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Year Number of Results
2011 1
2016 5
2017 2
2018 4
2021 2
2022 2
2023 2
2024 0

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17 results

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Page 1
Three-Country Snapshot of Ornithine Transcarbamylase Deficiency.
Seker Yilmaz B, Baruteau J, Arslan N, Aydin HI, Barth M, Bozaci AE, Brassier A, Canda E, Cano A, Chronopoulou E, Connolly GM, Damaj L, Dawson C, Dobbelaere D, Douillard C, Eminoglu FT, Erdol S, Ersoy M, Fang S, Feillet F, Gokcay G, Goksoy E, Gorce M, Inci A, Kadioglu B, Kardas F, Kasapkara CS, Kilic Yildirim G, Kor D, Kose M, Marelli C, Mundy H, O'Sullivan S, Ozturk Hismi B, Ramachandran R, Roubertie A, Sanlilar M, Schiff M, Sreekantam S, Stepien KM, Uzun Unal O, Yildiz Y, Zubarioglu T, Gissen P. Seker Yilmaz B, et al. Among authors: erdol s. Life (Basel). 2022 Oct 27;12(11):1721. doi: 10.3390/life12111721. Life (Basel). 2022. PMID: 36362876 Free PMC article.
Acrodermatitis dysmetabolica with argininosuccinate lyase deficiency.
Öztürk F, Ünlü CI, Sarıcaoğlu H, Aydoğan K, Erdöl Ş. Öztürk F, et al. Among authors: erdol s. Indian J Dermatol Venereol Leprol. 2023 Nov-Dec;89(6):927. doi: 10.25259/IJDVL_75_2023. Indian J Dermatol Venereol Leprol. 2023. PMID: 37317759 Free article. No abstract available.
Alkaptonuria in Turkey: Clinical and molecular characteristics of 66 patients.
Kisa PT, Gunduz M, Dorum S, Uzun OU, Cakar NE, Yildirim GK, Erdol S, Hismi BO, Tugsal HY, Ucar U, Gorukmez O, Gulten ZA, Kucukcongar A, Bulbul S, Sari I, Arslan N. Kisa PT, et al. Among authors: erdol s. Eur J Med Genet. 2021 May;64(5):104197. doi: 10.1016/j.ejmg.2021.104197. Epub 2021 Mar 18. Eur J Med Genet. 2021. PMID: 33746036
Clinical and Genetic Findings of Turkish Hypophosphatasia Cases.
Sağlam H, Erdöl Ş, Dorum S. Sağlam H, et al. Among authors: erdol s. J Clin Res Pediatr Endocrinol. 2017 Sep 1;9(3):229-236. doi: 10.4274/jcrpe.4549. Epub 2017 Jun 30. J Clin Res Pediatr Endocrinol. 2017. PMID: 28663156 Free PMC article.
17 results