Herguner OM - Search Results

1

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.

2

Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin.

Horoz OO, Mungan NO, Yildizdas D, Hergüner Ö, Ceylaner S, Kör D, Waterham H, Coskun T. Horoz OO, et al. J Pediatr Endocrinol Metab. 2016 Feb;29(2):227-31. doi: 10.1515/jpem-2015-0198. J Pediatr Endocrinol Metab. 2016. PMID: 26444347

3

Different Clinical Manifestations of Three Prime Repair Exonuclease 1 Mutation: A Case Series.

Incecik F, Balci S, Kisla Ekinci RM, Herguner OM, Bisgin A, Yilmaz M. Incecik F, et al. Among authors: herguner om. Ann Indian Acad Neurol. 2020 Sep-Oct;23(5):699-703. doi: 10.4103/aian.AIAN_469_18. Epub 2020 Dec 8. Ann Indian Acad Neurol. 2020. PMID: 33623276 Free PMC article.

4

Effect of Levetiracetam Usage on Serum Creatine Phosphokinase Concentration in Patients with Epilepsy.

Incecik F, Herguner OM, Besen S. Incecik F, et al. Among authors: herguner om. J Pediatr Neurosci. 2020 Apr-Jun;15(2):81-85. doi: 10.4103/jpn.JPN_133_18. Epub 2020 Jun 27. J Pediatr Neurosci. 2020. PMID: 33042235 Free PMC article.

5

Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child.

Ozcanyuz DG, Incecik F, Herguner OM, Mungan NO, Bozdogan ST. Ozcanyuz DG, et al. Among authors: herguner om. Ann Indian Acad Neurol. 2020 May-Jun;23(3):399-401. doi: 10.4103/aian.AIAN_536_19. Epub 2020 Jun 10. Ann Indian Acad Neurol. 2020. PMID: 32606554 Free PMC article. No abstract available.

6

Dynamic thiol/disulphide homeostasis in children with Duchenne muscular dystrophy.

Incecik F, Avcıoğlu G, Erel Ö, Neşelioğlu S, Hergüner OM. Incecik F, et al. Among authors: herguner om. Acta Neurol Belg. 2019 Jun;119(2):215-218. doi: 10.1007/s13760-018-01072-5. Epub 2019 Jan 3. Acta Neurol Belg. 2019. PMID: 30607902

7

Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay: A Turkish Child.

Incecik F, Hergüner OM, Bisgin A. Incecik F, et al. Among authors: herguner om. J Pediatr Neurosci. 2018 Jul-Sep;13(3):355-357. doi: 10.4103/JPN.JPN_8_18. J Pediatr Neurosci. 2018. PMID: 30271475 Free PMC article.

8

Late-Onset Leigh Syndrome due to NDUFV1 Mutation in a 10-Year-Old Boy Initially Presenting with Ataxia.

Incecik F, Herguner OM, Besen S, Bozdoğan ST, Mungan NO. Incecik F, et al. Among authors: herguner om. J Pediatr Neurosci. 2018 Apr-Jun;13(2):205-207. doi: 10.4103/jpn.JPN_138_17. J Pediatr Neurosci. 2018. PMID: 30090137 Free PMC article.

9

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.

10

Spinocerebellar Ataxia-21 in a Turkish Child.

Incecik F, Herguner OM, Willems P, Mungan NO. Incecik F, et al. Among authors: herguner om. Ann Indian Acad Neurol. 2018 Jan-Mar;21(1):68-70. doi: 10.4103/aian.AIAN_415_17. Ann Indian Acad Neurol. 2018. PMID: 29720801 Free PMC article.

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