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Clinical and bi-genomic DNA findings of patients suspected to have mitochondrial diseases.
Gedikbasi A, Toksoy G, Karaca M, Gulec C, Balci MC, Gunes D, Gunes S, Aslanger AD, Unverengil G, Karaman B, Basaran S, Demirkol M, Gokcay GF, Uyguner ZO. Gedikbasi A, et al. Among authors: unverengil g. Front Genet. 2023 Jun 12;14:1191159. doi: 10.3389/fgene.2023.1191159. eCollection 2023. Front Genet. 2023. PMID: 37377599 Free PMC article.
Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease.
Marais A, Bertoli-Avella AM, Beetz C, Altunoglu U, Alhashem A, Mohamed S, Alghamdi A, Willems P, Tsoutsou E, Fryssira H, Pons R, Almarzooq R, Karatoprak EY, Ayaz A, Ünverengil G, Calvo M, Yüksel Z, Bauer P. Marais A, et al. Among authors: unverengil g. Eur J Med Genet. 2022 Aug;65(8):104537. doi: 10.1016/j.ejmg.2022.104537. Epub 2022 Jun 9. Eur J Med Genet. 2022. PMID: 35690317
Post-COVID-19 vaccination inflammatory syndrome: A case report.
Durucan I, Guner S, Kilickiran Avci B, Unverengil G, Melikoglu M, Ugurlu S. Durucan I, et al. Among authors: unverengil g. Mod Rheumatol Case Rep. 2023 Jan 3;7(1):280-282. doi: 10.1093/mrcr/rxac041. Mod Rheumatol Case Rep. 2023. PMID: 35556127 Free PMC article.
Late-Onset Lipid Storage Myopathy with Fatal Hepatosteatosis.
Yavuz A, Ünverengil G, Yıldırım ANT, Maraşlı HŞ, Tuncer İ. Yavuz A, et al. Among authors: unverengil g. Eur J Case Rep Intern Med. 2020 Oct 7;7(12):001980. doi: 10.12890/2020_001980. eCollection 2020. Eur J Case Rep Intern Med. 2020. PMID: 33313013 Free PMC article.