Transgenerational transduction of MPTP-induced alterations in a Parkinson's disease mouse model von Alvarez-Fischer, D., Vernik, T., Vulinovic, F., Herrmann, A., Westenberger, A., Klein, C.

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Genetics of Parkinson's disease von Klein, Christine, Westenberger, Ana

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A novel DCC mutation and genetic heterogeneity in congenital mirror movements von Djarmati-Westenberger, A, Brüggemann, N, Espay, A J, Bhatia, K P, Klein, C

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Isolated lingual dystonia as a presenting symptom of X-linked dystonia parkinsonism von Dakay, D., Saranza, G., Leonardo, Z., Brüggemann, N., Westenberger, A.

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Non-motor manifestations of myoclonus dystonia on a mixed-ethnicity Filipino female with a novel sgce gene nonsense mutation: a case report von De Leon, M.A., Rosales, R., Klein, C., Westenberger, A.

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Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice von Keller, Annika, Westenberger, Ana, Sobrido, Maria J, García-Murias, Maria, Domingo, Aloysius, Sears, Renee L, Lemos, Roberta R, Ordoñez-Ugalde, Andres, Nicolas, Gael, da Cunha, José E Gomes, Rushing, Elisabeth J, Hugelshofer, Michael, Wurnig, Moritz C, Kaech, Andres, Reimann, Regina, Lohmann, Katja, Dobričić, Valerija, Carracedo, Angel, Petrović, Igor, Miyasaki, Janis M, Abakumova, Irina, Mäe, Maarja Andaloussi, Raschperger, Elisabeth, Zatz, Mayana, Zschiedrich, Katja, Klepper, Jörg, Spiteri, Elizabeth, Prieto, Jose M, Navas, Inmaculada, Preuss, Michael, Dering, Carmen, Janković, Milena, Paucar, Martin, Svenningsson, Per, Saliminejad, Kioomars, Khorshid, Hamid R K, Novaković, Ivana, Aguzzi, Adriano, Boss, Andreas, Le Ber, Isabelle, Defer, Gilles, Hannequin, Didier, Kostić, Vladimir S, Campion, Dominique, Geschwind, Daniel H, Coppola, Giovanni, Betsholtz, Christer, Klein, Christine, Oliveira, Joao R M

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Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease von Kim, Jonggeol Jeffrey, Vitale, Dan, Otani, Diego Véliz, Lian, Michelle Mulan, Heilbron, Karl, Iwaki, Hirotaka, Lake, Julie, Solsberg, Caroline Warly, Leonard, Hampton, Makarious, Mary B., Tan, Eng-King, Singleton, Andrew B., Bandres-Ciga, Sara, Noyce, Alastair J., Blauwendraat, Cornelis, Nalls, Mike A., Foo, Jia Nee, Mata, Ignacio

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GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians von Crea, Peter Wild, Noyce, Alastair J., Kauffman, Marcelo, Tavadyan, Zaruhi, Hunter, Julie, Rentería, Miguel E., Koks, Sulev, Rieder, Carlos, Awad, Paula Saffie, Fon, Ted, Olguin, Patricio, Chan, Piu, Luo, Wei, Arboleda, Gonzalo, Hernandez, Alvaro, Salama, Mohamed, Westenberger, Ana, Illarionova, Anastasia, Hopfner, Franziska, Madoev, Harutyun, Junker, Johanna, Fang, Zih‐Hua, Xiromerisiou, Georgia, Dagklis, Ioannis, Stefanis, Leonidas, Medina, Alex, Divya, KP, Rajan, Roopa, Borgohain, Rupam, Salari, Mehri, Quattrone, Andrea, Hattori, Nobutaka, Shiraishi, Tomotaka, Krüger, Rejko, Ahmad‐Annuar, Azlina, Norlinah, Mohamed Ibrahim, Azmin, Shahrul, Lim, Shen‐Yang, Ojha, Rajeev, Okubadejo, Njideka, Cornejo‐Olivas, Mario, Rosales, Raymond, Iakovenko, Elena, Bardien, Soraya, Jeon, Beomseok, Cubo, Esther, Beyer, Katrin, Zweier, Christiane, Tinkhauser, Gerd, Lin, Chin‐Hsien, Amouri, Rim, Başak, A. Nazlı, Genc, Gencer, Çakmak, Özgür Öztop, Ertan, Sibel, Grosset, Donald, Morris, Huw R, Williams, Nigel, Lewis, Patrick Alfryn, Weil, Rimona, Stott, Simon, Jasaityte, Simona, Obese, Vida, Espay, Alberto, O'Grady, Alyssa, Fiske, Brian, Jonas, Cabell, Cruchaga, Carlos, Pantazis, Caroline B., Blauwendraat, Cornelis, Vitale, Dan, Mata, Ignacio F., Sarmiento, Ignacio Juan Keller, Kim, Jonggeol Jeff, Jankovic, Joseph, Murphy, Kaileigh, Kieburtz, Karl, Andersh, Kate, Markopoulou, Katerina, Levine, Kristin S., Ibanez, Laura, Marsili, Luca, Makarious, Mary B, Nalls, Mike A., Mencacci, Niccolò Emanuele, Albin, Roger, Chowdhury, Sohini, Foroud, Tatiana, Njideka, Okubadejo, Sani, Abubakar, Uchechi, Agulanna, Rufus, Akinyemi, Abiodun, Bello, Daniel, Ezuduemoih, Evewero, Ikwenu, Morenikeji, Komolafe, Paul, Nwani, Franscisca, Nwaokorie, Godwin, Osaigbovo, Simon, Ozomma

