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IDENTIFICATION OF MIRNA PROFILING IN EPICARDIAL ADIPOSE TISSUE OF PATIENTS WITH ATHEROSCLEROSIS Guclu-Geyik, F.; Koseoglu, P.; Ozsoy, S. D.; Cetin, H. K.; Balkanay, O. O.; Yildiz, C. E.; Goksedef, D.; Coban, N.; Komurcu-Bayrak, A. E.; Erginel-Unaltuna, N. 分享 收藏
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, Gamze; Bilgic, Briar; Tufekcioglu, Zeynep; Unaltuna, Nihan Erginel; Hanagasi, Hasmet; Gurvit, Hakan; Singleton, Andrew; Hardy, John; Emre, Murat; Gulec, Cagri; Bras, Jose; Guerreiro, Rita; Lohmann, Ebba 分享 收藏
HPCA Confirmed as a Genetic Cause of DYT2-Like Dystonia Phenotype Atasu, Burcu; Hanagasi, Hasmet; Bilgic, Basar; Pak, Meltem; Erginel-Unaltuna, Nihan; Hauser, Ann-Kathrin; Guven, Gamze; Simon-Sanchez, Javier; Heutink, Peter; Gasser, Thomas; Lohmann, Ebba 分享 收藏
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Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey Kessler, Christoph; Atasu, Burcu; Hanagasi, Hasmet; Simon-Sanchez, Javier; Hauser, Ann-Kathrin; Pak, Meltem; Bilgic, Basar; Erginel-Unaltuna, Nihan; Gurvit, Hakan; Gasser, Thomas; Lohmann, Ebba 分享 收藏
Mutations in TYROBP are not a common cause of dementia in a Turkish cohort Darwent, Lee; Carmona, Susana; Lohmann, Ebba; Guven, Gamze; Kun-Rodrigues, Celia; Bilgic, Basar; Hanagasi, Hasmet; Gurvit, Hakan; Erginel-Unaltuna, Nihan; Pak, Meltem; Hardy, John; Singleton, Andrew; Bras, Jose; Guerreiro, Rita 分享 收藏
THE ROLE OF CYP19A1, ESR1 AND MIF GENES POLYMORPHIMS ON THE ANGIOGRAPHIC SEVERITY AND THE EXTENT OF ATHEROSCLEROTIC CORONARY ARTERY DISEASE Coban, Neslihan; Kaya, Aysem; Erkan, Aycan Fahri; Guclu-Geyik, Filiz; Ekici, Berkay; Ademoglu, Evin; Diker, Irem Yagmur; Can, Gunay; Erginel-Unaltuna, Nihan 分享 收藏
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Loss of VPS1 3C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy Lesage, Suzanne; Drouet, Valerie; Majounie, Elisa; Deramecourt, Vincent; Jacoupy, Maxime; Nicolas, Aude; Cormier-Dequaire, Florence; Hassoun, Sidi Mohamed; Pujol, Claire; Ciura, Sorana; Erpapazoglou, Zoi; Usenko, Tatiana; Maurage, Claude-Alain; Sahbatou, Mourad; Liebau, Stefan; Ding, Jinhui; Bilgic, Basar; Emre, Murat; Erginel-Unaltuna, Nihan; Guven, Gamze; Tison, Francois; Tranchant, Christine; Vidailhet, Marie; Corvol, Jean-Christophe; Krack, Paul; Leutenegger, Anne-Louise; Nalls, Michael A.; Hernandez, Dena G.; Heutink, Peter; Gibbs, J. Raphael; Hardy, John; Wood, Nicholas W.; Gasser, Thomas; Durr, Alexandra; Deleuze, Jean-Francois; Tazir, Meriem; Destee, Alain; Lohmann, Ebba; Kabashi, Edor; Singleton, Andrew; Corti, Olga; Brice, Alexis 分享 收藏
A new F-box protein 7 gene mutation causing typical Parkinson's disease Lohmann, Ebba; Coquel, Anne-Sophie; Honore, Aurelie; Gurvit, Hakan; Hanagasi, Hasmet; Emre, Murat; Leutenegger, Anne L.; Drouet, Valerie; Sahbatou, Mourad; Guven, Gamze; Erginel-Unaltuna, Nihan; Deleuze, Jean-Francois; Lesage, Suzanne; Brice, Alexis 分享 收藏
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