Resultats de la cerca - Haşmet Hanağası

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  1. 1
    A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family

    A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family per Rita Guerreiro, Başar Bılgıç, Gamze Güven, José Brás, Jonathan D. Rohrer, Ebba Lohmann, Haşmet Hanağası, Hakan Gürvıt, Murat Emre

    Publicat 2013
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  2. 2
    Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights

    Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights per Burcu Atasu, Javier Simón‐Sánchez, Haşmet Hanağası, Başar Bılgıç, Ann‐Kathrin Hauser, Gamze Güven, Peter Heutink, Thomas Gasser, Ebba Lohmann

    Publicat 2024
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  3. 3
    Association between Vitamin D Receptor Gene Polymorphism and Alzheimer's Disease

    Association between Vitamin D Receptor Gene Polymorphism and Alzheimer's Disease per Duygu Gezen‐Ak, Erdinç Dursun, Turan Ertan, Haşmet Hanağası, Hakan Gürvıt, Murat Emre, Engin Eker, Melek Öztürk, Funda Engin, Selma Yılmazer

    Publicat 2007
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  4. 4
    Vitamin D Receptor Gene Haplotype Is Associated with Late-Onset Alzheimer's Disease

    Vitamin D Receptor Gene Haplotype Is Associated with Late-Onset Alzheimer's Disease per Duygu Gezen‐Ak, Erdinç Dursun, Başar Bılgıç, Haşmet Hanağası, Turan Ertan, Hakan Gürvıt, Murat Emre, Engin Eker, Turgut Ulutin, Ömer Uysal, Selma Yılmazer

    Publicat 2012
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  5. 5
    Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement

    Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement per Rita Guerreiro, Ebba Lohmann, José Brás, J. Raphael Gibbs, Jonathan D. Rohrer, Nicole Gurunlian, Burcu Dursun, Başar Bılgıç, Haşmet Hanağası, Hakan Gürvıt, Murat Emre, Andrew Singleton, John Hardy

    Publicat 2013
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  6. 6
    Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease

    Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease per Rita Guerreiro, Ebba Lohmann, Emma Kinsella, José Brás, Nga Luu, Nicole Gurunlian, Burcu Dursun, Başar Bılgıç, Isabel Santana, Haşmet Hanağası, Hakan Gürvıt, J. Raphael Gibbs, Catarina R. Oliveira, Murat Emre, Andrew Singleton

    Publicat 2011
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  7. 7
    Early‐onset L‐dopa‐responsive parkinsonism with pyramidal signs due to <i>ATP13A2, PLA2G6, FBXO7</i> and <i>spatacsin</i> mutations

    Early‐onset L‐dopa‐responsive parkinsonism with pyramidal signs due to <i>ATP13A2, PLA2G6, FBXO7</i> and <i>spatacsin</i> mutations per Coro Paisán‐Ruíz, Rocio Guevara, Monica Federoff, Haşmet Hanağası, Farzad Sina, Elahe Elahi, Susanne A. Schneider, Petra Schwingenschuh, Nin Bajaj, Murat Emre, Andrew Singleton, John Hardy, Kailash P. Bhatia, Sebastian Brandner, Andrew J. Lees, Henry Houlden

    Publicat 2010
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  8. 8
    Analysis of Mutations in <i>AARS2</i> in a Series of <i>CSF1R</i>-Negative Patients With Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia

    Analysis of Mutations in <i>AARS2</i> in a Series of <i>CSF1R</i>-Negative Patients With Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia per David S. Lynch, Wei Jia Zhang, Rahul Lakshmanan, Justin Kinsella, Güneş Altıokka Uzun, Merih Karbay, Zeynep Tüfekçıoğlu, Haşmet Hanağası, Georgina Burke, Nicola Foulds, Simon Hammans, Anupam Bhattacharjee, Heather Wilson, Matthew Adams, Mark Walker, James A. R. Nicoll, Jeremy Chataway, Nick C. Fox, Indran Davagnanam, Rahul Phadke, Henry Houlden

    Publicat 2016
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  9. 9
    Quantitative Gait and Balance Outcomes for Ataxia Trials: Consensus Recommendations by the Ataxia Global Initiative Working Group on Digital-Motor Biomarkers

    Quantitative Gait and Balance Outcomes for Ataxia Trials: Consensus Recommendations by the Ataxia Global Initiative Working Group on Digital-Motor Biomarkers per Winfried Ilg, Sarah Milne, Tanja Schmitz‐Hübsch, Lisa Alcock, Lukas Beichert, Enrico Bertini, Norlinah Mohamed Ibrahim, Helen Dawes, Christopher M. Gómez, Haşmet Hanağası, Kirsi M. Kinnunen, Martina Minnerop, Andrea H. Németh, Jane Newman, Yi Shiau Ng, Clara Rentz, Bedia Samancı, Vrutangkumar V. Shah, Susanna Summa, Gessica Vasco, James McNames, Fay B. Horak

