Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 102

1.

Effects of levetiracetam and valproic acid treatment on liver function tests, plasma free carnitine and lipid peroxidation in childhood epilepsies.

Haznedar P, Doğan Ö, Albayrak P, Öz Tunçer G, Teber S, Deda G, Eminoglu FT.

Epilepsy Res. 2019 Jul;153:7-13. doi: 10.1016/j.eplepsyres.2019.03.009. Epub 2019 Mar 15.

PMID:
30925397
2.

A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene.

Tunçer GÖ, Teber S, Albayrak P, Kutluk MG, Deda G.

Turk Pediatri Ars. 2018 Dec 1;53(4):259-262. doi: 10.5152/TurkPediatriArs.2018.4197. eCollection 2018 Dec.

3.

Primary cardiac MYC/BCL6 double hit non-Hodgkin lymphoma.

Annibali O, Nenna A, Barbato R, Chello M, Sedati P, Bianchi A, Deda G, Avvisati G.

J Cardiol Cases. 2017 Dec 8;17(3):103-106. doi: 10.1016/j.jccase.2017.11.002. eCollection 2018 Mar.

4.

Hashimoto's encephalopathy presenting as pseudobulbar palsy.

Oz Tuncer G, Teber S, Kutluk MG, Albayrak P, Deda G.

Childs Nerv Syst. 2018 Jun;34(6):1251-1254. doi: 10.1007/s00381-018-3720-2. Epub 2018 Jan 24.

PMID:
29368307
5.

Assessment of optic disc and ganglion cell layer in diabetes mellitus type 2.

Pekel E, Tufaner G, Kaya H, Kaşıkçı A, Deda G, Pekel G.

Medicine (Baltimore). 2017 Jul;96(29):e7556. doi: 10.1097/MD.0000000000007556.

6.

Andersen-Tawil Syndrome with Early Onset Myopathy: 2 Cases.

Oz Tuncer G, Teber S, Kutluk MG, Albayrak P, Deda G.

J Neuromuscul Dis. 2017;4(1):93-95. doi: 10.3233/JND-160188. No abstract available.

PMID:
28106564
7.

Complete paralytic botulism mimicking a deep coma in a child.

Azapağası E, Kendirli T, Öz-Tuncer G, Albayrak P, Teber S, Deda G.

Turk J Pediatr. 2017;59(5):581-585. doi: 10.24953/turkjped.2017.05.012.

8.

The effects of risk factors on EEG and seizure in children with ADHD.

Kartal A, Aksoy E, Deda G.

Acta Neurol Belg. 2017 Mar;117(1):169-173. doi: 10.1007/s13760-016-0718-y. Epub 2016 Nov 7.

PMID:
27822696
9.

A celiac case mimicking mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).

Aksoy E, Tıraş-Teber S, Deda G.

Turk J Pediatr. 2016;58(6):662-665. doi: 10.24953/turkjped.2016.06.014.

10.

Neurological findings spectrum in Celiac disease.

Aksoy E, Tıraş-Teber S, Kansu A, Deda G, Kartal A.

Turk J Pediatr. 2016;58(3):233-240.

11.

Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency.

Dönmez-Demir B, Celkan T, Sarper N, Deda G, İnce E, Çalişkan Ü, Öztürk G, Karagün B, Küpesiz A, Tokgöz H, Akar N, Özdağ H.

Blood Coagul Fibrinolysis. 2016 Sep;27(6):637-44. doi: 10.1097/MBC.0000000000000383.

PMID:
26340456
12.

A rare cause of fatal pulmonary alveolar proteinosis: Niemann-Pick disease type C2 and a novel mutation.

Yaman A, Eminoğlu FT, Kendirli T, Ödek Ç, Ceylaner S, Kansu A, İnce E, Deda G.

J Pediatr Endocrinol Metab. 2015 Sep;28(9-10):1163-7. doi: 10.1515/jpem-2014-0358.

PMID:
26024245
13.

Composite mantle-cell lymphoma and classical Hodgkin lymphoma in a very old adult.

Giua R, Fontana D, Deda G, Bianchi A, Rabitti C, Antonelli Incalzi R.

J Am Geriatr Soc. 2015 Apr;63(4):824-6. doi: 10.1111/jgs.13355. No abstract available.

