Fatma Derya Bulut (Derya Bulut)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 12

Top Topics

Transcription Factor

End Stage Renal Disease

Top Venues

American journal of medical genetics. Part A

Metabolic brain disease

International journal of paediatric dentistry

Journal of paediatrics and child health

This page only lists publications with an associated author ORCID identifier.

Publications

Ezgi Burgac, İrem Kaplan, Burcu Köseci, Esra Kara, Deniz Kor, Fatma Derya Bulut, Anıl Atmıs, Ferhat Can Piskin, Sevcan Tuğ Bozdoğan, Gizem Ürel-Demir, Faruk Incecik, Halise Neslihan Onenli Mungan
Early diagnostic clues of mucolipidosis type II: Significance of radiological findings. American journal of medical genetics. Part A 194 (6) (2024)
Ezgi Burgac, İrem Kaplan, Burcu Köseci, Esra Kara, Deniz Kor, Fatma Derya Bulut, Anıl Atmıs, Ferhat Can Piskin, Sevcan Tuğ Bozdoğan, Gizem Ürel-Demir, Faruk Incecik, Halise Neslihan Onenli Mungan
Early diagnostic clues of mucolipidosis type II: Significance of radiological findings. American journal of medical genetics. Part A 194 (6) (2024)
Ezgi Burgac, İrem Kaplan, Burcu Köseci, Esra Kara, Deniz Kor, Fatma Derya Bulut, Anıl Atmıs, Ferhat Can Piskin, Sevcan Tuğ Bozdoğan, Gizem Ürel-Demir, Faruk Incecik, Halise Neslihan Onenli Mungan
Early diagnostic clues of mucolipidosis type II: Significance of radiological findings. American journal of medical genetics. Part A (2024)
Fatma Derya Bulut, Deniz Kor, Sebile Kılavuz, Ebru Cicek, Burcu Köseci, Esra Kara, Ezgi Burgac, İrem Kaplan, Halise Neslihan Onenli Mungan
Actions speak louder than words: Home visits and its effect on dietary adherence in patients with phenylketonuria. Journal of paediatrics and child health (2023)
Fatma Derya Bulut, Neslihan Ekşi Bozbulut, Özge Özalp, Buket Dalgiç, Neslihan Önenli Mungan, Habibe Koç Uçar, Gürsel Biberoğlu
Diagnostic value of plasma lysosphingolipids levels in a Niemann-Pick disease type C patient with transient neonatal cholestasis. Journal of pediatric endocrinology & metabolism : JPEM 35 (5) (2022)
Sebile Kılavuz, Sibel Basaran, Deniz Kor, Fatma Derya Bulut, Sevcan Erdem, Hüseyin Tuğsan Ballı, Muhammed Dağkıran, Serdar Ceylaner, Halise Neslihan Onenli Mungan
Morquio A syndrome and effect of enzyme replacement therapy in different age groups of Turkish patients: a case series. Orphanet journal of rare diseases 16 (1) (2021)
Sebile Kılavuz, Fatma Derya Bulut, Deniz Kor, Berna Seker Yilmaz, Neslihan Özcan, Faruk Incecik, Hasan Bilen Onan, Gülay Ceylaner, Halise Neslihan Onenli Mungan
The outcome of 41 Late-Diagnosed Turkish GA-1 Patients: A Candidate for the Turkish NBS. Neuropediatrics 52 (5) (2021)
Berna Seker Yilmaz, Deniz Kor, Fatma Derya Bulut, Sebile Kılavuz, Serdar Ceylaner, Halise Neslihan Onenli Mungan
Clinical and molecular findings in 37 Turkish patients with isolated methylmalonic acidemia Turkish journal of medical sciences 51 (3) (2021)
Fatma Derya Bulut, Semine Özdemir Dilek, Leman Damla Kotan, Eda Mengen Ucakturk, Fatih Gurbuz, Bilgin Yuksel
Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency Journal of clinical research in pediatric endocrinology 12 (3) (2020)
Volkan Çiftçi, Sebile Kılavuz, Fatma Derya Bulut, Halise Neslihan Onenli Mungan, Serdar Ceylaner, Muharrem Cem Dogan
Congenital erythropoietic porphyria with erythrodontia: A case report. International journal of paediatric dentistry 29 (4) (2019)
Fatma Derya Bulut, Deniz Kör, Berna Şeker-Yılmaz, Özlem Hergüner, Serdar Ceylaner, Ferda Özkınay, Sebile Kılavuz, Neslihan Önenli-Mungan
Four Gaucher disease type II patients with three novel mutations: a single centre experience from Turkey. Metabolic brain disease 33 (4) (2018)
Fatma Derya Bulut, Deniz Kör, Berna Şeker-Yılmaz, Gülen Gül-Mert, Sebile Kılavuz, Neslihan Önenli-Mungan
Turkish case of ethylmalonic encephalopathy misdiagnosed as short chain acyl-CoA dehydrogenase deficiency. Metabolic brain disease 33 (3) (2017)