Hochschule Zittau Görlitz

Funding evidence: The National Institute of Neurological Disorders and Stroke Clinical Trials Program

by Ravina, Bernard
Published in NeuroRX (2004)

Brain banking for neurodegenerative diseases

by Murphy, Diane D., Ravina, Bernard
Published in Current Opinion in Neurology (2003)

MR Findings in Subacute Combined Degeneration of the Spinal Cord : A Case of Reversible Cervical Myelopathy: A Case of Reversible Cervical Myelopathy

by Ravina, Bernard, Loevner, Laurie A., Bank, William
Published in American Journal of Roentgenology (2000)

Flexible Analytical Methods for Adding a Treatment Arm Mid-Study to an Ongoing Clinical Trial

by Elm, Jordan J., Palesch, Yuko Y., Koch, Gary G., Hinson, Vanessa, Ravina, Bernard, Zhao, Wenle
Published in Journal of Biopharmaceutical Statistics (2012)

Biosignatures for Parkinson’s Disease and Atypical Parkinsonian Disorders Patients

by Potashkin, Judith A., Santiago, Jose A., Ravina, Bernard M., Watts, Arthur, Leontovich, Alexey A.
Published in PLoS ONE (2012)

Finances of the publishers of the most highly cited US medical journals

by Dorsey, E. Ray, George, Benjamin P, Dayoub, Elias J, Ravina, Bernard M
Published in Journal of the Medical Library Association : JMLA (2011)

Human B Cell Differentiation Induced by Microbial Superantigens: Unselected Peripheral Blood Lymphocytes Secrete Polyclonal Immunoglobulin in Response toMycopusma ArthrztidzsMitoge...

by Crow, Mary K., Zagon, Gary, Chu, Zhongqiang, Ravina, Bernard, Tumang, Joseph R., Cole, Barry C., Friedman, Steven M.
Published in Autoimmunity (1993)

Improved stratification of ALS clinical trials using predicted survival

by Berry, James D., Taylor, Albert A., Beaulieu, Danielle, Meng, Lisa, Bian, Amy, Andrews, Jinsy, Keymer, Mike, Ennist, David L., Ravina, Bernard
Published in Annals of Clinical and Translational Neurology (2018)

Early Clinical Predictors of Treatment-Resistant and Functional Outcomes in Parkinson's Disease

by Kurlan, Roger, Ravina, Bernard, Eberly, Shirley, Lang, Anthony E., Tanner, Caroline M., Marek, Kenneth, Marder, Karen, Beck, James, Elliott, Robin, Oakes, David, Shoulson, Ira
Published in Movement Disorders Clinical Practice (2016)

Pharmacokinetics and pharmacodynamics of multiple doses of BG00010, a neurotrophic factor with anti-hyperalgesic effects, in patients with sciatica : PK/PD of the neurotrophic fact...

by Okkerse, Pieter, Hay, Justin L., Versage, Eve, Tang, Yongqiang, Galluppi, Gerald, Ravina, Bernard, Verma, Ajay, Williams, Leslie, Aycardi, Ernesto, Groeneveld, Geert Jan
Published in British Journal of Clinical Pharmacology (2016)

Virtual research visits and direct-to-consumer genetic testing in Parkinson’s disease

by Dorsey, E Ray, Darwin, Kristin C, Mohammed, Samara, Donohue, Sean, Tethal, Alyssa, Achey, Meredith A, Ward, Susan, Caughey, Elaine, Conley, Emily D, Eriksson, Nicholas, Ravina, Bernard
Published in DIGITAL HEALTH (2015)

Exercise-induced dystonia as a preceding symptom of familial Parkinson's disease

by Bruno, Michiko K., Ravina, Bernard, Garraux, Gaetan, Hallett, Mark, Ptacek, Louis, Singleton, Amanda, Johnson, Janel, Singleton, Andrew, Hanson, Melissa, Considine, Elaine, Gwinn-Hardy, Katrina
Published in Movement Disorders (2004)

A Bayesian mathematical model of motor and cognitive outcomes in Parkinson’s disease

by Hayete, Boris, Wuest, Diane, Laramie, Jason, McDonagh, Paul, Church, Bruce, Eberly, Shirley, Lang, Anthony, Marek, Kenneth, Runge, Karl, Shoulson, Ira, Singleton, Andrew, Tanner, Caroline, Khalil, Iya, Verma, Ajay, Ravina, Bernard
Published in PLOS ONE (2017)

Toward more efficient clinical trials for amyotrophic lateral sclerosis

by Cudkowicz, Merit E., Katz, Jon, Moore, Dan H., O’neill, Gilmore, Glass, Jonathan D., Mitsumoto, Hiroshi, Appel, Stanley, Ravina, Bernard, Kieburtz, Karl, Shoulson, Ira, Kaufmann, Petra, Khan, Jaffar, Simpson, Ericka, Shefner, Jeremy, Levin, Bruce, Cwik, Valerie, Schoenfeld, David, Aggarwal, Swati, McDermott, Michael P., Miller, Robert G.
Published in Amyotrophic Lateral Sclerosis (2010)

Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation

by Hague, Stephen, Rogaeva, Ekaterina, Hernandez, Dena, Gulick, Cindy, Singleton, Amanda, Hanson, Melissa, Johnson, Janel, Weiser, Roberto, Gallardo, Marisol, Ravina, Bernard, Gwinn-Hardy, Katrina, Crawley, Anthony, St. George-Hyslop, Peter H., Lang, Anthony E., Heutink, Peter, Bonifati, Vincenzo, Hardy, John, Singleton, Andrew
Published in Annals of Neurology (2003)

Association between α-synuclein blood transcripts and early, neuroimaging-supported Parkinson’s disease

by Locascio, Joseph J., Eberly, Shirley, Liao, Zhixiang, Liu, Ganqiang, Hoesing, Ashley N., Duong, Karen, Trisini-Lipsanopoulos, Ana, Dhima, Kaltra, Hung, Albert Y., Flaherty, Alice W., Schwarzschild, Michael A., Hayes, Michael T., Wills, Anne-Marie, Shivraj Sohur, U., Mejia, Nicte I., Selkoe, Dennis J., Oakes, David, Shoulson, Ira, Dong, Xianjun, Marek, Ken, Zheng, Bin, Ivinson, Adrian, Hyman, Bradley T., Growdon, John H., Sudarsky, Lewis R., Schlossmacher, Michael G., Ravina, Bernard, Scherzer, Clemens R.
Published in Brain (2015)

Meeting Report: Consensus Statement—Parkinson’s Disease and the Environment: Collaborative on Health and the Environment and Parkinson’s Action Network (CHE PAN) Conference 26–28 J...

by Bronstein, Jeff, Carvey, Paul, Chen, Honglei, Cory-Slechta, Deborah, DiMonte, Donato, Duda, John, English, Paul, Goldman, Samuel, Grate, Stephen, Hansen, Johnni, Hoppin, Jane, Jewell, Sarah, Kamel, Freya, Koroshetz, Walter, Langston, James W., Logroscino, Giancarlo, Nelson, Lorene, Ravina, Bernard, Rocca, Walter, Ross, George W., Schettler, Ted, Schwarzschild, Michael, Scott, Bill, Seegal, Richard, Singleton, Andrew, Steenland, Kyle, Tanner, Caroline M., Van Den Eeden, Stephen, Weisskopf, Marc
Published in Environmental Health Perspectives (2009)

Genetic risk of Parkinson disease and progression: : An analysis of 13 longitudinal cohorts: An analysis of 13 longitudinal cohorts

by Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L., Liu, Ganqiang, Maple-Grødem, Jodi, Corvol, Jean-Christophe, Pihlstrøm, Lasse, van Nimwegen, Marlies, Hutten, Samantha J., Nguyen, Khanh-Dung H., Rick, Jacqueline, Eberly, Shirley, Faghri, Faraz, Auinger, Peggy, Scott, Kirsten M., Wijeyekoon, Ruwani, Van Deerlin, Vivianna M., Hernandez, Dena G., Day-Williams, Aaron G., Brice, Alexis, Alves, Guido, Noyce, Alastair J., Tysnes, Ole-Bjørn, Evans, Jonathan R., Breen, David P., Estrada, Karol, Wegel, Claire E., Danjou, Fabrice, Simon, David K., Ravina, Bernard, Toft, Mathias, Heutink, Peter, Bloem, Bastiaan R., Weintraub, Daniel, Barker, Roger A., Williams-Gray, Caroline H., van de Warrenburg, Bart P., Van Hilten, Jacobus J., Scherzer, Clemens R., Singleton, Andrew B., Nalls, Mike A.
Published in Neurology Genetics (2019)

Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

by Robak, Laurie A, Jansen, Iris E, van Rooij, Jeroen, Uitterlinden, André G, Kraaij, Robert, Jankovic, Joseph, Heutink, Peter, Shulman, Joshua M, Nalls, Mike A, Plagnol, Vincent, Hernandez, Dena G, Sharma, Manu, Sheerin, Una-Marie, Saad, Mohamad, Simón-Sánchez, Javier, Schulte, Claudia, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Arepalli, Sampath, Barker, Roger, Ben-, Yoav, Berendse, Henk W, Berg, Daniela, Bhatia, Kailash, de Bie, Rob M A, Biffi, Alessandro, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M, Brockmann, Kathrin, Brooks, Janet, Burn, David J, Majounie, Elisa, Charlesworth, Gavin, Lungu, Codrin, Chen, Honglei, Chinnery, Patrick F, Chong, Sean, Clarke, Carl E, Cookson, Mark R, Mark Cooper, J, Corvol, Jean Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean-François, Deloukas, Panos, Deuschl, Günther, Dexter, David T, van Dijk, Karin D, Dillman, Allissa, Durif, Frank, Dürr, Alexandra, Edkins, Sarah, Evans, Jonathan R, Foltynie, Thomas, Dong, Jing, Gardner, Michelle, Raphael Gibbs, J, Goate, Alison, Gray, Emma, Guerreiro, Rita, Harris, Clare, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huang, Xuemei, Wurster, Isabel, Mätzler, Walter, Hudson, Gavin, Hunt, Sarah E, Huttenlocher, Johanna, Illig, Thomas, Jónsson, Pálmi V, Lambert, Jean-Charles, Langford, Cordelia, Lees, Andrew, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, Lungu, Codrin, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morris, Huw R, Morrison, Karen E, Escott-Price, Valentina, Mudanohwo, Ese, O’Sullivan, Sean S, Pearson, Justin, Perlmutter, Joel S, Pétursson, Hjörvar, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Ryten, Mina, Sawcer, Stephen, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Shulman, Joshua, Sidransky, Ellen, Smith, Colin, Spencer, Chris C A, Stefánsson, Hreinn, Bettella, Francesco, Stockton, Joanna D, Strange, Amy, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Tison, François, Trabzuni, Daniah, Traynor, Bryan J, Uitterlinden, André G, Velseboer, Daan, Vidailhet, Marie, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Williams-Gray, Caroline H, Winder-Rhodes, Sophie, Stefánsson, Kári, Martinez, Maria, Wood, Nicholas W, Hardy, John, Heutink, Peter, Brice, Alexis, Gasser, Thomas, Singleton, Andrew B
Published in Brain (2017)

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

by Holmans, Peter, Moskvina, Valentina, Jones, Lesley, Sharma, Manu, Vedernikov, Alexey, Buchel, Finja, Sadd, Mohamad, Bras, Jose M., Bettella, Francesco, Nicolaou, Nayia, Simón-Sánchez, Javier, Mittag, Florian, Gibbs, J. Raphael, Schulte, Claudia, Durr, Alexandra, Guerreiro, Rita, Hernandez, Dena, Brice, Alexis, Stefánsson, Hreinn, Majamaa, Kari, Gasser, Thomas, Heutink, Peter, Wood, Nicholas W., Martinez, Maria, Singleton, Andrew B., Nalls, Michael A., Hardy, John, Morris, Huw R., Williams, Nigel M., Arepalli, Sampath, Barker, Roger, Barrett, Jeffrey, Ben-Shlomo, Yoav, Berendse, Henk W., Berg, Daniela, Bhatia, Kailash, de Bie, Rob M.A., Biffi, Alessandro, Bloem, Bas, Brice, Alexis, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M., Brockmann, Kathrin, Brooks, Janet, Burn, David J., Charlesworth, Gavin, Chen, Honglei, Chinnery, Patrick F., Chong, Sean, Clarke, Carl E., Cookson, Mark R., Cooper, Jonathan M., Corvol, Jen-Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean Francois, Deloukas, Panagiotis, Deuschl, Günther, Dexter, David T., van Dijk, Karin D., Dillman, Allissa, Durif, Frank, Durr, Alexandra, Edkins, Sarah, Evans, Jonathan R., Foltynie, Thomas, Gao, Jianjun, Gardner, Michelle, Gasser, Thomas, Gibbs, J. Raphael, Goate, Alison, Gray, Emma, Guerreiro, Rita, Gústafsson, Ómar, Hardy, John, Harris, Clare, Hernandez, Dena G., Heutink, Peter, van Hilten, Jacobus J., Hofman, Albert, Hollenbeck, Albert, Holmans, Peter, Holton, Janice, Hu, Michele, Huber, Heiko, Hudson, Gavin, Hunt, Sarah E., Huttenlocher, Johanna, Illig, Thomas, Langford, Cordelia, Lees, Andrew, Lesage, Suzanne, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, Martinez, Maria, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morris, Huw, Morrison, Karen E., Moskvina, Valentina, Mudanohwo, Ese, Nalls, Michael A., Pearson, Justin, Perlmutter, Joel S., Pétursson, Hjörvar, Plagnol, Vincent, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Ryten, Mina, Saad, Mohamad, Sawcer, Stephen, Schapira, Anthony, Scheffer, Hans, Sharma, Manu, Shaw, Karen, Sheerin, Una-Marie, Shoulson, Ira, Schulte, Claudia, Sidransky, Ellen, Simón-Sánchez, Javier, Singleton, Andrew B., Smith, Colin, Stefánsson, Hreinn, Stefánsson, Kári, Steinberg, Stacy, Stockton, Joanna D., Sveinbjornsdottir, Sigurlaug, Talbot, Kevin, Tanner, Carlie M., Tashakkori-Ghanbaria, Avazeh, Tison, François, Trabzuni, Daniah, Traynor, Bryan J., Uitterlinden, André G., Velseboer, Daan, Vidailhet, Marie, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Williams-Gray, Caroline H., Winder-Rhodes, Sophie, Wood, Nicholas
Published in Human Molecular Genetics (2013)