PMID:
25900501
14.

Epilepsy and autoimmunity in pediatric patients.

Bektaş Ö, Jacobson L, Tutkak H, Karagöl S, Lang B, Clover L, Vincent A, Deda G.

Neuropediatrics. 2015 Feb;46(1):13-9. doi: 10.1055/s-0034-1389895. Epub 2014 Oct 7.

PMID:
25290722
15.

Anti-N-methyl-D-aspartate receptor encephalitis that developed after herpes encephalitis: a case report and literature review.

Bektaş Ö, Tanyel T, Kocabaş BA, Fitöz S, Ince E, Deda G.

Neuropediatrics. 2014 Dec;45(6):396-401. doi: 10.1055/s-0034-1387813. Epub 2014 Sep 27. Review.

PMID:
25261793
16.

Relationship of childhood headaches with preferences in leisure time activities, depression, anxiety and eating habits: A population-based, cross-sectional study.

Bektaş Ö, Uğur C, Gençtürk ZB, Aysev A, Sireli Ö, Deda G.

Cephalalgia. 2015 May;35(6):527-37. doi: 10.1177/0333102414547134. Epub 2014 Aug 22.

PMID:
25149505
17.

Cerebral sinovenous thrombosis in children and neonates: clinical experience, laboratory, treatment, and outcome.

Bektaş Ö, Teber S, Akar N, Uysal LZ, Arsan S, Atasay B, Deda G.

Clin Appl Thromb Hemost. 2015 Nov;21(8):777-82. doi: 10.1177/1076029614523491. Epub 2014 Feb 18.

PMID:
24550550
18.

Endothelial protein C receptor and pediatric arterial stroke.

Akar N, Karabıyık A, Deda G.

Turk J Haematol. 2013 Mar;30(1):37-9. doi: 10.4274/tjh.01488. Epub 2013 Mar 5.

19.

An unusual case of neurobrucellosis presenting as demyelination disorder.

Bektaş O, Ozdemir H, Yılmaz A, Fitöz S, Ciftçi E, Ince E, Aksoy E, Deda G.

Turk J Pediatr. 2013 Mar-Apr;55(2):210-3.

PMID:
24192684
20.

A novel protein C inhibitor gene mutation in pediatric stroke patients after bone marrow transplantation.

Torun D, Deda G, Ertem M, Uysal Z, Yılmaz E, Akar N.

Mol Biol Rep. 2013 Sep;40(9):5465-8. doi: 10.1007/s11033-013-2644-x. Epub 2013 May 14.

PMID:
23670045
21.

Valproic acid-induced acute pancreatitis and multiorgan failure in a child.

Yaman A, Kendirli T, Odek C, Bektaş O, Kuloğlu Z, Koloğlu M, Ince E, Deda G.

Pediatr Emerg Care. 2013 May;29(5):659-61. doi: 10.1097/PEC.0b013e31828ec2d5. Review.

PMID:
23640149
22.

Chloral hydrate and/or hydroxyzine for sedation in pediatric EEG recording.

Bektas O, Arıca B, Teber S, Yılmaz A, Zeybek H, Kaymak S, Deda G.

Brain Dev. 2014 Feb;36(2):130-6. doi: 10.1016/j.braindev.2013.03.002. Epub 2013 Apr 10.

PMID:
23582501
23.

An adolescent girl with hypertension and neuropsychiatric symptoms: questions.

Ozçakar ZB, Bolkent MG, Kavaz A, Oztürk BB, Deda G, Ekim M, Yalçınkaya F.

Pediatr Nephrol. 2013 Mar;28(3):427, 429-31. doi: 10.1007/s00467-012-2231-8. Epub 2012 Jun 29. No abstract available.

PMID:
22744768
24.

Electroencephalogram variations in pediatric migraines and tension-type headaches.

Ozkan M, Teber ST, Deda G.

Pediatr Neurol. 2012 Mar;46(3):154-7. doi: 10.1016/j.pediatrneurol.2011.11.016.

PMID:
22353289
25.

Hashimoto encephalopathy causing drug-resistant status epilepticus treated with plasmapheresis.

Bektas Ö, Yılmaz A, Kendirli T, Sıklar Z, Deda G.

