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Items: 1 to 50 of 86

1.

Affective theory of mind in human aging: is there any relation with executive functioning?

Yıldırım E, Soncu Büyükişcan E, Gürvit H.

Neuropsychol Dev Cogn B Aging Neuropsychol Cogn. 2019 Apr 17:1-13. doi: 10.1080/13825585.2019.1602706. [Epub ahead of print]

PMID:
30994403
2.

Association Between Inflammatory Markers and Cognitive Outcome in Patients with Acute Brain Dysfunction Due to Sepsis.

Orhun G, Tüzün E, Özcan PE, Ulusoy C, Yildirim E, Küçükerden M, Gürvit H, Ali A, Esen F.

Noro Psikiyatr Ars. 2019 Mar;56(1):63-70. doi: 10.29399/npa.23212. Epub 2018 Jul 10.

3.

Association between selected cholesterol-related gene polymorphisms and Alzheimer's disease in a Turkish cohort.

Guven G, Vurgun E, Bilgic B, Hanagasi H, Gurvit H, Ozer E, Lohmann E, Erginel-Unaltuna N.

Mol Biol Rep. 2019 Apr;46(2):1701-1707. doi: 10.1007/s11033-019-04619-8. Epub 2019 Jan 25.

PMID:
30684189
4.

Amyloid Beta Adsorption Problem with Transfer Plates in Amyloid Beta 1-42 IVD Kits.

Dursun E, Alaylıoğlu M, Bilgiç B, Hanağası H, Gürvit H, Emre M, Gezen-Ak D.

J Mol Neurosci. 2019 Apr;67(4):534-539. doi: 10.1007/s12031-019-1261-0. Epub 2019 Jan 11.

PMID:
30635782
5.

Development of somatic markers guiding decision-making along adolescence.

Sandor S, Gürvit H.

Int J Psychophysiol. 2019 Mar;137:82-91. doi: 10.1016/j.ijpsycho.2018.12.005. Epub 2018 Dec 15. No abstract available.

PMID:
30557572
6.

Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal Dementia.

Guven G, Bilgic B, Tufekcioglu Z, Erginel Unaltuna N, Hanagasi H, Gurvit H, Singleton A, Hardy J, Emre M, Gulec C, Bras J, Guerreiro R, Lohmann E.

J Alzheimers Dis. 2019;67(1):159-167. doi: 10.3233/JAD-180599.

7.

G82S polymorphism of receptor for advanced glycation end products gene and serum soluble RAGE levels in mild cognitive impairment and dementia of Alzheimer's type patients in Turkish population.

Ataç ZS, Alaylıoğlu M, Dursun E, Gezen-Ak D, Yılmazer S, Gürvit H.

J Clin Neurosci. 2019 Jan;59:197-201. doi: 10.1016/j.jocn.2018.10.072. Epub 2018 Oct 30.

PMID:
30389362
8.

Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span.

Yücel-Yılmaz D, Yücesan E, Yalnızoğlu D, Oğuz KK, Sağıroğlu MŞ, Özbek U, Serdaroğlu E, Bilgiç B, Erdem S, İşeri SAU, Hanağası H, Gürvit H, Özgül RK, Dursun A.

Brain Dev. 2018 Jun;40(6):458-464. doi: 10.1016/j.braindev.2018.02.013. Epub 2018 Mar 12.

PMID:
29544888
9.

[Effects of cerebral oxygen changes during coronary bypass surgery on postoperative cognitive dysfunction in elderly patients: a pilot study].

Şahan C, Sungur Z, Çamcı E, Sivrikoz N, Sayin Ö, Gurvit H, Şentürk M.

Rev Bras Anestesiol. 2018 Mar - Apr;68(2):142-148. doi: 10.1016/j.bjan.2017.10.005. Epub 2017 Dec 26. Portuguese.

10.

Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey.

