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Erratum to 'Response to early coenzyme Q10 supplementation is not sustained in CoQ10 deficiency caused by CoQ2 mutation' [Pediatric Neurology 88 (2018) 71-74].
Eroglu FK, Ozaltin F, Gönç N, Nalçacıoğlu H, Özçakar ZB, Yalnızoğlu D, Güçer Ş, Orhan D, Eminoğlu FT, Göçmen R, Alikaşifoğlu A, Topaloğlu R, Düzova A. Eroglu FK, et al. Among authors: gocmen r. Pediatr Neurol. 2019 May;94:84. doi: 10.1016/j.pediatrneurol.2018.12.017. Epub 2019 Feb 15. Pediatr Neurol. 2019. PMID: 30777605 No abstract available.
Further expanding the mutational spectrum of brain abnormalities, neurodegeneration, and dysosteosclerosis: A rare disorder with neurologic regression and skeletal features.
Kındış E, Simsek-Kiper PÖ, Koşukcu C, Taşkıran EZ, Göçmen R, Utine E, Haliloğlu G, Boduroğlu K, Alikaşifoğlu M. Kındış E, et al. Among authors: gocmen r. Am J Med Genet A. 2021 Jun;185(6):1888-1896. doi: 10.1002/ajmg.a.62179. Epub 2021 Mar 22. Am J Med Genet A. 2021. PMID: 33749994
Neurologic manifestations in children with COVID-19 from a tertiary center in Turkey and literature review.
Laçinel Gürlevik S, Günbey C, Ozsurekci Y, Oygar PD, Kesici S, Gocmen R, Aydin O, Temucin Ç, Tufan E, Terzi K, Baltu D, Ozturk TT, Teksam O, Ozen S, Oguz KK, Cengiz AB, Yalnızoglu D. Laçinel Gürlevik S, et al. Among authors: gocmen r. Eur J Paediatr Neurol. 2022 Mar;37:139-154. doi: 10.1016/j.ejpn.2022.02.003. Epub 2022 Feb 18. Eur J Paediatr Neurol. 2022. PMID: 35287009 Free PMC article. Review.
124 results