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Erdoğan Soyuçen

Observed names: E Soyucen, ERDOĞAN SOYUÇEN, Erdogan Soyucen, Erdogan Soyucen ., Erdoğan SOYUCEN, Erdoğan Soyucen, SOYUÇEN, ERDOĞAN
Institution: Akdeniz University
ORCID: 0000-0002-2500-7028
Observed ORCID: 0000-0002-2500-7028
OpenAlex ID: A5026073885
Differences in the gut microbiota of healthy children and those with type 1 diabetes
2013 · Erdogan Soyucen, Aynur Gulcan, et al. · Pediatrics International · 146
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Inherited metabolic disorders in T urkish patients with autism spectrum disorders
2015 · Ertugrul Kiykim, Cigdem Aktuglu Zeybek, et al. · Autism Research · 38
Hereditary tyrosinemia type 1 in T urkey: Twenty year single‐center experience
2014 · A Cigdem Aktuglu Zeybek, Ertugrul Kiykim, et al. · Pediatrics International · 34
Clinical, biochemical, and molecular insights into Cerebrotendinous Xanthomatosis: A nationwide study of 100 Turkish individuals
2024 · Tanyel Zubarioglu, Ertuğrul Kıykım, et al. · Molecular Genetics and Metabolism · 20
Sensitization of Children to Storage Mites in Kutahya, Turkey
2009 · Cihangir Akdemir, Erdogan Soyucen · Korean Journal of Parasitology · 16
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Outpatient treatment of propionic acidemia-associated hyperammonemia with N-carbamoyl-l-glutamate in an infant
2010 · Erdogan Soyucen, Esra Demirci, et al. · Clinical Therapeutics · 14
Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene
2016 · Banu Güzel Nur, Gamze Çelmeli, et al. · Journal of Clinical Research in Pediatric Endocrinology · 13
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Recurrence of carbamoyl phosphate synthetase 1 (CPS1) deficiency in Turkish patients: Characterization of a founder mutation by use of recombinant CPS1 from insect cells expression
2014 · Liyan Hu, Carmen Diez-Fernandez, et al. · Molecular Genetics and Metabolism · 10
Seroprevalence of autoimmune thyroiditis and celiac disease in children with insulin-dependent diabetes mellitus in the Thrace region of Turkey
2010 · Erdoğan SOYUCEN, Sema YILMAZ, et al. · The Turkish Journal of Gastroenterology · 10
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Presentation of two cases with hypermobility syndrome and review of the related literature.
2010 · S Toker, E Soyucen, et al. · PubMed · 8
MicroRNA profiling in lymphocytes and serum of tyrosinemia type-I patients
2013 · Omer Faruk Karatas, Esra Guzel, et al. · Molecular Biology Reports · 7
Long‐Term Outcomes of Chenodeoxycholic Acid Therapy for Cerebrotendinous Xanthomatosis: A Nationwide Study on Prognostic Factors and Treatment Response
2025 · Tanyel Zubarioglu, Banu Kadıoğlu‐Yılmaz, et al. · Journal of Inherited Metabolic Disease · 6
Benign joint hypermobility syndrome: A cause of childhood asthma?
2010 · Erdogan Soyucen, Fehim Esen · Medical Hypotheses · 6
Intestinal Mucormycosis in a Child With Maple Syrup Urine Disease After Orthotopic Liver Transplant
2022 · Erdem Cebisli, Nazan Ulgen-Tekerek, et al. · Experimental and Clinical Transplantation · 4
Long‐term results of liver transplantation for maple syrup urine disease: A single‐center experience in Turkey
2023 · Arzu Aras, Ali Avanaz, et al. · Pediatric Transplantation · 3
Liver transplantation from a live donor to a patient with maple syrup urine disease: Two case reports
2018 · Ahmet Basturk, Meryem Keceli, et al. · Türk Pediatri Arşivi · 3
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Clinical and laboratory outcomes of ketogenic versus glycine-restricted diet in nonketotic hyperglycinemia: A comparative study
2026 · Ayşe Ergül Bozacı, İzzet Erdal, et al. · Molecular Genetics and Metabolism · 2
Expert opinion on clinical presentation, diagnosis and treatment of infantile onset pompe disease: a delphi study in Türkiye
2025 · EKİN ÖZSAYDI AKTAŞOĞLU, ASLI İNCİ, et al. · TURKISH JOURNAL OF MEDICAL SCIENCES · 1
Mutual Relationship of Hepatitis C Virus Infection with Hepatitis B
2006 · Mehmet Rami Helvaci ., Erdogan Soyucen ., et al. · Journal of Medical Sciences(Faisalabad) · 1
Clinical, biochemical, and genetic perspectives in hepatic glycogen storage diseases: HEPA-GSD study
2026 · Özlem Ünal Uzun, Gülhan Karakaya Molla, et al. · Molecular Genetics and Metabolism
Development and Validation of a Multiplex LC-MS/MS Assay for Lysosphingolipid Quantification in the Diagnosis of Gaucher and Fabry Diseases
2026 · Halide Akbaş, Ayşe Ergül Bozacı, et al. · Inherited Metabolic Disorders and Nutrition
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A Single-Center Genotype-Phenotype Correlation Cohort Study of Hyperphenylalaninemia Patients: Genetic Analysis as a Deterministic Tool for Treatment Consistency
2025 · Alp Peker, Sezin Yakut Uzuner, et al. · Molecular Syndromology
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Fabry hastalığı Olan Hastalarda Gastrointestinal Bulgular
2023 · KARAKAYA MOLLA, GÜLHAN, KULU, BAHAR, et al. · Kocaeli Üniversitesi - AVESİS
Yetim (Orphan) Hastalıkları İlaçlarında İlerlemeler, Keşifler ve Sorunlar
2017 · Erdoğan Soyuçen, Murat Çağlar Erol · Turkiye Klinikleri Pharmacology - Special Topics
Canlı Donörden Akçaağaç Şurup İdrar Hastasına yapılan Karaciğer Transplantasyonu
2015 · KEÇELİ, MERYEM, YILMAZ, AYGEN, et al. · AYBU AVESIS
Works count: 34
Citation count: 342
H-index: 9
I10-index: 9
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