Kessler C, Atasu B, Hanagasi H, Simón-Sánchez J, Hauser AK, Pak M, Bilgic B, Erginel-Unaltuna N, Gurvit H, Gasser T, Lohmann E.

Parkinsonism Relat Disord. 2018 Mar;48:34-39. doi: 10.1016/j.parkreldis.2017.12.007. Epub 2017 Dec 9.

PMID:
29248340
11.

An assessment of Movement Disorder Society Task Force diagnostic criteria for mild cognitive impairment in Parkinson's disease.

Uysal-Cantürk P, Hanağası HA, Bilgiç B, Gürvit H, Emre M.

Eur J Neurol. 2018 Jan;25(1):148-153. doi: 10.1111/ene.13467. Epub 2017 Oct 16.

PMID:
28941002
12.

Mutations in TYROBP are not a common cause of dementia in a Turkish cohort.

Darwent L, Carmona S, Lohmann E, Guven G, Kun-Rodrigues C, Bilgic B, Hanagasi H, Gurvit H, Erginel-Unaltuna N, Pak M, Hardy J, Singleton A, Brás J, Guerreiro R.

Neurobiol Aging. 2017 Oct;58:240.e1-240.e3. doi: 10.1016/j.neurobiolaging.2017.06.019. Epub 2017 Jun 28.

13.

SYNE1 related cerebellar ataxia presents with variable phenotypes in a consanguineous family from Turkey.

Yucesan E, Ugur Iseri SA, Bilgic B, Gormez Z, Bakir Gungor B, Sarac A, Ozdemir O, Sagiroglu M, Gurvit H, Hanagasi H, Ozbek U.

Neurol Sci. 2017 Dec;38(12):2203-2207. doi: 10.1007/s10072-017-3049-8. Epub 2017 Jul 7.

PMID:
28687974
14.

Salience network engagement with the detection of morally laden information.

Sevinc G, Gurvit H, Spreng RN.

Soc Cogn Affect Neurosci. 2017 Jul 1;12(7):1118-1127. doi: 10.1093/scan/nsx035.

15.

[The effect of two different glycemic management protocols on postoperative cognitive dysfunction in coronary artery bypass surgery].

Kurnaz P, Sungur Z, Camci E, Sivrikoz N, Orhun G, Senturk M, Sayin O, Tireli E, Gurvit H.

Rev Bras Anestesiol. 2017 May - Jun;67(3):258-265. doi: 10.1016/j.bjan.2016.01.007. Epub 2017 Feb 27. Portuguese.

16.

Evaluation of cognitive performance in professional divers by means of event-related potentials and neuropsychology.

Ergen M, Uslu A, Caglar O, Akca-Kalem S, Cimsit M, Gurvit H.

Clin Neurophysiol. 2017 Apr;128(4):579-588. doi: 10.1016/j.clinph.2017.01.007. Epub 2017 Jan 29.

PMID:
28231476
17.

NMDA receptor encephalitis with cancer of unknown primary origin.

Çoban A, Gündoğdu G, Poyraz M, Yegen G, Demirtaş-Tatlıdede A, Bilgiç B, Hanagasi HA, Tüzün E, Gürvit H.

Tumori. 2016 Nov 11;102(Suppl. 2). doi: 10.5301/tj.5000447.

PMID:
26481863
18.

Cognitive and anatomical correlates of anosognosia in amnestic mild cognitive impairment and early-stage Alzheimer's disease.

Senturk G, Bilgic B, Arslan AB, Bayram A, Hanagasi H, Gurvit H, Emre M.

Int Psychogeriatr. 2017 Feb;29(2):293-302. doi: 10.1017/S1041610216001812. Epub 2016 Oct 26.

PMID:
27780496
19.

Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients.

Guven G, Lohmann E, Bras J, Gibbs JR, Gurvit H, Bilgic B, Hanagasi H, Rizzu P, Heutink P, Emre M, Erginel-Unaltuna N, Just W, Hardy J, Singleton A, Guerreiro R.