    Publicat 2023
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  10. 10
    Turkish inappropriate medication use in the elderly (TIME) criteria to improve prescribing in older adults: TIME-to-STOP/TIME-to-START

    Turkish inappropriate medication use in the elderly (TIME) criteria to improve prescribing in older adults: TIME-to-STOP/TIME-to-START per Gülistan Bahat, Birkan İlhan, Tuğba Erdoğan, Meltem Halil, Sumru Savaş, Zekeriya Ülger, Filiz Akyüz, Ahmet Kaya Bilge, Sibel Çakır, Kutay Demirkan, Mustafa Erelel, Kerim Güler, Haşmet Hanağası, Belgin İzgi, Ateş Kadıoğlu, Ayşe Karan, Işın Baral Kulaksızoğlu, Ali Mert, Savaş Öztürk, İlhan Satman, Mehmet Şükrü Sever, Tufan Tükek, Yağız Üresin, Önay Yalçın, Nilüfer Yeşilot, Meryem Merve Ören, Mehmet Akif Karan

    Publicat 2020
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  11. 11
    Responsiveness of the Scale for the Assessment and Rating of Ataxia and Natural History in 884 Recessive and Early Onset Ataxia Patients

    Responsiveness of the Scale for the Assessment and Rating of Ataxia and Natural History in 884 Recessive and Early Onset Ataxia Patients per Andreas Traschütz, Astrid Adarmes‐Gómez, Mathieu Anheim, Jonathan Baets, Bernard Brais, Cynthia Gagnon, Janina Gburek‐Augustat, Sarah Doss, Haşmet Hanağası, Christoph Kamm, Péter Klivényi, Thomas Klockgether, Thomas Klopstock, Martina Minnerop, Alexander Münchau, M. Renaud, Filippo M. Santorelli, Lüdger Schöls, Andreas Thieme, Stefan Vielhaber, Bart P.C. van de Warrenburg, Ginevra Zanni, R.-D Hilgers, Matthis Synofzik

    Publicat 2023
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  12. 12
    Characterization of Recessive Parkinson Disease in a Large Multicenter Study

    Characterization of Recessive Parkinson Disease in a Large Multicenter Study per Suzanne Lesage, Ariane Lunati, Marion Houot, Sawssan Ben Romdhan, Fabienne Clot, Christelle Tesson, Graziella Mangone, Benjamin Le Toullec, Thomas Courtin, Kathy Larcher, Mustapha Benmahdjoub, Mohamed Arezki, Ahmed Bouhouche, Mathieu Anheim, Emmanuel Roze, François Viallet, François Tison, Emmanuel Broussolle, Murat Emre, Haşmet Hanağası, Başar Bılgıç, Mériem Tazir, Mouna Ben Djebara, Riadh Gouider, Christine Tranchant, Marie Vidailhet, E. Le Guern, Olga Corti, Chokri Mhiri, Ebba Lohmann, Andrew Singleton, Jean‐Christophe Corvol, Alexis Brice

    Publicat 2020
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  13. 13
    The distinct genetic pattern of ALS in Turkey and novel mutations

    The distinct genetic pattern of ALS in Turkey and novel mutations per Aslıhan Özoğuz, Özgün Uyan, Güneş Birdal, Ceren Iskender, Ece Kartal, Suna Lahut, Özgür Ömür, Zeynep Sena Ağım, Aslı Gündoğdu Eken, Nesli Ece Şen, Pınar Kavak, Ceren Saygı, Peter C. Sapp, Pamela Keagle, Yeşim Parman, Ersin Tan, Filiz Koç, Feza Deymeer, Piraye Oflazer, Haşmet Hanağası, Hakan Gürvıt, Başar Bılgıç, Hacer Durmuş, Mustafa Ertaş, Dilcan Kotan, Mehmet Ali Akalın, Halil Güllüoğlu, Mehmet Zarifoğlu, Fikret Aysal, Nilgün Döşoğlu, Kaya Bilgüvar, Murat Günel, Özlem Keskin, Tahsin Akgün, Hilmi Özçelik, John E. Landers, Robert H. Brown, A. Nazlı Başak

    Publicat 2015
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  14. 14
    Clinico‐Genetic, Imaging and Molecular Delineation of <scp><i>COQ8A</i></scp>‐Ataxia: A Multicenter Study of 59 Patients