Pediatr Neurol. 2012 Feb;46(2):132-5. doi: 10.1016/j.pediatrneurol.2011.11.009.

PMID:
22264710
26.

Lipoprotein a levels in pediatric migraine.

Teber S, Bektas Ö, Yılmaz A, Aksoy E, Akar N, Deda G.

Pediatr Neurol. 2011 Oct;45(4):225-8. doi: 10.1016/j.pediatrneurol.2011.06.008.

PMID:
21907882
27.

Childhood migraine and hypercoagulopathy.

Teber S, Akar N, Deda G.

Br J Haematol. 2011 Nov;155(4):527-8. doi: 10.1111/j.1365-2141.2011.08718.x. Epub 2011 May 25. No abstract available.

PMID:
21615378
28.

A challenging review of childhood incontinence: rare complications of dysfunctional elimination syndrome in an epileptic boy.

Aydoğdu O, Burgu B, Teber S, Altugan S, Gökçe I, Deda G, Soygür T.

Turk J Pediatr. 2011 Jan-Feb;53(1):100-3. Review.

PMID:
21534350
29.

Fetal and neonatal cardiac rhabdomyomas: clinical presentation, outcome and association with tuberous sclerosis complex.

Atalay S, Aypar E, Uçar T, Altuğ N, Deda G, Teber S, Tutar E.

Turk J Pediatr. 2010 Sep-Oct;52(5):481-7.

PMID:
21434532
30.

Genoa syndrome and central diabetes insipidus: a case report.

Hacıhamdioğlu B, Şıklar Z, Savaş Erdeve Ş, Berberoğlu M, Deda G, Tıraş ST, Fitöz S, Öcal G.

J Clin Res Pediatr Endocrinol. 2010;2(2):89-91. doi: 10.4274/jcrpe.v2i2.89. Epub 2010 May 8.

31.

Treatment challenges in pediatric stroke patients.

Yılmaz A, Teber S, Bektaş O, Akar N, Uysal LZ, Aksoy E, Deda G.

Stroke Res Treat. 2010 Dec 28;2011:534362. doi: 10.4061/2011/534362.

32.

Congenital myotonic dystrophy associated with Moebius syndrome and double-outlet right ventricle.

Teber S, Sezer T, Aypar E, Kendirli T, Atalay S, Deda G.

Pediatr Int. 2010 Jun;52(3):501-2. doi: 10.1111/j.1442-200X.2010.03148.x. No abstract available.

PMID:
20723129
33.

Status epilepticus and capillary leak syndrome in a neonate related to perinatal hypoxic-ischemic encephalopathy.

Karagol BS, Erdeve O, Arsan S, Atasay B, Ekim M, Teber S, Deda G.

Indian J Pediatr. 2010 Apr;77(4):439-41. doi: 10.1007/s12098-010-0011-7. Epub 2010 Feb 8.

PMID:
20140779
34.

Lipoprotein (a) levels in childhood arterial ischemic stroke.

Teber S, Deda G, Akar N, Soylu K.

Clin Appl Thromb Hemost. 2010 Apr;16(2):214-7. doi: 10.1177/1076029609334124. Epub 2009 Sep 13.

PMID:
19752039
35.

EEG and MRI findings and their relation with intellectual disability in pervasive developmental disorders.

Unal O, Ozcan O, Oner O, Akcakin M, Aysev A, Deda G.

World J Pediatr. 2009 Aug;5(3):196-200. doi: 10.1007/s12519-009-0037-y. Epub 2009 Aug 20.

36.

Relationship between functional promoter polymorphism in the XBP1 gene (-116C/G) and atherosclerosis, ischemic stroke and hyperhomocysteinemia.

Yilmaz E, Akar R, Eker ST, Deda G, Adiguzel Y, Akar N.

Mol Biol Rep. 2010 Jan;37(1):269-72. doi: 10.1007/s11033-009-9674-4. Epub 2009 Aug 11.

PMID:
19669932
37.

Thrombophilic risk factors in epileptic children treated with valproic Acid.

Unal O, Deda G, Teber S, Ertem M, Akar N.

Pediatr Neurol. 2009 Feb;40(2):102-6. doi: 10.1016/j.pediatrneurol.2008.10.005.

