| Genotypic and phenotypic features in Turkish patients with classic nonketotic hyperglycinemia H Bayrak, Y Yıldız, A Olgaç, ÇS Kasapkara, A Küçükcongar, A Zenciroğlu, ... Metabolic Brain Disease 36, 1213-1222, 2021 | 8 | 2021 |
| Association Between Vitamin D Levels and COVID-19 Infection in Children: A Case-Control Study H Bayrak, D Öztürk, A Bolat, B Ünay Turkish Archives of Pediatrics 58 (3), 250, 2023 | 3 | 2023 |
| Pterin Profiling in Serum, Dried Blood Spot, and Urine Samples Using LC-MS/MS in Patients with Inherited Hyperphenylalaninemia RM Öktem, A İnci, H Bayrak, F Demir, G Biberoğlu, ME Maviş, GG Gürsu, ... Molecular Syndromology 15 (3), 185-193, 2024 | 1 | 2024 |
| A 7-year-old boy with scurvy owing to coeliac disease B Küçükalİ, H Bayrak, DG Yıldırım, A İnci, SA Bakkaloğlu, L Tümer Paediatrics and international child health, 1-5, 2024 | | 2024 |
| RMND1 Mutation Case Report and Literature Review H Bayrak, A Sezer, M Kılıç Molecular Syndromology, 1-8, 2024 | | 2024 |
| Current Advances of Treatment of Metabolic Myopathies H BAYRAK, FS EZGÜ Turkiye Klinikleri Pediatric Metabolism Diseases-Special Topics 5 (1), 105-108, 2024 | | 2024 |
| Inherited Metabolic Myopathies-2024 E Özsaydı Aktaşoğlu, L Tümer, A Yar Sağlam, D Usta Salımı, ... TÜRKİYE KLİNİKLERİ, 2024 | | 2024 |
| Expanding the Clinical and Genetic Features Associated with Combined Oxidative Phosphorylation Deficiency 11 Short Title: RMND1 Overview: A case report and review of the … H Bayrak, A Sezer, M Kılıç | | 2023 |
| SERAC1 gene mutation presented with markedly alpha fetoprotein elevation: case report H Bayrak, A Sezer, A Danış, SH Özhan, H Yıldız, M Kılıç Acta Neurologica Belgica, 1-3, 2023 | | 2023 |
| Hipotoni ve Mikrosefali ile Başvuran Bir PMM2-CDG Vakası SHAS ÖZHAN, A OLGAÇ, H BAYRAK, A SEZER, HA ÇELİK, E AKSOY, ... Turkiye Klinikleri Scientific Meetings 5 (3), 76-78, 2023 | | 2023 |
| RMND1 Mutation Case Report and Literature Review H Bayrak, A Sezer, M Kılıç Molecular Syndromology, 1-8, 0 | | |
| Pterin Profiling in Serum, Dry Blood Spot and Urine using LC-MS/MS in Patients with Hyperphenylalaninemia R ÖKTEM, A İNCİ, H Bayrak, F DEMİR, G BİBEROĞLU, M Mavis, İ OKUR, ... | | |
