Genetic screening of South African families with Parkinson's disease von Bardien, S, Braun, A, Van Coller, R, Hassan Amod, F, Carr, J, Moosa, S

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Identification of a common founder couple for 40 South African Afrikaner families with Parkinson's disease von Geldenhuys, Gerhard, Glanzmann, Brigitte, Lombard, Debbie, Boolay, Sihaam, Carr, Jonathan, Bardien, Soraya

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Inherited retinal disorders in South Africa and the clinical impact of evolving technologies von Roberts, L, Goliath, R, Rebello, G, Bardien, S, September, A V, Bartmann, L, Loubser, F, Greenberg, L J, Ramesar, R S

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Direct-to-consumer genetic testing: to test or not to test, that is the question von Dandara, Collet, Greenberg, Jacqui, Lambie, Lindsay, Lombard, Zane, Naicker, Thirona, Ramesar, Raj, Ramsay, Michele, Roberts, Lisa, Theron, Magda, Venter, Phillip, Bardien-Kruger, Soraya

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Factors influencing the development of early- or late-onset Parkinson's disease in a cohort of South African patients von DER MERWE, C. Van, HAYLETT, W, HARVEY, J, LOMBARD, D, BARDIEN, S, CARR, J

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A South African family with the mitochondrial A1555G mutation on haplogroup L0d von Human, H., Lombard, D., de Jong, G., Bardien, S.

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Novel non-sense GCH1 mutation in a South African family diagnosed with dopa-responsive dystonia von Bardien, S., Keyser, R., Lombard, D., Du Plessis, M., Human, H., Carr, J.

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Transformation of learning and teaching in rehabilitation sciences: A case study from South Africa, in Human Functioning von Visser, Monique, Oosthuizen, Helena, Louw, Alwyn J.N, Unger, Marianne, Keiller, Lianne, Inglis-Jassiem, Gakeemah, Hanekom, Susan D, de Beer, Alida, Gaskin, Ashley, Bardien, Faeza, Manas, Lorisha, Coetzee, Marisa, de Wit, Monique, Nizeyimana, Eugene, Dawood, Gouwa, Plastow, Nicola, Joseph, Conran, Louw, Quinette, Kloppers, Maatje, Bester, Juanita, Baxter, Anja, Denton, ELLA PRU, Koegelenberg, Ané, Burchell, Helena J, Simpson, Tayla-leigh, van Wyk, Marnie, Ernstzen, Dawn Verna, Schmutz, Anna M. S, Meyer, Ilse S, Filies, Gerard, Müller, Jana, Gerber, Berna, Berner, Karina, Pefile, Ntsikelelo, Charumbira, Maria Yvonne

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Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions von Schumacher‐Schuh, Artur Francisco, Bieger, Andrei, Okunoye, Olaitan, Mok, Kin Ying, Lim, Shen‐Yang, Bardien, Soraya, Ahmad‐Annuar, Azlina, Santos‐Lobato, Bruno Lopes, Strelow, Matheus Zschornack, Salama, Mohamed, Rao, Shilpa C., Zewde, Yared Zenebe, Dindayal, Saiesha, Azar, Jihan, Prashanth, Lingappa Kukkle, Rajan, Roopa, Noyce, Alastair J., Okubadejo, Njideka, Rizig, Mie, Lesage, Suzanne, Mata, Ignacio Fernandez