PMID:
19135623
38.

A note on homocysteine levels in children.

Tras ST, Deda G, Akar N.

Thromb Res. 2009 Mar;123(5):799. doi: 10.1016/j.thromres.2008.08.022. Epub 2008 Nov 8. No abstract available.

PMID:
18996573
39.

Tau and S100B proteins as biochemical markers of bilirubin-induced neurotoxicity in term neonates.

Okumus N, Turkyilmaz C, Onal EE, Atalay Y, Serdaroglu A, Elbeg S, Koc E, Deda G, Cansu A, Gunduz B.

Pediatr Neurol. 2008 Oct;39(4):245-52. doi: 10.1016/j.pediatrneurol.2008.07.004.

PMID:
18805362
40.

Protein Z G79A polymorphism in Turkish pediatriccerebral infarct patients.

Öztürk A, Eğin Y, Deda G, Teber S, Akar N.

Turk J Haematol. 2008 Sep 5;25(3):133-5.

PMID:
27264704
41.

The relation between cytokines, soluble endothelial protein C receptor, and factor VIII levels in Turkish pediatric stroke patients.

Yürürer D, Teber S, Deda G, Egin Y, Akar N.

Clin Appl Thromb Hemost. 2009 Oct;15(5):545-51. doi: 10.1177/1076029608319880. Epub 2008 Jun 29.

PMID:
18591180
42.

Hypophosphatasia associated with pseudotumor cerebri and respiratory insufficiency.

Teber S, Sezer T, Kafali M, Kendirli T, Siklar Z, Berberoglu M, Ocal G, Deda G.

Indian J Pediatr. 2008 Feb;75(2):186-8.

PMID:
18334804
43.

Juvenile form of myasthenia gravis presenting as recurrent pulmonary infection with atelectasis.

Unal O, Teber S, Kendirli T, Deda G, Anlar B.

Pediatr Int. 2007 Dec;49(6):1007-8.

PMID:
18045313
44.

Distal truncation of KCC3 in non-French Canadian HMSN/ACC families.

Salin-Cantegrel A, Rivière JB, Dupré N, Charron FM, Shekarabi M, Karéméra L, Gaspar C, Horst J, Tekin M, Deda G, Krause A, Lippert MM, Willemsen MA, Jarrar R, Lapointe JY, Rouleau GA.

Neurology. 2007 Sep 25;69(13):1350-5.

PMID:
17893295
45.

Severe muscle-eye-brain disease is associated with a homozygous mutation in the POMGnT1 gene.

Teber S, Sezer T, Kafali M, Manzini MC, Konuk Yüksel B, Tekin M, Fitöz S, Walsh CA, Deda G.

Eur J Paediatr Neurol. 2008 Mar;12(2):133-6. Epub 2007 Sep 18.

PMID:
17881266
46.

FXIII gene Val34Leu polymorphism in Turkish children with cerebral infarct.

Akar N, Dönmez B, Deda G.

J Child Neurol. 2007 Feb;22(2):222-4.

PMID:
17621488
47.

T102C polymorphism of the serotonin (5-HT) 2A receptor gene in Turkish children with cerebral infarct.

Dönmez BN, Teber S, Deda G, Akar N.

Turk J Haematol. 2007 Mar 5;24(1):14-7.

PMID:
27263479
48.

Prothrombin G20210A and A19911G mutations in Turkish pediatric stroke patients.

Yıldız Z, Deda G, Akar N.

Turk J Haematol. 2006 Dec 5;23(4):197-9.

PMID:
27265662
49.

EPCR gene A3 haplotype and elevated soluble endothelial protein C receptor (sEPCR) levels in Turkish pediatric stroke patients.

Ulu A, Gunal D, Tiras S, Egin Y, Deda G, Akar N.

Thromb Res. 2007;120(1):47-52. Epub 2006 Oct 5.

PMID:
17027065
50.

Pediatric stroke, homocysteine and MTHFR 677C-T and 1298 A-C.

Akar N, Deda G, Teber ST.

J Pediatr Hematol Oncol. 2006 Sep;28(9):632-3. No abstract available.

PMID:
17006274

Supplemental Content

Support Center