Güngör O - Search Results

1

Novel mutation in SUCLA2 identified on sequencing analysis.

Güngör O, Özkaya AK, Güngör G, Karaer K, Dilber C, Aydin K. Güngör O, et al. Among authors: gungor g. Pediatr Int. 2016 Jul;58(7):659-61. doi: 10.1111/ped.12921. Epub 2016 Mar 8. Pediatr Int. 2016. PMID: 26952923

2

Intracranial saccular aneurysm in a child with only persistent headache.

Güngör O, Özkaya AK, Dilber C, Çinar C. Güngör O, et al. J Child Neurol. 2015 Jun;30(7):916-8. doi: 10.1177/0883073814544362. Epub 2014 Aug 24. J Child Neurol. 2015. PMID: 25156664

3

A rare mutation in EIF2B4 gene in an epileptic child with vanishing white matter disease: a case report.

Gungor O, Ozkaya AK, Hirfanoglu T, Dilber C, Aydin K. Gungor O, et al. Genet Couns. 2015;26(1):41-6. Genet Couns. 2015. PMID: 26043506

4

A case of congenital insensitivity to pain with anhidrosis.

Özkaya AK, Güler E, Arık E, Namlı AR, Cevizli D, Güngör O. Özkaya AK, et al. Among authors: gungor o. Turk Pediatri Ars. 2014 Jun 1;49(2):177-9. doi: 10.5152/tpa.2014.1549. eCollection 2014 Jun. Turk Pediatri Ars. 2014. PMID: 26078659 Free PMC article. No abstract available.

5

Thalamic T2 hypointensity: a diagnostic clue for Tay-Sachs disease.

Güngör O, Güngör G, Yurttutan N, Dilber C. Güngör O, et al. Among authors: gungor g. Acta Neurol Belg. 2016 Jun;116(2):195-7. doi: 10.1007/s13760-015-0538-5. Epub 2015 Sep 4. Acta Neurol Belg. 2016. PMID: 26338066 No abstract available.

6

A RETT SYNDROME CASE WITH NOVEL NON-IDENTICAL MUTATION IN MECP2 GENE.

Güngör O, Kirik S, Cevizli D, Karaokur F, Ozer L, Uysal S, Dilber C. Güngör O, et al. Genet Couns. 2015;26(4):387-92. Genet Couns. 2015. PMID: 26852508

7

A new mutation in an infant with Krabbe disease accompanied by enlargement of the optic nerves.

Güngör O, Güngör G, Özkaya AK, Dilber C, Aydın K. Güngör O, et al. Among authors: gungor g. Acta Neurol Belg. 2017 Mar;117(1):319-321. doi: 10.1007/s13760-016-0637-y. Epub 2016 Apr 4. Acta Neurol Belg. 2017. PMID: 27040675 No abstract available.

8

A compound heterozygous EARS2 mutation associated with mild leukoencephalopathy with thalamus and brainstem involvement and high lactate (LTBL).

Güngör O, Özkaya AK, Şahin Y, Güngör G, Dilber C, Aydın K. Güngör O, et al. Among authors: gungor g. Brain Dev. 2016 Oct;38(9):857-61. doi: 10.1016/j.braindev.2016.04.002. Epub 2016 Apr 23. Brain Dev. 2016. PMID: 27117034

9

A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis.

Sahin Y, Güngör O, Ayaz A, Güngör G, Sahin B, Yaykasli K, Ceylaner S. Sahin Y, et al. Among authors: gungor g, gungor o. Brain Dev. 2017 Feb;39(2):166-170. doi: 10.1016/j.braindev.2016.09.002. Epub 2016 Sep 15. Brain Dev. 2017. PMID: 27640920

10

Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy.

Sahin Y, Güngör O, Gormez Z, Demirci H, Ergüner B, Güngör G, Dilber C. Sahin Y, et al. Among authors: gungor g, gungor o. Acta Neurol Belg. 2017 Mar;117(1):159-167. doi: 10.1007/s13760-016-0721-3. Epub 2016 Nov 14. Acta Neurol Belg. 2017. PMID: 27844444

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