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Embracing monogenic Parkinson's disease: the MJFF Global Genetic PD Cohort von Vollstedt, Eva‐Juliane, Schaake, Susen, Lohmann, Katja, Padmanabhan, Shalini, Brice, Alexis, Vidailhet, Marie, Wurster, Isabel, Hentati, Faycel, Mirelman, Anat, Chung, Sun Ju, Winkelmann, Juliane, Sue, Carolyn M., Kostic, Vladimir S., Giladi, Nir, Arkadir, David, Martikainen, Mika, Borges, Vanderci, Hertz, Jens Michael, Brighina, Laura, Spitz, Mariana, Riess, Olaf, Das, Parimal, Gatto, Emilia M., Petersen, Maria Skaalum, Hattori, Nobutaka, Illarioshkin, Sergey N., Valente, Enza Maria, Aasly, Jan O., Aasly, Anna, Alcalay, Roy N., Brockmann, Kathrin, Corvol, Jean‐Christophe, Klein, Christine, Fahn, Stanley, Foroud, Tatiana, Tolosa, Eduardo, Garrido, Alicia, Annesi, Grazia, Gagliardi, Monica, Stefanis, Leonidas, Ferreira, Joaquim J, Correia Guedes, Leonor, Avenali, Micol, Abramycheva, Natalya Y., Alvarez, Victoria, Menéndez‐González, Manuel, Jesús Maestre, Silvia, Gómez‐Garre, Pilar, Belin, Andrea Carmine, Ran, Caroline, Wszolek, Zbigniew K., Ross, Owen A., Jankovic, Joseph, Nishioka, Kenya, Funayama, Manabu, Clarimon, Jordi, Williams‐Gray, Caroline H., Camacho, Marta, Cornejo‐Olivas, Mario, Wu, Yih‐Ru, Morgadinho, Ana, Pulkes, Teeratorn, Termsarasab, Pichet, Kuhlenbäumer, Gregor, Kühn, Andrea A., Borngräber, Friederike, de Michele, Giuseppe, Zimprich, Alexander, Puschmann, Andreas, Mellick, George D., Dorszewska, Jolanta, Carr, Jonathan, Ferese, Rosangela, Gambardella, Stefano, Chase, Bruce, Markopoulou, Katerina, Satake, Wataru, Toda, Tatsushi, Rossi, Malco, Merello, Marcelo, Lynch, Timothy, Lim, Shen‐Yang, Ahmad‐Annuar, Azlina, Al‐Mubarak, Bashayer, Hanagasi, Hasmet, Koziorowski, Dariusz, Ertan, Sibel, Genç, Gençer, de Carvalho Aguiar, Patricia, Barkhuizen, Melinda, Pimentel, Marcia M.G., Bressman, Susan, Toft, Mathias, Appel‐Cresswell, Silke, Lang, Anthony E., Skorvanek, Matej, Boon, Agnita J.W., Krüger, Rejko, Sammler, Esther M., Tumas, Vitor

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Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study von Ross, Owen A, Dr, Soto-Ortolaza, Alexandra I, BSc, Heckman, Michael G, MS, Aasly, Jan O, Prof, Abahuni, Nadine, MD, Annesi, Grazia, Prof, Bacon, Justin A, BSc, Bardien, Soraya, PhD, Bozi, Maria, MD, Brice, Alexis, Prof, Brighina, Laura, MD, Van Broeckhoven, Christine, Prof, Carr, Jonathan, Prof, Chartier-Harlin, Marie-Christine, Prof, Dardiotis, Efthimios, MD, Dickson, Dennis W, Prof, Diehl, Nancy N, BS, Elbaz, Alexis, Prof, Ferrarese, Carlo, Prof, Ferraris, Alessandro, MD, Fiske, Brian, PhD, Gibson, J Mark, Prof, Gibson, Rachel, PhD, Hadjigeorgiou, Georgios M, MD, Hattori, Nobutaka, Prof, Ioannidis, John PA, Prof, Jasinska-Myga, Barbara, MD, Jeon, Beom S, Prof, Kim, Yun Joong, Prof, Klein, Christine, Prof, Kruger, Rejko, MD, Kyratzi, Elli, MD, Lesage, Suzanne, PhD, Lin, Chin-Hsien, MD, Lynch, Timothy, Prof, Maraganore, Demetrius M, Prof, Mellick, George D, PhD, Mutez, Eugénie, MD, Nilsson, Christer, Prof, Opala, Grzegorz, Prof, Park, Sung Sup, Prof, Puschmann, Andreas, MD, Quattrone, Aldo, Prof, Sharma, Manu, PhD, Silburn, Peter A, Prof, Sohn, Young Ho, Prof, Stefanis, Leonidas, MD, Tadic, Vera, MD, Theuns, Jessie, PhD, Tomiyama, Hiroyuki, MD, Uitti, Ryan J, Prof, Valente, Enza Maria, Prof, van de Loo, Simone, PhD, Vassilatis, Demetrios K, PhD, Vilariño-Güell, Carles, PhD, White, Linda R, Prof, Wirdefeldt, Karin, MD, Wszolek, Zbigniew K, Prof, Wu, Ruey-Meei, Prof, Farrer, Matthew J, Prof

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Clinical findings and genetic screening for copy number variation mutations in a cohort of South African patients with Parkinson's disease : research von Bardien, S., Mahne, A.C., Carr, J.A., Schutte, C-M

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Clinical findings and genetic screening for copy number variation mutations in a cohort of South African patients with Parkinson's disease : research von Mahne, A.C., Schutte, C-M, Carr, J.A., Bardien, S.

