Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 17

1.

Anti-N-methyl-d-aspartate (Anti-NMDA) receptor encephalitis: rapid and sustained clinical improvement with steroid therapy starting in the late phase.

Turkdoğan D, Orengul AC, Zaimoğlu S, Ekinci G.

J Child Neurol. 2014 May;29(5):684-7. doi: 10.1177/0883073813520497. Epub 2014 Feb 20.

PMID:
24563473
[PubMed - indexed for MEDLINE]
2.

Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy.

Møller RS, Weber YG, Klitten LL, Trucks H, Muhle H, Kunz WS, Mefford HC, Franke A, Kautza M, Wolf P, Dennig D, Schreiber S, Rückert IM, Wichmann HE, Ernst JP, Schurmann C, Grabe HJ, Tommerup N, Stephani U, Lerche H, Hjalgrim H, Helbig I, Sander T; EPICURE Consortium.

Epilepsia. 2013 Feb;54(2):256-64. doi: 10.1111/epi.12078. Epub 2013 Jan 7. Erratum in: Epilepsia. 2013 Dec;54(12):2232.

PMID:
23294455
[PubMed - indexed for MEDLINE]
3.

PRRT2 mutations are the major cause of benign familial infantile seizures.

Schubert J, Paravidino R, Becker F, Berger A, Bebek N, Bianchi A, Brockmann K, Capovilla G, Dalla Bernardina B, Fukuyama Y, Hoffmann GF, Jurkat-Rott K, Anttonen AK, Kurlemann G, Lehesjoki AE, Lehmann-Horn F, Mastrangelo M, Mause U, Müller S, Neubauer B, Püst B, Rating D, Robbiano A, Ruf S, Schroeder C, Seidel A, Specchio N, Stephani U, Striano P, Teichler J, Turkdogan D, Vigevano F, Viri M, Bauer P, Zara F, Lerche H, Weber YG.

Hum Mutat. 2012 Oct;33(10):1439-43. doi: 10.1002/humu.22126. Epub 2012 Jun 11.

PMID:
22623405
[PubMed - indexed for MEDLINE]
4.

Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies.

EPICURE Consortium, Leu C, de Kovel CG, Zara F, Striano P, Pezzella M, Robbiano A, Bianchi A, Bisulli F, Coppola A, Giallonardo AT, Beccaria F, Trenité DK, Lindhout D, Gaus V, Schmitz B, Janz D, Weber YG, Becker F, Lerche H, Kleefuss-Lie AA, Hallman K, Kunz WS, Elger CE, Muhle H, Stephani U, Møller RS, Hjalgrim H, Mullen S, Scheffer IE, Berkovic SF, Everett KV, Gardiner MR, Marini C, Guerrini R, Lehesjoki AE, Siren A, Nabbout R, Baulac S, Leguern E, Serratosa JM, Rosenow F, Feucht M, Unterberger I, Covanis A, Suls A, Weckhuysen S, Kaneva R, Caglayan H, Turkdogan D, Baykan B, Bebek N, Ozbek U, Hempelmann A, Schulz H, Rüschendorf F, Trucks H, Nürnberg P, Avanzini G, Koeleman BP, Sander T.

Epilepsia. 2012 Feb;53(2):308-18. doi: 10.1111/j.1528-1167.2011.03379.x. Epub 2012 Jan 13.

PMID:
22242659
[PubMed - indexed for MEDLINE]
5.

A prevalence study of restless legs syndrome in Turkish children and adolescents.

Turkdogan D, Bekiroglu N, Zaimoglu S.

Sleep Med. 2011 Apr;12(4):315-21. doi: 10.1016/j.sleep.2010.08.013. Epub 2011 Feb 19.

PMID:
21339085
[PubMed - indexed for MEDLINE]
6.

An association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic-clonic seizures.

Yalçin O, Baykan B, Ağan K, Yapici Z, Yalçin D, Dizdarer G, Türkdoğan D, Ozkara C, Unalp A, Uludüz D, Gül G, Kuşcu D, Ayta S, Tutkavul K, Comu S, Tatli B, Meral C, Bebek N, Cağlayan SH.

