sciences, Genetics, Pediatrics +16