Dopamine Agonist-Associated Hiccup in Parkinson’s Disease: A Case Report

por EMEKLİ, Ahmed Serkan, HANAGASI, Hasmet A.
Publicado 2019

Neuroimaging, Biomarkers, and Management of Dementia with Lewy Bodies

por Hanagasi, Hasmet A., Bilgiç, Başar, Emre, Murat
Publicado 2013

Anticholinergic Burden, Polypharmacy, and Cognition in Parkinson's Disease Patients with Mild Cognitive Impairment: A Cross-Sectional Observational Study

por Sumbul-Sekerci, Betul, Bilgic, Basar, Pasin, Ozge, Emre, Murat, Hanagasi, Hasmet A.
Publicado 2023

A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family()

por Guerreiro, Rita, Bilgic, Basar, Guven, Gamze, Brás, José, Rohrer, Jonathan, Lohmann, Ebba, Hanagasi, Hasmet, Gurvit, Hakan, Emre, Murat
Publicado 2013

Inflammation and regulatory T cell genes are differentially expressed in peripheral blood mononuclear cells of Parkinson’s disease patients

por Karaaslan, Zerrin, Kahraman, Özlem Timirci, Şanlı, Elif, Ergen, Hayriye Arzu, Ulusoy, Canan, Bilgiç, Başar, Yılmaz, Vuslat, Tüzün, Erdem, Hanağası, Haşmet Ayhan, Küçükali, Cem İsmail
Publicado 2021

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

por Giri, Anamika, Guven, Gamze, Hanagasi, Hasmet, Hauser, Ann-Kathrin, Erginul-Unaltuna, Nihan, Bilgic, Basar, Gurvit, Hakan, Heutink, Peter, Gasser, Thomas, Lohmann, Ebba, Simón-Sánchez, Javier
Publicado 2016

A comprehensive analysis of copy number variation in a Turkish dementia cohort

por Dehghani, Nadia, Guven, Gamze, Kun-Rodrigues, Celia, Gouveia, Catarina, Foster, Kalina, Hanagasi, Hasmet, Lohmann, Ebba, Samanci, Bedia, Gurvit, Hakan, Bilgic, Basar, Bras, Jose, Guerreiro, Rita
Publicado 2021

Evaluation of Incidence and Clinical Features of Antibody-Associated Autoimmune Encephalitis Mimicking Dementia

por Çoban, Arzu, İsmail Küçükali, Cem, Bilgiç, Başar, Yalçınkaya, Nazlı, Haytural, Hazal, Ulusoy, Canan, Turan, Selin, Çakır, Sibel, Üçok, Alp, Ünübol, Hüseyin, Hanagasi, Hasmet A., Gürvit, Hakan, Tüzün, Erdem
Publicado 2014

Genotype–Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature review

por Atasu, Burcu, Acarlı, Ayse Nur Ozdag, Bilgic, Basar, Baykan, Betül, Demir, Erol, Ozluk, Yasemin, Turkmen, Aydin, Hauser, Ann-Kathrin, Guven, Gamze, Hanagasi, Hasmet, Gurvit, Hakan, Emre, Murat, Gasser, Thomas, Lohmann, Ebba
Publicado 2022

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

por Guven, Gamze, Lohmann, Ebba, Bras, Jose, Gibbs, J. Raphael, Gurvit, Hakan, Bilgic, Basar, Hanagasi, Hasmet, Rizzu, Patrizia, Heutink, Peter, Emre, Murat, Erginel-Unaltuna, Nihan, Just, Walter, Hardy, John, Singleton, Andrew, Guerreiro, Rita
Publicado 2016

Multicenter study of levodopa carbidopa intestinal gel in Parkinson’s disease: the Turkish experience

por GÜLTEKİN, Murat, ULUKAN, Çağrı, TEZCAN, Sabiha, DOĞU, Okan, HANAĞASI, Haşmet, BİLGİÇ, Başar, BORA TOKÇAER, Ayşe, ÇAKMUR, Raif, ELİBOL, Bülent, MİRZA, Meral, İNCE GÜNAL, Dilek, ERER ÖZBEK, Çiğdem Sevda, KENANGİL, Gülay, YILMAZ KÜSBECİ, Özge, AKBOSTANCI, Muhittin Cenk
Publicado 2020

A new alpha-synuclein missense variant (Thr72Met) in two Turkish families with Parkinson’s disease

por 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
Publicado 2021

Turkish inappropriate medication use in the elderly (TIME) criteria to improve prescribing in older adults: TIME-to-STOP/TIME-to-START

por Bahat, Gulistan, Ilhan, Birkan, Erdogan, Tugba, Halil, Meltem, Savas, Sumru, Ulger, Zekeriya, Akyuz, Filiz, Bilge, Ahmet Kaya, Cakir, Sibel, Demirkan, Kutay, Erelel, Mustafa, Guler, Kerim, Hanagasi, Hasmet, Izgi, Belgin, Kadioglu, Ates, Karan, Ayse, Kulaksizoglu, Isin Baral, Mert, Ali, Ozturk, Savas, Satman, Ilhan, Sever, Mehmet Sukru, Tukek, Tufan, Uresin, Yagiz, Yalcin, Onay, Yesilot, Nilufer, Oren, Meryem Merve, Karan, Mehmet Akif
Publicado 2020

PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice

por Messerschmidt, Clemens, Foddis, Marco, Blumenau, Sonja, Müller, Susanne, Bentele, Kajetan, Holtgrewe, Manuel, Kun-Rodrigues, Celia, Alonso, Isabel, do Carmo Macario, Maria, Morgadinho, Ana Sofia, Velon, Ana Graça, Santo, Gustavo, Santana, Isabel, Mönkäre, Saana, Kuuluvainen, Liina, Schleutker, Johanna, Pöyhönen, Minna, Myllykangas, Liisa, Senatore, Assunta, Berchtold, Daniel, Winek, Katarzyna, Meisel, Andreas, Pavlovic, Aleksandra, Kostic, Vladimir, Dobricic, Valerija, Lohmann, Ebba, Hanagasi, Hasmet, Guven, Gamze, Bilgic, Basar, Bras, Jose, Guerreiro, Rita, Beule, Dieter, Dirnagl, Ulrich, Sassi, Celeste
Publicado 2021

The ARCA Registry: A Collaborative Global Platform for Advancing Trial Readiness in Autosomal Recessive Cerebellar Ataxias

por Traschütz, Andreas, Reich, Selina, Adarmes, Astrid D., Anheim, Mathieu, Ashrafi, Mahmoud Reza, Baets, Jonathan, Basak, A. Nazli, Bertini, Enrico, Brais, Bernard, Gagnon, Cynthia, Gburek-Augustat, Janina, Hanagasi, Hasmet A., Heinzmann, Anna, Horvath, Rita, de Jonghe, Peter, Kamm, Christoph, Klivenyi, Peter, Klopstock, Thomas, Minnerop, Martina, Münchau, Alexander, Renaud, Mathilde, Roxburgh, Richard H., Santorelli, Filippo M., Schirinzi, Tommaso, Sival, Deborah A., Timmann, Dagmar, Vielhaber, Stefan, Wallner, Michael, van de Warrenburg, Bart P., Zanni, Ginevra, Zuchner, Stephan, Klockgether, Thomas, Schüle, Rebecca, Schöls, Ludger, Synofzik, Matthis
Publicado 2021

Clinico‐Genetic, Imaging and Molecular Delineation of COQ8A ‐Ataxia: A Multicenter Study of 59 Patients

por Traschütz, Andreas, Schirinzi, Tommaso, Laugwitz, Lucia, Murray, Nathan H., Bingman, Craig A., Reich, Selina, Kern, Jan, Heinzmann, Anna, Vasco, Gessica, Bertini, Enrico, Zanni, Ginevra, Durr, Alexandra, Magri, Stefania, Taroni, Franco, Malandrini, Alessandro, Baets, Jonathan, de Jonghe, Peter, de Ridder, Willem, Bereau, Matthieu, Demuth, Stephanie, Ganos, Christos, Basak, A. Nazli, Hanagasi, Hasmet, Kurul, Semra Hiz, Bender, Benjamin, Schöls, Ludger, Grasshoff, Ute, Klopstock, Thomas, Horvath, Rita, van de Warrenburg, Bart, Burglen, Lydie, Rougeot, Christelle, Ewenczyk, Claire, Koenig, Michel, Santorelli, Filippo M., Anheim, Mathieu, Munhoz, Renato P., Haack, Tobias, Distelmaier, Felix, Pagliarini, David J., Puccio, Hélène, Synofzik, Matthis
Publicado 2020

Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Projec...

por Vollstedt, Eva-Juliane, Madoev, Harutyun, Aasly, Anna, Ahmad-Annuar, Azlina, Al-Mubarak, Bashayer, Alcalay, Roy N., Alvarez, Victoria, Amorin, Ignacio, Annesi, Grazia, Arkadir, David, Bardien, Soraya, Barker, Roger A., Barkhuizen, Melinda, Basak, A. Nazli, Bonifati, Vincenzo, Boon, Agnita, Brighina, Laura, Brockmann, Kathrin, Carmine Belin, Andrea, Carr, Jonathan, Clarimon, Jordi, Cornejo-Olivas, Mario, Correia Guedes, Leonor, Corvol, Jean-Christophe, Crosiers, David, Damásio, Joana, Das, Parimal, de Carvalho Aguiar, Patricia, De Rosa, Anna, Dorszewska, Jolanta, Ertan, Sibel, Ferese, Rosangela, Ferreira, Joaquim, Gatto, Emilia, Genç, Gençer, Giladi, Nir, Gómez-Garre, Pilar, Hanagasi, Hasmet, Hattori, Nobutaka, Hentati, Faycal, Hoffman-Zacharska, Dorota, Illarioshkin, Sergey N., Jankovic, Joseph, Jesús, Silvia, Kaasinen, Valtteri, Kievit, Anneke, Klivenyi, Peter, Kostic, Vladimir, Koziorowski, Dariusz, Kühn, Andrea A., Lang, Anthony E., Lim, Shen-Yang, Lin, Chin-Hsien, Lohmann, Katja, Markovic, Vladana, Martikainen, Mika Henrik, Mellick, George, Merello, Marcelo, Milanowski, Lukasz, Mir, Pablo, Öztop-Çakmak, Özgür, Pimentel, Márcia Mattos Gonçalves, Pulkes, Teeratorn, Puschmann, Andreas, Rogaeva, Ekaterina, Sammler, Esther M., Skaalum Petersen, Maria, Skorvanek, Matej, Spitz, Mariana, Suchowersky, Oksana, Tan, Ai Huey, Termsarasab, Pichet, Thaler, Avner, Tumas, Vitor, Valente, Enza Maria, van de Warrenburg, Bart, Williams-Gray, Caroline H., Wu, Ruey-Mei, Zhang, Baorong, Zimprich, Alexander, Solle, Justin, Padmanabhan, Shalini, Klein, Christine
Publicado 2023