PLoS One. 2016 Sep 15;11(9):e0162592. doi: 10.1371/journal.pone.0162592. eCollection 2016.

20.

Erratum to: GC and VDR SNPs and Vitamin D Levels in Parkinson's Disease: The Relevance to Clinical Features.

Gezen-Ak D, Alaylıoğlu M, Genç G, Gündüz A, Candaş E, Bilgiç B, Atasoy İL, Apaydın H, Kızıltan G, Gürvit H, Hanağası H, Ertan S, Yılmazer S, Dursun E.

Neuromolecular Med. 2017 Mar;19(1):175-180. doi: 10.1007/s12017-016-8426-6. No abstract available.

PMID:
27444632
21.

Vitamin D deficiency might pose a greater risk for ApoEɛ4 non-carrier Alzheimer's disease patients.

Dursun E, Alaylıoğlu M, Bilgiç B, Hanağası H, Lohmann E, Atasoy IL, Candaş E, Araz ÖS, Önal B, Gürvit H, Yılmazer S, Gezen-Ak D.

Neurol Sci. 2016 Oct;37(10):1633-43. doi: 10.1007/s10072-016-2647-1. Epub 2016 Jun 29.

PMID:
27357856
22.

GC and VDR SNPs and Vitamin D Levels in Parkinson's Disease: The Relevance to Clinical Features.

Gezen-Ak D, Alaylıoğlu M, Genç G, Gündüz A, Candaş E, Bilgiç B, Atasoy İL, Apaydın H, Kızıltan G, Gürvit H, Hanağası H, Ertan S, Yılmazer S, Dursun E.

Neuromolecular Med. 2017 Mar;19(1):24-40. doi: 10.1007/s12017-016-8415-9. Epub 2016 Jun 9. Erratum in: Neuromolecular Med. 2017 Mar;19(1):175-180.

PMID:
27282160
23.

PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism.

Giri A, Guven G, Hanagasi H, Hauser AK, Erginul-Unaltuna N, Bilgic B, Gurvit H, Heutink P, Gasser T, Lohmann E, Simón-Sánchez J.

Tremor Other Hyperkinet Mov (N Y). 2016 Mar 16;6:363. doi: 10.7916/D81G0M12. eCollection 2016.

24.

The Association Between Clusterin and APOE Polymorphisms and Late-Onset Alzheimer Disease in a Turkish Cohort.

Alaylıoğlu M, Gezen-Ak D, Dursun E, Bilgiç B, Hanağası H, Ertan T, Gürvit H, Emre M, Eker E, Uysal Ö, Yılmazer S.

J Geriatr Psychiatry Neurol. 2016 Jul;29(4):221-6. doi: 10.1177/0891988716640373. Epub 2016 Apr 12.

PMID:
27076484
25.

Serotonin transporter promoter polymorphism is associated with executive function impairments in patients with obsessive compulsive disorder.

Tükel R, Alkaş E, Gürvit H, Aslantaş Ertekin B, Ertekin E, Baran B, Akça Kalem Ş, Saruhan Direskeneli G.

Clin Neuropsychol. 2016 May;30(4):536-46. doi: 10.1080/13854046.2016.1162329. Epub 2016 Mar 17.

PMID:
26986829
26.

Adult-onset phenylketonuria with rapidly progressive dementia and parkinsonism.

Tufekcioglu Z, Cakar A, Bilgic B, Hanagasi H, Gurvit H, Emre M.

Neurocase. 2016 Jun;22(3):273-5. doi: 10.1080/13554794.2016.1142567. Epub 2016 Mar 10.

PMID:
26962957
27.

Expression changes of genes associated with apoptosis and survival processes in Parkinson's disease.

Yalçınkaya N, Haytural H, Bilgiç B, Özdemir Ö, Hanağası H, Küçükali Cİ, Özbek Z, Akcan U, İdrisoğlu HA, Gürvit H, Tüzün E.

