Sager SG - Search Results

1

A novel de novo TET3 loss-of-function variant in a Turkish boy presenting with neurodevelopmental delay and electrical status epilepticus during slow-wave sleep.

Sager SG, Turkyilmaz A, Gunbey HP, Karatoprak EY, Aslan ES, Akın Y. Sager SG, et al. Brain Dev. 2023 Feb;45(2):140-145. doi: 10.1016/j.braindev.2022.09.004. Epub 2022 Sep 30. Brain Dev. 2023. PMID: 36192301

2

Novel SH3PXD2B variant identified by whole-exome sequencing in a Turkish newborn with Frank-Ter Haar Syndrome.

Türkyilmaz A, Sager SG, Topcu B, Kaplan AT, Günbey HP, Akin Y. Türkyilmaz A, et al. Among authors: sager sg. Clin Dysmorphol. 2022 Jan 1;31(1):45-49. doi: 10.1097/MCD.0000000000000389. Clin Dysmorphol. 2022. PMID: 34538861 No abstract available.

3

Two New Cases of Primary Microcephaly with Neuronal Migration Defect Caused by Truncating Mutations in the ASPM Gene.

Türkyılmaz A, Sager SG. Türkyılmaz A, et al. Among authors: sager sg. Mol Syndromol. 2022 Feb;13(1):56-63. doi: 10.1159/000516201. Epub 2021 Sep 15. Mol Syndromol. 2022. PMID: 35221876 Free PMC article.

4

Efficacy of intravenous levetiracetam versus phenytoin in convulsive status epilepticus and acute repetitive seizures in children.

Köle MT, Sager SG, Zeynel H, Çağ Y, Akın Y. Köle MT, et al. Among authors: sager sg. Childs Nerv Syst. 2022 Jul;38(7):1357-1364. doi: 10.1007/s00381-022-05543-2. Epub 2022 Apr 30. Childs Nerv Syst. 2022. PMID: 35501510

5

Novel LNPK variant causes progressive cerebral atrophy: Expanding the clinical phenotype.

Türkyılmaz A, Sağer SG, Günbey HP, Akın Y. Türkyılmaz A, et al. Among authors: sager sg. Clin Genet. 2022 Sep;102(3):218-222. doi: 10.1111/cge.14166. Epub 2022 May 28. Clin Genet. 2022. PMID: 35599435

6

Evaluation of optical coherence tomography findings and visual evoked potentials in Charcot-Marie-Tooth disease.

Kaplan AT, Oskan Yalcin S, Sager SG, Türkyılmaz A, İnan R. Kaplan AT, et al. Among authors: sager sg. Int Ophthalmol. 2023 Jan;43(1):333-341. doi: 10.1007/s10792-022-02452-w. Epub 2022 Aug 12. Int Ophthalmol. 2023. PMID: 35953577

7

Calgary score and modified calgary score in the differential diagnosis between syncope and genetic generalized epilepsy in children.

Köle MT, Sağer SG, Batu U, Çetiner Çine N, Çağ Y, Akin Y. Köle MT, et al. Among authors: sager sg. Sci Rep. 2023 Jul 31;13(1):12376. doi: 10.1038/s41598-023-39338-5. Sci Rep. 2023. PMID: 37524730 Free PMC article.

8

Coexistence of longitudinally extensive transverse myelitis and diffuse midline glioma in the brainstem in an adolescent boy with acute flaccid paralysis.

Caliskan E, Sager SG, Yukselmis U, Kilic AK, Gunbey HP. Caliskan E, et al. Among authors: sager sg. Childs Nerv Syst. 2024 Jan;40(1):227-232. doi: 10.1007/s00381-023-06163-0. Epub 2023 Sep 22. Childs Nerv Syst. 2024. PMID: 37737897

9

Microstructural evaluation of the brain with advanced magnetic resonance imaging techniques in cases of electrical status epilepticus during sleep (ESES).

Düzkalir HG, Genç B, Sağer SG, Türkyilmaz A, Günbey HP. Düzkalir HG, et al. Among authors: sager sg. Turk J Med Sci. 2023 Oct 25;53(6):1840-1851. doi: 10.55730/1300-0144.5754. eCollection 2023. Turk J Med Sci. 2023. PMID: 38813507 Free PMC article.

10

A case of ocular flutter associated with sole anti-sulphatide antibody positivity: successful treatment with intravenous immunoglobulin in a pediatric patient.

Akcay M, Sager SG, Kaplan AT, Alomari O, Akin Y. Akcay M, et al. Among authors: sager sg. Acta Neurol Belg. 2024 Dec;124(6):2063-2065. doi: 10.1007/s13760-024-02645-3. Epub 2024 Sep 28. Acta Neurol Belg. 2024. PMID: 39342054

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