Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Molecular Genetics and Metabolism Reports|March 17, 2025
Carglumic acid as a treatment for persistent hyperammonemia in carnitine-acylcarnitine translocase deficiency: A case studyHanım Babazade, Tanyel Zubarioglu, Esma Uygur, et al.
Molecular Genetics and Metabolism|July 11, 2025
The clinical utility of short-term protein substitute use during intercurrent illness in BH4-responsive phenylketonuriaSelin Akbulut, Esma Uygur, Tanyel Zubarioglu, et al.
The Journal of Obstetrics and Gynaecology Research|July 27, 2026
Managing Pregnancy in Inherited Metabolic Disorders: Experience From a Single Tertiary Metabolic CenterElif İşler-Soylu, Tanyel Zubarioglu, Esma Uygur, et al.
Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|March 15, 2021
The Impact of Telemedicine for Monitoring and Treatment of Phenylketonuria Patients on Metabolic Outcome During Coronavirus Disease-19 OutbreakTanyel Zubarioglu, Duhan Hopurcuoglu, Esma Uygur, et al.
Turkish Archives of Pediatrics|August 1, 2026
Revealing BCKDK Deficiency Under Autism: A Case Report, Therapeutic Outcomes, and Literature ReviewHanım Babazade, Başak Günal, Kağan Çalişgan, et al.
Frontiers in Immunology|January 23, 2023
BNT162b2 COVID-19 vaccination elicited protective robust immune responses in pediatric patients with inborn errors of metabolismTanyel Zubarioglu, Harika Oyku Dinc, Duhan Hopurcuoglu, et al.
Journal of Paediatrics and Child Health|September 29, 2022
Safety of COVID-19 vaccines in children with inborn errors of metabolism in terms of developing metabolic decompensationTanyel Zubarioglu, Sinem Oral-Cebeci, Duhan Hopurcuoglu, et al.
Pageof 1