Søgeresultater - Samson Khachatryan
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Physicians’ beliefs about brain surgery for drug-resistant epilepsy: A global survey af Ali A. Asadi‐Pooya, Francesco Brigo, Eugen Trinka, Simona Lattanzi, Ioannis Karakis, Nirmeen A. Kishk, Kette D. Valente, Asel Jusupova, С Т Туруспекова, Anilú Daza‐Restrepo, Guilca Contreras, М А Кутлубаев, Alla Guekht, Abbas Rahimi Jaberi, Ghaieb Aljandeel, Yamile Calle‐López, Taoufik Alsaadi, Abdulaziz Ashkanani, Lakshmi Narasimhan Ranganathan, Abdullah Al‐Asmi, Samson Khachatryan, David Gigineishvili, Boulenouar Mesraoua, Naluca Mwendaweli
Udgivet 2022Artigo -
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The European Insomnia Guideline: An update on the diagnosis and treatment of insomnia 2023 af Dieter Riemann, Colin A. Espie, Ellemarije Altena, Erna Sif Arnardóttir, Chiara Baglioni, Claudio L. Bassetti, Célyne Bastien, Natālija Bērziņa-Novikova, Björn Bjorvatn, Dimitris Dikeos, Leja Dolenc‐Grošelj, Jason Ellis, Diego Garcı́a-Borreguero, Pierre A. Geoffroy, Michaela D. Gjerstad, Marta Gonçalves, Elisabeth Hertenstein, Kerstin Hoedlmoser, Tuuliki Hion, Brigitte Holzinger, Karolína Janků, Markus Jansson‐Fröjmark, Heli Järnefelt, Susanna Jernelöv, Poul Jennum, Samson Khachatryan, Lukas B. Krone, Simon D. Kyle, Jaap Lancee, Damien Léger, A. Lupuşor, Daniel Ruivo Marques, Christoph Nissen, Laura Palagini, Tiina Paunio, Lampros Perogamvros, Dirk Pevernagie, Manuel Schabus, Tamar Shochat, András Szentkirályi, Eus J.W. Van Someren, Annemieke van Straten, Adam Wichniak, Johan Verbraecken, Kai Spiegelhalder
Udgivet 2023Revisão -
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Cerebellar Volume and Disease Staging in Parkinson's Disease: An <scp>ENIGMA‐PD</scp> Study af Rebecca Kerestes, Max A. Laansma, Conor Owens‐Walton, Andrew Perry, Eva M. van Heese, Sarah Al–Bachari, Tim Anderson, Francesca Assogna, Ítalo Karmann Aventurato, Tim D. van Balkom, Henk W. Berendse, Kevin R.E. van den Berg, R. P. Betts, Ricardo Brioschi, Jonathan Carr, Fernando Cendes, K. Lyles Clark, John C. Dalrymple‐Alford, Michiel F. Dirkx, T. Jason Druzgal, Helena Durrant, Hedley Emsley, Gaëtan Garraux, Hamied Haroon, Rick C. Helmich, Odile A. van den Heuvel, Rafael Batista João, Martin E. Johansson, Samson Khachatryan, Christine Löchner, Corey T. McMillan, Tracy R. Melzer, Philip Mosley, Benjamin T. Newman, Peter Opriessnig, Laura M. Parkes, Clelia Pellicano, Fabrizio Piras, Toni L. Pitcher, Kathleen L. Poston, Mario Rango, Annerine Roos, Christian Rummel, Reinhold Schmidt, Petra Schwingenschuh, Lucas Scárdua Silva, Viktorija Smith, Letizia Squarcina, Dan J. Stein, Zaruhi Tavadyan, Chih‐Chien Tsai, Daniela Vecchio, Chris Vriend, Jiun‐Jie Wang, Roland Wiest, Clarissa Lin Yasuda, Christina B. Young, Neda Jahanshad, Paul M. Thompson, Ysbrand D. van der Werf, Ian H. Harding
Udgivet 2023Artigo -
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Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) af Clodagh Towns, Madeleine Richer, Simona Jasaityte, Eleanor J. Stafford, Julie Joubert, Tarek Antar, Alejandro Martínez-Carrasco, Mary B. Makarious, Bradford Casey, Dan Vitale, Kristin Levine, Hampton L. Leonard, Caroline B. Pantazis, Laurel A. Screven, Dena Hernández, Claire Wegel, Justin Solle, Mike A. Nalls, Cornelis Blauwendraat, Andrew Singleton, Manuela Tan, Hirotaka Iwaki, Huw R. Morris, Emilia Gatto, Marcelo Kauffman, Samson Khachatryan, Zaruhi Tavadyan, Claire E. Shepherd, Julie Hunter, Kishore R. Kumar, Melina Ellis, Miguel E. Rentería, Sulev Kõks, Alexander Zimprich, Artur Francisco Schumacher Schuh, Carlos