Neurosci Lett. 2016 Feb 26;615:72-7. doi: 10.1016/j.neulet.2016.01.029. Epub 2016 Jan 22.

PMID:
26806867
28.

The Central Biobank and Virtual Biobank of BIOMARKAPD: A Resource for Studies on Neurodegenerative Diseases.

Reijs BL, Teunissen CE, Goncharenko N, Betsou F, Blennow K, Baldeiras I, Brosseron F, Cavedo E, Fladby T, Froelich L, Gabryelewicz T, Gurvit H, Kapaki E, Koson P, Kulic L, Lehmann S, Lewczuk P, Lleó A, Maetzler W, de Mendonça A, Miller AM, Molinuevo JL, Mollenhauer B, Parnetti L, Rot U, Schneider A, Simonsen AH, Tagliavini F, Tsolaki M, Verbeek MM, Verhey FR, Zboch M, Winblad B, Scheltens P, Zetterberg H, Visser PJ.

Front Neurol. 2015 Oct 15;6:216. doi: 10.3389/fneur.2015.00216. eCollection 2015.

29.

Neuro-Behçet's Disease with Chorea.

Gür Özmen S, Hanağasi H, Gürvit H, Emre M, Akman Demir G.

Noro Psikiyatr Ars. 2015 Jun;52(2):200-201. doi: 10.5152/npa.2015.7316. Epub 2015 Jun 1.

30.

A new F-box protein 7 gene mutation causing typical Parkinson's disease.

Lohmann E, Coquel AS, Honoré A, Gurvit H, Hanagasi H, Emre M, Leutenegger AL, Drouet V, Sahbatou M, Guven G, Erginel-Unaltuna N, Deleuze JF, Lesage S, Brice A.

Mov Disord. 2015 Jul;30(8):1130-3. doi: 10.1002/mds.26266. Epub 2015 May 23.

PMID:
26010069
31.

The interleukin 1 alpha, interleukin 1 beta, interleukin 6 and alpha-2-macroglobulin serum levels in patients with early or late onset Alzheimer's disease, mild cognitive impairment or Parkinson's disease.

Dursun E, Gezen-Ak D, Hanağası H, Bilgiç B, Lohmann E, Ertan S, Atasoy İL, Alaylıoğlu M, Araz ÖS, Önal B, Gündüz A, Apaydın H, Kızıltan G, Ulutin T, Gürvit H, Yılmazer S.

J Neuroimmunol. 2015 Jun 15;283:50-7. doi: 10.1016/j.jneuroim.2015.04.014. Epub 2015 Apr 25.

PMID:
26004156
32.

Secondary paroxysmal kinesigenic dyskinesia associated with CLCN2 gene mutation.

Hanagasi HA, Bilgiç B, Abbink TE, Hanagasi F, Tüfekçioğlu Z, Gürvit H, Başak N, van der Knaap MS, Emre M.

Parkinsonism Relat Disord. 2015 May;21(5):544-6. doi: 10.1016/j.parkreldis.2015.02.013. Epub 2015 Feb 25. No abstract available.

PMID:
25745790
33.

The distinct genetic pattern of ALS in Turkey and novel mutations.

Özoğuz A, Uyan Ö, Birdal G, Iskender C, Kartal E, Lahut S, Ömür Ö, Agim ZS, Eken AG, Sen NE, Kavak P, Saygı C, Sapp PC, Keagle P, Parman Y, Tan E, Koç F, Deymeer F, Oflazer P, Hanağası H, Gürvit H, Bilgiç B, Durmuş H, Ertaş M, Kotan D, Akalın MA, Güllüoğlu H, Zarifoğlu M, Aysal F, Döşoğlu N, Bilguvar K, Günel M, Keskin Ö, Akgün T, Özçelik H, Landers JE, Brown RH, Başak AN.

Neurobiol Aging. 2015 Apr;36(4):1764.e9-1764.e18. doi: 10.1016/j.neurobiolaging.2014.12.032. Epub 2015 Jan 10.

34.

TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis.

Kleinberger G, Yamanishi Y, Suárez-Calvet M, Czirr E, Lohmann E, Cuyvers E, Struyfs H, Pettkus N, Wenninger-Weinzierl A, Mazaheri F, Tahirovic S, Lleó A, Alcolea D, Fortea J, Willem M, Lammich S, Molinuevo JL, Sánchez-Valle R, Antonell A, Ramirez A, Heneka MT, Sleegers K, van der Zee J, Martin JJ, Engelborghs S, Demirtas-Tatlidede A, Zetterberg H, Van Broeckhoven C, Gurvit H, Wyss-Coray T, Hardy J, Colonna M, Haass C.

Sci Transl Med. 2014 Jul 2;6(243):243ra86. doi: 10.1126/scitranslmed.3009093.

35.

Evaluation of incidence and clinical features of antibody-associated autoimmune encephalitis mimicking dementia.

Çoban A, Ismail Küçükali C, Bilgiç B, Yalçınkaya N, Haytural H, Ulusoy C, Turan S, Çakır S, Uçok A, Ünübol H, Hanagasi HA, Gürvit H, Tüzün E.

Behav Neurol. 2014;2014:935379. doi: 10.1155/2014/935379. Epub 2014 Mar 17.

36.

Supranuclear Gaze Abnormality in Sporadic-Creutzfeldt Jacob Disease.

Gür Özmen S, Gürvit H, Hanağasi HA, Alpsan Gökmen MH, Emre M.

Noro Psikiyatr Ars. 2014 Mar;51(1):91-92. doi: 10.4274/npa.y7341. Epub 2014 Mar 1. No abstract available.

37.

The Relationship of White Matter Hyperintensities with Depressive Symptoms and Daily Living Activities in Early-Stage Alzheimer's Disease Patients.

Bilgiç B, Bayram A, Hanağasi HA, Tümaç A, Uysal P, Şentürk G, Alpsan H, Lohmann E, Gürvit H, Emre M.

Noro Psikiyatr Ars. 2013 Dec;50(4):360-363. doi: 10.4274/Npa.y6603. Epub 2013 Dec 1.

38.

BDNF, TNFα, HSP90, CFH, and IL-10 serum levels in patients with early or late onset Alzheimer's disease or mild cognitive impairment.

Gezen-Ak D, Dursun E, Hanağası H, Bilgiç B, Lohman E, Araz ÖS, Atasoy IL, Alaylıoğlu M, Önal B, Gürvit H, Yılmazer S.

J Alzheimers Dis. 2013;37(1):185-95. doi: 10.3233/JAD-130497.

PMID:
23948885
39.

Novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family.

Guerreiro R, Bilgic B, Guven G, Brás J, Rohrer J, Lohmann E, Hanagasi H, Gurvit H, Emre M.

Neurobiol Aging. 2013 Dec;34(12):2890.e1-5. doi: 10.1016/j.neurobiolaging.2013.06.005. Epub 2013 Jul 17. Review.

40.

Non-convulsive status epilepticus associated with glutamic acid decarboxylase antibody.

Cikrikçili U, Ulusoy C, Turan S, Yildiz S, Bilgiç B, Hanagasi H, Baykan B, Tüzün E, Gürvit H.

Clin EEG Neurosci. 2013 Jul;44(3):232-6. doi: 10.1177/1550059412459330.

PMID:
23820312
41.

Reduced orexin-A levels in frontotemporal dementia: possible association with sleep disturbance.

Çoban A, Bilgiç B, Lohmann E, Küçükali Cİ, Benbir G, Karadeniz D, Hanagasi HA, Tüzün E, Gürvit H.

Am J Alzheimers Dis Other Demen. 2013 Sep;28(6):606-11. doi: 10.1177/1533317513494453. Epub 2013 Jun 27.

PMID:
23813609
42.

Akinetic mutism without a structural prefrontal lesion.

Demirtas-Tatlidede A, Bahar SZ, Gurvit H.

Cogn Behav Neurol. 2013 Jun;26(2):59-62. doi: 10.1097/WNN.0b013e31829bd4f5.

PMID:
23812168
43.

COMT Val158Met polymorphism and executive functions in obsessive-compulsive disorder.

Tükel R, Gürvit H, Öztürk N, Özata B, Ertekin BA, Ertekin E, Baran B, Kalem ŞA, Büyükgök D, Direskeneli GS.

J Neuropsychiatry Clin Neurosci. 2013 Summer;25(3):214-21. doi: 10.1176/appi.neuropsych.12040103.

PMID:
23774999
44.

Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement.

Guerreiro RJ, Lohmann E, Brás JM, Gibbs JR, Rohrer JD, Gurunlian N, Dursun B, Bilgic B, Hanagasi H, Gurvit H, Emre M, Singleton A, Hardy J.

JAMA Neurol. 2013 Jan;70(1):78-84. doi: 10.1001/jamaneurol.2013.579.

45.

A rare dementing disease: adult neuronal ceroid lipofuscinoses.

Babacan-Yildiz G, Hanagasi H, Gurvit H, Sirin G, Solakoglu S, Kucuk OS.

J Neuropsychiatry Clin Neurosci. 2012 Fall;24(4):493-8. doi: 10.1176/appi.neuropsych.11080182.

PMID:
23224458
46.

Vitamin D receptor gene haplotype is associated with late-onset Alzheimer's disease.

Gezen-Ak D, Dursun E, Bilgiç B, Hanağasi H, Ertan T, Gürvit H, Emre M, Eker E, Ulutin T, Uysal O, Yilmazer S.

Tohoku J Exp Med. 2012 Nov;228(3):189-96.

47.

Brain-derived neurotrophic factor gene Val66Met polymorphism and cognitive function in obsessive-compulsive disorder.

Tükel R, Gürvit H, Ozata B, Oztürk N, Ertekin BA, Ertekin E, Baran B, Kalem SA, Büyükgök D, Direskeneli GS.

Am J Med Genet B Neuropsychiatr Genet. 2012 Oct;159B(7):850-8. doi: 10.1002/ajmg.b.32092. Epub 2012 Aug 22.

PMID:
22911909
48.

EFNS-ENS Guidelines on the diagnosis and management of disorders associated with dementia.

Sorbi S, Hort J, Erkinjuntti T, Fladby T, Gainotti G, Gurvit H, Nacmias B, Pasquier F, Popescu BO, Rektorova I, Religa D, Rusina R, Rossor M, Schmidt R, Stefanova E, Warren JD, Scheltens P; EFNS Scientist Panel on Dementia and Cognitive Neurology.

Eur J Neurol. 2012 Sep;19(9):1159-79. doi: 10.1111/j.1468-1331.2012.03784.x.

PMID:
22891773
49.

Cognitive impairment in neuro-Behcet's disease and multiple sclerosis: a comparative study.

Gündüz T, Emir Ö, Kürtüncü M, Mutlu M, Tumaç A, Akca S, Coban O, Bahar S, Öktem-Tanör Ö, Tüzün E, Eraksoy M, Gürvit H, Akman-Demir G.

Int J Neurosci. 2012 Nov;122(11):650-6. doi: 10.3109/00207454.2012.704454. Epub 2012 Jul 12.

PMID:
22720779
50.

Dysexecutive syndrome: a specific pattern of cognitive impairment in systemic sclerosis.

Yilmaz N, Mollahasanoglu A, Gurvit H, Can M, Tuncer N, Inanc N, Yavuz S.

Cogn Behav Neurol. 2012 Jun;25(2):57-62. doi: 10.1097/WNN.0b013e3182593c75.

PMID:
22596111

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