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Aminoglycoside-induced hearing loss in HIV-positive and HIV-negative multidrug-resistant tuberculosis patients von Harris, Tashneem, Bardien, Soraya, Schaaf, H Simon, Petersen, Lucretia, De Jong, Greetje, Fagan, Johannes J

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Clinical findings and genetic screening for copy number variation mutations in a cohort of South African patients with Parkinson's disease von Mahne, Anna Cecelia, Carr, Jonathan A, Bardien, Soraya, Schutte, Clara Maria

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Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors von Liu, Hui, Dehestani, Mohammad, Blauwendraat, Cornelis, Makarious, Mary B., Leonard, Hampton, Kim, Jonggeol J., Schulte, Claudia, Noyce, Alastair, Jacobs, Benjamin M., Foote, Isabelle, Sharma, Manu, Koks, Sulev, Mellick, George D, Pirker, Walter, Zimprich, Alexander, Lang, Anthony E, Rogaeva, Ekaterina, Taba, Pille, Brice, Alexis, Chartier‐Harlin, Marie‐Christine, Corvol, Jean‐Christophe, Domenighetti, Cloé, Elbaz, Alexis, Lesage, Suzanne, Mutez, Eugenie, Sugier, Pierre‐Emmanuel, Sreelatha, Ashwin Ashok Kumar, Grover, Sandeep, Brockmann, Kathrin, Deutschländer, Angela B, Gasser, Thomas, Krüger, Jens, Lichtner, Peter, Radivojkov‐Blagojevic, Milena, Schulte, Claudia, Sharma, Manu, Dardiotis, Efthimos, Hadjigeorgiou, Georges M, Simitsi, Athina Maria, Stefanis, Leonidas, Annesi, Grazia, Brighina, Laura, Ferrarese, Carlo, Petrucci, Simona, Pezzoli, Gianni, Quattrone, Andrea, Straniero, Letizia, Gagliardi, Monica, Valente, Enza Maria, Zecchinelli, Anna, Hattori, Nobutaka, Nakayama, Akiyoshi, Matsuo, Hirotaka, Nishioka, Kenya, Bobbili, Dheeraj, Kruger, Rejko, Landoulsi, Zied, May, Patrick, Pavelka, Lukas, Bloem, Bastiaan R, Warrenburg, Bart PC, Aasly, Jan, Pihlstrøm, Lasse, Toft, Mathias, Ferreira, Joaquim J, Guedes, Leonor Correia, Bardien, Soraya, Carr, Jonathan, Chung, Sun Ju, Kim, Yun Joong, Diez‐Fairen, Monica, Ezquerra, Mario, Pastor, Pau, Tolosa, Eduardo, Belin, Andrea C, Pedersen, Nancy L, Puschmann, Andreas, Ran, Caroline, Rödström, Emil Y, Wirdefeldt, Karin, Clarke, Carl E, Morrison, Karen E, Tan, Manuela, Edsall, Connor, Farrer, Matt J, Krainc, Dimitri, Singleton, Andrew B, Burbulla, Lena F, Hernandez, Dena G, Nalls, Mike, Singleton, Andrew, Gasser, Thomas, Bandres‐Ciga, Sara

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Using global team science to identify genetic parkinson's disease worldwide von Vollstedt, Eva‐Juliane, Klein, Christine, Ahmad‐Annuar, Azlina, Al‐Mubarak, Bashayer, Annesi, Grazia, Barber, Thomas R., Bardien, Soraya, Başak, A. Nazlı, Bhatia, Kailash, Binkofski, Ferdinand, Bozi, Maria, Brice, Alexis, Brighina, Laura, Brockmann, Kathrin, Brücke, Thomas, Chen‐Plotkin, Alice, Ju Chung, Sun, Clark, Lorraine, Corvol, Jean‐Christophe, Cosentino, Carlos, Cras, Patrick, Crosiers, David, De Michele, Giuseppe, De Rosa, Anna, Erer, Sevda, Ertan, Sibel, Farrer, Matthew, Fiala, Ondrej, Foroud, Tatiana, Friedman, Andrzej, Frigerio, Roberta, Garraux, Gaetan, Gomez‐Esteban, Juan Carlos, Hardy, John, Hassan, Anhar, Hedera, Peter, Hentati, Faycal, Inca‐Martinez, Miguel, Infante, Jon, Jankovic, Joseph, Jesús, Silvia, Kasten, Meike, Kataoka, Hiroshi, Kim, Yun Joong, Koziorowski, Dariusz, Krüger, Rejko, Krygowska‐Wajs, Anna, Kulisevsky, Jaime, Lai, Dongbing, Lang, Anthony, LeDoux, Mark, Lesage, Suzanne, Lim, Shen‐Yang, Lin, Chin‐Hsien, Lopera, Francisco, Lopez, Grisel, Lu, Chin‐Song, Lynch, Tim, Maraganore, Demetrius, Marder, Karen, Mazzetti, Pilar, Mirelman, Anat, Morris, Huw, Naito, Anna, Ozelius, Laurie J., Padmanabhan, Shalini, Paisán‐Ruiz, Coro, Petkovic, Sonja, Petrucci, Simona, Pimentel, Márcia, Pirker, Walter, Pulkes, Teeratorn, Puschmann, Andreas, Quattrone, Aldo, Sammler, Esther, Sazci, Ali, Schrag, Anette, Sharma, Manu, Sidransky, Ellen, Petersen, Maria Skaalum, Sue, Carolyn M., Swan, Matthew, Swanberg, Maria, Taba, Pille, Tan, Manuela, Tan, Ai Huey, Tan, Eng‐King, Tayebi, Nahid, Thaler, Avner, Thomas, Astrid, Toda, Tatsushi, Torres, Luis, Valente, Enza Maria, Van Broeckhoven, Christine, Wood, Nicholas W., Wszolek, Zbigniew K., Wu, Ruey‐Meei, Yoshino, Hiroyo, Zhang, Baorong, Zimprich, Alexander

