Hergüner ÖM - Search Results

1

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: herguner om. J Neuromuscul Dis. 2023;10(5):915-924. doi: 10.3233/JND-230046. J Neuromuscul Dis. 2023. PMID: 37355912 Free PMC article.

2

Factors affecting epilepsy development and epilepsy prognosis in cerebral palsy.

Mert GG, Incecik F, Altunbasak S, Herguner O, Mert MK, Kiris N, Unal I. Mert GG, et al. Pediatr Neurol. 2011 Aug;45(2):89-94. doi: 10.1016/j.pediatrneurol.2011.03.001. Pediatr Neurol. 2011. PMID: 21763948

3

Prognostic significance of failure of the initial antiepileptic drug in children with benign childhood epilepsy with centrotemporal spikes.

Incecik F, Altunbasak S, Herguner OM, Mert G, Sahan D. Incecik F, et al. Among authors: herguner om. Brain Dev. 2015 Jan;37(1):66-70. doi: 10.1016/j.braindev.2014.02.008. Epub 2014 Mar 20. Brain Dev. 2015. PMID: 24657010

4

Risk of recurrence after discontinuation of antiepileptic drug therapy in children with epilepsy.

Incecik F, Herguner OM, Altunbasak S, Mert G, Kiris N. Incecik F, et al. Among authors: herguner om. J Pediatr Neurosci. 2014 May;9(2):100-4. doi: 10.4103/1817-1745.139262. J Pediatr Neurosci. 2014. PMID: 25250060 Free PMC article.

5

Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database.

Yılmaz Ü, Anlar B, Gücüyener K; Turkish Pediatric Multiple Sclerosis Study Group. Yılmaz Ü, et al. Eur J Paediatr Neurol. 2017 Nov;21(6):864-872. doi: 10.1016/j.ejpn.2017.06.004. Epub 2017 Jun 29. Eur J Paediatr Neurol. 2017. PMID: 28694135

6

Neuro-ichthyotic Syndromes: A Case Series.

Incecık F, Herguner OM, Ozbek MN, Gungor S, Yılmaz M, Rizzo WB, Mert GG. Incecık F, et al. Among authors: herguner om. J Pediatr Neurosci. 2018 Jan-Mar;13(1):34-38. doi: 10.4103/JPN.JPN_54_17. J Pediatr Neurosci. 2018. PMID: 29899769 Free PMC article.

7

Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience.

Bilge S, Mert GG, Hergüner Ö, Özcanyüz D, Bozdoğan ST, Kaya Ö, Havalı C. Bilge S, et al. Ital J Pediatr. 2022 Sep 8;48(1):169. doi: 10.1186/s13052-022-01349-9. Ital J Pediatr. 2022. PMID: 36076253 Free PMC article.

8

Clinical Features and Molecular Genetics of Autosomal Recessive Ataxia in the Turkish Population.

Incecik F, Herguner OM, Mungan NO. Incecik F, et al. Among authors: herguner om. J Pediatr Neurosci. 2020 Apr-Jun;15(2):86-89. doi: 10.4103/jpn.JPN_145_18. Epub 2020 Jun 27. J Pediatr Neurosci. 2020. PMID: 33042236 Free PMC article.

9

A Cytogenetic Study of Turkish Children with Global Developmental Delay.

Demirhan O, Hergüner Ö, Tunç E. Demirhan O, et al. J Pediatr Genet. 2022 Dec 1;13(2):99-105. doi: 10.1055/s-0042-1758872. eCollection 2024 Jun. J Pediatr Genet. 2022. PMID: 38721584 Free PMC article.

10

A Turkish family with Sjögren-Larsson syndrome caused by a novel ALDH3A2 mutation.

Incecık F, Herguner OM, Rizzo WB, Altunbasak S. Incecık F, et al. Among authors: herguner om. Ann Indian Acad Neurol. 2013 Jul;16(3):425-7. doi: 10.4103/0972-2327.116927. Ann Indian Acad Neurol. 2013. PMID: 24101836 Free PMC article.

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