    Clinico‐Genetic, Imaging and Molecular Delineation of <scp><i>COQ8A</i></scp>‐Ataxia: A Multicenter Study of 59 Patients per Andreas Traschütz, Tommaso Schirinzi, Lucia Laugwitz, Nathan H. Murray, C.A. Bingman, Selina Reich, Jan Marco Kern, Anna Heinzmann, Gessica Vasco, Enrico Bertini, Ginevra Zanni, Alexandra Dürr, Stefania Magri, Franco Taroni, Alessandro Malandrini, Jonathan Baets, Peter De Jonghe, Willem De Ridder, Matthieu Béreau, Stephanie Demuth, Christos Ganos, A. Nazlı Başak, Haşmet Hanağası, Semra Hız Kurul, Benjamin Bender, Lüdger Schöls, Ute Grasshoff, Thomas Klopstock, Rita Horváth, Bart van de Warrenburg, Lydie Bürglen, Christelle Rougeot, Claire Ewenczyk, Michel Kœnig, Filippo M. Santorelli, Mathieu Anheim, Renato P. Munhoz, Tobias B. Haack, Felix Distelmaier, David J. Pagliarini, Hélène Puccio, Matthis Synofzik

    Publicat 2020
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  15. 15
    Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Project

    Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Projec... per Eva‐Juliane Vollstedt, Harutyun Madoev, Anna Aasly, Azlina Ahmad‐Annuar, Bashayer Al‐Mubarak, Roy N. Alcalay, Victoria Álvarez, Ignacio Amorín, Grazia Annesi, David Arkadir, Soraya Bardien, Roger A. Barker, Melinda Barkhuizen, A. Nazlı Başak, Vincenzo Bonifati, Agnita J.W. Boon, Laura Brighina, Kathrin Brockmann, Andrea Carmine Belin, Jonathan Carr, Jordi Clarimón, Mario Cornejo‐Olivas, Leonor Correia Guedes, Jean‐Christophe Corvol, David Crosiers, Joana Damásio, Parimal Das, Patrícia de Carvalho Aguiar, Anna De Rosa, Jolanta Dorszewska, Sibel Ertan, Rosangela Ferese, Joaquim J. Ferreira, Emilia Gatto, Gençer Genç, Nir Giladi, Pilar Gómez‐Garre, Haşmet Hanağası, Nobutaka Hattori, Fayçal Hentati, Dorota Hoffman‐Zacharska, С. Н. Иллариошкин, Joseph Jankovic, Silvia Jesús, Valtteri Kaasinen, Anneke J.A. Kievit, Péter Klivényi, Vladimir Kostić, Dariusz Koziorowski, Andrea A. Kühn, Anthony E. Lang, Shen‐Yang Lim, Chin‐Hsien Lin, Katja Lohmann, Vladana Marković, Mika H. Martikainen, George D. Mellick, Marcelo Merello, Łukasz Milanowski, Pablo Mir, Özgür Öztop Çakmak, Márcia Mattos Gonçalves Pimentel, Teeratorn Pulkes, Andreas Puschmann, Ekaterina Rogaeva, Esther Sammler, Maria Skaalum Petersen, Matěj Škorvánek, Mariana Spitz, Oksana Suchowersky, Ai Huey Tan, Pichet Termsarasab, Avner Thaler, Vítor Tumas, Enza Maria Valente, Bart P.C. van de Warrenburg, Caroline H. Williams‐Gray, Ruey-Mei Wu, Baorong Zhang, Alexander Zimprich, Justin Solle, Shalini Padmanabhan, Christine Klein

    Publicat 2023
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  16. 16
    Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson’s disease study

    Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson’s disease study per Ana Westenberger, Volha Skrahina, Tatiana Usnich, Christian Beetz, Eva-Juliane Vollstedt, Björn‐Hergen Laabs, Jefri J Paul, Filipa Curado, Snezana Skobalj, Hanaa Gaber, Maria Olmedillas, Xenia Bogdanovic, Najim Ameziane, Nathalie Schell, Jan Aasly, Mitra Afshari, Pinky Agarwal, Jason Aldred, Fernando Alonso‐Frech, Roderick Anderson, Rui Araújo, David Arkadir, Micol Avenali, Mehmet Balal, Sandra Benizri, Sagari Betté, Perminder Bhatia, Michael Bonello, Pedro Braga‐Neto, Sarah Brauneis, Francisco Cardoso, Francesco Cavallieri, Joseph Claßen, Lisa J. Cohen, Della Coletta, David Crosiers, Paskal Cullufi, Khashayar Dashtipour, Meltem Demirkıran, Patrícia de Carvalho Aguiar, Anna De Rosa, Ruth Djaldetti, Okan Doğu, Maria Gabriela dos Santos Ghilardi, Carsten Eggers, Bülent Elibol, Aaron Ellenbogen, Sibel Ertan, G Fabiani, Björn Falkenburger, S. Farrow, Tsviya Fay-Karmon, Gerald J Ferencz, Erich Talamoni Fonoff, Yára Dadalti Fragoso, Gençer Genç, A Gorospe, Francisco Grandas, Doreen Gruber, Mark Gudesblatt, Tanya Gurevich, Johann Hagenah, Haşmet Hanağası, Sharon Hassin-Baer, Robert A. Hauser, Jorge Hernández‐Vara, Birgit Herting, Vanessa K. Hinson, Elliot Hogg, Joshua Shulman, Eduardo Hummelgen, Kelly Hussey, Jon Infante, Stuart Isaacson, Serge Jaumà, Natalia Koleva‐Alazeh, Gregor Kuhlenbäumer, Andrea A. Kühn, Irene Litvan, Lydia López Manzanares, McKenzie Luxmore, Sujeena Manandhar, V. Marcaud, Katerina Markopoulou, Connie Marras, Mark McKenzie, Michele Matarazzo, Marcelo Merello, Brit Mollenhauer, John C. Morgan, Stephen Mullin, Thomas Musacchio, Bennett Myers, Anna Negrotti, Anette Nieves, Zeev Nitsan, Nader Oskooilar, Özgür Öztop Çakmak, Gian Pal, Nicola Pavese

    Publicat 2024
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  17. 17
    Embracing Monogenic Parkinson's Disease: The <scp>MJFF</scp> Global Genetic <scp>PD</scp> Cohort

    Embracing Monogenic Parkinson's Disease: The <scp>MJFF</scp> Global Genetic <scp>PD</scp> Cohort per Eva‐Juliane Vollstedt, Susen Schaake, Katja Lohmann, Shalini Padmanabhan, Alexis Brice, Suzanne Lesage, Christelle Tesson, Marie Vidailhet, Isabel Wurster, F. Hentati, Anat Mirelman, Nir Giladi, Karen Marder, Cheryl Waters, Stanley Fahn, Meike Kasten, Norbert Brüggemann, Max Borsche, Tatiana Foroud, Eduardo Tolosa, Alícia Garrido, Grazia Annesi, Monica Gagliardi, Maria Bozi, Leonidas Stefanis, Joaquim J. Ferreira, Leonor Correia Guedes, Micol Avenali, Simona Petrucci, Lorraine N. Clark, E. Yu. Fedotova, Natalya Abramycheva, Victoria Álvarez, Manuel Menéndez‐González, S. Jesús Maestre, Pilar Gómez‐Garre, Pablo Mir, Andrea Carmine Belin, Caroline Ran, Chin‐Hsien Lin, Ming‐Che Kuo, David Crosiers, Zbigniew K. Wszołek, Owen A. Ross, Joseph Jankovic, Kenya Nishioka, Manabu Funayama, Jordi Clarimón, Caroline H. Williams‐Gray, Marta Camacho, Mario Cornejo‐Olivas, Luis Torres-Ramírez, Yih‐Ru Wu, Guey‐Jen Lee‐Chen, Ana Morgadinho, Teeratorn Pulkes, Pichet Termsarasab, Daniela Berg, Gregor Kuhlenbäumer, Andrea A. Kühn, Friederike Borngräber, Giuseppe De Michele, Anna De Rosa, Alexander Zimprich, Andreas Puschmann, George D. Mellick, Jolanta Dorszewska, Jonathan Carr, Rosangela Ferese, Stefano Gambardella, Bruce A. Chase, Katerina Markopoulou, Wataru Satake, Tatsushi Toda, Malco Rossi, Marcelo Merello, Timothy Lynch, Diana A. Olszewska, Shen‐Yang Lim, Azlina Ahmad‐Annuar, Ai Huey Tan, Bashayer Al‐Mubarak, Haşmet Hanağası, Dariusz Koziorowski, Sibel Ertan, Gençer Genç, Patrícia de Carvalho Aguiar, Melinda Barkhuizen, Márcia Mattos Gonçalves Pimentel, Rachel Saunders‐Pullman, Bart van de Warrenburg, Susan Bressman, Mathias Toft, Silke Appel‐Cresswell, Anthony E. Lang, Matěj Škorvánek, Agnita J.W. Boon, Rejko Krüger, Esther Sammler, Vítor Tumas

    Publicat 2023
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