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Atay Vural
Atay Vural
Koç University & Koç University Research Center for Translational Medicine
在 ku.edu.tr 的电子邮件经过验证
标题
引用次数
引用次数
年份
Pericyte contraction induced by oxidative-nitrative stress impairs capillary reflow despite successful opening of an occluded cerebral artery
M Yemisci, Y Gursoy-Ozdemir, A Vural, A Can, K Topalkara, T Dalkara
Nature medicine 15 (9), 1031-1037, 2009
8322009
A nanomedicine transports a peptide caspase-3 inhibitor across the blood–brain barrier and provides neuroprotection
H Karatas, Y Aktas, Y Gursoy-Ozdemir, E Bodur, M Yemisci, S Caban, ...
Journal of Neuroscience 29 (44), 13761-13769, 2009
2382009
Autoantibodies against the node of Ranvier in seropositive chronic inflammatory demyelinating polyneuropathy: diagnostic, pathogenic, and therapeutic relevance
A Vural, K Doppler, E Meinl
Frontiers in immunology 9, 1029, 2018
1212018
The detrimental effect of aging on leptomeningeal collaterals in ischemic stroke
EM Arsava, A Vural, E Akpinar, R Gocmen, S Akcalar, KK Oguz, ...
Journal of Stroke and Cerebrovascular Diseases 23 (3), 421-426, 2014
922014
The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public
RAA van der Spek, W van Rheenen, SL Pulit, KP Kenna, ...
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 20 (5-6), 432-440, 2019
712019
Anti–pan-neurofascin IgG3 as a marker of fulminant autoimmune neuropathy
H Stengel, A Vural, AM Brunder, A Heinius, L Appeltshauser, B Fiebig, ...
Neurology: Neuroimmunology & Neuroinflammation 6 (5), e603, 2019
682019
Identification of circulating MOG-specific B cells in patients with MOG antibodies
S Winklmeier, M Schlüter, M Spadaro, FS Thaler, A Vural, R Gerhards, ...
Neurology: Neuroimmunology & Neuroinflammation 6 (6), 625, 2019
512019
Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis
A Al Khleifat, A Iacoangeli, JJFA Van Vugt, H Bowles, M Moisse, ...
NPJ genomic medicine 7 (1), 8, 2022
362022
Association of pyrin mutations and autoinflammation with complex phenotype hidradenitis suppurativa: a case–control study
S Vural, M Gündoğdu, E Gökpınar İli, CD Durmaz, A Vural, ...
British Journal of Dermatology 180 (6), 1459-1467, 2019
352019
Features of MOG required for recognition by patients with MOG antibody-associated disorders
C Macrini, R Gerhards, S Winklmeier, L Bergmann, S Mader, M Spadaro, ...
Brain 144 (8), 2375-2389, 2021
332021
Cerebellar cognitive-affective syndrome preceding ataxia associated with complex extrapyramidal features in a Turkish SCA48 family
R Palvadeau, ZE Kaya-Güleç, G Şimşir, A Vural, Ö Öztop-Çakmak, ...
neurogenetics 21, 51-58, 2020
262020
Antiepileptic treatment for anti‐NMDA receptor encephalitis: the need for video‐EEG monitoring
N Dericioglu, A Vural, P Acar, N Agayeva, V Ismailova, A Kurne, E Saka, ...
Epileptic disorders 15 (2), 166-170, 2013
262013
Poloxamer-188 and citicoline provide neuronal membrane integrity and protect membrane stability in cortical spreading depression
T Yıldırım, A Eylen, S Lule, SE Erdener, A Vural, H Karatas, MF Ozveren, ...
International Journal of Neuroscience 125 (12), 941-946, 2015
252015
Retinal degeneration is associated with brain volume reduction and prognosis in radiologically isolated syndrome
A Vural, S Okar, A Kurne, G Sayat-Gürel, NP Acar, E Karabulut, KK Oğuz, ...
Multiple Sclerosis Journal 26 (1), 38-47, 2020
232020
Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families
C Kocoglu, A Gundogdu, G Kocaman, P Kahraman-Koytak, K Uluc, ...
Neurology: Genetics 4 (1), e218, 2018
232018
Central neurogenic hyperventilation in anti-NMDA receptor encephalitis
A Vural, EM Arsava, N Dericioglu, MA Topcuoglu
Internal Medicine 51 (19), 2789-2792, 2012
232012
The glycosylation site of myelin oligodendrocyte glycoprotein affects autoantibody recognition in a large proportion of patients
I Marti Fernandez, C Macrini, M Krumbholz, PJ Hensbergen, ...
Frontiers in immunology 10, 1189, 2019
222019
The influence of N-desmethylclozapine and clozapine on recognition memory and BDNF expression in hippocampus
A Ertuğrul, H Özdemir, A Vural, T Dalkara, HY Meltzer, E Saka
Brain research bulletin 84 (2), 144-150, 2011
172011
A practical approach to ichthyoses with systemic manifestations
S Saral, A Vural, A Wollenberg, T Ruzicka
Clinical Genetics 91 (6), 799-812, 2017
152017
A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID
F Akçimen, A Vural, H Durmuş, A Çakar, H Houlden, YG Parman, ...
Journal of human genetics 64 (11), 1141-1144, 2019
142019
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