Fatma Derya Bulut - Pediatric Metabolism and Nutrition Department, Çukurova University

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论文共 71 篇作者统计合作学者相似作者

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Pediatric Cardiomyopathies from the Landscape of Inherited Metabolic Disorders in Southeastern Turkey

Fadli Demir, Ezgi Topal,Fatma Derya Bulut,Sevcan Erdem,Deniz Kor,Anil Atmis,Sevcan Tug Bozdogan,Atil Bisgin,Neslihan Onenli Mungan,Nazan Ozbarlas

IRANIAN JOURNAL OF PEDIATRICS（2024）

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Clinical, Biochemical, and Molecular Insights into Cerebrotendinous Xanthomatosis: A Nationwide Study of 100 Turkish Individuals

Tanyel Zubarioglu,Ertugrul Kiykim,Engin Kose,Fatma Tuba Eminoglu,Pelin Teke Kisa,Mehmet Cihan Balci,Isil Ozer,Asli Inci, Kubra Cilesiz,Ebru Canda,Havva Yazici, Burcu Ozturk-Hismi,Fatma Derya Bulut,Sevil Dorum,Abdurrahman Akgun, Guel Yalcin-Cakmakli,Gonca Kilic-Yildirim,Erdogan Soyucen,Aylin Akcali, Dilek Gunes,Asli Durmus,Aysegul Gunduz,cigdem Seher Kasapkara,Emine Goksoy,Halil Tuna Akar,Melike Ersoy,Sahin Erdol,Yilmaz Yildiz, Hasmet Ayhan Hanagasi,Nur Arslan,Cigdem Aktuglu-Zeybek

MOLECULAR GENETICS AND METABOLISMno. 2 (2024)

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Early Diagnostic Clues of Mucolipidosis Type II: Significance of Radiological Findings

Ezgi Burgac,Irem Kaplan,Burcu Koseci,Esra Kara,Deniz Kor,Fatma Derya Bulut,Anil Atmis, Ferhatcan Piskin,Sevcan Tug Bozdogan,Gizem Urel Demir,Faruk Incecik,Neslihan Onenli Mungan

AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 6 (2024)

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Actions Speak Louder Than Words: Home Visits and Its Effect on Dietary Adherence in Patients with Phenylketonuria

Fatma Derya Bulut,Deniz Kor,Sebile Kilavuz,Ebru Cicek,Burcu Koseci,Esra Kara,Ezgi Burgac,Irem Kaplan,Neslihan Onenli Mungan

JOURNAL OF PAEDIATRICS AND CHILD HEALTH（2023）

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Expanding the Phenotypic Landscape of Gaucher Disease Type 3c with a Novel Entity - Transient Neonatal Cholestasis

Fatma Derya Bulut,Deniz Kor,Sebile Kilavuz,Berna Seker Yilmaz,Irem Kaplan,Faruk Ekinci,Ezgi Burgac,Ilknur Varol,Burcu Koseci,Sevcan Tug Bozdogan,Esra Kara,Fadli Demir,Ali Deniz,Fatih Temiz,Neslihan Onenli Mungan

European journal of medical geneticsno. 6 (2023): 104764-104764

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Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders

Sebile Kilavuz,Derya Bulut,Deniz Kor,Berna Seker Yilmaz,Atil Bisgin,Fadli Demir,Bahriye Atmis,Derya Alabaz,Neslihan Mungan,Mustafa Yilmaz

JOURNAL OF CHILD - COCUK DERGISIno. 3 (2023): 233-242

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3D YAZICILAR ÜZERİNE YAPILAN ARAŞTIRMALARIN İNCELENMESİ

Bilge Yılmaz,Fatma Derya Bulut

The journal of international social research and educationno. Year: 7 - Number: 2 (2023): 45-54

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Taliglucerase-alfa Experience with 34 Gaucher Disease Patients from Turkey

Neslihan Onenli Mungan,Mahmut Coker,Gonca Kilic Yildirim,Ozlem Unal Uzun,Melike Ersoy,Ayse Cigdem Aktuglu Zeybek, Seda Gunes,Nur Arslan,Leyla Tumer, Mustafa Kilic,Tuba Eminoglu, Mehmet Gunduz, Mehmet Keskin,Deniz Kor,Ebru Canda,Derya Bulut, Sema Kalkan Ucar

Molecular genetics and metabolismno. 2 (2023): 107252-107252

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A NOVEL VARIATION OF GAMT IN CEREBRAL CREATINE DEFICIENCY SYNDROME, FIRST COMPLETE HOMOZYGOUS DELETION OF GAMT

Habibe Koc Ucar,Fatma Derya Bulut,Berrak Bilginer Gurbuz,Okan Dilek,Ilker Guney

Genetikano. 1 (2023): 415-426

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Perspectives of Adult Patients with Lysosomal Storage Diseases on the Transition from Pediatric to Adult Healthcare in Turkey

Fatma Derya Bulut,Gulsah Seydaoglu,Deniz Kor,Sebile Kilavuz,Asli Boz,Neslihan Onenli Mungan

Archives de Pédiatrieno. 7 (2023): 450-454

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