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Şahin Erdöl

Observed names: Prof. Dr Şahin Erdöl, Sahin Erdol, Şahin ERDÖL
Observed institution: Bursa Uludağ Üni̇versi̇tesi̇
ORCID: 0000-0003-4402-9609
Observed ORCID: 0000-0003-4402-9609
OpenAlex ID: A5012190043
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
Massive ascites in a canakinumab resistant case with MVA leading to bone marrow transplantation
2016 · Sahin Erdol, Sukru Cekic, et al. · Rheumatology International · 20
Three-Country Snapshot of Ornithine Transcarbamylase Deficiency
2022 · Berna Seker Yilmaz, Julien Baruteau, et al. · Life · 19
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Use of complementary and alternative medicine in patients with inherited metabolic disease
2018 · Sahin Erdol, Halil Saglam · Journal of Pediatric Endocrinology and Metabolism · 19
Alkaptonuria in Turkey: Clinical and molecular characteristics of 66 patients
2021 · Pelin Teke Kisa, Mehmet Gunduz, et al. · European Journal of Medical Genetics · 16
Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?
2016 · Ivo Barić, Sahin Erdol, et al. · JIMD Reports · 16
Clinical and Genetic Findings of Turkish Hypophosphatasia Cases
2017 · Halil Sağlam, Şahin Erdöl, et al. · Journal of Clinical Research in Pediatric Endocrinology · 14
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An Unusual Case of LCHAD Deficiency Presenting With a Clinical Picture of Hemophagocytic Lymphohistiocytosis: Secondary HLH or Coincidence?
2016 · Sahin Erdol, Mehmet Ture, et al. · Journal of Pediatric Hematology/Oncology · 13
A Turkish Patient With Succinyl-CoA:3-Oxoacid CoA Transferase Deficiency Mimicking Diabetic Ketoacidosis
2016 · Sahin Erdol, Mehmet Ture, et al. · Journal of Inborn Errors of Metabolism and Screening · 12
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Long-term outcome in children with nutritional vitamin B12 deficiency
2011 · Melike Sezgin Evim, Sahin Erdol, et al. · Turkish Journal of Hematology · 11
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Vitamin B12 deficiency associated with hyperbilirubinemia and cholestasis in infants
2018 · Sahin Erdol, Taner Ozgur · Pakistan Journal of Medical Sciences · 7
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Endocrine Dysfunctions in Patients with Inherited Metabolic Diseases
2016 · Şahin Erdöl, Halil Sağlam · Journal of Clinical Research in Pediatric Endocrinology · 7
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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
Chromhidrosis due to exogenous oxidizing heavy metals: Clinical and laboratory findings
2018 · Sahin Erdol, Sabahattin Karakaya, et al. · Pediatric Dermatology · 6
Evaluation of 700 patients referred with a preliminary diagnosis of biotinidase deficiency by the national newborn metabolic screening program: a single-center experience
2023 · Sahin Erdol, Tugba Akbey Kocak, et al. · Journal of Pediatric Endocrinology and Metabolism · 5
Acrodermatitis dysmetabolica with argininosuccinate lyase deficiency
2023 · Ferdi Öztürk, Cansu Irmak Ünlü, et al. · Indian Journal of Dermatology Venereology and Leprology · 2
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Evaluation of patients with phenylalanine metabolism disorder: a single center experience
2022 · Sahin Erdol, Huseyin Bilgin · Journal of Pediatric Endocrinology and Metabolism · 2
Comparison of plasmapheresis with medical apheresis in terms of efficacy and cost in the acute treatment of hypertriglyceridemia in children with lipoprotein lipase deficiency
2021 · Sahin Erdol, Huseyin Bilgin, et al. · Journal of Pediatric Endocrinology and Metabolism · 2
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Mukopolisakkaridoz Hastalarının Geriye Yönelik Olarak Değerlendirilmesi: Tek Merkez Deneyimi
2021 · Hüseyin BİLGİN, Şahin ERDÖL · Uludağ Üniversitesi Tıp Fakültesi Dergisi · 2
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An Important Public Health Problem: Vitamin B12 Deficiency
2017 · Şahin Erdöl · Güncel Pediatri · 2
Celiac Disease Presenting with Biotinidase Deficiency and Paraplegia
2016 · Sahin Erdol, Halil Saglam, et al. · The Indian Journal of Pediatrics · 2
Talasemi Majorlü Vakalarda Endokrin Komplikasyonların Değerlendirilmesi
2008 · Birol Baytan, Halil Sağlam, et al. · Güncel Pediatri · 2
Profiles of paediatric patients experiencing stroke-like episodes associated with mitochondrial disease
2025 · Gülhan Karakaya Molla, Prof. Dr Özlem Ünal Uzun, et al. · Frontiers in Neurology · 1
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Clinical spectrum and genetic landscape of MTHFR deficiency: a cohort study including novel variants
2026 · Ozge Kamer Karalar Pekuz, Pelin Teke Kisa, et al. · Neurological Sciences
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
Works count: 40
Citation count: 206
H-index: 10
I10-index: 10
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