Tanyel Zübarioğlu

Expert opinion on diagnosing, treating and managing patients with cerebrotendinous xanthomatosis (CTX): a modified Delphi study

Bianca M. L. Stelten, Maria Teresa Dotti, Aad Verrips et al. · Orphanet Journal of Rare Diseases · 2021 · 62 citations · Full text

Medicine, Internal Medicine, Neurology +13

Inherited metabolic disorders in<scp>T</scp>urkish patients with autism spectrum disorders

Ayşe Çiğdem Aktuğlu Zeybek, Tanyel Zübarioğlu, Şerif Cansever et al. · Autism Research · 2015 · 36 citations

Life Sciences, Pediatrics, Human Genetics +12

Hereditary tyrosinemia type 1 in <scp>T</scp>urkey: Twenty year single‐center experience

Ayşe Çiğdem Aktuğlu Zeybek, Erdoğan Soyuçen, Şerif Cansever et al. · Pediatrics International · 2014 · 33 citations

Medicine, Neurology, Oncology +16

Early diagnosed cerebrotendinous xanthomatosis patients: clinical, neuroradiological characteristics and therapy results of a single center from Turkey

Tanyel Zübarioğlu, Gözde Yeşil, Duhan Demircioglu et al. · Acta Neurologica Belgica · 2017 · 31 citations

Medicine, Neurology, Radiology +6

The Impact of Telemedicine for Monitoring and Treatment of Phenylketonuria Patients on Metabolic Outcome During Coronavirus Disease-19 Outbreak

Tanyel Zübarioğlu, Duhan Hopurcuoğlu, Esma Uygur et al. · Telemedicine Journal and e-Health · 2021 · 23 citations

Computing, Infectious Diseases, Pharmacotherapy +9