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Items: 19

1.

Genetic and phenotypic features of patients with childhood ataxias diagnosed by next-generation sequencing gene panel.

Arslan EA, Öncel İ, Ceylan AC, Topçu M, Topaloğlu H.

Brain Dev. 2019 Sep 4. pii: S0387-7604(18)30608-9. doi: 10.1016/j.braindev.2019.08.004. [Epub ahead of print]

PMID:
31493945
2.

Changes in Serum Valproate and Levetiracetam Levels Related to Sex Steroids in Adolescent Girls.

Şahin S, Yılmaz SA, Cansu A, Kamaşak T, Arslan EA, Kaklıkkaya N.

Pediatr Neurol. 2019 Jul;96:76-78. doi: 10.1016/j.pediatrneurol.2019.03.010. Epub 2019 Mar 21. No abstract available.

PMID:
31023605
3.

An investigation of the ocular toxic effects of levetiracetam therapy in children with epilepsy.

Diler Durgut B, Turk A, Acar Arslan E, Kamasak T, Sahin S, Dilber B, Turkcan Soguksulu T, Cansu A.

Childs Nerv Syst. 2019 May;35(5):769-774. doi: 10.1007/s00381-019-04076-5. Epub 2019 Feb 20.

PMID:
30783756
4.

Vitamin D protects against hippocampal apoptosis related with seizures induced by kainic acid and pentylenetetrazol in rats.

Şahin S, Gürgen SG, Yazar U, İnce İ, Kamaşak T, Acar Arslan E, Diler Durgut B, Dilber B, Cansu A.

Epilepsy Res. 2019 Jan;149:107-116. doi: 10.1016/j.eplepsyres.2018.12.005. Epub 2018 Dec 15.

PMID:
30584976
5.

Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders.

Ceylan AC, Citli S, Erdem HB, Sahin I, Acar Arslan E, Erdogan M.

Mol Cytogenet. 2018 Sep 24;11:54. doi: 10.1186/s13039-018-0402-4. eCollection 2018.

6.

A rare cause of chronic ataxia in childhood: ganglioneuroma.

Arslan EA, Kamaşak T, Turgut BD, Saygın İ, Sarıhan H, Cansu A.

World J Pediatr. 2018 Apr;14(2):204-206. doi: 10.1007/s12519-018-0141-y. Epub 2018 Mar 12. No abstract available.

PMID:
29532434
7.

Childhood hereditary ataxias: experience from a tertiary referral university hospital in Turkey.

Arslan EA, Göçmen R, Oğuz KK, Konuşkan GD, Serdaroğlu E, Topaloğlu H, Topçu M.

Acta Neurol Belg. 2017 Dec;117(4):857-865. doi: 10.1007/s13760-017-0786-7. Epub 2017 Apr 29.

PMID:
28456889
8.

SUDEP: The First Case Series in Turkey.

Güngör M, Acar Arslan E, Tezer Filik Fİ, Saygi S.

Noro Psikiyatr Ars. 2016 Mar;53(1):67-71. doi: 10.5152/npa.2015.7553. Epub 2016 Mar 1.

9.

Effect of Biperiden Treatment in Acute Orofacial and Extremity Dyskinesia With Methylphenidate Therapy.

Arslan EA, Arslan E, Kilinç A, Göksu Ö.

Pediatr Emerg Care. 2018 Nov;34(11):e217-e218. doi: 10.1097/PEC.0000000000001102.

PMID:
28328695
10.

Comparison of the serum cytokine levels before and after adrenocorticotropic hormone (ACTH) therapy in patients with infantile spasm.

Türe E, Kamaşak T, Cora M, Şahin S, Arslan EA, Kaklıkaya N, Cansu A.

Seizure. 2016 Oct;41:112-5. doi: 10.1016/j.seizure.2016.06.021. Epub 2016 Jul 30.

11.

Genes for spinocerebellar ataxia with blindness and deafness (SCABD/SCAR3, MIM# 271250 and SCABD2).

Guissart C, Drouot N, Oncel I, Leheup B, Gershoni-Barush R, Muller J, Ferdinandusse S, Larrieu L, Anheim M, Arslan EA, Claustres M, Tranchant C, Topaloglu H, Koenig M.

Eur J Hum Genet. 2016 Aug;24(8):1154-9. doi: 10.1038/ejhg.2015.259. Epub 2015 Dec 16.

12.

Cerebral Venous Sinus Thrombosis with Internal Jugular Venous Thrombosis in a Male Patient with Nephrotic Syndrome.

Hacifazlioglu C, Arslan E, Arslan EA, Buyukserbetci G.

Turk Neurosurg. 2015;25(6):980-3. doi: 10.5137/1019-5149.JTN.11355-14.1.

13.

A case of neurocutaneous melanosis and neuroimaging findings.

Gocmen R, Guler E, Arslan EA.

J Radiol Case Rep. 2015 Mar 31;9(3):1-6. doi: 10.3941/jrcr.v9i3.2141. eCollection 2015 Mar.

14.

Stimulus-induced myoclonus treated effectively with clonazepam in genetically confirmed Coffin-Lowry syndrome.

Arslan EA, Ceylaner S, Turanlı G.

Epilepsy Behav Case Rep. 2014 Nov 25;2:196-8. doi: 10.1016/j.ebcr.2014.09.007. eCollection 2014.

15.

Wernicke encephalopathy due to thiamine deficiency after surgery on a child with duodenal stenosis.

Arslan EA, Ekinci S, Akkuş PZ, Göçmen R, Haliloğlu G.

Pediatr Neurol. 2014 Dec;51(6):840-2. doi: 10.1016/j.pediatrneurol.2014.08.034. Epub 2014 Sep 4.

PMID:
25303868
16.

Intraspinal lipomas without associated spinal dysraphism.

Arslan E, Kuzeyli K, Acar Arslan E.

Iran Red Crescent Med J. 2014 May;16(5):e11423. doi: 10.5812/ircmj.11423. Epub 2014 May 5.

17.

Delayed diagnosis of cleidocranial dysplasia in an adult: a case report.

Gömleksiz C, Arslan E, Arslan S, Pusat S, Arslan EA.

Acta Med Acad. 2014;43(1):92-6. doi: 10.5644/ama2006-124.106.

18.

Absence of exon 17 c.2970-2872delAAT mutation in Turkish NF1 patients with mild phenotype.

Terzi YK, Sirin B, Serdaroglu E, Anlar B, Aysun S, Hosgor G, Arslan EA, Ayter S.

Childs Nerv Syst. 2011 Dec;27(12):2113-6. doi: 10.1007/s00381-011-1512-z. Epub 2011 Jul 6.

PMID:
21732117
19.

Recurrent lumbar spinal intradural enterogenous cyst: a case report.

Arslan E, Cakir E, Kuzeyli K, Guvercin AR, Gazioglu G, Arslan EA, Reis A.

Turk Neurosurg. 2010 Jul;20(3):402-5. doi: 10.5137/1019-5149.JTN.1992-09.3.

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