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Clinical and molecular genetic findings of hereditary Parkinson's patients from Turkey Emekli, Inci; Tepgec, Fatih; Samanci, Bedia; Toksoy, Guven; Kina, Gizem Hasanogullari; Tufekcioglu, Zeynep; Basaran, Seher; Bilgic, Basar; Gurvit, I. Hakan; Emre, Murat; Uyguner, Zehra Oya; Hanagasi, Hasmet A. 分享 收藏
Frequency of frontotemporal dementia-related gene variants in Turkey 土耳其额颞叶痴呆相关基因变异的频率 Artan, Sevilhan; Gokalp, Ebru Erzurumluoglu; Samanci, Bedia; Adapinar, Demet Ozbabalik; Bas, Hasan; Tepgec, Fatih; Ekenel, Emilia Qomi; Cilingir, Oguz; Bilgic, Basar; Gurvit, Hakan; Hanagasi, Hasmet Ayhan; Kocagil, Sinem; Aras, Beyhan Durak; Uyguner, Oya; Emre, Murat 分享 收藏
A new alpha-synuclein missense variant (Thr72Met) in two Turkish families with Parkinson's disease 在两个患有帕金森氏病的土耳其家庭中，一种新的 α-突触核蛋白错义变体 (Thr72Met) Fevga, Christina; Park, Yangshin; Lohmann, Ebba; Kievit, Anneke J.; Breedveld, Guido J.; Ferraro, Federico; de Boer, Leon; van Minkelen, Rick; Hanagasi, Hasmet; Boon, Agnita; Wang, Wei; Petsko, Gregory A.; Hoang, Quyen Q.; Emre, Murat; Bonifati, Vincenzo 分享 收藏
Functional Connectivity Analysis in Heterozygous Glucocerebrosidase Mutation Carriers Sezgin, Mine; Kicik, Ani; Bilgic, Basar; Kurt, Elif; Bayram, Ali; Hanagasi, Hasmet; Tepgec, Fatih; Toksoy, Guven; Gurvit, Hakan; Uyguner, Oya; Gokcay, Gulden; Demiralp, Tamer; Emre, Murat 分享 收藏
Characterization of Recessive Parkinson Disease in a Large Multicenter Study Lesage, Suzanne; Lunati, Ariane; Houot, Marion; Ben Romdhan, Sawssan; Clot, Fabienne; Tesson, Christelle; Mangone, Graziella; Le Toullec, Benjamin; Courtin, Thomas; Larcher, Kathy; Benmahdjoub, Mustapha; Arezki, Mohamed; Bouhouche, Ahmed; Anheim, Mathieu; Roze, Emmanuel; Viallet, Francois; Tison, Francois; Broussolle, Emmanuel; Emre, Murat; Hanagasi, Hasmet; Bilgic, Basar; Tazir, Meriem; Ben Djebara, Mouna; Gouider, Riadh; Tranchant, Christine; Vidailhet, Marie; Le Guern, Eric; Corti, Olga; Mhiri, Chokri; Lohmann, Ebba; Singleton, Andrew; Corvol, Jean-Christophe; Brice, Alexis 分享 收藏
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Research criteria for the diagnosis of prodromal dementia with Lewy bodies McKeith, Ian G.; Ferman, Tanis J.; Thomas, Alan J.; Blanc, Frederic; Boeve, Bradley F.; Fujishiro, Hiroshige; Kantarci, Kejal; Muscio, Cristina; O'Brien, John T.; Postuma, Ronald B.; Aarsland, Dag; Ballard, Clive; Bonanni, Laura; Donaghy, Paul; Emre, Murat; Galvin, James E.; Galasko, Douglas; Goldman, Jennifer G.; Gomperts, Stephen N.; Honig, Lawrence S.; Ikeda, Manabu; Leverenz, James B.; Lewis, Simon J. G.; Marder, Karen S.; Masellis, Mario; Salmon, David P.; Taylor, John Paul; Tsuang, Debby W.; Walker, Zuzana; Tiraboschi, Pietro 分享 收藏
Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family Kuipers, Demy J. S.; Tufekcioglu, Zeynep; Bilgic, Basar; Olgiati, Simone; Dremmen, Marjolein H. G.; van IJcken, Wilfred F. J.; Breedveld, Guido J.; Mancini, Grazia M. S.; Hanagasi, Hasmet A.; Emre, Murat; Bonifati, Vincenzo 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
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The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN Olgiati, Simone; Dogu, Okan; Tufekcioglu, Zeynep; Diler, Yunus; Saka, Esen; Gultekin, Murat; Kaleagasi, Hakan; Kuipers, Demy; Graafland, Josja; Breedveld, Guido J.; Quadri, Marialuisa; Surmeli, Reyhan; Sunter, Gulin; Dogan, Tugrul; Yalcin, Aye Destina; Bilgic, Basar; Elibol, Bulent; Emre, Murat; Hanagasi, Hasmet A.; Bonifati, Vincenzo 分享 收藏
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A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family Hanagasi, Hasmet A.; Giri, Anamika; Kartal, Ece; Guven, Gamze; Bilgic, Basar; Hauser, Ann-Kathrin; Emre, Murat; Heutink, Peter; Basak, Nazh; Gasser, Thomas; Simon-Sanchez, Javier; Lohmann, Ebba 分享 收藏
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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