Yıldırım M - Search Results

1

A Novel Variant of the CTSD Gene Associated with Juvenile-onset Neuronal Ceroid Lipofuscinosis Type 10: A Case Report and Literature Review.

Çiçek S, Yıldırım M, Tabanlı FP, Köse E, Bektaş Ö, Teber S. Çiçek S, et al. Among authors: yildirim m. Cerebellum. 2024 Dec 10;24(1):7. doi: 10.1007/s12311-024-01773-z. Cerebellum. 2024. PMID: 39656415 Review.

2

Status dystonicus associated with CLN8 disease.

Yıldırım M, Köse E, Keçeli AM, Balasar Ö, Şimşek N. Yıldırım M, et al. Brain Dev. 2021 Apr;43(4):571-575. doi: 10.1016/j.braindev.2020.12.005. Epub 2020 Dec 24. Brain Dev. 2021. PMID: 33358637

3

Levetiracetam monotherapy in children with epilepsy: Experience from a tertiary pediatric neurology center.

Yıldırım M, Bektaş Ö, Akıncı Göktaş Ö, Yüksel MF, Şahin S, Tıraş Teber S. Yıldırım M, et al. Epilepsy Behav. 2021 Mar;116:107745. doi: 10.1016/j.yebeh.2020.107745. Epub 2021 Jan 25. Epilepsy Behav. 2021. PMID: 33508749

4

Hypomelanosis of Ito presenting with unilateral dilation of Virchow-Robin spaces: a case report.

Uçar Çİ, Yıldırım M, Sayar Y, Şahin S, Teber ST. Uçar Çİ, et al. Among authors: yildirim m. Childs Nerv Syst. 2021 Sep;37(9):2931-2934. doi: 10.1007/s00381-021-05083-1. Epub 2021 Feb 13. Childs Nerv Syst. 2021. PMID: 33585955

5

A sydenham chorea attack associated with COVID-19 infection.

Yüksel MF, Yıldırım M, Bektaş Ö, Şahin S, Teber S. Yüksel MF, et al. Among authors: yildirim m. Brain Behav Immun Health. 2021 May;13:100222. doi: 10.1016/j.bbih.2021.100222. Epub 2021 Feb 16. Brain Behav Immun Health. 2021. PMID: 33615279 Free PMC article.

6

Therapeutic plasma exchange in clinical pediatric neurology practice: Experience from a tertiary referral hospital.

Yıldırım M, Bektaş Ö, Botan E, Şahin S, Gurbanov A, Teber S, Kendirli T. Yıldırım M, et al. Clin Neurol Neurosurg. 2021 Aug;207:106823. doi: 10.1016/j.clineuro.2021.106823. Epub 2021 Jul 17. Clin Neurol Neurosurg. 2021. PMID: 34304066

7

Mild congenital myopathy due to a novel variation in SPEG gene.

Yildirim M, Balasar O, Kose E, Dogan MT. Yildirim M, et al. Intractable Rare Dis Res. 2021 Aug;10(3):220-222. doi: 10.5582/irdr.2021.01034. Intractable Rare Dis Res. 2021. PMID: 34466346 Free PMC article.

8

Intracranial Calcification Associated with 3-Methylcrotonyl-CoA Carboxylase Deficiency.

Şahin S, Yıldırım M, Bektaş Ö, Sürücü Kara İ, Ceylan AC, Teber S. Şahin S, et al. Among authors: yildirim m. Mol Syndromol. 2021 Oct;12(6):393-398. doi: 10.1159/000517272. Epub 2021 Aug 26. Mol Syndromol. 2021. PMID: 34899149 Free PMC article.

9

The diagnostic challenges of congenital mirror movements and hand stereotypies in a case with TUBB3-associated tubulinopathy.

Yeniay Süt N, Yıldırım M, Bektaş Ö, Altıntaş M, Teber S. Yeniay Süt N, et al. Among authors: yildirim m. Acta Neurol Belg. 2022 Feb;122(1):251-253. doi: 10.1007/s13760-021-01858-0. Epub 2022 Jan 3. Acta Neurol Belg. 2022. PMID: 34981407 No abstract available.

10

A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the TRIT1 Gene.

Yıldırım M, Bektaş Ö, Tunçez E, Yeniay Süt N, Sayar Y, Öncül Ü, Teber S. Yıldırım M, et al. Mol Syndromol. 2022 Feb;13(2):139-145. doi: 10.1159/000518373. Epub 2021 Sep 30. Mol Syndromol. 2022. PMID: 35418828 Free PMC article.

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