Roberto de Mello Rieder, Paula Saffie Awad, Vítor Tumas, Sarah Camargos, Edward A. Fon, Oury Monchi, Ted Fon, Benjamin Pizarro Galleguillos, Marcelo Miranda, M. Leonor Bustamante, Patricio Olguı́n, Pedro Chaná, Beisha Tang, Huifang Shang, Jifeng Guo, Piu Chan, Wei Luo, Gonzálo Arboleda, Jorge Orozco, Marlene Jiménez-Del-Río, Álvaro Hernández-Flores, Mohamed Salama, Walaa A. Kamel, Yared Z. Zewde, Alexis Brice, Jean‐Christophe Corvol, Ana Westenberger, Anastasia Illarionova, Brit Mollenhauer, Christine Klein, Eva‐Juliane Vollstedt, Franziska Hopfner, Günter U. Höglinger, Harutyun Madoev, Joanne Trinh, Johanna Junker, Katja Lohmann, Lara M. Lange, Manu Sharma, Sergiu Groppa, Thomas Gasser, Zih‐Hua Fang, Albert Akpalu, Georgia Xiromerisiou, Georgios Hadjigorgiou, Ioannis E. Dagklis, Ioannis Tarnanas, Leonidas Stefanis, María Stamelou, Efthymios Dadiotis, Alex Medina, Germaine Hiu-Fai Chan, Nancy Y. Ip, Nelson Yuk-Fai Cheung, Phillip Chan, Xiaopu Zhou, Asha Kishore, Divya KP, Pramod Kumar Pal, Prashanth Lingappa Kukkle, Roopa Rajan, Rupam Borgohain, Mehri Salari, Andrea Quattrone, Enza Maria Valente
Udgivet 2023Artigo -
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Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) af Lara M. Lange, Micol Avenali, Melina Ellis, Anastasia Illarionova, Ignacio Juan Keller Sarmiento, Ai Huey Tan, Harutyun Madoev, Caterina Galandra, Johanna Junker, Karisha Roopnarain, Justin Solle, Claire Wegel, Zih‐Hua Fang, Peter Heutink, Kishore R. Kumar, Shen‐Yang Lim, Enza Maria Valente, Mike A. Nalls, Cornelis Blauwendraat, Andrew Singleton, Niccolò E. Mencacci, Katja Lohmann, Christine Klein, Emilia Gatto, Marcelo Kauffman, Samson Khachatryan, Zaruhi Tavadyan, Claire E. Shepherd, Julie Hunter, Kishore R. Kumar, Melina Ellis, Miguel E. Rentería, Sulev Kõks, Alexander Zimprich, Artur Francisco Schumacher Schuh, Carlos Roberto de Mello Rieder, Paula Saffie Awad, Vítor Tumas, Sarah Camargos, Edward A. Fon, Oury Monchi, Ted Fon, Benjamin Pizarro Galleguillos, Marcelo Miranda, M. Leonor Bustamante, Patricio Olguı́n, Pedro Chaná, Beisha Tang, Huifang Shang, Jifeng Guo, Piu Chan, Wei Luo, Gonzálo Arboleda, Jorge Orozco, Marlene Jiménez-Del-Río, Alvaro G. Hernandez, Mohamed Salama, Walaa A. Kamel, Yared Z. Zewde, Alexis Brice, Jean‐Christophe Corvol, Ana Westenberger, Anastasia Illarionova, Brit Mollenhauer, Christine Klein, Eva‐Juliane Vollstedt, Franziska Hopfner, Günter U. Höglinger, Harutyun Madoev, Joanne Trinh, Johanna Junker, Katja Lohmann, Lara M. Lange, Manu Sharma, Sergiu Groppa, Thomas Gasser, Zih‐Hua Fang, Albert Akpalu, Georgia Xiromerisiou, Georgios Hadjigorgiou, Ioannis E. Dagklis, Ioannis Tarnanas, Leonidas Stefanis, María Stamelou, Efthymios Dadiotis, Alex Medina, Germaine Hiu-Fai Chan, Nancy Y. Ip, Nelson Yuk-Fai Cheung, Phillip Chan, Xiaopu Zhou, Asha Kishore, Divya KP, Pramod Kumar Pal, Prashanth Lingappa Kukkle, Roopa Rajan, Rupam Borgohain, Mehri Salari, Andrea Quattrone, Enza Maria Valente
Udgivet 2023Errata/Corrigenda -
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Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease af Jonggeol Jeffrey Kim, Dan Vitale, Diego Véliz Otani, Michelle Mulan Lian, Karl Heilbron, Stella Aslibekyan, Adam Auton, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Paul J. Cannon, Daniella Coker, Gabriel Cuéllar-Partida, Devika Dhamija, Sayantan Das, Sarah L. Elson, Nicholas Eriksson, Teresa Filshtein, Alison Fitch, Kipper Fletez‐Brant, Pierre Fontanillas, Will Freyman, Julie M. Granka, Alejandro Hernandez, Barry Hicks, David A. Hinds, Ethan M. Jewett, Yunxuan Jiang, Katelyn Kukar, Alan Kwong, Keng‐Han