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Adaptive finite element solution of eigenvalue problems: Balancing of discretization and iteration error von Rannacher, R., Westenberger, A., Wollner, W.

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Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) von Lange, LM, Avenali, M, Ellis, M, Illarionova, A, Keller Sarmiento, IJ, Tan, AH, Madoev, H, Galandra, C, Junker, J, Roopnarain, K, Solle, J, Wegel, C, Fang, ZH, Heutink, P, Kumar, KR, Lim, SY, Valente, EM, Nalls, M, Blauwendraat, C, Singleton, A, Mencacci, N, Lohmann, K, Klein, C, Gatto, EM, Kauffman, M, Khachatryan, S, Tavadyan, Z, Shepherd, CE, Hunter, J, Kumar, K, Rentería, ME, Koks, S, Zimprich, A, Schumacher-Schuh, AF, Rieder, C, Awad, PS, Tumas, V, Camargos, S, Fon, EA, Monchi, O, Fon, T, Galleguillos, BP, Miranda, M, Bustamante, ML, Olguin, P, Chana, P, Tang, B, Shang, H, Guo, J, Chan, P, Luo, W, Arboleda, G, Orozco, J, del Rio, MJ, Hernandez, A, Salama, M, Kamel, WA, Zewde, YZ, Brice, A, Corvol, JC, Westenberger, A, Mollenhauer, B, Vollstedt, EJ, Hopfner, F, Höglinger, G, Trinh, J, Sharma, M, Groppa, S, Gasser, T, Akpalu, A, Xiromerisiou, G, Hadjigorgiou, G, Dagklis, I, Tarnanas, I, Stefanis, L, Stamelou, M, Dadiotis, E, Medina, A, Chan, GHF, Ip, N, Cheung, NYF, Zhou, X, Kishore, A, Kp, D, Pal, P, Kukkle, PL, Rajan, R, Borgohain, R, Salari, M, Quattrone, A

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4 - Hydrogen-fueled aeroplanes von Godula-Jopek, A., Westenberger, A.

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Filtering solution to the out-of-sequence measurement problem with colored and correlated noise von Westenberger, A., Muntzinger, M., Dietmayer, K.

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Phenotypic insights into ADCY5-associated disease von Chang, FC, Westenberger, A, Dale, RC, Smith, M, Pall, HS, Perez-Dueñas, B, Grattan-Smith, P, Ouvrier, RA, Mahant, N, Hanna, BC, Hunter, M, Lawson, JA, Max, C, Sachdev, R, Meyer, E, Crimmins, D, Pryor, D, Morris, JG, Münchau, A, Grozeva, D, Carss, KJ, Raymond, L, Kurian, MA, Klein, C, Fung, VS

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Innovative design emphasizes easy access von Westenberger, John A

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Unraveling Primary Familial Brain Calcification Mechanisms: Are NAA60 and SLC20A2 Partners in Crime? von Brand, Max, Westenberger, Ana

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Essential phenotypes of NOTCH2NLC-related repeat expansion disorder von Westenberger, Ana, Klein, Christine

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The evolving spectrum of PRRT2-associated paroxysmal diseases von Ebrahimi-Fakhari, Darius, Saffari, Afshin, Westenberger, Ana, Klein, Christine

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LRRK2 Loss‐of‐Function Variants: When Less Is More von Usnich, Tatiana, Westenberger, Ana

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Hybridization vessel rotator von WESTENBERGER, JOHN A, KAPKA, ANTHONY S, MANZARI, RICHARD

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Failure of AI projects: understanding the critical factors von Westenberger, Jens, Schuler, Kajetan, Schlegel, Dennis

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