Epilepsia. 2011 May;52(5):975-83. doi: 10.1111/j.1528-1167.2010.02970.x. Epub 2011 Feb 14.

PMID:
21320115
[PubMed - indexed for MEDLINE]
7.

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance.

Dibbens LM, Mullen S, Helbig I, Mefford HC, Bayly MA, Bellows S, Leu C, Trucks H, Obermeier T, Wittig M, Franke A, Caglayan H, Yapici Z; EPICURE Consortium, Sander T, Eichler EE, Scheffer IE, Mulley JC, Berkovic SF.

Hum Mol Genet. 2009 Oct 1;18(19):3626-31. doi: 10.1093/hmg/ddp311. Epub 2009 Jul 10.

PMID:
19592580
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Characteristic and overlapping features of migraine and tension-type headache.

Turkdogan D, Cagirici S, Soylemez D, Sur H, Bilge C, Turk U.

Headache. 2006 Mar;46(3):461-8.

PMID:
16618264
[PubMed - indexed for MEDLINE]
9.

Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine.

Vanmolkot KR, Kors EE, Turk U, Turkdogan D, Keyser A, Broos LA, Kia SK, van den Heuvel JJ, Black DF, Haan J, Frants RR, Barone V, Ferrari MD, Casari G, Koenderink JB, van den Maagdenberg AM.

Eur J Hum Genet. 2006 May;14(5):555-60.

PMID:
16538223
[PubMed - indexed for MEDLINE]
Free Article
10.

Auditory neuropathy in hyperbilirubinemia: is there a correlation between serum bilirubin, neuron-specific enolase levels and auditory neuropathy?

Akman I, Ozek E, Kulekci S, Türkdogan D, Cebeci D, Akdaş F.

Int J Audiol. 2004 Oct;43(9):516-22.

PMID:
15726842
[PubMed - indexed for MEDLINE]
11.

Subdural EEG patterns in children with taylor-type cortical dysplasia: comparison with nondysplastic lesions.

Turkdogan D, Duchowny M, Resnick T, Jayakar P.

J Clin Neurophysiol. 2005 Jan-Feb;22(1):37-42.

PMID:
15689711
[PubMed - indexed for MEDLINE]
12.

Involvement of sympathetic reflex activity in patients with acute and chronic stroke: A comparison with functional motor capacity.

Muslumanoglu L, Aki S, Turkdogan D, Us O, Akyuz G.

Arch Phys Med Rehabil. 2004 Mar;85(3):470-3.

PMID:
15031835
[PubMed - indexed for MEDLINE]
13.

Visual and auditory event related potentials in epileptic children: a comparison with normal and abnormal MRI findings.

Turkdogan D, Us O, Akyuz G.

Brain Dev. 2003 Sep;25(6):396-400.

PMID:
12907272
[PubMed - indexed for MEDLINE]
14.

Evaluation of vestibular functions in children with vertigo attacks.

Uneri A, Turkdogan D.

Arch Dis Child. 2003 Jun;88(6):510-1.

PMID:
12765917
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Lipid peroxidation and antioxidative enzyme activities in childhood epilepsy.

Turkdogan D, Toplan S, Karakoc Y.

J Child Neurol. 2002 Sep;17(9):673-6.

PMID:
12503643
[PubMed - indexed for MEDLINE]
16.

Phenytoin toxicity with mandibular tremor secondary to intravenous administration.

Türkdogan D, Onat F, Türe U, Pamir N.

Int J Clin Pharmacol Ther. 2002 Jan;40(1):18-9.

PMID:
11837377
[PubMed - indexed for MEDLINE]
17.

Continuous muscle fiber activity syndrome.

Calişkan M, Türkdogan D, Ozmen M, Cantez T, Baslo A, Apak S.

Acta Paediatr Jpn. 1995 Feb;37(1):94-6.

PMID:
7754777
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk