Follow
Hakan Gurvit
Title
Cited by
Cited by
Year
TREM2 Variants in Alzheimer's Disease
R Guerreiro, A Wojtas, J Bras, M Carrasquillo, E Rogaeva, E Majounie, ...
New England Journal of Medicine 368 (2), 117-27, 2013
30392013
TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis
G Kleinberger, Y Yamanishi, M Suárez-Calvet, E Czirr, E Lohmann, ...
Science translational medicine 6 (243), 243ra86-243ra86, 2014
7222014
EFNS‐ENS Guidelines on the diagnosis and management of disorders associated with dementia
S Sorbi, J Hort, T Erkinjuntti, T Fladby, G Gainotti, H Gurvit, B Nacmias, ...
European Journal of Neurology 19 (9), 1159-1179, 2012
3962012
Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia–like syndrome without bone involvement
RJ Guerreiro, E Lohmann, JM Brás, JR Gibbs, JD Rohrer, N Gurunlian, ...
JAMA neurology 70 (1), 78-84, 2013
3852013
Comparative analysis of event-related potentials during Go/NoGo and CPT: decomposition of electrophysiological markers of response inhibition and sustained attention
E Kirmizi-Alsan, Z Bayraktaroglu, H Gurvit, YH Keskin, M Emre, ...
Brain research 1104 (1), 114-128, 2006
3042006
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 …
E Dursun, D Gezen-Ak, H Hanağası, B Bilgiç, E Lohmann, S Ertan, ...
Journal of neuroimmunology 283, 50-57, 2015
2592015
Neuropsychological patterns and language deficits in 20 consecutive cases of autopsy-confirmed Alzheimer's disease
BH Price, H Gurvit, S Weintraub, C Geula, E Leimkuhler, M Mesulam
Archives of neurology 50 (9), 931-937, 1993
2371993
The prevalence of dementia in an urban Turkish population
H Gurvit, M Emre, S Tinaz, B Bilgic, H Hanagasi, H Sahin, E Gurol, ...
American Journal of Alzheimer's Disease & Other Dementias® 23 (1), 67-76, 2008
2312008
Association between vitamin D receptor gene polymorphism and Alzheimer's disease
D Gezen-Ak, E Dursun, T Ertan, H Hanagasi, H Gürvit, M Emre, E Eker, ...
The Tohoku journal of experimental medicine 212 (3), 275-282, 2007
2272007
BDNF, TNFα, HSP90, CFH, and IL-10 serum levels in patients with early or late onset Alzheimer's disease or mild cognitive impairment
D Gezen-Ak, E Dursun, H Hanağası, B Bilgiç, E Lohman, ÖS Araz, ...
Journal of Alzheimer's Disease 37 (1), 185-195, 2013
2072013
Cognitive impairment in amyotrophic lateral sclerosis: evidence from neuropsychological investigation and event-related potentials
HA Hanagasi, IH Gurvit, N Ermutlu, G Kaptanoglu, S Karamursel, ...
Cognitive Brain Research 14 (2), 234-244, 2002
1982002
Seven-year follow-up of neurologic involvement in Behçet syndrome
G Akman-Demir, B Baykan-Kurt, P Serdaroǧlu, H Gürvit, S Yurdakul, ...
Archives of neurology 53 (7), 691-694, 1996
1471996
Neuropsychological function in obsessive-compulsive disorder
R Tükel, H Gürvit, BA Ertekin, S Oflaz, E Ertekin, B Baran, ŞA Kalem, ...
Comprehensive psychiatry 53 (2), 167-175, 2012
1422012
The effects of rasagiline on cognitive deficits in Parkinson's disease patients without dementia: a randomized, double‐blind, placebo‐controlled, multicenter study
HA Hanagasi, H Gurvit, P Unsalan, H Horozoglu, N Tuncer, A Feyzioglu, ...
Movement Disorders 26 (10), 1851-1858, 2011
1402011
Neuropsychological follow-up of 12 patients with neuro-Behçet disease
Ö Öktem-Tanör, B Baykan-Kurt, IH Gürvit, G Akman-Demir, P Serdaroğlu
Journal of neurology 246, 113-119, 1999
1401999
Pain is common in Parkinson's disease
HA Hanagasi, S Akat, H Gurvit, J Yazici, M Emre
Clinical neurology and neurosurgery 113 (1), 11-13, 2011
1352011
A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family
R Guerreiro, B Bilgic, G Guven, J Brás, J Rohrer, E Lohmann, H Hanagasi, ...
Neurobiology of aging 34 (12), 2890. e1-2890. e5, 2013
1252013
Vitamin D receptor gene haplotype is associated with late-onset Alzheimer's disease
D Gezen-Ak, E Dursun, B Bilgic, H Hanagasi, T Ertan, H Gürvit, M Emre, ...
The Tohoku journal of experimental medicine 228 (3), 189-196, 2012
1182012
Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease
RJ Guerreiro, E Lohmann, E Kinsella, JM Brás, N Luu, N Gurunlian, ...
Neurobiology of aging 33 (5), 1008. e17-1008. e23, 2012
1172012
The distinct genetic pattern of ALS in Turkey and novel mutations
A Özoğuz, Ö Uyan, G Birdal, C Iskender, E Kartal, S Lahut, Ö Ömür, ...
Neurobiology of aging 36 (4), 1764. e9-1764. e18, 2015
1052015
The system can't perform the operation now. Try again later.
Articles 1–20