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The commercial genetic testing landscape for Parkinson's disease von Cook, Lola, Schulze, Jeanine, Verbrugge, Jennifer, Beck, James C., Marder, Karen S., Saunders-Pullman, Rachel, Klein, Christine, Naito, Anna, Alcalay, Roy N., Brice, Alexis, Kumeh, Amasi, West, Andrew B., Singleton, Andrew, Naito, Anna, Schüle, Birgitt, Fiske, Brian, Gabbert, Carolin, Marras, Connie, Blauwendraat, Cornelis, Thaxton, Courtney, Alessi, Dario, Craig, David, Fon, Edward A., Forbes, Emily, Valente, Enza Maria, Sammler, Esther, Chao, Gill, Riboldi, Giulietta, Elloumi, Houda Zghal, Mata, Ignacio, Beck, James C., Fong, Jamie C., Corvol, Jean-Christophe, Schulze, Jeanine, Verbrugge, Jennifer, Shulman, Joshua, Peterschmitt, Judith, Marder, Karen, Lohmann, Katja, Nudelman, Kelly, Lange, Lara, Cook, Lola, Cookson, Mark R., Nance, Martha, Farrer, Matthew, Grigorian, Melina, Schwarzschild, Michael A., Mencacci, Niccolo, Ross, Owen, Mistry, Pramod, Hodges, Priscila, Blake, Rachel, Saunders-Pullman, Rachel, Alcalay, Roy N., Sardi, S. Pablo, Farhan, Sali, Strom, Samuel, Padmanabhan, Shalini, Mohan, Shruthi, Longerich, Simonne, Schneider, Susanne, Lesage, Suzanne, Bardakjian, Tanya, Foroud, Tatiana, Courtin, Thomas, Tropea, Thomas, Liu, Yunlong, Gan-Or, Ziv, Shalash, Ali S., Hall, Anne, Thaler, Avner, Sue, Carolyn M., Mascalzoni, Deborah, Raymond, Deborah, Gatto, Emilia Mabel, Pal, Gian D., König, Inke, Novakovic, Ivana, Merello, Marcelo, Salari, Mehri, Mencacci, Niccolo Emanuele, Hattori, Nobutaka, Suchowersky, Oksana, Bardien, Soraya, Chung, Sun Ju, Simuni, Tatyana, Lynch, Timothy, Bonifati, Vincenzo

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eVOC: a controlled vocabulary for unifying gene expression data von Kelso, Janet, Visagie, Johann, Theiler, Gregory, Christoffels, Alan, Bardien, Soraya, Smedley, Damian, Otgaar, Darren, Greyling, Gary, Jongeneel, C Victor, McCarthy, Mark I, Hide, Tania, Hide, Winston

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Apoptosis-Inducing Signal Sequence Mutation in Carbonic Anhydrase IV Identified in Patients with the RP17 Form of Retinitis Pigmentosa von Rebello, George, Ramesar, Rajkumar, Vorster, Alvera, Roberts, Lisa, Ehrenreich, Liezle, Oppon, Ekow, Gama, Dumisani, Bardien, Soraya, Greenberg, Jacquie, Bonapace, Giuseppe, Waheed, Abdul, Shah, Gul N., Sly, William S.

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