Lin, Bianca A. Llamas, Maya Lowe, Jey C. McCreight, Matthew H. McIntyre, Steven J. Micheletti, Meghan E. Moreno, Priyanka Nandakumar, Dominique T. Nguyen, Elizabeth S. Noblin, Jared O’Connell, Aaron A. Petrakovitz, G. David Poznik, Alexandra Reynoso, Madeleine Schloetter, Morgan Schumacher, Anjali J. Shastri, Janie F. Shelton, Jingchunzi Shi, Suyash Shringarpure, Qiaojuan Jane Su, Susana A. Tat, Christophe Toukam Tchakouté, Vinh Tran, Joyce Y. Tung, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton, Corinna D. Wong, Hirotaka Iwaki, Julie Lake, Caroline Warly Solsberg, Hampton L. Leonard, Mary B. Makarious, Eng‐King Tan, Andrew Singleton, Sara Bandrés‐Ciga, Alastair Noyce, Emilia Gatto, Marcelo Kauffman, Samson Khachatryan, Zaruhi Tavadyan, Claire E. Shepherd, Julie Hunter, Kishore R. Kumar, Melina Ellis, Miguel E. Rentería, Sulev Kõks, Alexander Zimprich, Artur Francisco Schumacher Schuh, Carlos Roberto de Mello Rieder, Paula Saffie Awad, Vítor Tumas, Sarah Camargos, Edward A. Fon, Oury Monchi, Ted Fon, Benjamin Pizarro Galleguillos, Marcelo Miranda, M. Leonor Bustamante, Patricio Olguı́n, Pedro Chaná, Beisha Tang, Huifang Shang, Jifeng Guo, Piu Chan, Wei Luo
Udgivet 2023Revisão -
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The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population af Lara M. Lange, Kristin Levine, Susan H. Fox, Connie Marras, Nazish Rafique, Nicole Kuznetsov, Dan Vitale, Hirotaka Iwaki, Katja Lohmann, Luca Marsili, Alberto J. Espay, Peter Bauer, Christian Beetz, Jessica Martin, Stewart A. Factor, Lenora A. Higginbotham, Honglei Chen, Hampton L. Leonard, Mike A. Nalls, Niccolò E. Mencacci, Huw R. Morris, Andrew Singleton, Christine Klein, Cornelis Blauwendraat, Zih‐Hua Fang, Emilia Gatto, Marcelo Kauffman, Samson Khachatryan, Zaruhi Tavadyan, Claire E. Shepherd, Julie Hunter, Kishore R. Kumar, Melina Ellis, Miguel E. Rentería, Sulev Kõks, Alexander Zimprich, Artur Francisco Schumacher Schuh, Carlos Roberto de Mello Rieder, Paula Saffie Awad, Vítor Tumas, Sarah Camargos, Edward A. Fon, Oury Monchi, Ted Fon, Benjamin Pizarro Galleguillos, Patricio Olguı́n, Marcelo Miranda, M. Leonor Bustamante, Pedro Chaná, Beisha Tang, Huifang Shang, Jifeng Guo, Piu Chan, Wei Luo, Gonzálo Arboleda, Jorge Orozco, Marlene Jiménez-Del-Río, Álvaro Hernández-Flores, Mohamed Salama, Walaa A. Kamel, Yared Z. Zewde, Alexis Brice, Jean‐Christophe Corvol, Ana Westenberger, Eva‐Juliane Vollstedt, Harutyun Madoev, Joanne Trinh, Johanna Junker, Anastasia Illarionova, Brit Mollenhauer, Franziska Hopfner, Günter U. Höglinger, Manu Sharma, Thomas Gasser, Sergiu Groppa, Albert Akpalu, Georgia Xiromerisiou, Georgios Hadjigorgiou, Efthymios Dadiotis, Ioannis E. Dagklis, Ioannis Tarnanas, Leonidas Stefanis, María Stamelou, Alex Medina, Germaine Hiu-Fai Chan, Nelson Yuk-Fai Cheung, Nancy Y. Ip, Phillip Chan, Xiaopu Zhou, Asha Kishore, Divya KP, Pramod Kr. Pal, Prashanth Lingappa Kukkle, Roopa Rajan, Rupam Borgohain, Mehri Salari, Andrea Quattrone, Monica Gagliardi, Enza Maria Valente, Micol Avenali
Udgivet 2025Artigo
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Relaterede emner
Medicine
Internal medicine
Disease
Biology
Genetics
Neuroscience
Parkinson's disease
Epilepsy
Gene
Genotype
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Psychiatry
Psychology
1000 Genomes Project
Audiology
Bioinformatics
Cerebellar hemisphere
Cerebellum
Computer science
Demographics
Demography
Drug Resistant Epilepsy
Environmental health
Epilepsy surgery
Expression quantitative trait loci
Family medicine
Genetic association
Genome
Genome-wide association study
Genotyping