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Sahin Erdol
Sahin Erdol
Verified email at uludag.edu.tr
Title
Cited by
Cited by
Year
A Turkish patient with succinyl-CoA: 3-oxoacid CoA transferase deficiency mimicking diabetic ketoacidosis
S Erdol, M Ture, T Yakut, H Saglam, H Sasai, E Abdelkreem, H Otsuka, ...
Journal of Inborn Errors of Metabolism and Screening 4, 2326409816651281, 2016
162016
Massive ascites in a canakinumab resistant case with MVA leading to bone marrow transplantation
S Erdol, S Cekic, SC Kılıc, H Saglam, SS Kılıc
Rheumatology international 36, 1011-1013, 2016
152016
Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?
I Barić, S Erdol, H Saglam, M Lovrić, R Belužić, O Vugrek, HJ Blom, ...
JIMD Reports, Volume 31, 101-106, 2016
142016
An unusual case of LCHAD deficiency presenting with a clinical picture of hemophagocytic lymphohistiocytosis: secondary HLH or coincidence?
S Erdol, M Ture, B Baytan, T Yakut, H Saglam
Journal of Pediatric Hematology/Oncology 38 (8), 661-662, 2016
132016
Alkaptonuria in Turkey: Clinical and molecular characteristics of 66 patients
PT Kisa, M Gunduz, S Dorum, OU Uzun, NE Cakar, GK Yildirim, S Erdol, ...
European journal of medical genetics 64 (5), 104197, 2021
112021
Use of complementary and alternative medicine in patients with inherited metabolic disease
S Erdol, H Saglam
Journal of Pediatric Endocrinology and Metabolism 31 (10), 1091-1098, 2018
92018
Vitamin B12 deficiency associated with hyperbilirubinemia and cholestasis in infants
S Erdol, T Ozgur
Pakistan Journal of Medical Sciences 34 (3), 714, 2018
92018
Chromhidrosis due to exogenous oxidizing heavy metals: Clinical and laboratory findings
S Erdol, S Karakaya, H Saglam, O Tarim
Pediatric dermatology 35 (4), 448-452, 2018
62018
Endocrine dysfunctions in patients with inherited metabolic diseases
Ş Erdöl, H Sağlam
Journal of clinical research in pediatric endocrinology 8 (3), 330, 2016
62016
Three-country snapshot of ornithine Transcarbamylase deficiency
B Seker Yilmaz, J Baruteau, N Arslan, HI Aydin, M Barth, AE Bozaci, ...
Life 12 (11), 1721, 2022
52022
Evaluation of 700 patients referred with a preliminary diagnosis of biotinidase deficiency by the national newborn metabolic screening program: a single-center experience
S Erdol, TA Kocak, H Bilgin
Journal of Pediatric Endocrinology and Metabolism 36 (6), 555-560, 2023
32023
Novel mutation of the electron transferring flavoprotein dehydrogenase (ETFDH) gene in the isolated myopathic form of coenzyme Q10 deficiency
O Gorukmez, O Gorukmez, SO Sag, S Erdol, H Saglam, T Yakut
Genet Couns Geneva Switz 26, 259-62, 2015
22015
An Important Public Health Problem: Vitamin B12 Deficiency/Onemli Bir Halk Sagligi Problemi: Vitamin B12 Eksikligi.
S Erdol
The Journal of Current Pediatrics 15 (2), 30-37, 2017
12017
Celiac Disease Presenting with Biotinidase Deficiency and Paraplegia
S Erdol, H Saglam, TO Basarır, MS Okan
The Indian Journal of Pediatrics 83, 596-597, 2016
12016
Evaluation of patients with phenylalanine metabolism disorder: a single center experience
S Erdol, H Bilgin
Journal of Pediatric Endocrinology and Metabolism 35 (4), 463-467, 2022
2022
Comparison of plasmapheresis with medical apheresis in terms of efficacy and cost in the acute treatment of hypertriglyceridemia in children with lipoprotein lipase deficiency
S Erdol, H Bilgin, H Saglam
Journal of Pediatric Endocrinology and Metabolism 34 (11), 1419-1424, 2021
2021
Lysinuric protein intolerance and HOIP deficiency in a boy: SLCA7A and RNF31 gene disruptions
L Aliyeva, S Erdol, O Gorukmez, B Turkgenc, H Gurkan, Y Yarali, B Baytan, ...
Journal of Biotechnology 280, S20, 2018
2018
Outcomes of mitochondrial derived diseases: a single-center experience
S Erdol, H Saglam
Journal of Pediatric Endocrinology and Metabolism 31 (4), 399-405, 2018
2018
Evaluation of endocrine complications in patients with thalassemia major/Talasemi majorlu vakalarda endokrin komplikasyonlarin degerlendirilmesi
B Baytan, H Saglam, S Erdol, AN Beyazit, T Ozgur, AM Gunes, U Gunay
The Journal of Current Pediatrics, 58-66, 2008
2008
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Articles 1–19