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Corrigendum to "Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes" [Europ. J. Paediatr. Neurol. 41 (2022) 8-18 doi.org/10.1016/j.ejpn.2022.08.006].
Yılmaz Ü, Gücüyener K, Yavuz M, Ibrahim Oncel, Canpolat M, Saltık S, Ünver O, Çıtak Kurt AN, Tosun A, Yılmaz S, Özgör B, İlknur Erol, Öztoprak Ü, Elitez DA, Çobanoğulları Direk M, Bodur M, Teber S, Anlar B; Turkish Pediatric Multiple Sclerosis Study Group. Yılmaz Ü, et al. Eur J Paediatr Neurol. 2024 Dec 2:S1090-3798(24)00172-7. doi: 10.1016/j.ejpn.2024.11.006. Online ahead of print. Eur J Paediatr Neurol. 2024. PMID: 39627061 No abstract available.
Clinical and Genetic Spectrum of Myotonia Congenita in Turkish Children.
Öz Tunçer G, Sanri A, Aydin S, Hergüner ÖM, Özgün N, Kömür M, İçağasioğlu DF, Toker RT, Yilmaz S, Arslan EA, Güngör M, Kutluk G, Erol İ, Mert GG, Polat BG, Aksoy A. Öz Tunçer G, et al. Among authors: toker rt. J Neuromuscul Dis. 2023;10(5):915-924. doi: 10.3233/JND-230046. J Neuromuscul Dis. 2023. PMID: 37355912 Free PMC article.
Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes.
Yılmaz Ü, Gücüyener K, Yavuz M, Öncel İ, Canpolat M, Saltık S, Ünver O, Çıtak Kurt AN, Tosun A, Yılmaz S, Özgör B, Erol İ, Öztoprak Ü, Elitez DA, Direk MÇ, Bodur M, Teber S, Anlar B; Turkish Pediatric Multiple Sclerosis Study Group. Yılmaz Ü, et al. Eur J Paediatr Neurol. 2022 Nov;41:8-18. doi: 10.1016/j.ejpn.2022.08.006. Epub 2022 Sep 1. Eur J Paediatr Neurol. 2022. PMID: 36137476
A rare case of juvenile amyotrophic lateral sclerosis.
Bodur M, Toker RT, Başak AN, Okan MS. Bodur M, et al. Among authors: toker rt. Turk J Pediatr. 2021;63(3):495-499. doi: 10.24953/turkjped.2021.03.017. Turk J Pediatr. 2021. PMID: 34254495 Free article.
[Chronic tophaceous gout].
Toker R, Flusser D, Hertzanu Y, Sukenik S. Toker R, et al. Harefuah. 1997 Jun 1;132(11):759-61, 823. Harefuah. 1997. PMID: 9223816 Hebrew.
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