Search Results - Salari, Laura

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    Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) by Richer, Madeleine, Antar, Tarek, Makarious, Mary B, Levine, Kristin, Leonard, Hampton, Hernandez, Dena G, Blauwendraat, Cornelis, Singleton, Andrew B, Tan, Manuela, Iwaki, Hirotaka, Morris, Huw R, Shepherd, Claire E, Hunter, Julie, Kumar, Kishore, Ellis, Melina, Rentería, Miguel E, Schumacher-Schuh, Artur F, Rieder, Carlos, Camargos, Sarah, Fon, Edward A, Chana, Pedro, Guo, Jifeng, Luo, Wei, Orozco, Jorge, del Rio, Marlene Jimenez, Hernandez, Alvaro, Kamel, Walaa A, Brice, Alexis, Corvol, Jean-Christophe, Mollenhauer, Brit, Klein, Christine, Hopfner, Franziska, Madoev, Harutyun, Trinh, Joanne, Groppa, Sergiu, Gasser, Thomas, Hadjigorgiou, Georgios, Stamelou, Maria, Dadiotis, Efthymios, Medina, Alex, Ip, Nancy, Cheung, Nelson Yuk-Fai, Kp, Divya, Pal, Pramod, Kukkle, Prashanth Lingappa, Quattrone, Andrea, Avenali, Micol, Kaishibayeva, Gulnaz, Tay, Yi Wen, Ojha, Rajeev, Anderson, Tim J, Pitcher, Toni L, Sanyaolu, Arinola, Pihlstrøm, Lasse, Doquenia, Maria Leila, Rosales, Raymond, Vinuela, Angel, Iakovenko, Elena, Mubarak, Bashayer Al, Bardien, Soraya, Kim, Yun Joong, Periñan, Maria Teresa, Pastor, Pau, Wu, Hsiu-Chuan, Wu, Ruey-Meei, Wu, Yihru, Başak, A. Nazlı, Schrag, Anette, Bale, Claire, Hardy, John, Mok, Kin Ying, Wood, Nicholas, Williams, Nigel, Okunoye, Olaitan, Weil, Rimona, Jasaitye, Simona, O’Grady, Alyssa, Sobering, Andrew K, Jonas, Cabell, Comart, Charisse, Wegel, Claire, Hall, Deborah, Hernandez, Dena, Shulman, Joshua, Solle, Justin C, Nuytemans, Karen, Chahine, Lana M, Screven, Laurel, Marsili, Luca, Kuhl, Maggie, Dean, Marissa, Mencacci, Niccolò Emanuele, Albin, Roger, Alcalay, Roy, Lubbe, Steven, Foroud, Tatiana, Sherer, Todd, Song, Yeajin, Nguyen, Duan, Nguyen, Toan

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